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Phase 2 trial of tremelimumab in patients with metastatic urothelial cancer previously treated with programmed death 1/programmed death ligand 1 blockade.
Miller, Eric J; Rose, Tracy L; Maughan, Benjamin L; Milowsky, Matthew I; Bilen, Mehmet A; Carthon, Bradley C; Gao, Xin; Rapisuwon, Suthee; Zhao, Qianqian; Yu, Menggang; Agarwal, Neeraj; Galsky, Matthew D.
Afiliação
  • Miller EJ; Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai/Tisch Cancer Institute, New York, New York, USA.
  • Rose TL; Division of Oncology, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Maughan BL; Division of Hematology and Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
  • Milowsky MI; Division of Oncology, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Bilen MA; Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Carthon BC; Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.
  • Gao X; Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Rapisuwon S; Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.
  • Zhao Q; Department of Internal Medicine, Division of Hematology/Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Yu M; Division of Hematology and Medical Oncology, Georgetown Lombardi Comprehensive Cancer Center, Medstar Georgetown University Hospital, Washington, DC, USA.
  • Agarwal N; Department of Biostatistics and Medical Informatics, University of Wisconsin Carbone Cancer Center, Madison, Wisconsin, USA.
  • Galsky MD; Department of Biostatistics and Medical Informatics, University of Wisconsin Carbone Cancer Center, Madison, Wisconsin, USA.
Cancer ; 130(9): 1642-1649, 2024 May 01.
Article em En | MEDLINE | ID: mdl-38180804
ABSTRACT

INTRODUCTION:

Programmed 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.

METHODS:

The 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.

RESULTS:

Twenty-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.

CONCLUSIONS:

High 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células de Transição / Anticorpos Monoclonais Humanizados / Antígeno B7-H1 Limite: Humans Idioma: En Revista: Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células de Transição / Anticorpos Monoclonais Humanizados / Antígeno B7-H1 Limite: Humans Idioma: En Revista: Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos