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Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immunotherapy for the treatment of melanoma, version 3.0.
Pavlick, Anna C; Ariyan, Charlotte E; Buchbinder, Elizabeth I; Davar, Diwakar; Gibney, Geoffrey T; Hamid, Omid; Hieken, Tina J; Izar, Benjamin; Johnson, Douglas B; Kulkarni, Rajan P; Luke, Jason J; Mitchell, Tara C; Mooradian, Meghan J; Rubin, Krista M; Salama, April Ks; Shirai, Keisuke; Taube, Janis M; Tawbi, Hussein A; Tolley, J Keith; Valdueza, Caressa; Weiss, Sarah A; Wong, Michael K; Sullivan, Ryan J.
Afiliação
  • Pavlick AC; Weill Cornell Medicine, New York, New York, USA acp9008@med.cornell.edu.
  • Ariyan CE; Department of Surgery Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Buchbinder EI; Melanoma Disease Center, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
  • Davar D; Hillman Cancer Center, University of Pittsburg Medical Center, Pittsburgh, Pennsylvania, USA.
  • Gibney GT; Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington, District of Columbia, USA.
  • Hamid O; The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate, Los Angeles, California, USA.
  • Hieken TJ; Department of Surgery and Comprehensive Cancer Center, Mayo Clinic, Rochester, Minnesota, USA.
  • Izar B; Department of Medicine, Division of Hematology/Oncology, Columbia University Medical Center, New York, New York, USA.
  • Johnson DB; Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Kulkarni RP; Departments of Dermatology, Oncological Sciences, Biomedical Engineering, and Center for Cancer Early Detection Advanced Research, Knight Cancer Institute, OHSU, Portland, Oregon, USA.
  • Luke JJ; Operative Care Division, VA Portland Health Care System (VAPORHCS), Portland, Oregon, USA.
  • Mitchell TC; Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Mooradian MJ; Abramson Cancer Center, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Rubin KM; Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Salama AK; Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Shirai K; Department of Medicine, Division of Medical Oncology, Duke University, Durham, Carolina, USA.
  • Taube JM; Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Tawbi HA; Department of Dermatology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Tolley JK; Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Valdueza C; Patient Advocate, Melanoma Research Alliance, Washington, DC, USA.
  • Weiss SA; Cutaneous Oncology Program, Weill Cornell Medicine, New York, New York, USA.
  • Wong MK; Department of Medical Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
  • Sullivan RJ; Patient Advocate, Melanoma Research Alliance, Washington, DC, USA.
J Immunother Cancer ; 11(10)2023 10.
Article em En | MEDLINE | ID: mdl-37852736
ABSTRACT
Since the first approval for immune checkpoint inhibitors (ICIs) for the treatment of cutaneous melanoma more than a decade ago, immunotherapy has completely transformed the treatment landscape of this chemotherapy-resistant disease. Combination regimens including ICIs directed against programmed cell death protein 1 (PD-1) with anti-cytotoxic T lymphocyte antigen-4 (CTLA-4) agents or, more recently, anti-lymphocyte-activation gene 3 (LAG-3) agents, have gained regulatory approvals for the treatment of metastatic cutaneous melanoma, with long-term follow-up data suggesting the possibility of cure for some patients with advanced disease. In the resectable setting, adjuvant ICIs prolong recurrence-free survival, and neoadjuvant strategies are an active area of investigation. Other immunotherapy strategies, such as oncolytic virotherapy for injectable cutaneous melanoma and bispecific T-cell engager therapy for HLA-A*0201 genotype-positive uveal melanoma, are also available to patients. Despite the remarkable efficacy of these regimens for many patients with cutaneous melanoma, traditional immunotherapy biomarkers (ie, programmed death-ligand 1 expression, tumor mutational burden, T-cell infiltrate and/or microsatellite stability) have failed to reliably predict response. Furthermore, ICIs are associated with unique toxicity profiles, particularly for the highly active combination of anti-PD-1 plus anti-CTLA-4 agents. The Society for Immunotherapy of Cancer (SITC) convened a panel of experts to develop this clinical practice guideline on immunotherapy for the treatment of melanoma, including rare subtypes of the disease (eg, uveal, mucosal), with the goal of improving patient care by providing guidance to the oncology community. Drawing from published data and clinical experience, the Expert Panel developed evidence- and consensus-based recommendations for healthcare professionals using immunotherapy to treat melanoma, with topics including therapy selection in the advanced and perioperative settings, intratumoral immunotherapy, when to use immunotherapy for patients with BRAFV600-mutated disease, management of patients with brain metastases, evaluation of treatment response, special patient populations, patient education, quality of life, and survivorship, among others.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos