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Immune adverse events (irAEs) with adjuvant ipilimumab in melanoma, use of immunosuppressants and association with outcome: ECOG-ACRIN E1609 study analysis.
Tarhini, Ahmad A; Kang, Ni; Lee, Sandra J; Hodi, F Stephen; Cohen, Gary I; Hamid, Omid; Hutchins, Laura F; Sosman, Jeffrey A; Kluger, Harriet M; Eroglu, Zeynep; Koon, Henry B; Lawrence, Donald P; Kendra, Kari L; Minor, David R; Lee, Carrie B; Albertini, Mark R; Flaherty, Lawrence E; Petrella, Teresa M; Streicher, Howard; Sondak, Vernon K; Kirkwood, John M.
Afiliação
  • Tarhini AA; Departments of Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Center Inc, Tampa, Florida, USA ahmad.tarhini@moffitt.org.
  • Kang N; Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts, USA.
  • Lee SJ; Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts, USA.
  • Hodi FS; Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Cohen GI; Greater Baltimore Medical Center, Baltimore, Maryland, USA.
  • Hamid O; The Angeles Clinic & Research Institute, A Cedars Sinai Affiliate, Los Angeles, California, USA.
  • Hutchins LF; Department of Medicine, University of Arkansas for Medical Sciences (UAMS), Little Rock, Arkansas, USA.
  • Sosman JA; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, USA.
  • Kluger HM; Department of Medicine, Yale University, New Haven, Connecticut, USA.
  • Eroglu Z; Departments of Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Center Inc, Tampa, Florida, USA.
  • Koon HB; Case Western Reserve University, Cleveland, Ohio, USA.
  • Lawrence DP; Massachusetts General Hospital, Boston, MA, USA.
  • Kendra KL; Ohio State University, Columbus, OH, USA.
  • Minor DR; Sutter-California Pacific Medical Center, San Francisco, California, USA.
  • Lee CB; University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Albertini MR; University of Wisconsin, Madison, Wisconsin, USA.
  • Flaherty LE; Wayne State University and Karmanos Cancer Institute, Detroit, Michigan, USA.
  • Petrella TM; Odette Cancer Center, Toronta, Ontario, Canada.
  • Streicher H; National Cancer Institute, Rockville, MD, USA.
  • Sondak VK; Departments of Cutaneous Oncology and Immunology, H. Lee Moffitt Cancer Center and Research Center Inc, Tampa, Florida, USA.
  • Kirkwood JM; UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
J Immunother Cancer ; 9(5)2021 05.
Article em En | MEDLINE | ID: mdl-33963015
ABSTRACT

BACKGROUND:

The impact of immune-related adverse events (irAEs) occurring from adjuvant use of immunotherapy and of their management on relapse-free survival (RFS) and overall survival (OS) outcomes is currently not well understood. PATIENTS AND

METHODS:

E1609 enrolled 1673 patients with resected high-risk melanoma and evaluated adjuvant ipilimumab 3 mg/kg (ipi3) and 10 mg/kg (ipi10) versus interferon-α. We investigated the association of irAEs and of use of immunosuppressants with RFS and OS for patients treated with ipilimumab (n=1034).

RESULTS:

Occurrence of grades 1-2 irAEs was associated with RFS (5 years 52% (95% CI 47% to 56%) vs 41% (95% CI 31% to 50%) with no AE; p=0.006) and a trend toward improved OS (5 years 75% (95% CI 71% to 79%) compared with 67% (95% CI 56% to 75%) with no AE; p=0.064). Among specific irAEs, grades 1-2 rash was most significantly associated with RFS (p=0.002) and OS (p=0.003). In multivariate models adjusting for prognostic factors, the most significant associations were seen for grades 1-2 rash with RFS (p<0.001, HR=0.70) and OS (p=0.01, HR=0.71) and for grades 1-2 endocrine+rash with RFS (p<0.001, HR=0.66) and OS (p=0.008, HR=0.7). Overall, grades 1-2 irAEs had the best prognosis in terms of RFS and OS and those with grades 3-4 had less RFS benefits and no OS advantage over no irAE. Patients experiencing grades 3-4 irAE had significantly higher exposure to corticosteroids and immunosuppressants than those with grades 1-2 (92% vs 60%; p<0.001), but no significant associations were found between corticosteroid and immunosuppressant use and RFS or OS. In investigating the impact of non-corticosteroid immunosuppressants, although there were trends toward better RFS and OS favoring cases who were not exposed, no significant associations were found.

CONCLUSIONS:

Rash and endocrine irAEs were independent prognostic factors of RFS and OS in patients treated with adjuvant ipilimumab. Patients experiencing lower grade irAEs derived the most benefit, but we found no significant evidence supporting a negative impact of high dose corticosteroids and immunosuppressants more commonly used to manage grades 3-4 irAEs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Adjuvantes Imunológicos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Ipilimumab / Inibidores de Checkpoint Imunológico / Imunossupressores / Melanoma Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / 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: Neoplasias Cutâneas / Adjuvantes Imunológicos / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Ipilimumab / Inibidores de Checkpoint Imunológico / Imunossupressores / Melanoma Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / 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