Combination treatment
Human clinical use of a chimeric poliovirus construct has demonstrated excellent anti-tumor effect. Combination with immune checkpoint inhibitors increases the anti-tumor effect. Tumors of different types are susceptible to the combination treatment, including but not limited to melanoma, glioglastoma, renal cell carcinoma, prostate cancer, breast cancer, lung cancer, medulloblastoma, and colorectal cancer.
1. A method of treating a tumor in a patient to achieve a therapeutic anti-tumor effect, wherein the tumor expresses NECL5 (nectin-like protein 5), comprising:
administering to the patient a chimeric poliovirus construct comprising a Sabin type I strain of poliovirus with a human rhinovirus 2 (HRV2) internal ribosome entry site (IRES) in said poliovirus' 5′ untranslated region between said poliovirus' cloverleaf and said poliovirus' open reading frame; and
administering an immune checkpoint inhibitor to the patient, whereby the patient is treated.
2. The method of claim 1 wherein the tumor is a glioblastoma.
3. The method of claim 1 wherein the tumor is an astrocytoma or an oligodendroglioma.
4. The method of claim 1 wherein the tumor is an astro-oligodendroglioma.
5. The method of claim 1 wherein the tumor is a renal cell carcinoma.
6. The method of claim 1 wherein the tumor is urostate tumor.
7. The method of claim 1 wherein the tumor is a bladder tumor.
8. The method of claim 1 wherein the tumor is an esophagus and/or a stomach tumor.
9. The method of claim 1 wherein the tumor is a pancreas tumor.
10. The method of claim 1 wherein the tumor is a colorectal tumor.
11. The method of claim 1 wherein the tumor is a liver or gall bladder tumor.
12. The method of claim 1 wherein the tumor is a breast tumor.
13. The method of claim 1 wherein the tumor is a medulloblastoma.
14. The method of claim 1 wherein the tumor is a lung tumor.
15. The method of claim 1 wherein the tumor is a head and neck tumor.
16. The method of claim 1 wherein the tumor is a melanoma.
17. The method of claim 1 wherein the tumor is a sarcoma.
18. The method of claim 1 wherein the chimeric poliovirus construct is administered by intracerebral infusion with convection enhanced delivery.
19. The method of claim 1 wherein the chimeric poliovirus construct is administered directly to the tumor.
20. The method of claim 1 wherein the checkpoint inhibitor is an anti-PD-1 antibody.
21. The method of claim 1 wherein the checkpoint inhibitor is an anti-PDL-1 antibody.
22. The method of claim 1 wherein the checkpoint inhibitor is an anti-CTLA4 antibody.
23. The method of claim 1 wherein the checkpoint inhibitor is an anti-LAG-3 antibody.
24. The method of claim 1 wherein the checkpoint inhibitor is an anti-TIM-3 antibody.
25. The method of claim 1 wherein the immune checkpoint inhibitor is administered within 30 days of administering the chimeric poliovirus construct.
26. The method of claim 1 wherein the immune checkpoint inhibitor is administered within 7 days of administering the chimeric poliovirus construct.
27. The method of claim 1 wherein the chimeric poliovirus construct is PVS-RIPO.