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Considerations for treatment duration in responders to immune checkpoint inhibitors.
Marron, Thomas U; Ryan, Aideen E; Reddy, Sangeetha M; Kaczanowska, Sabina; Younis, Rania H; Thakkar, Dipti; Zhang, Jiajia; Bartkowiak, Todd; Howard, Rachel; Anderson, Kristin G; Olson, Daniel; Naqash, Abdul Rafeh; Patel, Ravi B; Sachdev, Esha; Rodriguez-Ruiz, Maria E; Sheffer, Michal; Church, Sarah; Fuhrman, Christopher; Overacre-Delgoffe, Abigail; Nguyen, Rosa; Florou, Vaia; Thaxton, Jessica E; Aggen, David H; Guerriero, Jennifer L.
Afiliação
  • Marron TU; Department of Medicine, Division of Hematology Oncology, Mount Sinai School of Medicine, New York, New York, USA.
  • Ryan AE; Discipline of Pharmacology & Therapeutics, Lambe Institute for Translational Medicine, National University of Ireland, Galway, Ireland.
  • Reddy SM; The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Kaczanowska S; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Younis RH; Department of Oncology and Diagnostic Sciences, School of Dentistry, and the Tumor Immunology and Immunotherapy Division UMGBCCC, University of Maryland, Baltimore, Maryland, USA.
  • Thakkar D; Department of Oral Pathology, Faculty of Dentistry, Alexandria University, Alexandria, Egypt.
  • Zhang J; Department of Pharmacology, Hummingbird Bioscience, Singapore.
  • Bartkowiak T; Bloomberg Kimmel Institute for Cancer Immunotherapy, Johns Hopkins, Baltimore, Maryland, USA.
  • Howard R; Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee, USA.
  • Anderson KG; Health Informatics, H Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
  • Olson D; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Naqash AR; Department of Immunology, University of Washington, Seattle, WA, USA.
  • Patel RB; Department of Medicine, The University of Chicago Comprehensive Cancer Center, Chicago, Illinois, USA.
  • Sachdev E; Division of Cancer Treatment And Diagnosis, National Cancer Institute, Bethesda, Maryland, USA.
  • Rodriguez-Ruiz ME; Department of Radiation Oncology, University of Pittsburgh Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
  • Sheffer M; Department of Medicine, Division of Oncology, University of Southern California, Los Angeles, California, USA.
  • Church S; Radiation Oncology, Clinica Universidad de Navarra Departamento de Oncologia Medica, Pamplona, Spain.
  • Fuhrman C; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Overacre-Delgoffe A; Transitional Sciences, NanoString Technologies Inc, Seattle, Washington, USA.
  • Nguyen R; Transitional Sciences, NanoString Technologies Inc, Seattle, Washington, USA.
  • Florou V; Department of Immunology, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Thaxton JE; Pediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
  • Aggen DH; Internal Medicine, Huntsman Cancer Institute, Salt Lake City, Utah, USA.
  • Guerriero JL; Department of Orthopedics and Physical Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
J Immunother Cancer ; 9(3)2021 03.
Article em En | MEDLINE | ID: mdl-33653801
ABSTRACT
Immune checkpoint inhibitors (ICIs) have improved overall survival for cancer patients, however, optimal duration of ICI therapy has yet to be defined. Given ICIs were first used to treat patients with metastatic melanoma, a condition that at the time was incurable, little attention was initially paid to how much therapy would be needed for a durable response. As the early immunotherapy trials have matured past 10 years, a significant per cent of patients have demonstrated durable responses; it is now time to determine whether patients have been overtreated, and if durable remissions can still be achieved with less therapy, limiting the physical and financial toxicity associated with years of treatment. Well-designed trials are needed to identify optimal duration of therapy, and to define biomarkers to predict who would benefit from shorter courses of immunotherapy. Here, we outline key questions related to health, financial and societal toxicities of over treating with ICI and present four unique clinical trials aimed at exposing criteria for early cessation of ICI. Taken together, there is a serious liability to overtreating patients with ICI and future work is warranted to determine when it is safe to stop ICI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article