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Multicenter phase II trial (SWOG S1609, cohort 51) of ipilimumab and nivolumab in metastatic or unresectable angiosarcoma: a substudy of dual anti-CTLA-4 and anti-PD-1 blockade in rare tumors (DART).
Wagner, Michael J; Othus, Megan; Patel, Sandip P; Ryan, Chris; Sangal, Ashish; Powers, Benjamin; Budd, G Thomas; Victor, Adrienne I; Hsueh, Chung-Tsen; Chugh, Rashmi; Nair, Suresh; Leu, Kirsten M; Agulnik, Mark; Sharon, Elad; Mayerson, Edward; Plets, Melissa; Blanke, Charles; Streicher, Howard; Chae, Young Kwang; Kurzrock, Razelle.
Afiliação
  • Wagner MJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA wagnermj@uw.edu.
  • Othus M; Medical Oncology, University of Washington, Seattle, Washington, USA.
  • Patel SP; SWOG Statistical and Data Management Center/Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Ryan C; Department of Medicine, UCSD Moores Cancer Center, La Jolla, California, USA.
  • Sangal A; Department of Medicine, OHSU, Portland, Oregon, USA.
  • Powers B; Western Regional Medical Center, Goodyear, Arizona, USA.
  • Budd GT; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, Kansas, USA.
  • Victor AI; Hematology and Medical Oncology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Hsueh CT; Department of Medicine, University of Rochester, Rochester, New York, USA.
  • Chugh R; Loma Linda University, Loma Linda, California, USA.
  • Nair S; Department of Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Leu KM; Lehigh Valley Health Network, Allentown, Pennsylvania, USA.
  • Agulnik M; Nebraska Methodist Health System, Omaha, Nebraska, USA.
  • Sharon E; Medical Oncology & Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, California, USA.
  • Mayerson E; Department of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Plets M; Cancer Therapy Evaluation Program, National Cancer Institute, Bethesda, Maryland, USA.
  • Blanke C; SWOG Statistical and Data Management Center/Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Streicher H; SWOG Statistical and Data Management Center/Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Chae YK; Department of Medicine, OHSU, Portland, Oregon, USA.
  • Kurzrock R; SWOG, Portland, Oregon, USA.
J Immunother Cancer ; 9(8)2021 08.
Article em En | MEDLINE | ID: mdl-34380663
ABSTRACT

PURPOSE:

Angiosarcoma is a rare aggressive endothelial cell cancer with high mortality. Isolated reports suggest immune checkpoint inhibition efficacy in angiosarcoma, but no prospective studies have been published. We report results for angiosarcoma treated with ipilimumab and nivolumab as a cohort of an ongoing rare cancer study.

METHODS:

This is a prospective, open-label, multicenter phase II clinical trial of ipilimumab (1 mg/kg intravenously every 6 weeks) plus nivolumab (240 mg intravenously every 2 weeks) for metastatic or unresectable angiosarcoma. Primary endpoint was objective response rate (ORR) per RECIST 1.1. Secondary endpoints include progression-free (PFS) and overall survival, and toxicity. A two-stage design was used.

RESULTS:

Overall, there were 16 evaluable patients. Median age was 68 years (range, 25-81); median number of prior lines of therapy, 2. Nine patients had cutaneous and seven non-cutaneous primary tumors. ORR was 25% (4/16). Sixty per cent of patients (3/5) with primary cutaneous scalp or face tumors attained a confirmed response. Six-month PFS was 38%. Altogether, 75% of patients experienced an adverse event (AE) (at least possibly related to drug) (25% grade 3-4 AE); 68.8%, an immune-related AE (irAE) (2 (12.5%), grade 3 or 4 irAEs (alanine aminotransferase/aspartate aminotransferase increase and diarrhea)). There were no grade 5 toxicities. One of seven patients in whom tumor mutation burden (TMB) was assessed showed a high TMB (24 mutations/mb); that patient achieved a partial response (PR). Two of three patients with PDL1 immunohistochemistry assessed had high PDL1 expression; one achieved a PR.

CONCLUSION:

The combination of ipilimumab and nivolumab demonstrated an ORR of 25% in angiosarcoma, with three of five patients with cutaneous tumors of the scalp or face responding. Ipilimumab and nivolumab warrant further investigation in angiosarcoma. TRIAL REGISTRATION NUMBER NCT02834013.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Doenças Raras / Antígeno CTLA-4 / Hemangiossarcoma Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Immunother Cancer Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Doenças Raras / Antígeno CTLA-4 / Hemangiossarcoma Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Immunother Cancer Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos