File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence

TitleCancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence
Authors
KeywordsCancer-related cognitive impairment
CAR T cell
Chimeric antigen receptor T cell therapy
Hematologic malignancies
Immunotherapy
Neurotoxicity
Issue Date22-Mar-2025
PublisherSpringer
Citation
Supportive Care in Cancer, 2025, v. 33, n. 4 How to Cite?
Abstract

Purpose: Cancer-related cognitive impairment is one of the symptoms of neurotoxicity among patients receiving chimeric antigen receptor (CAR) T cell therapy. Evidence of the overall estimated prevalence of cancer-related cognitive impairment following CAR T-cell therapy among patients with hematologic malignancies at short-term and long-term follow-ups is lacking. This review aimed to summarize the cognitive functioning status and estimate the prevalence of cancer-related cognitive impairment at follow-up within 1 month, 1 to 12 months, and > 12 months after CAR T cell therapy. Methods: PubMed, Cochrane Library, EMBASE, CINAHL Plus, Web of Science, and PsycINFO via ProQuest from inception through August 2024. Studies that reported on cognitive impairment among patients receiving CAR T cell therapy with valid measures were included. Data on cognitive impairment prevalence were pooled using a random-effects model. Results: In total, 16 studies involving 1407 patients were included. The pooled cancer-related cognitive impairment prevalence rates assessed using neuropsychological tests at the follow-up timepoints (< 1 month, 1–12 months, and > 12 months) were 24% [95% prediction interval (PI) 16–33%], 33% (95%, PI 9–64%), and 35% (95%, PI 23–48%), respectively. The prevalence estimates assessed using other measures were ranging from 4 to 38% across different timepoints. The leave-one-out meta-analyses quantified the impact of these potential outliers on the estimation of the overall prevalence. Conclusions: The findings stress the importance of developing targeted interventions to prevent or manage cognitive impairment in cancer patients during both short-term and long-term follow-up periods. This review also highlights the need for further research in this area to improve our understanding of the disease mechanisms and implement preventive strategies for managing cancer-related cognitive impairment.


Persistent Identifierhttp://hdl.handle.net/10722/355651
ISSN
2023 Impact Factor: 2.8
2023 SCImago Journal Rankings: 1.007
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHo, Mu Hsing-
dc.contributor.authorCheung, Denise Shuk Ting-
dc.contributor.authorWang, Tongyao-
dc.contributor.authorWang, Lizhen-
dc.contributor.authorWong, Justin Wei Ho-
dc.contributor.authorLin, Chia Chin-
dc.date.accessioned2025-04-26T00:35:22Z-
dc.date.available2025-04-26T00:35:22Z-
dc.date.issued2025-03-22-
dc.identifier.citationSupportive Care in Cancer, 2025, v. 33, n. 4-
dc.identifier.issn0941-4355-
dc.identifier.urihttp://hdl.handle.net/10722/355651-
dc.description.abstract<p>Purpose: Cancer-related cognitive impairment is one of the symptoms of neurotoxicity among patients receiving chimeric antigen receptor (CAR) T cell therapy. Evidence of the overall estimated prevalence of cancer-related cognitive impairment following CAR T-cell therapy among patients with hematologic malignancies at short-term and long-term follow-ups is lacking. This review aimed to summarize the cognitive functioning status and estimate the prevalence of cancer-related cognitive impairment at follow-up within 1 month, 1 to 12 months, and > 12 months after CAR T cell therapy. Methods: PubMed, Cochrane Library, EMBASE, CINAHL Plus, Web of Science, and PsycINFO via ProQuest from inception through August 2024. Studies that reported on cognitive impairment among patients receiving CAR T cell therapy with valid measures were included. Data on cognitive impairment prevalence were pooled using a random-effects model. Results: In total, 16 studies involving 1407 patients were included. The pooled cancer-related cognitive impairment prevalence rates assessed using neuropsychological tests at the follow-up timepoints (< 1 month, 1–12 months, and > 12 months) were 24% [95% prediction interval (PI) 16–33%], 33% (95%, PI 9–64%), and 35% (95%, PI 23–48%), respectively. The prevalence estimates assessed using other measures were ranging from 4 to 38% across different timepoints. The leave-one-out meta-analyses quantified the impact of these potential outliers on the estimation of the overall prevalence. Conclusions: The findings stress the importance of developing targeted interventions to prevent or manage cognitive impairment in cancer patients during both short-term and long-term follow-up periods. This review also highlights the need for further research in this area to improve our understanding of the disease mechanisms and implement preventive strategies for managing cancer-related cognitive impairment.</p>-
dc.languageeng-
dc.publisherSpringer-
dc.relation.ispartofSupportive Care in Cancer-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCancer-related cognitive impairment-
dc.subjectCAR T cell-
dc.subjectChimeric antigen receptor T cell therapy-
dc.subjectHematologic malignancies-
dc.subjectImmunotherapy-
dc.subjectNeurotoxicity-
dc.titleCancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1007/s00520-025-09356-2-
dc.identifier.scopuseid_2-s2.0-105000809424-
dc.identifier.volume33-
dc.identifier.issue4-
dc.identifier.eissn1433-7339-
dc.identifier.isiWOS:001449817300002-
dc.identifier.issnl0941-4355-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats