METHODS AND SYSTEMS FOR EVALUATING THE SENSITIVITY OR RESISTANCE OF TUMOR SPECIMENS TO CHEMOTHERAPEUTIC AGENTS
The present invention provides methods, systems, and kits for evaluating the sensitivity and/or resistance of tumor specimens to one or a combination of chemotherapeutic agents. Particularly, the invention provides malignant cell gene signatures that are predictive of a tumor's response to candidate chemotherapeutic regimens.
1 . A method for preparing a gene expression profile indicative of drug-sensitivity or drug-resistance, comprising:
extracting RNA from a patient tumor specimen or cells cultured therefrom, and
determining the level of expression for at least 10 genes listed in one of Tables 1-10, thereby preparing the gene expression profile.
2 . The method of claim 1 , wherein the tumor is derived from a tissue selected from breast, ovaries, lung, colon, skin, prostate, kidney, endometrium, nasopharynx, pancreas, head and neck, kidney, and brain.
3 . (canceled)
4 . (canceled)
5 . The method of claim 1 , wherein the tumor specimen is a breast tumor specimen, and the breast tumor specimen is optionally determined to be ER+ or ER−.
6 . The method of claim 1 , wherein the patient has primary cancer.
7 . The method of claim 1 , wherein the patient has recurrent cancer.
8 . The method of claim 1 , wherein the patient is a candidate for treatment with a combination selected from: cyclophosphamide, doxorubicin, fluorouracil, and paclitaxel (TFAC); cyclophosphamide and epirubicin (EC); fluorouracil, cyclophosphamide and doxrubicin (FAC); cyclophosphamide and doxorubicin (AC); cyclophosphamide, docetaxel, and doxorubicin (ACT), cyclophosphamide, docetaxel, epirubicin, and fluorouracil, (TFEC), docetaxel and fluorouracil (DX).
9 . The method of claim 1 , wherein the RNA is extracted from a tumor specimen.
10 . The method of claim 9 , wherein the tumor specimen is formalin-fixed and paraffin-embedded.
11 . The method of claim 1 , wherein the RNA is extracted from cultured cells derived from the tumor specimen.
12 . (canceled)
13 . (canceled)
14 . The method of claim 1 , wherein the levels of expression are determined by hybridizing nucleic acids to oligonucleotide probes, by RT-PCR, or by direct mRNA capture.
15 . (canceled)
16 . (canceled)
17 . (canceled)
18 . (canceled)
19 . The method of claim 1 , wherein the gene expression profile comprises the level of expression for at least about 100 genes listed in one of Tables 1-10.
20 . The method of claim 1 , wherein the gene expression profile comprises the level of expression for at least about 200 genes listed in one of Tables 1-10.
21 - 28 . (canceled)
29 . A method for evaluating the sensitivity of a tumor to one or a combination of chemotherapeutic agents, comprising:
preparing a gene expression profile for a tumor specimen according to claim 1 ; and
determining the presence of at least one gene expression signature indicative of drug-sensitivity or drug-resistance, thereby classifying the profile as a drug-sensitive or drug-resistant profile, wherein the gene signature is based on in vitro chemosensitivity of cell lines.
30 . (canceled)
31 . (canceled)
32 . The method of claim 29 , wherein the gene expression signature is predictive of efficacy for one or more of treatment with TFAC, EC, FEC, AC, ACT, TFEC, or DX.
33 . The method of claim 29 , wherein the gene expression profile is classified by using one or more of Principal Components Analysis, Naïve Bayes, Support Vector Machines, Nearest Neighbors, Decision Trees, Logistic, Artificial Neural Networks, and Rule-based schemes.
34 . The method of claim 29 , wherein the gene expression signature is predictive of survival, pathological complete response (pCR), reduction in tumor size, or duration of progression free interval upon treatment with a chemotherapeutic agent or combination.
35 . (canceled)
36 . A computer system for performing the method of claim 1 .
37 . A probe array or probe set for performing the method of claim 1 .