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Beyond the storm - subacute toxicities and late effects in children receiving CAR T cells.
Shalabi, Haneen; Gust, Juliane; Taraseviciute, Agne; Wolters, Pamela L; Leahy, Allison B; Sandi, Carlos; Laetsch, Theodore W; Wiener, Lori; Gardner, Rebecca A; Nussenblatt, Veronique; Hill, Joshua A; Curran, Kevin J; Olson, Timothy S; Annesley, Colleen; Wang, Hao-Wei; Khan, Javed; Pasquini, Marcelo C; Duncan, Christine N; Grupp, Stephan A; Pulsipher, Michael A; Shah, Nirali N.
Afiliación
  • Shalabi H; Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
  • Gust J; Seattle Children's Research Institute, Seattle, WA, USA.
  • Taraseviciute A; Department of Pediatrics, University of Washington Seattle, Seattle, WA, USA.
  • Wolters PL; Cancer and Blood Disease Institute, Children's Hospital Los Angeles, Los Angeles, CA, USA.
  • Leahy AB; Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
  • Sandi C; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Laetsch TW; Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
  • Wiener L; St. Baldrick's Foundation, Monrovia, CA, USA.
  • Gardner RA; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Nussenblatt V; Department of Pediatrics and Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
  • Hill JA; Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
  • Curran KJ; Seattle Children's Research Institute, Seattle, WA, USA.
  • Olson TS; Department of Pediatrics, University of Washington Seattle, Seattle, WA, USA.
  • Annesley C; National Institute of Allergy and Infectious Disease, Clinical Center, NIH, Bethesda, MD, USA.
  • Wang HW; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Khan J; Department of Medicine, University of Washington, Seattle, WA, USA.
  • Pasquini MC; Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Duncan CN; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Grupp SA; Seattle Children's Research Institute, Seattle, WA, USA.
  • Pulsipher MA; Department of Pediatrics, University of Washington Seattle, Seattle, WA, USA.
  • Shah NN; Laboratory of Pathology, NCI, NIH, Bethesda, MD, USA.
Nat Rev Clin Oncol ; 18(6): 363-378, 2021 06.
Article en En | MEDLINE | ID: mdl-33495553
ABSTRACT
As clinical advances with chimeric antigen receptor (CAR) T cells are increasingly described and the potential for extending their therapeutic benefit grows, optimizing the implementation of this therapeutic modality is imperative. The recognition and management of cytokine release syndrome (CRS) marked a milestone in this field; however, beyond the understanding gained in treating CRS, a host of additional toxicities and/or potential late effects of CAR T cell therapy warrant further investigation. A multicentre initiative involving experts in paediatric cell therapy, supportive care and/or study of late effects from cancer and haematopoietic stem cell transplantation was convened to facilitate the comprehensive study of extended CAR T cell-mediated toxicities and establish a framework for new systematic investigations of CAR T cell-related adverse events. Together, this group identified six key focus areas extended monitoring of neurotoxicity and neurocognitive function, psychosocial considerations, infection and immune reconstitution, other end organ toxicities, evaluation of subsequent neoplasms, and strategies to optimize remission durability. Herein, we present the current understanding, gaps in knowledge and future directions of research addressing these CAR T cell-related outcomes. This systematic framework to study extended toxicities and optimization strategies will facilitate the translation of acquired experience and knowledge for optimal application of CAR T cell therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoterapia Adoptiva / Neoplasias Tipo de estudio: Etiology_studies Límite: Child / Humans Idioma: En Revista: Nat Rev Clin Oncol Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoterapia Adoptiva / Neoplasias Tipo de estudio: Etiology_studies Límite: Child / Humans Idioma: En Revista: Nat Rev Clin Oncol Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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