English
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(en)A method of providing a prognosis of breast cancer is conducted by analyzing the expression of a group of genes. Gene expression profiles in a variety of medium such as microarrays are included as are kits that contain them.
1.ApplicationNumber: US-92388807-A
1.PublishNumber: US-2010009861-A1
2.Date Publish: 20100114
3.Inventor: WANG YIXIN
4.Inventor Harmonized: WANG YIXIN(US)
5.Country: US
6.Claims:
(en)A method of providing a prognosis of breast cancer is conducted by analyzing the expression of a group of genes. Gene expression profiles in a variety of medium such as microarrays are included as are kits that contain them.
7.Description:
(en)BACKGROUND
This invention relates to prognostics for breast cancer based on the gene expression profiles of biological samples.
In breast cancers, prognosis is determined primarily by the presence or absence of metastases in draining axillary lymph nodes. However, in approximately one third of women with breast cancer who have negative lymph nodes, the disease recurs and about one third of patients with positive lymph nodes are free of disease ten years after local or regional therapy. Furthermore, an increasing proportion of breast cancers are being diagnosed at an early stage because of increased awareness and wider use of screening modalities. Universal application of systematic therapy to these patients often leads to over-treatment. According to the St Gallen and NIH consensus, 70-80% of the Stage I and II patients would not have developed distant metastases without adjuvant treatment and may potentially suffer from the side effects. These data highlight the need for more sensitive and specific prognostic assays that could significantly reduce the number of patients that receive unnecessary treatment.
Tumor size and lymphatic or vascular invasion have been found to be of significant prognostic value in several studies. Quantitative pathological features, i.e. nuclear morphology, DNA content and proliferative activity may further demarcate tumors that have a high chance of micrometastases. Known molecular genetic changes that affect patient outcome include Her2/NEU over-expression, DNA amplifications, p53 mutations, ER/PR status, uPA and PAI expression. Because the metastatic cascade is a complex process that includes multiple steps, single factors that contribute to tumor process have limitations for prognostic assessment. The gene expression profiles of this invention will provide increased prognostic power.
SUMMARY OF THE INVENTION
The invention is a method of assessing the likelihood of a recurrence or metastasis of breast cancer in a patient diagnosed with or treated for breast cancer. The method involves the analysis of a gene expression profile,
In one aspect of the invention, the gene expression profile includes 56 genes In yet other aspects of the invention, the profiles comprise those of at least 45 genes, 26 genes, 13 genes, and 6 genes respectively.
Articles used in practicing the methods are also an aspect of the invention. Such articles include gene expression profiles or representations of them that are fixed in machine-readable media such as computer readable media.
Articles used to identify gene expression profiles can also include substrates or surfaces (such as microarrays) to capture and/or indicate the presence, absence, or degree of gene expression.
In yet another aspect of the invention, kits include reagents for conducting the gene expression analysis prognostic of breast cancer recurrence or metastasis.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a standard Kaplan-Meier Plot constructed from the patient data as a training set as described in the Examples.
FIG. 2 is a standard Kaplan-Meier Plot constructed from the patient data as a testing set as described in the Examples.
FIG. 3 is a standard Kaplan-Meier Plot constructed from the patient data of 54 patients (training and testing data combined) using a 56-gene expression profile.
DETAILED DESCRIPTION
The mere presence or absence of particular nucleic acid sequences in a tissue sample has only rarely been found to have diagnostic or prognostic value. Information about the expression of various proteins, peptides or mRNA, on the other hand, is increasingly viewed as important. The mere presence of nucleic acid sequences having the potential to express proteins, peptides, or mRNA (such sequences referred to as “genes”) within the genome by itself is not determinative of whether a protein, peptide, or mRNA is expressed in a given cell. Whether or not a given gene capable of expressing proteins, peptides, or mRNA does so and to what extent such expression occurs, if at all, is determined by a variety of complex factors. Irrespective of difficulties in understanding and assessing these factors, assaying gene expression can provide useful information about the occurrence of important events such as tumerogenesis, metastasis, apoptosis, and other clinically relevant phenomena. Relative indications of the degree to which genes are active or inactive can be found in gene expression profiles. The gene expression profiles of this invention are used to provide a prognosis and treat patients for breast cancer.
Sample preparation requires the collection of patient samples. Patient samples used in the inventive method are those that are suspected of containing diseased cells such as epithelial cells taken from a breast or lymph node sample or from surgical margins. One useful technique for obtaining suspect samples is Laser Capture Microdisection (LCM). LCM technology provides a way to select the cells to be studied, minimizing variability caused by cell type heterogeneity. Consequently, moderate or small changes in gene expression between normal and cancerous cells can be readily detected. In a preferred method, the samples comprise circulating epithelial cells extracted from peripheral blood. These can be obtained according to a number of methods but the most preferred method is the magnetic separation technique described in U.S. Pat. No. 6,136,182 assigned to Immunivest Corp which is incorporated herein by reference. Once the sample containing the cells of interest has been obtained, RNA is extracted and amplified and a gene expression profile is obtained, preferably via micro-array, for genes in the appropriate portfolios.
Preferred methods for establishing gene expression profiles include determining the amount of RNA that is produced by a gene that can code for a protein or peptide. This is accomplished by reverse transcriptase PCR (RT-PCR), competitive RT-PCR, real time RT-PCR, differential display RT-PCR, Northern Blot analysis and other related tests. While it is possible to conduct these techniques using individual PCR reactions, it is best to amplify complimentary DNA (cDNA) or complimentary RNA (cRNA) produced from mRNA and analyze it via microarray. A number of different array configurations and methods for their production are known to those of skill in the art and are described in U.S. patents such as: U.S. Pat. Nos. 5,445,934; 5,532,128; 5,556,752; 5,242,974; 5,384,261; 5,405,783; 5,412,087; 5,424,186; 5,429,807; 5,436,327; 5,472,672; 5,527,681; 5,529,756; 5,545,531; 5,554,501; 5,561,071; 5,571,639; 5,593,839; 5,599,695; 5,624,711; to 5,658,734; and 5,700,637; the disclosures of which are incorporated herein by reference.
Microarray technology allows for the measurement of the steady-state mRNA level of thousands of genes simultaneously thereby presenting a powerful tool for identifying effects such as the onset, arrest, or modulation of uncontrolled cell proliferation. Two microarray technologies are currently in wide use. The first are cDNA arrays and the second are oligonucleotide arrays. Although differences exist in the construction of these chips, essentially all downstream data analysis and output are the same The product of these analyses are typically measurements of the intensity of the signal received from a labeled probe used to detect a cDNA sequence from the sample that hybridizes to a nucleic acid sequence at a known location on the microarray. Typically, the intensity of the signal is proportional to the quantity of cDNA, and thus mRNA, expressed in the sample cells. A large number of such techniques are available and useful. Preferred methods for determining gene expression can he found in U.S. Pat. No. 6,271,002 to Linsley, et al.; U.S. Pat. No. 6,218,122 to Friend, et al.; U.S. Pat. No. 6,218,114 to Peck, et al.; and U.S. Pat. No. 6,004,755 to Wang, et al., the disclosure of each of which is incorporated herein by reference.
Analysis of the expression levels is conducted by comparing such intensities. This is best done by generating a ratio matrix of the expression intensities of genes in a test sample versus those in a control sample. For instance, the gene expression intensities from a diseased tissue can be compared with the expression intensities generated from normal tissue of the same type (e.g., diseased breast tissue sample vs. normal breast tissue sample). A ratio of these expression intensities indicates the fold-change in gene expression between the test and control samples.
Gene expression profiles can also be displayed in a number of ways. The most common method is to arrange a raw fluorescence intensities or ratio matrix into a graphical dendogram where columns indicate test samples and rows indicate genes. The data is arranged so genes that have similar expression profiles are proximal to each other. The expression ratio for each gene is visualized as a color. For example, a ratio less than one (indicating down-regulation) may appear in the blue portion of the spectrum while a ratio greater than one (indicating up-regulation) may appear as a color in the red portion of the spectrum. Commercially available computer software programs are available to display such data including “GENESPRINT” from Silicon Genetics, Inc. and “DISCOVERY” and “INFER” software from Partek, Inc.
Modulated genes used in the methods of the invention are described in the Examples. The genes that are differentially expressed are either up regulated or down regulated in patients with a relapse of breast cancer relative to those without a relapse. Up regulation and down regulation are relative terms meaning that a detectable difference (beyond the contribution of noise in the system used to measure it) is found in the amount of expression of the genes relative to some baseline. In this case, the baseline is the measured gene expression of a non-relapsing patient. The genes of interest in the diseased cells (from the relapsing patients) are then either up regulated or down regulated relative to the baseline level using the same measurement method. Diseased, in this context, refers to an alteration of the state of a body that interrupts or disturbs, or has the potential to disturb, proper performance of bodily functions as occurs with the uncontrolled proliferation of cells. Someone is diagnosed with a disease when some aspect of that person's genotype or phenotype is consistent with the presence of the disease. However, the act of conducting a diagnosis or prognosis includes the determination of disease/status issues such as determining the likelihood of relapse or metastasis and therapy monitoring. In therapy monitoring, clinical judgments are made regarding the effect of a given course of therapy by comparing the expression of genes over time to determine whether the gene expression profiles have changed or are changing to patterns more consistent with normal tissue.
Preferably, levels of up and down regulation are distinguished based on fold changes of the intensity measurements of hybridized microarray probes. A 2.0 fold difference is preferred for making such distinctions or a p-value less than 0.05. That is, before a gene is said to be differentially expressed in diseased/relapsing versus normal/non-relapsing cells, the diseased cell is found to yield at least 2 times more, or 2 times less intensity than the normal cells. The greater the fold difference, the more preferred is use of the gene as a diagnostic or prognostic tool. Genes selected for the gene expression profiles of the instant invention have expression levels that result in the generation of a signal that is distinguishable from those of the normal or non-modulated genes by an amount that exceeds background using clinical laboratory instrumentation.
Statistical values can be used to confidently distinguish modulated from non-modulated genes and noise. Statistical tests find the genes most significantly different between diverse groups of samples. The Student's t-test is an example of a robust statistical test that can be used to find significant differences between two groups. The lower the p-value, the more compelling the evidence that the gene is showing a difference between the different groups. Nevertheless, since microarrays measure more than one gene at a time, tens of thousands of statistical tests may be asked at one time. Because of this, one is unlikely to see small p-values just by chance and adjustments for this using a Sidak correction as well as a randomization/permutation experiment can be made. A p-value less than 0.05 by the t-test is evidence that the gene is significantly different. More compelling evidence is a p-value less then 0.05 after the Sidak correction is factored in. For a large number of samples in each group, a p-value less than 0.05 after the randomization/permutation test is the most compelling evidence of a significant difference.
Another parameter that can be used to select genes that generate a signal that is greater than that of the non-modulated gene or noise is the use of a measurement of absolute signal difference. Preferably, the signal generated by the modulated gene expression is at least 20% different than those of the normal or non-modulated gene (on an absolute basis). It is even more preferred that such genes produce expression patterns that are at least 30% different than those of normal or non-modulated genes.
Genes can he grouped so that information obtained about the set of genes in the group provides a sound basis for making a clinically relevant judgment such as a diagnosis, prognosis, or treatment choice. These sets of genes make up the portfolios of the invention. In this case, the judgments supported by the portfolios involve breast cancer. As with most diagnostic markers, it is often desirable to use the fewest number of markers sufficient to make a correct medical judgment. This prevents a delay in treatment pending further analysis as well inappropriate use of time and resources.
Preferably, portfolios are established such that the combination of genes in the portfolio exhibit improved sensitivity and specificity relative to individual genes or randomly selected combinations of genes. In the context of the instant invention, the sensitivity of the portfolio can be reflected in the fold differences exhibited by a gene's expression in the diseased state relative to the normal state. Specificity can be reflected in statistical measurements of the correlation of the signaling of gene expression with the condition of interest For example, standard deviation can be a used as such a measurement. In considering a group of genes for inclusion in a portfolio, a small standard deviation in expression measurements correlates with greater specificity. Other measurements of variation such as correlation coefficients can also be used in this capacity.
A preferred method of establishing gene expression portfolios is through the use of optimization algorithms such as the mean variance algorithm widely used in establishing stock portfolios. This method is described in detail in the patent application entitled “Selection of Markers” by Tim Jatkoe, et. al., filed on Mar. 21, 2003 (application Ser. No. 10/394,087, incorporated herein by reference). Essentially, the method calls for the establishment of a set of inputs (stocks in financial applications, expression as measured by intensity here) that will optimize the return (e.g., signal that is generated) one receives for using it while minimizing the variability of the return. Many commercial software programs are available to conduct such operations. “Wagner Associates Mean-Variance Optimization Application”, referred to as “Wagner Software” throughout this specification, is preferred. This software uses functions from the “Wagner Associates Mean-Variance Optimization Library” to determine an efficient frontier and optimal portfolios.
Use of this type of software requires that microarray data (i.e. intensity measurements) be transformed so that it can be treated as an input in the way stock return and risk measurements are used when the software is used for its intended financial analysis purposes.
The process of portfolio selection and characterization of an unknown is summarized as follows:
1. Choose baseline class 2. Calculate mean, and standard deviation of each gene for baseline class samples 3. Calculate (X*Standard Deviation+Mean) for each gene. This is the baseline reading from which all other samples will be compared. X is a stringency variable with higher values of X being more stringent than lower. 4. Calculate ratio between each Experimental sample versus baseline reading calculated in step 3. 5. Transform ratios such that ratios less than 1 are negative (eg. using Log base 10). (Down regulated genes now correctly have negative values necessary for MV optimization). 6. These transformed ratios are used as inputs in place of the asset returns that are normally used in the software application. 7. The software will plot the efficient frontier and return an optimized portfolio at any point along the efficient frontier. 8. Choose a desired return or variance on the efficient frontier. 9. Calculate the Portfolio's Value for each sample by summing the multiples of each gene's intensity value by the weight generated by the portfolio selection algorithm. 10. Calculate a boundary value by adding the mean Portfolio Value for Baseline groups to the multiple of Y and the Standard Deviation of the Baseline's Portfolio Values. Values greater than this boundary value shall be classified as the Experimental Class. 11. Optionally one can reiterate this process until best prediction accuracy is obtained.
Alternatively, genes can first be pre-selected by identifying those genes whose expression shows some minimal level of differentiation. The pre-selection in this alternative method is preferably based on a threshold given by
1
≤
(
μ
t
-
μ
n
)
(
σ
t
+
σ
n
)
,
where μ t is the mean of the subset known to possess the disease or condition, μ n is the mean of the subset of normal samples, and σ t +σ n represent the combined standard deviations. A signal to noise cutoff can also be used by pre-selecting the data according to a relationship such as
0.5
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
.
This ensures that genes that are pre-selected based on their differential modulation are differentiated in a clinically significant way. That is, above the noise level of instrumentation appropriate to the task of measuring the diagnostic parameters. For each marker pre-selected according to these criteria, a matrix is established in which columns represents samples, rows represent markers and each element is a normalized intensity measurement for the expression of that marker according to the relationship
(
μ
t
-
I
)
μ
t
where I is the intensity measurement.
It is also possible to set additional boundary conditions to define the optimal portfolios. For example, portfolio size can be limited to a fixed range or number of markers. This can be done either by making data pre-selection criteria more stringent
(
e
.
g
,
.8
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
instead
of
0.5
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
)
or by using programming features such as restricting portfolio size. One could, for example, set the boundary condition that the efficient frontier is to be selected from among only the most optimal 10 genes. One could also use all of the genes pre-selected for determining the efficient frontier and then limit the number of genes selected (e.g., no more than 10).
The process of selecting a portfolio can also include the application of heuristic rules. Preferably, such rules are formulated based on biology and an understanding of the technology used to produce clinical results. More preferably, they are applied to output from the optimization method. For example, the mean variance method of portfolio selection can be applied to microarray data for a number of genes differentially expressed in subjects with breast cancer. Output from the method would be an optimized set of genes that could include some genes that are expressed in peripheral blood as well as in diseased tissue. If samples used in the testing method are obtained from peripheral blood and certain genes differentially expressed in instances of breast cancer could also be differentially expressed in peripheral blood, then a heuristic rule can be applied in which a portfolio is selected from the efficient frontier excluding those that are differentially expressed in peripheral blood. Of course, the rule can be applied prior to the formation of the efficient frontier by, for example, applying the rule during data pre-selection.
Other heuristic rules can be applied that are not necessarily related to the biology in question. For example, one can apply the rule that only a given percentage of the portfolio can be represented by a particular gene or genes. Commercially available software such as the Wagner Software readily accommodates these types of heuristics. This can be useful, for example, when factors other than accuracy and precision (e.g., anticipated licensing fees) have an impact on the desirability of including one or more genes.
One method of the invention involves comparing gene expression profiles for various genes (or portfolios) to ascribe prognoses. The gene expression profiles of each of the genes comprising the portfolio are fixed in a medium such as a computer readable medium. This can take a number of forms. For example, a table can be established into which the range of signals (e.g., intensity measurements) indicative of disease/relapse is input. Actual patient data can then be compared to the values in the table to determine whether the patient samples are normal or diseased. In a more sophisticated embodiment, patterns of the expression signals (e.g., flourescent intensity) are recorded digitally or graphically. The gene expression patterns from the gene portfolios used in conjunction with patient samples are then compared to the expression patterns. Pattern comparison software can then be used to determine whether the patient samples have a pattern indicative of recurrence of the disease. Of course, these comparisons can also be used to determine whether the patient is not likely to experience disease recurrence. The expression profiles of the samples are then compared to the portfolio of a control cell. If the sample expression patterns are consistent with the expression pattern for recurrence of a breast cancer then (in the absence of countervailing medical considerations) the patient is treated as one would treat a relapse patient. If the sample expression patterns are consistent with the expression pattern from the normal/control cell then the patient is diagnosed negative for breast cancer.
Numerous well known methods of pattern recognition are available. The following references provide some examples:
Weighted Voting:
Golub, T R., Slonim, D K., Tamaya, P., Huard, C., Gaasenbeek, M., Mesirov, J P., Coller, H., Loh, L., Downing, J R., Caligiuri, M A., Bloomfield, C D., Lander, E S. Molecular classification of cancer: class discovery and class prediction by gene expression monitoring. Science 286:531-537, 1999
Support Vector Machines:
Su, A I., Welsh, J B., Sapinoso, L M., Kern, S G., Dimitrov, P., Lapp, H., Schultz, P G., Powell, S M., Moskaluk, C A., Frierson, H F. Jr., Hampton, G M. Molecular classification of human carcinomas by use of gene expression signatures. Cancer Research 61:7388-93, 2001 Ramaswamy, S., Tamayo, P., Ritkin, R., Mukherjee, S., Yeang, C H., Angelo, M., Ladd, C., Reich, M., Latulippe, E., Mesirov, J P., Poggio, T., Gerald, W., Loda, M., Lander, E S., Gould, T R. Multiclass cancer diagnosis using tumor gene expression signatures Proceedings of the National Academy of Sciences of the USA 98:15149-15154, 2001
K-Nearest Neighbors:
Ramaswamy, S., Tamayo, P., Rifkin, R., Mukherjee, S., Yeang, C H., Angelo, M., Ladd, C., Reich, M., Latulippe, E., Mesirov, J P., Poggio, T., Gerald, W., Loda, M., Lander, E S., Gould, T R. Multiclass cancer diagnosis using tumor gene expression signatures Proceedings of the National Academy of Sciences of the USA 98:15149-15154, 2001
Correlation Coefficients:
van't Veer L I, Dai H, van de Vijver M J, He Y D, Hart A A, Mao M, Peterse H L, van der Kooy K, Marton M J, Witeveen A T, Schreiber G J, Kerthoven R M, Roberts C, Linsley P S, Bernards R, Friend S H. Gene expression profiling predicts clinical outcome of breast cancer. Nature, Jan. 31, 2002;415(6871):530-6.
The gene expression profiles of this invention can also be used in conjunction with other non-genetic diagnostic methods useful in cancer diagnosis, prognosis, or treatment monitoring. For example, in some circumstances it is beneficial to combine the diagnostic power of the gene expression based methods described above with data from conventional markers such as serum protein markers. A range of such markers exists including such analytes as Estrogen Receptor (ER) with ER+ results indicating a greater likelihood of recurrence or metastasis. Other markers such as the protein (or peptides) produced by the estrogen regulated gene sequence pLIV1 can be used in this capacity as described in U.S. Pat. No. 5,693,465 (incorporated by reference in this specification). In one such method, blood is periodically taken from a treated patient and then subjected to an enzyme immunoassay for one or more serum markers. When the concentration of the marker(s) suggests the return of tumors or failure of therapy, a sample source amenable to gene expression analysis is taken. Where a suspicious mass exists, a fine needle aspirate is taken and gene expression profiles of cells taken from the mass are then analyzed as described above. Alternatively, tissue samples may be taken from areas adjacent to the tissue from which a tumor was previously removed. This approach can be particularly useful when other testing produces ambiguous results.
Articles of this invention include representations of the gene expression profiles useful for treating, diagnosing, prognosticating, and otherwise assessing diseases. These profile representations are reduced to a medium that can be automatically read by a machine such as computer readable media (magnetic, optical, and the like). The articles can also include instructions for assessing the gene expression profiles in such media. For example, the articles may comprise a CD ROM having computer instructions for comparing gene expression profiles of the portfolios of genes described above. The articles may also have gene expression profiles digitally recorded therein so that they may be compared with gene expression data from patient samples. Alternatively, the profiles can be recorded in different representational format. A graphical recordation is one such format. Clustering algorithms such as those incorporated in “DISCOVERY” and “INFER” software from Partek, Inc. mentioned above can best assist in the visualization of such data.
Different types of articles of manufacture according to the invention are media or formatted assays used to reveal gene expression profiles. These can comprise, for example, microarrays in which sequence complements or probes are affixed to a matrix to which the sequences indicative of the genes of interest combine creating a readable determinant of their presence. Alternatively, articles according to the invention can be fashioned into reagent kits for conducting hybridization, amplification, and signal generation indicative or the level of expression or the genes of interest for detecting breast cancer.
Kits made according to the invention include formatted assays for determining the gene expression profiles. These can include all or some of the materials needed to conduct the assays such as reagents and instructions.
The invention is further illustrated by the following non-limiting examples.
Examples
Genes analyzed according to this invention are typically related to full-length nucleic acid sequences that code for the production of a protein or peptide. One skilled in the art will recognize that identification of full-length sequences is not necessary from an analytical point of view That is, portions of the sequences or ESTs can be selected according to well-known principles for which probes can be designed to assess gene expression for the corresponding gene.
Example 1
Sample Handling and LCM
Fresh frozen tissue samples were collected from patients who had surgery for breast tumors. The samples that were used were from 149 Stage I and II patients (staged according to standard clinical diagnostics and pathology). Clinical outcome of the patients was known. Seventy four of the patients have remained disease-free for more than seven years while seventy five patients had distant metastases within four years. One hundred and three patients were lymph node negative while forty six were lymph node positive.
The tissues were snap frozen in liquid nitrogen within 20-30 minutes of harvesting, and stored at −80C.° thereafter. For laser capture, the samples were cut (6 μm), and one section was mounted on a glass slide, and the second on film (P.A.L.M.), which had been fixed onto a glass slide (Micro Slides Colorfrost, VWR Scientific, Media, Pa.). The section mounted on a glass slide was after fixed in cold acetone, and stained with Mayer's Haematoxylin (Sigma, St. Louis, Mo.). A pathologist analyzed the samples for diagnosis and grade. The clinical stage was estimated from the accompanying surgical pathology and clinical reports to verify the staging of the tumor. The section mounted on film was after fixed for five minutes in 100% ethanol, counter stained for 1 minute in eosin/100% ethanol (100 μg of Eosin in 100 ml of dehydrated ethanol), quickly soaked once in 100% ethanol to remove the free stain, and air dried for 10 minutes.
Before use in LCM, the membrane (LPC-MEMBRANE PEN FOIL 1.35 μm No 8100, P.A.L.M. GmbH Mikrolaser Technologie, Bernried, Germany) and slides were pretreated to abolish RNases, and to enhance the attachment of the tissue sample onto the film. Briefly, the slides were washed in DEP H 2 O, and the film was washed in RNase AWAY (Molecular Bioproducts, Inc., San Diego, Calif.) and rinsed in DEP H 2 O. After attaching the film onto the glass slides, the slides were baked at +120° C. for 8 hours, treated with TI-SAD (Diagnostic Products Corpotation, Los Angeles, Calif., 1:50 in DEP H 2 O, filtered through cotton wool), and incubated at +37° C. for 30 minutes. Immediately before use, a 10 μl aliquot of RNase inhibitor solution (Rlasin Inhibitor 2500 U=33 U/μl N211A, Promega GmbH, Mannheim, Germany, 0.5 μl in 400 μl of freezing solution, containing 0.15 mol NaCl, 10 mmol Tris pH 8.0, 0.25 mmol dithiothreitol) was spread onto the film, where the tissue sample was to be mounted.
The tissue sections mounted on film were used for LCM. Approximately 2000 epithelial cells/sample were captured using the PALM Robot-Microbeam technology (P.A.L.M. Mikrolaser Technologie, Carl Zeiss, Inc., Thomwood, N.Y.), coupled into Zeiss Axioven 135 microscope (Carl Zeiss Jena GmbH, Jena, Germany). The surrounding stroma in the normal mucosa, and the occasional intervening stromal components in cancer samples, were included. The captured cells were put in tubes in 100% ethanol and preserved at −80° C.
Example 2
RNA Extraction and Amplification
Zymo-Spin Column (Zymo Research, Orange, Calif. 92867) was used to extract total RNA from the LCM captured samples. About 2 ng of total RNA was resuspended in 10 ul of water and 2 rounds of the T7 RNA polymerase based amplification were performed to yield about 50 ug of amplified RNA.
Example 3
cDNA Microarray Hybridization and Quantitation
A set of cDNA microarrays consisting of approximately 23,000 human cDNA clones was used to test the samples by use of the humanU133a chip obtained and commercially available from Affymetrix, Inc. Total RNA obtained and prepared as outlined above and applied to the chips and analyzed by Agilent BioAnalyzer according to the manufacturer's protocol. All 149 samples passed the quality control standards and the data were used for marker selection.
Marker selection was performed by analyzing the 103 lymph node negative patients. Genes that allow the discrimination of distant metastases and survivors were identified using Cox proportional hazard model. Chip intensity data was analyzed using MAS Version 5.0 software commercially available from Affymetrix, Inc. (“MAS 5.0”). An unsupervised analysis was first conducted followed by a supervised analysis.
The chip intensity data obtained as described was the input for the unsupervised clustering software commercially available as PARTEK version 5.1 software. This unsupervised clustering algorithm identified a group of 22 patients with a significant low expression of many genes including estrogen receptor. ER/PR are known prognostic factors for poor outcome in breast cancer so this group of 22 patients were excluded from subsequent analysis to identify additional factors (gene markers) with independent value as prognostic indicators. The remaining 81 patients were further filtered to remove potential effects of the well-characterized prognostic indicators of age and tumor size. Twenty-seven patients older than 55 years or having tumors larger than 5 cm were thus excluded too.
A Cox proportional hazard model was used for gene selection. In each cycle of the total 31 cycles, each of the 31 patients in the training set was held out, the remaining 26 patients were used in the univariate Cox model regression to assess the strength of association of gene expression with the patient survival time. The strength of such association was evaluated by the corresponding estimated standardized parameter estimate and P value returned from the Cox model regression. P value of 0.01 was used as the threshold to select top genes from each cycle of the leave-one-out gene selection. The top genes selected from each cycle were then compared in order to select those genes that showed up at least 28 times in the total of 31 leave-one-out gene selection cycles. A total of 56 genes were
Modulation
(Standardized
Gene
Coefficient)
P. value
Sequence I.D. No.
216516_at
−2.7708
0.0056
Sequence I.D.. No. 32
211646_at
−2.7853
0.0053
Sequence I.D.. No. 33
219463_at
−2.7860
0.0053
Serquence I.D. No. 34
204532_x_at
−2.7921
0.0052
Sequence I.D. No. 35
210365_at
−2.7931
0.0052
Sequence I.D.. No. 36
222098_s_at
−2.8121
0.0049
Sequence I.D.. No. 37
212800_at
−2.8267
0.0047
Sequence I.D.. No. 38
205582_s_at
−2.8350
0.0046
Sequence I.D.. No. 39:
219096_at
−2.8393
0.0045
Sequence I.D.. No. 40
216944_s_at
−2.8667
0.0041
Sequence I.D.. No. 41
208923_at
−2.8766
0.0040
Sequence I.D.. No. 42
209309_at
−2.9149
0.0036
Sequence I.D.. No. 43
207981_s_at
−2.9294
0.0034
Sequence I.D.. No. 44
210160_at
−2.9448
0.0032
Sequence I.D.. No. 45
206862_at
−2.9676
0.0030
Sequence I.D.. No. 46
213110_s_at
−2.9857
0.0028
Sequence I.D.. No. 47
201906_s_at
−3.0124
0.0026
Sequence I.D.. No. 48
201057_s_at
−3.0133
0.0026
Sequence I.D.. No. 49
220798_x_at
−3.0270
0.0025
Sequence I.D.. No. 50
218650_at
−3.0513
0.0023
Sequence I.D.. No. 51
220986_s_at
−3.2095
0.0013
Sequence I.D.. No. 52
214451_at
−3.4431
0.0006
Sequence I.D.. No. 53
203844_at
−3.4965
0.0005
Sequence I.D.. No. 54
202966_at
−3.5864
0.0003
Sequence I.D.. No. 55
Construction of a multiple-gene predictor: The prediction index is defined as the sum of the product of the 56 genes' expression values (log 10 based) and their corresponding cox model parameter estimates. The parameter estimate from the cox models measures the hazard ratio of the patient when the gene expression value increases. Therefore, patients with high scores using the index have poor survival outcomes. This prediction index was applied to the training set to obtain an estimate of the prediction accuracy ( FIG. 1 ).
Cross-validation and evaluation of predictor: Performance of the predictor should be determined on an independent data set because most classification selected. Gene expression for those genes having Seq. ID No 1 to 26 and Seq ID No. 56 were up-regulated at least two fold and genes having Seq. ID No 27 to 55 were down regulated at least two fold.
TABLE 1 Breast Cancer Prognostic Gene Markers. Modulation (Standardized Gene Coefficient) P. value Sequence I.D. No. 202984_s_at 3.8521 0.0001 Sequence I.D. No.: 1 208777_s_at 3.4922 0.0005 Sequence I.D. No. 2. 222133_s_at 3.1841 0.0015 Sequence I.D. No. 3 218185_s_at 3.1379 0.0017 Sequence I.D. No. 4 219571_s_at 3.1131 0.0019 Sequence I.D.. No. 5 201138_s_at 3.1075 0.0019 Sequence I.D.. No. 6 209155_s_at 3.1018 0.0019 Sequence I.D.. No. 7 212468_at 0.0019 0.0022 Sequence I.D.. No. 8 217593_at 0.0019 0.0022 Sequence I.D.. No. 9 212973_at 3.0325 0.0024 Sequence I.D.. No. 10 202971_s_at 2.9994 0.0027 Sequence I.D.. No. 11 204444_at 2.9926 0.0028 Sequence I.D.. No. 12 205169_at 2.9911 0.0028 Sequence I.D.. No. 13 219751_at 2.9707 0.0030 Sequence I.D.. No. 14 217988_at 2.9649 0.0030 Sequence I.D.. No. 15 212942_s_at 2.9460 0.0032 Sequence I.D.. No. 16 208993_s_at 2.9423 0.0033 Sequence I.D.. No. 17 219105_x_at 2.9324 0.0034 Sequence I.D.. No. 18 220085_at 2.9001 0.0037 Sequence I.D.. No. 19 206640_x_at 2.8799 0.0040 Sequence I.D. No. 20 205062_x_at 2.8663 0.0042 Sequence I.D. No. 21 209385_s_at 2.8115 0.0049 Sequence I.D.. No. 22 AFFX-M27830_5_at 2.7868 0.0053 Sequence I.D.. No. 56 215170_s_at 2.7814 0.0054 Sequence I.D.. No. 23 207663_x_at 2.7634 0.0057 Sequence I.D.. No. 24 212229_s_at 2.7422 0.0061 Sequence I.D.. No. 25 215206_at 2.7317 0.0063 Sequence I.D.. No. 26 206241_at −2.7281 0.0064 Sequence I.D.. No. 27 219813_at −2.7406 0.0061 Sequence I.D.. No. 28 210969_at −2.7522 0.0059 Sequence I.D.. No. 29 207865_s_at −2.7691 0.0056 Sequence I.D.. No. 30 202520_s_at −2.7702 0.0056 Sequence I.D.. No. 31
methods work well on the examples that were used in their establishment. The 23 patients testing set was used to assess prediction accuracy. The cutoff for the classification is determined using the ROC, curve with 90% sensitivity. With the selected cutoff, the numbers of correct prediction for relapse and survival patients in the test set are summarized in (Table 1). The Kaplan-Meier curve was constructed on the predicted relapsers and survivors ( FIG. 2 ).
Overall prediction: Gene expression profiling of 54 Stage I and II breast cancer patients led to identification of 56 genes that have differential expression in these patients. Thirty-six of the patients have remained disease-free for more than 7 years while 27 patients had distant metasteses within 4 years. Using the 56-gene predictor, 22 of the 27 relapse patients and 27 of 36 disease-free patients were identified correctly. This result represents a sensitivity of 82% and a specificity of 75%. The positive predictive value is 71% and the negative predictive value is 84% (Table 2), The Kaplan-Meier curve was constructed on the predicted distant metastases and survivors ( FIG. 3 ).
An independent study was previously published (Van't Veer et al. Nature 415, 530-535. Vijver et al., NEJM 347, 1999-2009) in which a 70-gene predictor was constructed to predict patient outcomes in Stage I and II lymph node negative breast cancer. Only one gene overlaps between the 70 0 gene of the Van't Veer et al. study and the 56-gene predictor of this specification.
TABLE 2
Prediction accuracy based on testing set using 56-gene predictor.
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
6
Sensitivity
91%
Specificity
50%
TABLE 3
Prediction accuracy based on all patients using 56-gene predictor.
Study
Prediction
Number of Sample
Correct
Relapse
25
23
Survivor
29
23
Sensitivity
92%
Specificity
79%
Example 4
Further Portfolios
The 56 gene portfolio was subjected to different treatments to fashion further portfolios that provide clinically significant benefits with fewer numbers of gene expression signatures for analysis.
a. In a first treatment, correlation coefficients among the 56 genes were calculated by Spearman rank correlation and Pearson's correlation. Using 0.7 as the correlation cutoff, a portfolio of 45 modulated genes was established. The genes are shown in Table 4.
b. In a second treatment, the 56 genes were tested with t-tests using either the training or testing dataset. The genes that displayed significant p values (<0.05) in both training and testing data were selected as a portfolio. A portfolio of 26 modulated genes was thus established. The genes are shown in Table 5.
c. The 26 gene portfolio of (b) and Table 5 were then evaluated based on the known biological functions of the genes in the portfolio. Those having a biological relationship to a metastatic pathway were selected. A portfolio of 13 modulated genes was thus established. The genes are shown in Table 6.
d. A two gene pair exhibiting the best classification performance was selected from the 56 gene portfolio. In serial, one additional gene was added to the portfolio and tested to determine whether the addition of that signature improved the overall classification accuracy in both training set and testing set of the two gene combination. This procedure was repeated until no further improvement was achieved. A portfolio of 6 modulated genes was established. The genes are shown in Table 7.
The sensitivity and specificity for each of the portfolios shown in Tables 4-7 was determined based on predicted versus known outcomes for the samples described above. These values are shown in Tables 8-11.
TABLE 4
45 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
220986_s_at
−3.2095
Seq. I.D. No. 52
220798_x_at
−3.0270
Seq. I.D. No. 50
220085_at
2.9001
Seq. I.D. No. 19
219751_at
2.9707
Seq. I.D. No. 14
219105_x_at
2.9324
Seq. I.D. No. 18
218650_at
−3.0513
Seq. I.D. No. 51
214451_at
−3.4431
Seq. I.D. No. 53
212973_at
3.0325
Seq. I.D. No. 10
208993_s_at
2.9423
Seq. I.D. No. 17
205582_s_at
−2.8350
Seq. I.D. No. 39
205169_at
2.9911
Seq. I.D. No. 13
203844_at
−3.4965
Seq. I.D. No. 54
202984_s_at
3.8521
Seq. I.D. No. 1
202966_at
−3.5864
Seq. I.D. No. 55
201057_s_at
−3.0133
Seq. I.D. No. 49
222133_s_at
3.1841
Seq. I.D. No. 3
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
212942_s_at
2.9460
Seq. I.D. No. 16
210160_at
−2.9448
Seq. I.D. No. 45
209155_s_at
3.1018
Seq. I.D. No. 7
204444_at
2.9926
Seq. I.D. No. 12
202971_s_at
2.9994
Seq. I.D. No. 11
201138_s_at
3.1075
Seq. I.D. No. 6
222098_s_at
−2.8121
Seq. I.D. No. 37
219813_at
−2.7406
Seq. I.D. No. 28
216944_s_at
−2.8667
Seq. I.D. No. 41
215206_at
2.7317
Seq. I.D. No. 26
212800_at
−2.8267
Seq. I.D. No. 38
212229_s_at
2.7422
Seq. I.D. No. 25
211646_at
−2.7853
Seq. I.D. No. 33
210365_at
−2.7931
Seq. I.D. No. 36
209385_s_at
2.8115
Seq. I.D. No. 22
209309_at
−2.9149
Seq. I.D. No. 43
208923_at
−2.8766
Seq. I.D. No. 42
207663_x_at
2.7634
Seq. I.D. No. 24
205062_x_at
2.8663
Seq. I.D. No. 21
202520_s_at
−2.7702
Seq. I.D. No. 31
AFFX-M27830_5_at
2.7868
Seq. I.D. No. 56
216516_at
−2.7708
Seq. I.D. No. 32
215170_s_at
2.7814
Seq. I.D. No. 23
210969_at
−2.7522
Seq. I.D. No. 29
207981_s_at
−2.9294
Seq. I.D. No. 44
206241_at
−2.7281
Seq. I.D. No. 27
204532_x_at
−2.7921
Seq. I.D. No. 35
TABLE 5
26 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
205169_at
2.9911
Seq. I.D. No. 13
203844_at
−3.4965
Seq. I.D. No. 54
205062_x_at
2.8663
Seq. I.D. No. 21
202971_s_at
2.9994
Seq. I.D. No. 11
201906_s_at
−3.0124
Seq. I.D. No. 48
212942_s_at
2.9460
Seq. I.D. No. 16
206862_at
−2.9676
Seq. I.D. No. 46
202966_at
−3.5864
Seq. I.D. No. 55
201057_s_at
−3.0133
Seq. I.D. No. 49
219105_x_at
2.9324
Seq. I.D. No. 18
217593_at
3.0584
Seq. I.D. No. 9
202520_s_at
−2.7702
Seq. I.D. No. 31
210365_at
−2.7931
Seq. I.D. No. 36
215206_at
2.7317
Seq. I.D. No. 26
212229_s_at
2.7422
Seq. I.D. No. 25
211646_at
−2.7853
Seq. I.D. No. 33
219813_at
−2.7406
Seq. I.D. No. 28
216944_s_at
−2.8667
Seq. I.D. No. 41
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
213110_s_at
−2.9857
Seq. I.D. No. 47
212468_at
3.0663
Seq. I.D. No. 8
208993_s_at
2.9423
Seq. I.D. No. 17
208777_s_at
3.4922
Seq. I.D. No. 2
220085_at
2.9001
Seq. I.D. No. 19
219751_at
2.9707
Seq. I.D. No. 14
TABLE 6
13 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
202971_s_at
2.9994
Seq. I.D. No. 11
201906_s_at
−3.0124
Seq. I.D. No. 48
206862_at
−2.9676
Seq. I.D. No. 46
202966_at
−3.5864
Seq. I.D. No. 55
219105_x_at
2.9324
Seq. I.D. No. 18
210365_at
−2.7931
Seq. I.D. No. 36
212229_s_at
2.7422
Seq. I.D. No. 25
219813_at
−2.7406
Seq. I.D. No. 28
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
213110_s_at
−2.9857
Seq. I.D. No. 47
208777_s_at
3.4922
Seq. I.D. No. 2
220085_at
2.9001
Seq. I.D. No. 19
TABLE 7
6 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
205169_at
2.9911
Seq. I.D. No. 13
202966_at
−3.5864
Seq. I.D. No. 55
206862_at
−2.9676
Seq. I.D. No. 46
219105_x_at
2.9324
Seq. I.D. No. 18
205062_x_at
2.8663
Seq. I.D. No. 21
201138_s_at
3.1075
Seq. I.D. No. 6
TABLE 8
45-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
6
Sensitivity
91%
Specificity
50%
TABLE 9
26-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
10
Sensitivity
91%
Specificity
83%
TABLE 10
13-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
8
Sensitivity
91%
Specificity
67%
TABLE 11
6-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
8
Sensitivity
91%
Specificity
67%
1.PublishNumber: US-2010009861-A1
2.Date Publish: 20100114
3.Inventor: WANG YIXIN
4.Inventor Harmonized: WANG YIXIN(US)
5.Country: US
6.Claims:
(en)A method of providing a prognosis of breast cancer is conducted by analyzing the expression of a group of genes. Gene expression profiles in a variety of medium such as microarrays are included as are kits that contain them.
7.Description:
(en)BACKGROUND
This invention relates to prognostics for breast cancer based on the gene expression profiles of biological samples.
In breast cancers, prognosis is determined primarily by the presence or absence of metastases in draining axillary lymph nodes. However, in approximately one third of women with breast cancer who have negative lymph nodes, the disease recurs and about one third of patients with positive lymph nodes are free of disease ten years after local or regional therapy. Furthermore, an increasing proportion of breast cancers are being diagnosed at an early stage because of increased awareness and wider use of screening modalities. Universal application of systematic therapy to these patients often leads to over-treatment. According to the St Gallen and NIH consensus, 70-80% of the Stage I and II patients would not have developed distant metastases without adjuvant treatment and may potentially suffer from the side effects. These data highlight the need for more sensitive and specific prognostic assays that could significantly reduce the number of patients that receive unnecessary treatment.
Tumor size and lymphatic or vascular invasion have been found to be of significant prognostic value in several studies. Quantitative pathological features, i.e. nuclear morphology, DNA content and proliferative activity may further demarcate tumors that have a high chance of micrometastases. Known molecular genetic changes that affect patient outcome include Her2/NEU over-expression, DNA amplifications, p53 mutations, ER/PR status, uPA and PAI expression. Because the metastatic cascade is a complex process that includes multiple steps, single factors that contribute to tumor process have limitations for prognostic assessment. The gene expression profiles of this invention will provide increased prognostic power.
SUMMARY OF THE INVENTION
The invention is a method of assessing the likelihood of a recurrence or metastasis of breast cancer in a patient diagnosed with or treated for breast cancer. The method involves the analysis of a gene expression profile,
In one aspect of the invention, the gene expression profile includes 56 genes In yet other aspects of the invention, the profiles comprise those of at least 45 genes, 26 genes, 13 genes, and 6 genes respectively.
Articles used in practicing the methods are also an aspect of the invention. Such articles include gene expression profiles or representations of them that are fixed in machine-readable media such as computer readable media.
Articles used to identify gene expression profiles can also include substrates or surfaces (such as microarrays) to capture and/or indicate the presence, absence, or degree of gene expression.
In yet another aspect of the invention, kits include reagents for conducting the gene expression analysis prognostic of breast cancer recurrence or metastasis.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a standard Kaplan-Meier Plot constructed from the patient data as a training set as described in the Examples.
FIG. 2 is a standard Kaplan-Meier Plot constructed from the patient data as a testing set as described in the Examples.
FIG. 3 is a standard Kaplan-Meier Plot constructed from the patient data of 54 patients (training and testing data combined) using a 56-gene expression profile.
DETAILED DESCRIPTION
The mere presence or absence of particular nucleic acid sequences in a tissue sample has only rarely been found to have diagnostic or prognostic value. Information about the expression of various proteins, peptides or mRNA, on the other hand, is increasingly viewed as important. The mere presence of nucleic acid sequences having the potential to express proteins, peptides, or mRNA (such sequences referred to as “genes”) within the genome by itself is not determinative of whether a protein, peptide, or mRNA is expressed in a given cell. Whether or not a given gene capable of expressing proteins, peptides, or mRNA does so and to what extent such expression occurs, if at all, is determined by a variety of complex factors. Irrespective of difficulties in understanding and assessing these factors, assaying gene expression can provide useful information about the occurrence of important events such as tumerogenesis, metastasis, apoptosis, and other clinically relevant phenomena. Relative indications of the degree to which genes are active or inactive can be found in gene expression profiles. The gene expression profiles of this invention are used to provide a prognosis and treat patients for breast cancer.
Sample preparation requires the collection of patient samples. Patient samples used in the inventive method are those that are suspected of containing diseased cells such as epithelial cells taken from a breast or lymph node sample or from surgical margins. One useful technique for obtaining suspect samples is Laser Capture Microdisection (LCM). LCM technology provides a way to select the cells to be studied, minimizing variability caused by cell type heterogeneity. Consequently, moderate or small changes in gene expression between normal and cancerous cells can be readily detected. In a preferred method, the samples comprise circulating epithelial cells extracted from peripheral blood. These can be obtained according to a number of methods but the most preferred method is the magnetic separation technique described in U.S. Pat. No. 6,136,182 assigned to Immunivest Corp which is incorporated herein by reference. Once the sample containing the cells of interest has been obtained, RNA is extracted and amplified and a gene expression profile is obtained, preferably via micro-array, for genes in the appropriate portfolios.
Preferred methods for establishing gene expression profiles include determining the amount of RNA that is produced by a gene that can code for a protein or peptide. This is accomplished by reverse transcriptase PCR (RT-PCR), competitive RT-PCR, real time RT-PCR, differential display RT-PCR, Northern Blot analysis and other related tests. While it is possible to conduct these techniques using individual PCR reactions, it is best to amplify complimentary DNA (cDNA) or complimentary RNA (cRNA) produced from mRNA and analyze it via microarray. A number of different array configurations and methods for their production are known to those of skill in the art and are described in U.S. patents such as: U.S. Pat. Nos. 5,445,934; 5,532,128; 5,556,752; 5,242,974; 5,384,261; 5,405,783; 5,412,087; 5,424,186; 5,429,807; 5,436,327; 5,472,672; 5,527,681; 5,529,756; 5,545,531; 5,554,501; 5,561,071; 5,571,639; 5,593,839; 5,599,695; 5,624,711; to 5,658,734; and 5,700,637; the disclosures of which are incorporated herein by reference.
Microarray technology allows for the measurement of the steady-state mRNA level of thousands of genes simultaneously thereby presenting a powerful tool for identifying effects such as the onset, arrest, or modulation of uncontrolled cell proliferation. Two microarray technologies are currently in wide use. The first are cDNA arrays and the second are oligonucleotide arrays. Although differences exist in the construction of these chips, essentially all downstream data analysis and output are the same The product of these analyses are typically measurements of the intensity of the signal received from a labeled probe used to detect a cDNA sequence from the sample that hybridizes to a nucleic acid sequence at a known location on the microarray. Typically, the intensity of the signal is proportional to the quantity of cDNA, and thus mRNA, expressed in the sample cells. A large number of such techniques are available and useful. Preferred methods for determining gene expression can he found in U.S. Pat. No. 6,271,002 to Linsley, et al.; U.S. Pat. No. 6,218,122 to Friend, et al.; U.S. Pat. No. 6,218,114 to Peck, et al.; and U.S. Pat. No. 6,004,755 to Wang, et al., the disclosure of each of which is incorporated herein by reference.
Analysis of the expression levels is conducted by comparing such intensities. This is best done by generating a ratio matrix of the expression intensities of genes in a test sample versus those in a control sample. For instance, the gene expression intensities from a diseased tissue can be compared with the expression intensities generated from normal tissue of the same type (e.g., diseased breast tissue sample vs. normal breast tissue sample). A ratio of these expression intensities indicates the fold-change in gene expression between the test and control samples.
Gene expression profiles can also be displayed in a number of ways. The most common method is to arrange a raw fluorescence intensities or ratio matrix into a graphical dendogram where columns indicate test samples and rows indicate genes. The data is arranged so genes that have similar expression profiles are proximal to each other. The expression ratio for each gene is visualized as a color. For example, a ratio less than one (indicating down-regulation) may appear in the blue portion of the spectrum while a ratio greater than one (indicating up-regulation) may appear as a color in the red portion of the spectrum. Commercially available computer software programs are available to display such data including “GENESPRINT” from Silicon Genetics, Inc. and “DISCOVERY” and “INFER” software from Partek, Inc.
Modulated genes used in the methods of the invention are described in the Examples. The genes that are differentially expressed are either up regulated or down regulated in patients with a relapse of breast cancer relative to those without a relapse. Up regulation and down regulation are relative terms meaning that a detectable difference (beyond the contribution of noise in the system used to measure it) is found in the amount of expression of the genes relative to some baseline. In this case, the baseline is the measured gene expression of a non-relapsing patient. The genes of interest in the diseased cells (from the relapsing patients) are then either up regulated or down regulated relative to the baseline level using the same measurement method. Diseased, in this context, refers to an alteration of the state of a body that interrupts or disturbs, or has the potential to disturb, proper performance of bodily functions as occurs with the uncontrolled proliferation of cells. Someone is diagnosed with a disease when some aspect of that person's genotype or phenotype is consistent with the presence of the disease. However, the act of conducting a diagnosis or prognosis includes the determination of disease/status issues such as determining the likelihood of relapse or metastasis and therapy monitoring. In therapy monitoring, clinical judgments are made regarding the effect of a given course of therapy by comparing the expression of genes over time to determine whether the gene expression profiles have changed or are changing to patterns more consistent with normal tissue.
Preferably, levels of up and down regulation are distinguished based on fold changes of the intensity measurements of hybridized microarray probes. A 2.0 fold difference is preferred for making such distinctions or a p-value less than 0.05. That is, before a gene is said to be differentially expressed in diseased/relapsing versus normal/non-relapsing cells, the diseased cell is found to yield at least 2 times more, or 2 times less intensity than the normal cells. The greater the fold difference, the more preferred is use of the gene as a diagnostic or prognostic tool. Genes selected for the gene expression profiles of the instant invention have expression levels that result in the generation of a signal that is distinguishable from those of the normal or non-modulated genes by an amount that exceeds background using clinical laboratory instrumentation.
Statistical values can be used to confidently distinguish modulated from non-modulated genes and noise. Statistical tests find the genes most significantly different between diverse groups of samples. The Student's t-test is an example of a robust statistical test that can be used to find significant differences between two groups. The lower the p-value, the more compelling the evidence that the gene is showing a difference between the different groups. Nevertheless, since microarrays measure more than one gene at a time, tens of thousands of statistical tests may be asked at one time. Because of this, one is unlikely to see small p-values just by chance and adjustments for this using a Sidak correction as well as a randomization/permutation experiment can be made. A p-value less than 0.05 by the t-test is evidence that the gene is significantly different. More compelling evidence is a p-value less then 0.05 after the Sidak correction is factored in. For a large number of samples in each group, a p-value less than 0.05 after the randomization/permutation test is the most compelling evidence of a significant difference.
Another parameter that can be used to select genes that generate a signal that is greater than that of the non-modulated gene or noise is the use of a measurement of absolute signal difference. Preferably, the signal generated by the modulated gene expression is at least 20% different than those of the normal or non-modulated gene (on an absolute basis). It is even more preferred that such genes produce expression patterns that are at least 30% different than those of normal or non-modulated genes.
Genes can he grouped so that information obtained about the set of genes in the group provides a sound basis for making a clinically relevant judgment such as a diagnosis, prognosis, or treatment choice. These sets of genes make up the portfolios of the invention. In this case, the judgments supported by the portfolios involve breast cancer. As with most diagnostic markers, it is often desirable to use the fewest number of markers sufficient to make a correct medical judgment. This prevents a delay in treatment pending further analysis as well inappropriate use of time and resources.
Preferably, portfolios are established such that the combination of genes in the portfolio exhibit improved sensitivity and specificity relative to individual genes or randomly selected combinations of genes. In the context of the instant invention, the sensitivity of the portfolio can be reflected in the fold differences exhibited by a gene's expression in the diseased state relative to the normal state. Specificity can be reflected in statistical measurements of the correlation of the signaling of gene expression with the condition of interest For example, standard deviation can be a used as such a measurement. In considering a group of genes for inclusion in a portfolio, a small standard deviation in expression measurements correlates with greater specificity. Other measurements of variation such as correlation coefficients can also be used in this capacity.
A preferred method of establishing gene expression portfolios is through the use of optimization algorithms such as the mean variance algorithm widely used in establishing stock portfolios. This method is described in detail in the patent application entitled “Selection of Markers” by Tim Jatkoe, et. al., filed on Mar. 21, 2003 (application Ser. No. 10/394,087, incorporated herein by reference). Essentially, the method calls for the establishment of a set of inputs (stocks in financial applications, expression as measured by intensity here) that will optimize the return (e.g., signal that is generated) one receives for using it while minimizing the variability of the return. Many commercial software programs are available to conduct such operations. “Wagner Associates Mean-Variance Optimization Application”, referred to as “Wagner Software” throughout this specification, is preferred. This software uses functions from the “Wagner Associates Mean-Variance Optimization Library” to determine an efficient frontier and optimal portfolios.
Use of this type of software requires that microarray data (i.e. intensity measurements) be transformed so that it can be treated as an input in the way stock return and risk measurements are used when the software is used for its intended financial analysis purposes.
The process of portfolio selection and characterization of an unknown is summarized as follows:
1. Choose baseline class 2. Calculate mean, and standard deviation of each gene for baseline class samples 3. Calculate (X*Standard Deviation+Mean) for each gene. This is the baseline reading from which all other samples will be compared. X is a stringency variable with higher values of X being more stringent than lower. 4. Calculate ratio between each Experimental sample versus baseline reading calculated in step 3. 5. Transform ratios such that ratios less than 1 are negative (eg. using Log base 10). (Down regulated genes now correctly have negative values necessary for MV optimization). 6. These transformed ratios are used as inputs in place of the asset returns that are normally used in the software application. 7. The software will plot the efficient frontier and return an optimized portfolio at any point along the efficient frontier. 8. Choose a desired return or variance on the efficient frontier. 9. Calculate the Portfolio's Value for each sample by summing the multiples of each gene's intensity value by the weight generated by the portfolio selection algorithm. 10. Calculate a boundary value by adding the mean Portfolio Value for Baseline groups to the multiple of Y and the Standard Deviation of the Baseline's Portfolio Values. Values greater than this boundary value shall be classified as the Experimental Class. 11. Optionally one can reiterate this process until best prediction accuracy is obtained.
Alternatively, genes can first be pre-selected by identifying those genes whose expression shows some minimal level of differentiation. The pre-selection in this alternative method is preferably based on a threshold given by
1
≤
(
μ
t
-
μ
n
)
(
σ
t
+
σ
n
)
,
where μ t is the mean of the subset known to possess the disease or condition, μ n is the mean of the subset of normal samples, and σ t +σ n represent the combined standard deviations. A signal to noise cutoff can also be used by pre-selecting the data according to a relationship such as
0.5
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
.
This ensures that genes that are pre-selected based on their differential modulation are differentiated in a clinically significant way. That is, above the noise level of instrumentation appropriate to the task of measuring the diagnostic parameters. For each marker pre-selected according to these criteria, a matrix is established in which columns represents samples, rows represent markers and each element is a normalized intensity measurement for the expression of that marker according to the relationship
(
μ
t
-
I
)
μ
t
where I is the intensity measurement.
It is also possible to set additional boundary conditions to define the optimal portfolios. For example, portfolio size can be limited to a fixed range or number of markers. This can be done either by making data pre-selection criteria more stringent
(
e
.
g
,
.8
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
instead
of
0.5
≤
(
μ
t
-
MAX
n
)
(
σ
t
+
σ
n
)
)
or by using programming features such as restricting portfolio size. One could, for example, set the boundary condition that the efficient frontier is to be selected from among only the most optimal 10 genes. One could also use all of the genes pre-selected for determining the efficient frontier and then limit the number of genes selected (e.g., no more than 10).
The process of selecting a portfolio can also include the application of heuristic rules. Preferably, such rules are formulated based on biology and an understanding of the technology used to produce clinical results. More preferably, they are applied to output from the optimization method. For example, the mean variance method of portfolio selection can be applied to microarray data for a number of genes differentially expressed in subjects with breast cancer. Output from the method would be an optimized set of genes that could include some genes that are expressed in peripheral blood as well as in diseased tissue. If samples used in the testing method are obtained from peripheral blood and certain genes differentially expressed in instances of breast cancer could also be differentially expressed in peripheral blood, then a heuristic rule can be applied in which a portfolio is selected from the efficient frontier excluding those that are differentially expressed in peripheral blood. Of course, the rule can be applied prior to the formation of the efficient frontier by, for example, applying the rule during data pre-selection.
Other heuristic rules can be applied that are not necessarily related to the biology in question. For example, one can apply the rule that only a given percentage of the portfolio can be represented by a particular gene or genes. Commercially available software such as the Wagner Software readily accommodates these types of heuristics. This can be useful, for example, when factors other than accuracy and precision (e.g., anticipated licensing fees) have an impact on the desirability of including one or more genes.
One method of the invention involves comparing gene expression profiles for various genes (or portfolios) to ascribe prognoses. The gene expression profiles of each of the genes comprising the portfolio are fixed in a medium such as a computer readable medium. This can take a number of forms. For example, a table can be established into which the range of signals (e.g., intensity measurements) indicative of disease/relapse is input. Actual patient data can then be compared to the values in the table to determine whether the patient samples are normal or diseased. In a more sophisticated embodiment, patterns of the expression signals (e.g., flourescent intensity) are recorded digitally or graphically. The gene expression patterns from the gene portfolios used in conjunction with patient samples are then compared to the expression patterns. Pattern comparison software can then be used to determine whether the patient samples have a pattern indicative of recurrence of the disease. Of course, these comparisons can also be used to determine whether the patient is not likely to experience disease recurrence. The expression profiles of the samples are then compared to the portfolio of a control cell. If the sample expression patterns are consistent with the expression pattern for recurrence of a breast cancer then (in the absence of countervailing medical considerations) the patient is treated as one would treat a relapse patient. If the sample expression patterns are consistent with the expression pattern from the normal/control cell then the patient is diagnosed negative for breast cancer.
Numerous well known methods of pattern recognition are available. The following references provide some examples:
Weighted Voting:
Golub, T R., Slonim, D K., Tamaya, P., Huard, C., Gaasenbeek, M., Mesirov, J P., Coller, H., Loh, L., Downing, J R., Caligiuri, M A., Bloomfield, C D., Lander, E S. Molecular classification of cancer: class discovery and class prediction by gene expression monitoring. Science 286:531-537, 1999
Support Vector Machines:
Su, A I., Welsh, J B., Sapinoso, L M., Kern, S G., Dimitrov, P., Lapp, H., Schultz, P G., Powell, S M., Moskaluk, C A., Frierson, H F. Jr., Hampton, G M. Molecular classification of human carcinomas by use of gene expression signatures. Cancer Research 61:7388-93, 2001 Ramaswamy, S., Tamayo, P., Ritkin, R., Mukherjee, S., Yeang, C H., Angelo, M., Ladd, C., Reich, M., Latulippe, E., Mesirov, J P., Poggio, T., Gerald, W., Loda, M., Lander, E S., Gould, T R. Multiclass cancer diagnosis using tumor gene expression signatures Proceedings of the National Academy of Sciences of the USA 98:15149-15154, 2001
K-Nearest Neighbors:
Ramaswamy, S., Tamayo, P., Rifkin, R., Mukherjee, S., Yeang, C H., Angelo, M., Ladd, C., Reich, M., Latulippe, E., Mesirov, J P., Poggio, T., Gerald, W., Loda, M., Lander, E S., Gould, T R. Multiclass cancer diagnosis using tumor gene expression signatures Proceedings of the National Academy of Sciences of the USA 98:15149-15154, 2001
Correlation Coefficients:
van't Veer L I, Dai H, van de Vijver M J, He Y D, Hart A A, Mao M, Peterse H L, van der Kooy K, Marton M J, Witeveen A T, Schreiber G J, Kerthoven R M, Roberts C, Linsley P S, Bernards R, Friend S H. Gene expression profiling predicts clinical outcome of breast cancer. Nature, Jan. 31, 2002;415(6871):530-6.
The gene expression profiles of this invention can also be used in conjunction with other non-genetic diagnostic methods useful in cancer diagnosis, prognosis, or treatment monitoring. For example, in some circumstances it is beneficial to combine the diagnostic power of the gene expression based methods described above with data from conventional markers such as serum protein markers. A range of such markers exists including such analytes as Estrogen Receptor (ER) with ER+ results indicating a greater likelihood of recurrence or metastasis. Other markers such as the protein (or peptides) produced by the estrogen regulated gene sequence pLIV1 can be used in this capacity as described in U.S. Pat. No. 5,693,465 (incorporated by reference in this specification). In one such method, blood is periodically taken from a treated patient and then subjected to an enzyme immunoassay for one or more serum markers. When the concentration of the marker(s) suggests the return of tumors or failure of therapy, a sample source amenable to gene expression analysis is taken. Where a suspicious mass exists, a fine needle aspirate is taken and gene expression profiles of cells taken from the mass are then analyzed as described above. Alternatively, tissue samples may be taken from areas adjacent to the tissue from which a tumor was previously removed. This approach can be particularly useful when other testing produces ambiguous results.
Articles of this invention include representations of the gene expression profiles useful for treating, diagnosing, prognosticating, and otherwise assessing diseases. These profile representations are reduced to a medium that can be automatically read by a machine such as computer readable media (magnetic, optical, and the like). The articles can also include instructions for assessing the gene expression profiles in such media. For example, the articles may comprise a CD ROM having computer instructions for comparing gene expression profiles of the portfolios of genes described above. The articles may also have gene expression profiles digitally recorded therein so that they may be compared with gene expression data from patient samples. Alternatively, the profiles can be recorded in different representational format. A graphical recordation is one such format. Clustering algorithms such as those incorporated in “DISCOVERY” and “INFER” software from Partek, Inc. mentioned above can best assist in the visualization of such data.
Different types of articles of manufacture according to the invention are media or formatted assays used to reveal gene expression profiles. These can comprise, for example, microarrays in which sequence complements or probes are affixed to a matrix to which the sequences indicative of the genes of interest combine creating a readable determinant of their presence. Alternatively, articles according to the invention can be fashioned into reagent kits for conducting hybridization, amplification, and signal generation indicative or the level of expression or the genes of interest for detecting breast cancer.
Kits made according to the invention include formatted assays for determining the gene expression profiles. These can include all or some of the materials needed to conduct the assays such as reagents and instructions.
The invention is further illustrated by the following non-limiting examples.
Examples
Genes analyzed according to this invention are typically related to full-length nucleic acid sequences that code for the production of a protein or peptide. One skilled in the art will recognize that identification of full-length sequences is not necessary from an analytical point of view That is, portions of the sequences or ESTs can be selected according to well-known principles for which probes can be designed to assess gene expression for the corresponding gene.
Example 1
Sample Handling and LCM
Fresh frozen tissue samples were collected from patients who had surgery for breast tumors. The samples that were used were from 149 Stage I and II patients (staged according to standard clinical diagnostics and pathology). Clinical outcome of the patients was known. Seventy four of the patients have remained disease-free for more than seven years while seventy five patients had distant metastases within four years. One hundred and three patients were lymph node negative while forty six were lymph node positive.
The tissues were snap frozen in liquid nitrogen within 20-30 minutes of harvesting, and stored at −80C.° thereafter. For laser capture, the samples were cut (6 μm), and one section was mounted on a glass slide, and the second on film (P.A.L.M.), which had been fixed onto a glass slide (Micro Slides Colorfrost, VWR Scientific, Media, Pa.). The section mounted on a glass slide was after fixed in cold acetone, and stained with Mayer's Haematoxylin (Sigma, St. Louis, Mo.). A pathologist analyzed the samples for diagnosis and grade. The clinical stage was estimated from the accompanying surgical pathology and clinical reports to verify the staging of the tumor. The section mounted on film was after fixed for five minutes in 100% ethanol, counter stained for 1 minute in eosin/100% ethanol (100 μg of Eosin in 100 ml of dehydrated ethanol), quickly soaked once in 100% ethanol to remove the free stain, and air dried for 10 minutes.
Before use in LCM, the membrane (LPC-MEMBRANE PEN FOIL 1.35 μm No 8100, P.A.L.M. GmbH Mikrolaser Technologie, Bernried, Germany) and slides were pretreated to abolish RNases, and to enhance the attachment of the tissue sample onto the film. Briefly, the slides were washed in DEP H 2 O, and the film was washed in RNase AWAY (Molecular Bioproducts, Inc., San Diego, Calif.) and rinsed in DEP H 2 O. After attaching the film onto the glass slides, the slides were baked at +120° C. for 8 hours, treated with TI-SAD (Diagnostic Products Corpotation, Los Angeles, Calif., 1:50 in DEP H 2 O, filtered through cotton wool), and incubated at +37° C. for 30 minutes. Immediately before use, a 10 μl aliquot of RNase inhibitor solution (Rlasin Inhibitor 2500 U=33 U/μl N211A, Promega GmbH, Mannheim, Germany, 0.5 μl in 400 μl of freezing solution, containing 0.15 mol NaCl, 10 mmol Tris pH 8.0, 0.25 mmol dithiothreitol) was spread onto the film, where the tissue sample was to be mounted.
The tissue sections mounted on film were used for LCM. Approximately 2000 epithelial cells/sample were captured using the PALM Robot-Microbeam technology (P.A.L.M. Mikrolaser Technologie, Carl Zeiss, Inc., Thomwood, N.Y.), coupled into Zeiss Axioven 135 microscope (Carl Zeiss Jena GmbH, Jena, Germany). The surrounding stroma in the normal mucosa, and the occasional intervening stromal components in cancer samples, were included. The captured cells were put in tubes in 100% ethanol and preserved at −80° C.
Example 2
RNA Extraction and Amplification
Zymo-Spin Column (Zymo Research, Orange, Calif. 92867) was used to extract total RNA from the LCM captured samples. About 2 ng of total RNA was resuspended in 10 ul of water and 2 rounds of the T7 RNA polymerase based amplification were performed to yield about 50 ug of amplified RNA.
Example 3
cDNA Microarray Hybridization and Quantitation
A set of cDNA microarrays consisting of approximately 23,000 human cDNA clones was used to test the samples by use of the humanU133a chip obtained and commercially available from Affymetrix, Inc. Total RNA obtained and prepared as outlined above and applied to the chips and analyzed by Agilent BioAnalyzer according to the manufacturer's protocol. All 149 samples passed the quality control standards and the data were used for marker selection.
Marker selection was performed by analyzing the 103 lymph node negative patients. Genes that allow the discrimination of distant metastases and survivors were identified using Cox proportional hazard model. Chip intensity data was analyzed using MAS Version 5.0 software commercially available from Affymetrix, Inc. (“MAS 5.0”). An unsupervised analysis was first conducted followed by a supervised analysis.
The chip intensity data obtained as described was the input for the unsupervised clustering software commercially available as PARTEK version 5.1 software. This unsupervised clustering algorithm identified a group of 22 patients with a significant low expression of many genes including estrogen receptor. ER/PR are known prognostic factors for poor outcome in breast cancer so this group of 22 patients were excluded from subsequent analysis to identify additional factors (gene markers) with independent value as prognostic indicators. The remaining 81 patients were further filtered to remove potential effects of the well-characterized prognostic indicators of age and tumor size. Twenty-seven patients older than 55 years or having tumors larger than 5 cm were thus excluded too.
A Cox proportional hazard model was used for gene selection. In each cycle of the total 31 cycles, each of the 31 patients in the training set was held out, the remaining 26 patients were used in the univariate Cox model regression to assess the strength of association of gene expression with the patient survival time. The strength of such association was evaluated by the corresponding estimated standardized parameter estimate and P value returned from the Cox model regression. P value of 0.01 was used as the threshold to select top genes from each cycle of the leave-one-out gene selection. The top genes selected from each cycle were then compared in order to select those genes that showed up at least 28 times in the total of 31 leave-one-out gene selection cycles. A total of 56 genes were
Modulation
(Standardized
Gene
Coefficient)
P. value
Sequence I.D. No.
216516_at
−2.7708
0.0056
Sequence I.D.. No. 32
211646_at
−2.7853
0.0053
Sequence I.D.. No. 33
219463_at
−2.7860
0.0053
Serquence I.D. No. 34
204532_x_at
−2.7921
0.0052
Sequence I.D. No. 35
210365_at
−2.7931
0.0052
Sequence I.D.. No. 36
222098_s_at
−2.8121
0.0049
Sequence I.D.. No. 37
212800_at
−2.8267
0.0047
Sequence I.D.. No. 38
205582_s_at
−2.8350
0.0046
Sequence I.D.. No. 39:
219096_at
−2.8393
0.0045
Sequence I.D.. No. 40
216944_s_at
−2.8667
0.0041
Sequence I.D.. No. 41
208923_at
−2.8766
0.0040
Sequence I.D.. No. 42
209309_at
−2.9149
0.0036
Sequence I.D.. No. 43
207981_s_at
−2.9294
0.0034
Sequence I.D.. No. 44
210160_at
−2.9448
0.0032
Sequence I.D.. No. 45
206862_at
−2.9676
0.0030
Sequence I.D.. No. 46
213110_s_at
−2.9857
0.0028
Sequence I.D.. No. 47
201906_s_at
−3.0124
0.0026
Sequence I.D.. No. 48
201057_s_at
−3.0133
0.0026
Sequence I.D.. No. 49
220798_x_at
−3.0270
0.0025
Sequence I.D.. No. 50
218650_at
−3.0513
0.0023
Sequence I.D.. No. 51
220986_s_at
−3.2095
0.0013
Sequence I.D.. No. 52
214451_at
−3.4431
0.0006
Sequence I.D.. No. 53
203844_at
−3.4965
0.0005
Sequence I.D.. No. 54
202966_at
−3.5864
0.0003
Sequence I.D.. No. 55
Construction of a multiple-gene predictor: The prediction index is defined as the sum of the product of the 56 genes' expression values (log 10 based) and their corresponding cox model parameter estimates. The parameter estimate from the cox models measures the hazard ratio of the patient when the gene expression value increases. Therefore, patients with high scores using the index have poor survival outcomes. This prediction index was applied to the training set to obtain an estimate of the prediction accuracy ( FIG. 1 ).
Cross-validation and evaluation of predictor: Performance of the predictor should be determined on an independent data set because most classification selected. Gene expression for those genes having Seq. ID No 1 to 26 and Seq ID No. 56 were up-regulated at least two fold and genes having Seq. ID No 27 to 55 were down regulated at least two fold.
TABLE 1 Breast Cancer Prognostic Gene Markers. Modulation (Standardized Gene Coefficient) P. value Sequence I.D. No. 202984_s_at 3.8521 0.0001 Sequence I.D. No.: 1 208777_s_at 3.4922 0.0005 Sequence I.D. No. 2. 222133_s_at 3.1841 0.0015 Sequence I.D. No. 3 218185_s_at 3.1379 0.0017 Sequence I.D. No. 4 219571_s_at 3.1131 0.0019 Sequence I.D.. No. 5 201138_s_at 3.1075 0.0019 Sequence I.D.. No. 6 209155_s_at 3.1018 0.0019 Sequence I.D.. No. 7 212468_at 0.0019 0.0022 Sequence I.D.. No. 8 217593_at 0.0019 0.0022 Sequence I.D.. No. 9 212973_at 3.0325 0.0024 Sequence I.D.. No. 10 202971_s_at 2.9994 0.0027 Sequence I.D.. No. 11 204444_at 2.9926 0.0028 Sequence I.D.. No. 12 205169_at 2.9911 0.0028 Sequence I.D.. No. 13 219751_at 2.9707 0.0030 Sequence I.D.. No. 14 217988_at 2.9649 0.0030 Sequence I.D.. No. 15 212942_s_at 2.9460 0.0032 Sequence I.D.. No. 16 208993_s_at 2.9423 0.0033 Sequence I.D.. No. 17 219105_x_at 2.9324 0.0034 Sequence I.D.. No. 18 220085_at 2.9001 0.0037 Sequence I.D.. No. 19 206640_x_at 2.8799 0.0040 Sequence I.D. No. 20 205062_x_at 2.8663 0.0042 Sequence I.D. No. 21 209385_s_at 2.8115 0.0049 Sequence I.D.. No. 22 AFFX-M27830_5_at 2.7868 0.0053 Sequence I.D.. No. 56 215170_s_at 2.7814 0.0054 Sequence I.D.. No. 23 207663_x_at 2.7634 0.0057 Sequence I.D.. No. 24 212229_s_at 2.7422 0.0061 Sequence I.D.. No. 25 215206_at 2.7317 0.0063 Sequence I.D.. No. 26 206241_at −2.7281 0.0064 Sequence I.D.. No. 27 219813_at −2.7406 0.0061 Sequence I.D.. No. 28 210969_at −2.7522 0.0059 Sequence I.D.. No. 29 207865_s_at −2.7691 0.0056 Sequence I.D.. No. 30 202520_s_at −2.7702 0.0056 Sequence I.D.. No. 31
methods work well on the examples that were used in their establishment. The 23 patients testing set was used to assess prediction accuracy. The cutoff for the classification is determined using the ROC, curve with 90% sensitivity. With the selected cutoff, the numbers of correct prediction for relapse and survival patients in the test set are summarized in (Table 1). The Kaplan-Meier curve was constructed on the predicted relapsers and survivors ( FIG. 2 ).
Overall prediction: Gene expression profiling of 54 Stage I and II breast cancer patients led to identification of 56 genes that have differential expression in these patients. Thirty-six of the patients have remained disease-free for more than 7 years while 27 patients had distant metasteses within 4 years. Using the 56-gene predictor, 22 of the 27 relapse patients and 27 of 36 disease-free patients were identified correctly. This result represents a sensitivity of 82% and a specificity of 75%. The positive predictive value is 71% and the negative predictive value is 84% (Table 2), The Kaplan-Meier curve was constructed on the predicted distant metastases and survivors ( FIG. 3 ).
An independent study was previously published (Van't Veer et al. Nature 415, 530-535. Vijver et al., NEJM 347, 1999-2009) in which a 70-gene predictor was constructed to predict patient outcomes in Stage I and II lymph node negative breast cancer. Only one gene overlaps between the 70 0 gene of the Van't Veer et al. study and the 56-gene predictor of this specification.
TABLE 2
Prediction accuracy based on testing set using 56-gene predictor.
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
6
Sensitivity
91%
Specificity
50%
TABLE 3
Prediction accuracy based on all patients using 56-gene predictor.
Study
Prediction
Number of Sample
Correct
Relapse
25
23
Survivor
29
23
Sensitivity
92%
Specificity
79%
Example 4
Further Portfolios
The 56 gene portfolio was subjected to different treatments to fashion further portfolios that provide clinically significant benefits with fewer numbers of gene expression signatures for analysis.
a. In a first treatment, correlation coefficients among the 56 genes were calculated by Spearman rank correlation and Pearson's correlation. Using 0.7 as the correlation cutoff, a portfolio of 45 modulated genes was established. The genes are shown in Table 4.
b. In a second treatment, the 56 genes were tested with t-tests using either the training or testing dataset. The genes that displayed significant p values (<0.05) in both training and testing data were selected as a portfolio. A portfolio of 26 modulated genes was thus established. The genes are shown in Table 5.
c. The 26 gene portfolio of (b) and Table 5 were then evaluated based on the known biological functions of the genes in the portfolio. Those having a biological relationship to a metastatic pathway were selected. A portfolio of 13 modulated genes was thus established. The genes are shown in Table 6.
d. A two gene pair exhibiting the best classification performance was selected from the 56 gene portfolio. In serial, one additional gene was added to the portfolio and tested to determine whether the addition of that signature improved the overall classification accuracy in both training set and testing set of the two gene combination. This procedure was repeated until no further improvement was achieved. A portfolio of 6 modulated genes was established. The genes are shown in Table 7.
The sensitivity and specificity for each of the portfolios shown in Tables 4-7 was determined based on predicted versus known outcomes for the samples described above. These values are shown in Tables 8-11.
TABLE 4
45 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
220986_s_at
−3.2095
Seq. I.D. No. 52
220798_x_at
−3.0270
Seq. I.D. No. 50
220085_at
2.9001
Seq. I.D. No. 19
219751_at
2.9707
Seq. I.D. No. 14
219105_x_at
2.9324
Seq. I.D. No. 18
218650_at
−3.0513
Seq. I.D. No. 51
214451_at
−3.4431
Seq. I.D. No. 53
212973_at
3.0325
Seq. I.D. No. 10
208993_s_at
2.9423
Seq. I.D. No. 17
205582_s_at
−2.8350
Seq. I.D. No. 39
205169_at
2.9911
Seq. I.D. No. 13
203844_at
−3.4965
Seq. I.D. No. 54
202984_s_at
3.8521
Seq. I.D. No. 1
202966_at
−3.5864
Seq. I.D. No. 55
201057_s_at
−3.0133
Seq. I.D. No. 49
222133_s_at
3.1841
Seq. I.D. No. 3
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
212942_s_at
2.9460
Seq. I.D. No. 16
210160_at
−2.9448
Seq. I.D. No. 45
209155_s_at
3.1018
Seq. I.D. No. 7
204444_at
2.9926
Seq. I.D. No. 12
202971_s_at
2.9994
Seq. I.D. No. 11
201138_s_at
3.1075
Seq. I.D. No. 6
222098_s_at
−2.8121
Seq. I.D. No. 37
219813_at
−2.7406
Seq. I.D. No. 28
216944_s_at
−2.8667
Seq. I.D. No. 41
215206_at
2.7317
Seq. I.D. No. 26
212800_at
−2.8267
Seq. I.D. No. 38
212229_s_at
2.7422
Seq. I.D. No. 25
211646_at
−2.7853
Seq. I.D. No. 33
210365_at
−2.7931
Seq. I.D. No. 36
209385_s_at
2.8115
Seq. I.D. No. 22
209309_at
−2.9149
Seq. I.D. No. 43
208923_at
−2.8766
Seq. I.D. No. 42
207663_x_at
2.7634
Seq. I.D. No. 24
205062_x_at
2.8663
Seq. I.D. No. 21
202520_s_at
−2.7702
Seq. I.D. No. 31
AFFX-M27830_5_at
2.7868
Seq. I.D. No. 56
216516_at
−2.7708
Seq. I.D. No. 32
215170_s_at
2.7814
Seq. I.D. No. 23
210969_at
−2.7522
Seq. I.D. No. 29
207981_s_at
−2.9294
Seq. I.D. No. 44
206241_at
−2.7281
Seq. I.D. No. 27
204532_x_at
−2.7921
Seq. I.D. No. 35
TABLE 5
26 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
205169_at
2.9911
Seq. I.D. No. 13
203844_at
−3.4965
Seq. I.D. No. 54
205062_x_at
2.8663
Seq. I.D. No. 21
202971_s_at
2.9994
Seq. I.D. No. 11
201906_s_at
−3.0124
Seq. I.D. No. 48
212942_s_at
2.9460
Seq. I.D. No. 16
206862_at
−2.9676
Seq. I.D. No. 46
202966_at
−3.5864
Seq. I.D. No. 55
201057_s_at
−3.0133
Seq. I.D. No. 49
219105_x_at
2.9324
Seq. I.D. No. 18
217593_at
3.0584
Seq. I.D. No. 9
202520_s_at
−2.7702
Seq. I.D. No. 31
210365_at
−2.7931
Seq. I.D. No. 36
215206_at
2.7317
Seq. I.D. No. 26
212229_s_at
2.7422
Seq. I.D. No. 25
211646_at
−2.7853
Seq. I.D. No. 33
219813_at
−2.7406
Seq. I.D. No. 28
216944_s_at
−2.8667
Seq. I.D. No. 41
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
213110_s_at
−2.9857
Seq. I.D. No. 47
212468_at
3.0663
Seq. I.D. No. 8
208993_s_at
2.9423
Seq. I.D. No. 17
208777_s_at
3.4922
Seq. I.D. No. 2
220085_at
2.9001
Seq. I.D. No. 19
219751_at
2.9707
Seq. I.D. No. 14
TABLE 6
13 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
202971_s_at
2.9994
Seq. I.D. No. 11
201906_s_at
−3.0124
Seq. I.D. No. 48
206862_at
−2.9676
Seq. I.D. No. 46
202966_at
−3.5864
Seq. I.D. No. 55
219105_x_at
2.9324
Seq. I.D. No. 18
210365_at
−2.7931
Seq. I.D. No. 36
212229_s_at
2.7422
Seq. I.D. No. 25
219813_at
−2.7406
Seq. I.D. No. 28
219096_at
−2.8393
Seq. I.D. No. 40
218185_s_at
3.1379
Seq. I.D. No. 4
213110_s_at
−2.9857
Seq. I.D. No. 47
208777_s_at
3.4922
Seq. I.D. No. 2
220085_at
2.9001
Seq. I.D. No. 19
TABLE 7
6 Gene Set
Modulation
(Standardized
Gene
Coefficient)
Sequence I.D. No.
205169_at
2.9911
Seq. I.D. No. 13
202966_at
−3.5864
Seq. I.D. No. 55
206862_at
−2.9676
Seq. I.D. No. 46
219105_x_at
2.9324
Seq. I.D. No. 18
205062_x_at
2.8663
Seq. I.D. No. 21
201138_s_at
3.1075
Seq. I.D. No. 6
TABLE 8
45-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
6
Sensitivity
91%
Specificity
50%
TABLE 9
26-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
10
Sensitivity
91%
Specificity
83%
TABLE 10
13-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
8
Sensitivity
91%
Specificity
67%
TABLE 11
6-gene Prognostic Portfolio
Study
Prediction
Number of Sample
Correct
Relapse
11
10
Survivor
12
8
Sensitivity
91%
Specificity
67%
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