Sensitivity test to predict efficacy of anti-cancer therapies
The present disclosure provides methods for determining the sensitivity of cancerous cells to various anti-cancer therapies and predicting the efficacy of these therapies. Specifically, the present disclosure provides methods for predicting the efficacy of one or more candidate anti-cancer therapies in a patient, based on determining the sensitivity of the patient's cancerous cells after exposure to candidate anti-cancer therapies in vitro. The disclosure further provides methods for predicting the efficacy of candidate anti-cancer therapies by using an in vitro sensitivity test of the patient's cancerous cells and a surrogate in vivo efficacy test of the patient's cancerous cells grafted into a surrogate host. The disclosure further provides methods for selecting the most efficacious anti-cancer therapy(s) for a patient, thereby avoiding ineffective or unnecessary treatments.
1. A method for determining the sensitivity of a patient's cancerous cells to a candidate anti-cancer therapy, comprising:
(a) exposing a sample of the patient's cancerous cells to the candidate anti-cancer therapy in vitro, wherein the candidate anti-cancer therapy comprises a G2 checkpoint-abrogating peptidomimetic selected from the group consisting of CBP500 (SEQ ID NO: 25), CBP501 (SEQ ID NO: 26), CBP504 (SEQ ID NO: 29), CBP505 (SEQ ID NO: 30), CBP506 (SEQ ID NO: 31), CBP510 (SEQ ID NO: 32), CBP511 (SEQ ID NO: 33), CBP512 (SEQ ID NO: 34), and CBP603 (SEQ ID NO: 37);
(b) measuring the DNA content of each cancerous cell in the sample after exposure to the candidate anti-cancer therapy; and
(c) determining the cell cycle distribution of the sample after exposure to the candidate anti-cancer therapy;
wherein a change in the cell cycle distribution of the sample after exposure to the candidate anti-cancer therapy indicates sensitivity of the patient's cancerous cells to the therapy.
2. A method for determining the sensitivity of a patient's cancerous cells to a candidate anti-cancer therapy, comprising:
(a) exposing a sample of the patient's cancerous cells to the candidate anti-cancer therapy in vitro, wherein the candidate anti-cancer therapy comprises a combination therapy comprising a DNA-damaging agent and a G2 checkpoint-abrogating agent, wherein the DNA-damaging agent is cisplatin (CDDP) and the G2 checkpoint-abrogating agent is CBP501 (SEQ ID NO: 26);
(b) measuring the DNA content of each cancerous cell in the sample after exposure to the candidate anti-cancer therapy; and
(c) determining the cell cycle distribution of the sample after exposure to the candidate anti-cancer therapy;
wherein a change in the cell cycle distribution of the sample after exposure to the candidate anti-cancer therapy indicates sensitivity of the patient's cancerous cells to the therapy.