Diagnosis, grading and management of toxicities from immunotherapies in children, adolescents and young adults with cancer

医学 嵌合抗原受体 癌症 临床试验 细胞因子释放综合征 肿瘤科 内科学 免疫疗法 移植 造血干细胞移植 癌症免疫疗法 重症监护医学
作者
Dristhi Ragoonanan,Sajad Khazal,Hisham Abdel‐Azim,David McCall,Branko Cuglievan,Francesco Paolo Tambaro,Ali Ahmad,Courtney M. Rowan,Cristina Gutiérrez,Keri Schadler,Shulin Li,Matteo Di Nardo,Linda Chi,Alison Gulbis,Basirat Shoberu,Maria E. Mireles,Jennifer McArthur,Neena Kapoor,Jeffrey D. Miller,Julie C. Fitzgerald
出处
期刊:Nature Reviews Clinical Oncology [Nature Portfolio]
卷期号:18 (7): 435-453 被引量:43
标识
DOI:10.1038/s41571-021-00474-4
摘要

Cancer immunotherapies are associated with remarkable therapeutic response rates but also with unique and severe toxicities, which potentially result in rapid deterioration in health. The number of clinical applications for novel immune effector-cell therapies, including chimeric antigen receptor (CAR)-expressing cells, and other immunotherapies, such as immune-checkpoint inhibitors, is increasing. In this Consensus Statement, members of the Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network Hematopoietic Cell Transplantation-Cancer Immunotherapy (HCT-CI) Subgroup, Paediatric Diseases Working Party (PDWP) of the European Society of Blood and Marrow Transplantation (EBMT), Supportive Care Committee of the Pediatric Transplantation and Cellular Therapy Consortium (PTCTC) and MD Anderson Cancer Center CAR T Cell Therapy-Associated Toxicity (CARTOX) Program collaborated to provide updated comprehensive recommendations for the care of children, adolescents and young adults receiving cancer immunotherapies. With these recommendations, we address emerging toxicity mitigation strategies, we advocate for the characterization of baseline organ function according to age and discipline-specific criteria, we recommend early critical care assessment when indicated, with consideration of reversibility of underlying pathology (instead of organ failure scores) to guide critical care interventions, and we call for researchers, regulatory agencies and sponsors to support and facilitate early inclusion of young patients with cancer in well-designed clinical trials.

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