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CAR-T therapy pulmonary adverse event profile: a pharmacovigilance study based on FAERS database (2017-2023).
Shi, Jing; Liu, Xinya; Jiang, Yun; Gao, Mengjiao; Yu, Jian; Zhang, Yuanming; Wu, Li.
Affiliation
  • Shi J; Xinjiang Medical University, Urumqi, China.
  • Liu X; Department of Oncology Cardiology, Xinjiang Medical University Cancer Hospital, Urumqi, China.
  • Jiang Y; Xinjiang Medical University, Urumqi, China.
  • Gao M; The Fifth Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Yu J; Department of Oncology Cardiology, Xinjiang Medical University Cancer Hospital, Urumqi, China.
  • Zhang Y; Department of Oncology Cardiology, Xinjiang Medical University Cancer Hospital, Urumqi, China.
  • Wu L; Department of Oncology Cardiology, Xinjiang Medical University Cancer Hospital, Urumqi, China.
Front Pharmacol ; 15: 1434231, 2024.
Article in En | MEDLINE | ID: mdl-39234101
ABSTRACT

Background:

Chimeric antigen receptor T-cell (CAR-T) therapy, a rapidly emerging treatment for cancer that has gained momentum since its approval by the FDA in 2017, involves the genetic engineering of patients' T cells to target tumors. Although significant therapeutic benefits have been observed, life-threatening adverse pulmonary events have been reported.

Methods:

Using SAS 9.4 with MedDRA 26.1, we retrospectively analyzed data from the Food and Drug Administration's Adverse Event Reporting System (FAERS) database, covering the period from 2017 to 2023. The analysis included the Reporting Odds Ratio Proportional Reporting Ratio Information Component and Empirical Bayes Geometric Mean to assess the association between CAR-T cell therapy and adverse pulmonary events (PAEs).

Results:

The FAERS database recorded 9,400 adverse events (AEs) pertaining to CAR-T therapies, of which 940 (10%) were PAEs. Among these CAR-T cell-related AEs, hypoxia was the most frequently reported (344 cases), followed by respiratory failure (127 cases). Notably, different CAR-T cell treatments demonstrated varying degrees of association with PAEs. Specifically, Tisa-cel was associated with severe events including respiratory failure and hypoxia, whereas Axi-cel was strongly correlated with both hypoxia and tachypnea. Additionally, other CAR-T therapies, namely, Brexu-cel, Liso-cel, Ide-cel, and Cilta-cel, have also been linked to distinct PAEs. Notably, the majority of these PAEs occurred within the first 30 days post-treatment. The fatality rates varied among the different CAR-T therapies, with Tisa-cel exhibiting the highest fatality rate (43.6%), followed by Ide-cel (18.8%).

Conclusion:

This study comprehensively analyzed the PAEs reported in the FAERS database among recipients of CAR-T cell therapy, revealing conditions such as hypoxia, respiratory failure, pleural effusion, and atelectasis. These CAR-T cell therapy-associated events are clinically significant and merit the attention of clinicians and researchers.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol / Frontiers in pharmacology Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol / Frontiers in pharmacology Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland