Your browser doesn't support javascript.
loading
Phase IB study of ziv-aflibercept plus pembrolizumab in patients with advanced solid tumors.
Rahma, Osama E; Tyan, Kevin; Giobbie-Hurder, Anita; Brohl, Andrew S; Bedard, Philippe L; Renouf, Daniel J; Sharon, Elad; Streicher, Howard; Hathaway, Emma; Cunningham, Rachel; Manos, Michael; Severgnini, Mariano; Rodig, Scott; Stephen Hodi, F.
Afiliação
  • Rahma OE; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA osamae_rahma@dfci.harvard.edu.
  • Tyan K; Harvard Medical School, Boston, Massachusetts, USA.
  • Giobbie-Hurder A; Harvard Medical School, Boston, Massachusetts, USA.
  • Brohl AS; Division of Biostatistics, Department of Data Sciences, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Bedard PL; Sarcoma Department and Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA.
  • Renouf DJ; Division of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
  • Sharon E; Cancer and Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Streicher H; Cancer Therapy Evaluation Program, National Cancer Institute, Bethesda, Maryland, USA.
  • Hathaway E; Cancer Therapy Evaluation Program, National Cancer Institute, Bethesda, Maryland, USA.
  • Cunningham R; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Manos M; Center for Immuno-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Severgnini M; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Rodig S; Center for Immuno-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Stephen Hodi F; Center for Immuno-Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
J Immunother Cancer ; 10(3)2022 03.
Article em En | MEDLINE | ID: mdl-35264434
BACKGROUND: The combination of antiangiogenic agents with immune checkpoint inhibitors could potentially overcome immune suppression driven by tumor angiogenesis. We report results from a phase IB study of ziv-aflibercept plus pembrolizumab in patients with advanced solid tumors. METHODS: This is a multicenter phase IB dose-escalation study of the combination of ziv-aflibercept (at 2-4 mg/kg) plus pembrolizumab (at 2 mg/kg) administered intravenously every 2 weeks with expansion cohorts in programmed cell death protein 1 (PD-1)/programmed death-ligand 1(PD-L1)-naïve melanoma, renal cell carcinoma (RCC), microsatellite stable colorectal cancer (CRC), and ovarian cancer. The primary objective was to determine maximum tolerated dose (MTD) and recommended dose of the combination. Secondary endpoints included overall response rate (ORR) and overall survival (OS). Exploratory objectives included correlation of clinical efficacy with tumor and peripheral immune population densities. RESULTS: Overall, 33 patients were enrolled during dose escalation (n=3) and dose expansion (n=30). No dose-limiting toxicities were reported in the initial dose level. Ziv-aflibercept 4 mg/kg plus pembrolizumab 2 mg/kg every 2 weeks was established as the MTD. Grade ≥3 adverse events occurred in 19/33 patients (58%), the most common being hypertension (36%) and proteinuria (18%). ORR in the dose-expansion cohort was 16.7% (5/30, 90% CI 7% to 32%). Complete responses occurred in melanoma (n=2); partial responses occurred in RCC (n=1), mesothelioma (n=1), and melanoma (n=1). Median OS was as follows: melanoma, not reached (NR); RCC, 15.7 months (90% CI 2.5 to 15.7); CRC, 3.3 months (90% CI 0.6 to 3.4); ovarian, 12.5 months (90% CI 3.8 to 13.6); other solid tumors, NR. Activated tumor-infiltrating CD8 T cells at baseline (CD8+PD1+), high CD40L expression, and increased peripheral memory CD8 T cells correlated with clinical response. CONCLUSION: The combination of ziv-aflibercept and pembrolizumab demonstrated an acceptable safety profile with antitumor activity in solid tumors. The combination is currently being studied in sarcoma and anti-PD-1-resistant melanoma. TRIAL REGISTRATION NUMBER: NCT02298959.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Limite: Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article