Neuropsychiatric manifestations following chimeric antigen receptor T cell therapy for cancer: a systematic review of clinical outcomes and management strategies
Нейропсихиатрические проявления после терапии рака Т-клетками с химерным антигенным рецептором: систематический обзор клинических исходов и стратегий лечения
2024-12-01
SCID: 54.1/fay3pjpb
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CAR-T cell therapyimmune effector cell-associated neurotoxicity syndromeneuropsychological symptomsneurotoxicitysystematic review
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Abstract (AI)
BACKGROUND: Chimeric antigen receptor (CAR)-T cell therapy has emerged as a transformative modality in the treatment of patients with cancer. However, it is increasingly evident that this therapeutic approach is not without its challenges. The unique nature of CAR-T cells as living drugs introduces a distinct set of side effects. As the application of CAR-T cell therapy expands to treat a broader range of diseases, it becomes increasingly important to devise effective strategies for handling the associated toxicities. Challenges in treating patients with CAR-T cells include addressing complications such as cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, and cytopenias. This comprehensive review seeks to systematically identify, categorize and elucidate all previously described neurological and psychological side effects associated with CAR-T cell therapy, shedding light on the pertinent laboratory findings that underscore these phenomena. METHODS: PubMed, Springer Link, and ScienceDirect were systematically searched for empirical studies on adult patients with cancer receiving CAR-T cell therapy for hemato-oncological malignancies. Quality assessment was conducted using Version 2 of the Cochrane risk-of-bias tool (RoB 2) for randomized trials and adherence to the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) checklist for observational studies. The synthesis of findings was conducted via a narrative approach, consolidating the diverse array of data into a coherent framework. RESULTS: From an initial pool of 2,276 citations, 546 studies met the inclusion criteria, exhibiting a rich tapestry of heterogeneity in terms of study characteristics and patient samples. The incidence of neuropsychological symptoms varied notably across different CAR-T cell products and hematological malignancies. Among the most frequently reported neuropsychological symptoms were aphasia, attention deficits, impaired consciousness, and disorientation, alongside a constellation of other symptoms including confusion, cognitive impairment, memory loss, writing difficulties, fatigue, headache, agitation, tremor, seizures, and psychomotor retardation. Early intervention strategies, including corticosteroids and tocilizumab, have shown the potential to reduce the intensity of neuropsychological symptoms and prevent their progression to critical complications. CONCLUSION: These insights underscore the imperative of extending neuropsychological assessments beyond the conventional Immune Effector Cell-Associated Encephalopathy score framework.
Key Findings
1
Frequently reported manifestations included aphasia, attention deficits, and impaired consciousness, alongside recognized immune effector cell-associated neurotoxicity.
2
Included studies showed substantial heterogeneity in study designs, patient samples, and reported outcomes, complicating direct comparisons across CAR-T therapies.
3
Reported neuropsychological symptom incidence varied substantially according to CAR-T cell product and underlying hematological malignancy.
4
The review synthesized neurological and psychological adverse effects together with pertinent laboratory findings and management strategies using a narrative approach.
5
The systematic review identified 546 eligible studies from 2,276 citations examining neuropsychiatric outcomes after CAR-T therapy in adults with hematological cancers.
Research Object
Adult patients with cancer receiving chimeric antigen receptor (CAR)-T cell therapy for hematologic malignancies
Research Subject
Neurological and psychological adverse effects, associated laboratory findings, and their clinical management following CAR-T cell therapy
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2024-12-01
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