Phase 2 trial of tremelimumab in patients with metastatic urothelial cancer previously treated with programmed death 1/programmed death ligand 1 blockade

Author:

Miller Eric J.1ORCID,Rose Tracy L.2,Maughan Benjamin L.3ORCID,Milowsky Matthew I.2ORCID,Bilen Mehmet A.45ORCID,Carthon Bradley C.45,Gao Xin6,Rapisuwon Suthee7,Zhao Qianqian8,Yu Menggang8,Agarwal Neeraj3,Galsky Matthew D.1

Affiliation:

1. Division of Hematology and Medical Oncology Icahn School of Medicine at Mount Sinai/Tisch Cancer Institute New York New York USA

2. Division of Oncology University of North Carolina Chapel Hill North Carolina USA

3. Division of Hematology and Medical Oncology Huntsman Cancer Institute University of Utah Salt Lake City Utah USA

4. Department of Hematology and Medical Oncology Emory University School of Medicine Atlanta Georgia USA

5. Winship Cancer Institute of Emory University Atlanta Georgia USA

6. Department of Internal Medicine Division of Hematology/Oncology Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA

7. Division of Hematology and Medical Oncology Georgetown Lombardi Comprehensive Cancer Center Medstar Georgetown University Hospital Washington DC USA

8. Department of Biostatistics and Medical Informatics University of Wisconsin Carbone Cancer Center Madison Wisconsin USA

Abstract

AbstractIntroductionProgrammed death 1 (PD‐1)/programmed death ligand 1 (PD‐L1) blockade has changed the landscape of treatment for metastatic urothelial cancer, but single‐agent cytotoxic T‐lymphocyte–associated protein 4 (CTLA‐4) blockade in metastatic urothelial cancer has been underexplored. A prior phase 2 trial of tremelimumab in PD‐1/PD‐L1–blockade naive patients with metastatic urothelial cancer revealed activity comparable to that observed with PD‐1/PD‐L1 blockade raising the hypothesis that these classes of immune checkpoint inhibitors might be non‐cross‐resistant.MethodsThe current phase 2 trial treated patients with PD‐1/PD‐L1 blockade‐resistant metastatic urothelial cancer with single‐agent tremelimumab (750 mg intravenously every 28 days for up to 7 cycles). The primary end point was objective response rate.ResultsTwenty‐six patients were enrolled and 24 patients were evaluable for response. The objective response rate was 8.3%, composed of a total of two partial responses that lasted 10.9 and 24.0 months. Stable disease was observed in another 20.8% of patients, with a median duration of stable disease of 5.4 months. Diarrhea occurred in 15 patients (58%), elevated hepatic transaminases occurred in seven patients (27%), and adrenal insufficiency occurred in two patients (8%); one patient died after experiencing immune‐related hepatitis.ConclusionsHigh dose CTLA‐4 blockade in patients with PD‐1/PD‐L1–resistant metastatic urothelial cancer has modest activity and is associated with treatment‐related toxicity similar to prior reports.

Publisher

Wiley

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