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Article: Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence
| Title | Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence |
|---|---|
| Authors | |
| Keywords | Cancer-related cognitive impairment CAR T cell Chimeric antigen receptor T cell therapy Hematologic malignancies Immunotherapy Neurotoxicity |
| Issue Date | 22-Mar-2025 |
| Publisher | Springer |
| 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 Identifier | http://hdl.handle.net/10722/355651 |
| ISSN | 2023 Impact Factor: 2.8 2023 SCImago Journal Rankings: 1.007 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ho, Mu Hsing | - |
| dc.contributor.author | Cheung, Denise Shuk Ting | - |
| dc.contributor.author | Wang, Tongyao | - |
| dc.contributor.author | Wang, Lizhen | - |
| dc.contributor.author | Wong, Justin Wei Ho | - |
| dc.contributor.author | Lin, Chia Chin | - |
| dc.date.accessioned | 2025-04-26T00:35:22Z | - |
| dc.date.available | 2025-04-26T00:35:22Z | - |
| dc.date.issued | 2025-03-22 | - |
| dc.identifier.citation | Supportive Care in Cancer, 2025, v. 33, n. 4 | - |
| dc.identifier.issn | 0941-4355 | - |
| dc.identifier.uri | http://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.language | eng | - |
| dc.publisher | Springer | - |
| dc.relation.ispartof | Supportive Care in Cancer | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.subject | Cancer-related cognitive impairment | - |
| dc.subject | CAR T cell | - |
| dc.subject | Chimeric antigen receptor T cell therapy | - |
| dc.subject | Hematologic malignancies | - |
| dc.subject | Immunotherapy | - |
| dc.subject | Neurotoxicity | - |
| dc.title | Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence | - |
| dc.type | Article | - |
| dc.description.nature | published_or_final_version | - |
| dc.identifier.doi | 10.1007/s00520-025-09356-2 | - |
| dc.identifier.scopus | eid_2-s2.0-105000809424 | - |
| dc.identifier.volume | 33 | - |
| dc.identifier.issue | 4 | - |
| dc.identifier.eissn | 1433-7339 | - |
| dc.identifier.isi | WOS:001449817300002 | - |
| dc.identifier.issnl | 0941-4355 | - |
