Combination therapy for treating cancer
The present disclosure provides methods of treating cancer in a patient. The method comprises administering to the patient an effective amount of a compound of Formula (Ia) or (Ib), or a pharmaceutically acceptable salt thereof, and an effective amount of an immunomodulatory agent. Also provided herein are compositions and kits for performing the methods described herein. In another aspect, the method comprises administering to the patient an effective amount of a compound of Formula (Ia) or (Ib), or a pharmaceutically acceptable salt thereof, and an effective amount of radiation therapy.
1 . A method of treating a cancer related to arginase activity in a patient comprising administering to the patient an effective amount of a compound of Formula (Ia1) or (Ib1), or a pharmaceutically acceptable salt thereof, and an effective amount of an immunomodulatory agent;
wherein
R 1 is —H or —C(O)CH(R 1a )NHR 1b ,
R 1a is selected from —H, —(C 1 -C 6 ) alkyl and CH 2 OR 1c ;
R 1b is —H; or alternatively, R 1a and R 1b , together with the atom to which they are attached, form a 5-membered heterocyclic ring; and
R 1c is H or —CH 3 .
2 . The method of claim 1 , wherein
R 1 is —H or —C(O)CH(R 1a )NH 2 ; and
R 1a is selected from —H or —(C 1 -C 6 ) alkyl.
3 . The method of claim 1 , wherein the compound of Formula (Ia1) or (Ib1) is represented by:
wherein R 2 is selected from —H or —(C 1 -C 4 ) alkyl.
4 . The method of claim 1 , wherein the compound of Formula (Ia1) or (Ib1) is selected from:
5 . The method of claim 1 , wherein the immunomodulatory agent is an immune checkpoint inhibitor or an immunostimulant.
6 . The method of claim 5 , wherein the immune checkpoint inhibitor is a CTLA-4 receptor inhibitor, a PD-1 receptor inhibitor, a PD-L1 inhibitor, a PD-L2 inhibitor, a NKG2A receptor inhibitor, or a combination thereof.
7 . The method of claim 5 , wherein the immunostimulant is a TLR3 agonist.
8 . The method of claim 5 , wherein the immune checkpoint inhibitor is an antibody or antigen-binding fragment thereof.
9 . The method of claim 5 , wherein the immune checkpoint inhibitor is an anti-CTLA-4 receptor antibody, an anti-PD-1 receptor antibody, an anti-PD-L1 antibody, an anti-PD-L2 antibody, an anti-NKG2A receptor antibody, or a combination thereof.
10 . The method of claim 9 , wherein the immune checkpoint inhibitor is durvalumab, tremelimumab, monalizumab, or a combination thereof.
11 . The method of claim 1 , wherein the cancer is a breast cancer, a bladder cancer, a head and neck cancer, a non-small cell lung cancer, a small cell lung cancer, a colorectal cancer, a gastrointestinal stromal tumor, a gastroesophageal carcinoma, a renal cell cancer, a prostate cancer, a liver cancer, a colon cancer, a pancreatic cancer, an ovarian cancer, a melanoma, A non-Hodgkin's lymphoma, a cutaneous T-cell lymphoma, multiple myeloma, acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), chronic myeloid leukemia (CML), chronic lymphocytic leukaemia (CLL), chronic myelomonocytic leukemia (CMML), and diffuse large B-cell lymphoma (DLBCL).
12 . A pharmaceutical product comprising i) a compound of Formula (Ia1) or (Ib1), or a pharmaceutically acceptable salt thereof, and ii) an immunomodulatory agent;
wherein
R 1 is —H or —C(O)CH(R 1a )NHR 1b ;
R 1a is selected from —H, —(C 1 -C 6 ) alkyl and CH 2 OR 1c ,
R 1b is —H; or alternatively, R 1a and R 1b , together with the atom to which they are attached, form a 5-membered heterocyclic ring; and
R 1c is H or —CH 3 .
13 . The pharmaceutical product of claim 12 , wherein the compound of Formula (Ia1) or (Ib1), or a pharmaceutically acceptable salt thereof and the immunomodulatory agent are present in a single dosage form.
14 . The pharmaceutical product of claim 12 , wherein the compound of Formula (Ia1) or (Ib1), or a pharmaceutically acceptable salt thereof and the immunomodulatory agent are present in separate dosage forms.
15 . A method of treating a cancer related to arginase activity in a patient comprising administering to the patient an effective amount of a compound of Formula (Ia1) or (Ib1), or a pharmaceutically acceptable salt thereof, and an effective amount of radiation therapy;
wherein
R 1 is —H or —C(O)CH(R 1a )NHR 1b ;
R 1a is selected from —H, —(C 1 -C 6 ) alkyl and CH 2 OR 1c ,
R 1b is —H; or alternatively, R 1a and R 1b , together with the atom to which they are attached, form a 5-membered heterocyclic ring; and
R 1c is H or —CH 3 .
16 . The method of claim 15 , wherein the compound of Formula (Ia1) or (Ib1) is represented by:
wherein R 2 is selected from —H or —(C 1 -C 4 ) alkyl.
17 . The method of claim 15 , wherein the radiation therapy is fractionated radiation therapy.
18 . The method of claim 15 , further comprising administering to the patient an effective amount of an immunomodulatory agent.
19 . The method of claim 18 , wherein the immunomodulatory agent is a CTLA-4 receptor inhibitor, a PD-1 receptor inhibitor, a PD-L1 inhibitor, a PD-L2 inhibitor, a NKG2A receptor inhibitor, or a combination thereof.