Abstract 58P
Background
Chimeric Antigen Receptor T-cell (CAR-T) therapies have revolutionized the treatment of certain hematologic malignancies. Despite their efficacy, these therapies are associated with significant adverse effects, including cardiotoxicity. Understanding the incidence, risk factors, and management strategies for CAR-T therapy-related cardiotoxicity is crucial for optimizing patient outcomes and improving safety profiles.
Methods
A systematic review and meta-analysis were conducted by searching PubMed, Embase, and Cochrane databases for studies published up to June 2024 that reported on cardiovascular outcomes in patients undergoing CAR-T therapy. Inclusion criteria were studies that provided detailed information on the incidence of cardiotoxic events, associated risk factors, and management strategies. Data were extracted independently by two reviewers and pooled using random-effects models to account for heterogeneity among studies. Subgroup analyses were performed to identify specific risk factors and effective management approaches.
Results
A total of 25 studies comprising 3,500 patients were included in the meta-analysis. The pooled incidence of cardiotoxic events among CAR-T therapy recipients was 18% (95% CI: 12%-25%). The most common cardiovascular complications were heart failure (10%), arrhythmias (6%), and myocardial infarction (2%). Risk factors significantly associated with increased cardiotoxicity included pre-existing cardiovascular disease (OR: 3.5, 95% CI: 2.1-5.8), older age (OR: 2.0, 95% CI: 1.3-3.2), and higher doses of CAR-T cells (OR: 1.8, 95% CI: 1.1-3.0). Effective management strategies identified included the use of beta-blockers, ACE inhibitors, and careful monitoring of cardiac function throughout the treatment course.
Conclusions
CAR-T cell therapies, while highly effective for treating hematologic malignancies, present a significant risk of cardiotoxicity. This meta-analysis highlights the importance of identifying high-risk patients and implementing proactive management strategies to mitigate these risks. Future research should focus on refining CAR-T protocols to minimize cardiotoxic effects and improve patient outcomes.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
195P - Anti-CTLA4 therapy leads to early expansion of peripheral Th17 population and induction of Th1 cytokines
Presenter: Mari Nakazawa
Session: Poster Display session
196P - Single-cell analysis of stage-I high-grade serous ovarian carcinoma reveals the essential role of regulatory T cells in early tumor establishment
Presenter: Joanna Mikulak
Session: Poster Display session
197P - Comprehensive immunoprofiling of the intratumoral and peripheral T cell receptor gene repertoire in triple-negative breast cancer patients
Presenter: Antonios Mingos
Session: Poster Display session
198P - Association of types of treatment modalities with expression of T Lymphocytes (CD4, CD8, Treg) in breast cancer patients and their clinical outcome
Presenter: Arshi Rizwan
Session: Poster Display session
Resources:
Abstract
199P - Cancer neutrophil encyclopedia: A deep dive into antigen-presenting warriors
Presenter: Yingcheng Wu
Session: Poster Display session
Resources:
Abstract
200P - CXCR1+ neutrophil infiltration orchestrates response to third-generation EGFR-TKI in EGFR mutant NSCLC
Presenter: Haowei Wang
Session: Poster Display session
Resources:
Abstract
201P - Underlying mechanisms of neutrophil-mediated immunosuppression and resistance to treatment in breast cancer: Further evidence that these cells matter
Presenter: Bruna Filipa Correia
Session: Poster Display session
202P - Mining tumor infiltrating B cells to discover antibody-target pairs and develop novel therapies
Presenter: Matthieu Delince
Session: Poster Display session
203P - Targeting IL-33 reprograms tumor microenvironment and potentiates antitumor response to anti-PD-L1 immunotherapy
Presenter: Xuyao Zhang
Session: Poster Display session
204P - Deciphering the crosstalk between tumor and circulating immune microenvironment in advanced NSCLC patients undergoing immunotherapy
Presenter: Prisca Tamarozzi
Session: Poster Display session