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Prolonged haematologic toxicity in CAR-T-cell therapy: A review

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WILEY
DOI: 10.1111/jcmm.17930

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CAR-T-cell therapy; management; mechanism; prolonged haematologic toxicity

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Chimeric antigen receptor-T-cell (CAR-T-cell) therapy is a promising immunotherapy for relapsed/refractory haematologic malignancies, but prolonged haematologic toxicity (PHT) is a common yet underestimated side effect. The incidence, risk factors, and management of PHT vary across studies due to heterogeneity in populations, CAR-T cells used, diseases treated, and definitions of PHT. This review aims to provide narrative and evidence-based insights into PHT following CAR-T-cell therapy to enhance systematic understanding and treatment strategies.
Chimeric antigen receptor-T-cell (CAR-T-cell) therapy is a novel immunotherapy with encouraging results for treatment of relapsed/refractory haematologic malignancies. With increasing use, our understanding of immune-mediated side effects such as cytokine release syndrome and neurotoxicity has improved; nevertheless, prolonged haematologic toxicity (PHT), with a high incidence rate, remains underrecognized. Owing to heterogeneity in populations, the CAR-T cells used and diseases treated as well as differences in the definition of PHT, its rate, risk factors and management vary across studies. In this review, we provide a narrative of PHT occurring in patients following CAR-T-cell therapy; evidence of PHT treatment strategies is also presented, with the aim of contributing to systematic understanding of PHT.

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