Combination therapy with an anti-CD25 antibody-drug conjugate
The present disclosure relates to combination therapies for the treatment of pathological conditions, such as cancer. In particular, the present disclosure relates to combination therapies comprising treatment with an Antibody Drug Conjugate (ADC) and a secondary agent.
1. A method for treating cancer in an individual, the method comprising administering to the individual an effective amount of ADCX25 and a PD1 antagonist; wherein ADCX25 has the following chemical structure:
and wherein Ab is an antibody that binds to CD25 which comprises (a) a heavy chain having the amino acid sequence of SEQ ID NO. 1, and (b) a light chain having the amino acid sequence of SEQ ID NO. 2.
2. The method of claim 1 , wherein the treatment comprises administering ADCX25 before the PD1 antagonist, simultaneous with the PD1 antagonist, or after the PD1 antagonist.
3. The method of claim 1 , wherein the treatment further comprises administering a chemotherapeutic agent.
4. The method of claim 1 , wherein the individual is a human.
5. The method of claim 1 , wherein the individual has cancer.
6. The method of claim 5 , wherein the cancer is characterised by the presence of a neoplasm comprising both CD25+ and CD25− cells.
7. The method of claim 5 , wherein the cancer is characterised by the presence of a neoplasm comprising CD25− neoplastic cells.
8. The method of claim 5 , wherein the cancer or neoplasm is all or part of a solid tumour.
9. The method of claim 5 , wherein the cancer expresses CD25 or CD25+ tumour-associated non-tumour cells.
10. The method of claim 5 , wherein the cancer exhibits a low level of surface expression of CD25.
11. The method of claim 5 , wherein the cancer is selected from: Hodgkin's and non-Hodgkin's Lymphoma, diffuse large B-cell lymphoma (DLBCL), follicular lymphoma, (FL), Mantle Cell lymphoma (MCL), chronic lymphatic lymphoma (CLL), Marginal Zone B-cell lymphoma (MZBL); Hairy cell leukemia (HCL), Hairy cell leukemia variant (HCL-v), Acute Myeloid Leukaemia (AML), Acute Lymphoblastic Leukaemia (ALL), Philadelphia chromosome-positive ALL (Ph+ALL), Philadelphia chromosome-negative ALL (Ph−ALL); pancreatic cancer, breast cancer, colorectal cancer, gastric cancer, oesophageal cancer, melanoma, non-small cell lung cancer, ovarian cancer, hepatocellular carcinoma, renal cell carcinoma, and head and neck cancer.
12. The method of claim 1 , wherein the PD1 antagonist is selected from pembrolizumab, nivolumab, MEDI0680, PDR001 (spartalizumab), Camrelizumab, AUNP12, Pidilizumab Cemiplimab (REGN-2810), AMP-224, BGB-A317 (Tisleizumab), and BGB-108.
13. The method of claim 1 , wherein the PD1 antagonist is pembrolizumab.