Method of normalizing the neutrophil to lymphocyte ratio in cancer patients with a selective glucocorticoid receptor antagonist
Methods for treating a cancer patient with a neutrophil-to-lymphocyte ratio (NLR) greater than 3 are disclosed, comprising administering a nonsteroidal glucocorticoid receptor antagonist (GRA) to such a cancer patient, effective to reduce the patient's NLR. The methods include administering a nonsteroidal GRA and a cancer treatment to such a cancer patient, effective to reduce the patient's NLR and enhance the treatment of the cancer patient. The GRA may be orally administered. The nonsteroidal GRA may be a nonsteroidal compound comprising a heteroaryl ketone fused azadecalin structure (e.g., relacorilant) or an octahydro fused azadecalin structure (e.g., exicorilant). The cancer treatment may include chemotherapy, immunotherapy, radiation therapy, administration of an anti-angiogenic agent, administration of a growth factor inhibitor, and surgery. The methods may enhance the cancer treatment, improve the prognosis of the cancer patient, improve the survival of the cancer patient, and provide beneficial clinical effects and advantages to the patient.
1. A method of reducing the neutrophil-to-lymphocyte ratio (NLR) by at least 10% as compared to the baseline NLR in a cancer patient suffering from pancreatic cancer, ovarian cancer, or having an advanced solid tumor or metastatic tumor and having a baseline NLR greater than 3, said baseline NLR being determined from a blood sample obtained from said patient prior to administration of a cancer treatment to the patient;
Wherein NLR is determined by a) measuring the absolute neutrophil count obtained from a blood sample obtained from said cancer patient to determine a value of said absolute neutrophil count, b) measuring the absolute lymphocyte count obtained from said blood sample obtained from said cancer patient to determine a value of said absolute neutrophil count, and c) dividing the value of said absolute neutrophil count by the value of said absolute lymphocyte count, wherein NLR is the quotient resulting from said dividing;
the method comprising:
administering an effective amount of the nonsteroidal selective glucocorticoid receptor antagonist (GRA) relacorilant, (R)-(1-(4-fluorophenyl)-6-((1-methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone, which has the structure:
and
administering an effective amount of a cancer treatment comprising a taxane chemotherapeutic, to said cancer patient,
whereby the NLR of said cancer patient determined after administration of relacorilant and said cancer treatment is reduced by at least 10% as compared to the baseline NLR.
2. The method of claim 1 , wherein said administration of said cancer treatment and administration of relacorilant is effective to reduce the tumor load of the patient.
3. The method of any of claim 1 , wherein said neutrophil-to-lymphocyte ratio (NLR) of said cancer patient is reduced to about 3 or less.
4. The method of claim 1 , wherein the method further comprises administration of an immunotherapeutic agent.
5. The method of claim 4 , wherein the immunotherapeutic agent comprises an antibody directed against a protein target selected from PD-1, PD-L1, CTKA4, LAG3, B7-H3, B7-H4, OX-40, CD137, and TIM3.
6. The method of claim 1 , wherein said reducing NLR by at least 10 % as compared to said baseline NLR is effective to enhance the response to cancer treatment in a cancer patient receiving cancer treatment and having a neutrophil-to-lymphocyte ratio of greater than 3, wherein said enhancing is as compared to the response in the absence of the present method, the method comprising:
administering an effective amount of a nab-paclitaxel and an effective amount of a relacorilant to said cancer patient,
whereby the cancer patient's NLR is reduced and the cancer patient's response to cancer treatment is enhanced.
7. The method of claim 6 , wherein the patient exhibits a partial response to the cancer treatment and GRA treatment, wherein said partial response is an improvement as compared to the patient's response to the cancer treatment alone,
whereby the cancer patient's NLR is reduced and the cancer patient's response to cancer treatment is enhanced.
8. The method of claim 6 , wherein the patient exhibits a complete response to the cancer treatment and GRA treatment, wherein said complete response is an improvement as compared to the patient's response to the cancer treatment alone,
whereby the cancer patient's NLR is reduced and the cancer patient's response to cancer treatment is enhanced.