Methods for treating cancer using anti-PD-1 antibodies
US-9492540-B2 · Nov 15, 2016 · US
US10138299B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10138299-B2 |
| Application number | US-201816006473-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 12, 2018 |
| Priority date | May 15, 2012 |
| Publication date | Nov 27, 2018 |
| Grant date | Nov 27, 2018 |
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The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
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What is claimed is: 1. A method of treating a tumor in a human subject in need thereof, comprising administering to the subject about 10 mg/kg of an anti-PD-L1 antibody every 2 weeks, wherein the anti-PD-L1 antibody is administered intravenously over 60 minutes infusion; wherein the tumor is derived from a bladder cancer of; and wherein the tumor is refractory to a platinum based chemotherapy. 2. The method of claim 1 , wherein the tumor is advanced. 3. The method of claim 1 , wherein the tumor is locally advanced. 4. The method of claim 1 , wherein the tumor is metastatic. 5. The method of claim 1 , wherein the treatment lasts more than 12 weeks. 6. The method of claim 1 , wherein the anti-PD-L1 antibody is formulated in a pharmaceutical composition. 7. The method of claim 6 , wherein the pharmaceutical composition further comprises a pharmaceutically acceptable salt, an anti-oxidant, an aqueous carrier, a non-aqueous carrier, or any combination thereof. 8. The method of claim 7 , wherein the salt comprises a sodium salt. 9. The method of claim 7 , wherein the salt comprises sodium chloride. 10. The method of claim 1 , wherein at least 1% of tumor cells exhibit membrane PD-L1 expression. 11. The method of claim 1 , wherein at least 5% of tumor cells exhibit membrane PD-L1 expression. 12. The method of claim 1 , further comprising administering an anti-cancer agent. 13. The method of claim 2 , further comprising administering an anti-cancer agent. 14. The method of claim 3 , further comprising administering an anti-cancer agent. 15. The method of claim 4 , further comprising administering an anti-cancer agent. 16. The method of claim 15 , further comprising administering an anti-cancer agent. 17. The method of claim 12 , wherein the anti-cancer agent is a chemotherapy. 18. The method of claim 12 , wherein the anti-cancer agent is a radiotherapy. 19. The method of claim 13 , wherein the anti-cancer agent is a chemotherapy. 20. The method of claim 13 , wherein the anti-cancer agent is a radiotherapy. 21. The method of claim 14 , wherein the anti-cancer agent is a chemotherapy. 22. The method of claim 14 , wherein the anti-cancer agent is a radiotherapy. 23. The method of claim 1 , wherein the platinum-based chemotherapy is a platinum-based doublet chemotherapy. 24. The method of claim 1 , wherein the platinum-based chemotherapy comprises cisplatin, carboplatin, or both. 25. The method of claims 1 , wherein the subject is administered an antihistamine prior to the anti-PD-L1 antibody.
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