Reagents and methods for use in cancer diagnosis, classification and therapy
View Patent ↗Methods and reagents for classifying tumors and for identifying new tumor classes and subclasses. Methods for correlating tumor class or subclass with therapeutic regimen or outcome, for identifying appropriate (new or known) therapies for particular classes or subclasses, and for predicting outcomes based on class or subclass. New therapeutic agents and methods for the treatment of cancer.
1. A method of assessing the likelihood that a patient having an ovarian tumor will die from ovarian cancer or have a recurrence, the method comprising steps of:
contacting a tumor sample from a patient with an ovarian tumor with a panel of one or more antibodies, wherein the panel comprises an antibody to a biomarker with SEQ ID NO. 1; and
assessing the likelihood that the patient will die from ovarian cancer or have a recurrence based upon detection of binding of the panel to the tumor sample, wherein across a population of patients with ovarian tumors, a higher level of binding of the antibody to a biomarker with SEQ ID NO. 1 is indicative of a higher likelihood that the patient will die from ovarian cancer or have a recurrence.
2. The method of claim 1 , wherein the step of assessing comprises assessing the likelihood that the patient will die from ovarian cancer.
3. The method of claim 1 , wherein the step of assessing comprises assessing the likelihood that the patient will have a recurrence.
4. A method of assessing the likelihood that a patient having an ovarian tumor will die from ovarian cancer or have a recurrence, the method comprising steps of:
contacting a tumor sample from a patient with an ovarian tumor with a panel of one or more antibodies, wherein the panel comprises an antibody to a biomarker with SEQ ID NO. 2; and
assessing the likelihood that the patient will die from ovarian cancer or have a recurrence based upon detection of binding of the panel to the tumor sample, wherein across a population of patients with ovarian tumors, a higher level of binding of the antibody to a biomarker with SEQ ID NO. 2 is indicative of a higher likelihood that the patient will die from ovarian cancer or have a recurrence.
5. The method of claim 4 , wherein the step of assessing comprises assessing the likelihood that the patient will die from ovarian cancer.
6. The method of claim 4 , wherein the step of assessing comprises assessing the likelihood that the patient will have a recurrence.
7. A method of assessing the likelihood that a patient having an ovarian tumor will die from ovarian cancer or have a recurrence, the method comprising steps of:
contacting a tumor sample from a patient with an ovarian tumor with a panel of one or more antibodies, wherein the panel comprises an antibody to a biomarker with SEQ ID NO. 3; and
assessing the likelihood that the patient will die from ovarian cancer or have a recurrence based upon detection of binding of the panel to the tumor sample, wherein across a population of patients with ovarian tumors, a higher level of binding of the antibody to a biomarker with SEQ ID NO. 3 is indicative of a lower likelihood that the patient will die from ovarian cancer or have a recurrence.
8. The method of claim 7 , wherein the step of assessing comprises assessing the likelihood that the patient will die from ovarian cancer.
9. The method of claim 7 , wherein the step of assessing comprises assessing the likelihood that the patient will have a recurrence.