A real-world study of oxaliplatin-induced hypersensitivity in colorectal cancer treatment based on the pharmacovigilance system in China: a cohort study
- PMID: 40672070
- PMCID: PMC12260960
- DOI: 10.21037/jgo-2025-312
A real-world study of oxaliplatin-induced hypersensitivity in colorectal cancer treatment based on the pharmacovigilance system in China: a cohort study
Abstract
Background: Oxaliplatin (OXA), a third-generation platinum-based chemotherapeutic agent, is commonly used in the treatment of colorectal cancer (CRC). However, there is growing recognition that OXA induced hypersensitivity poses a challenge to the continuity and safety of patient treatment. However, the risk factors for OXA-induced hypersensitivity reactions (HSRs) are not clear. This study aimed to investigate the incidence, characteristics, severity, and risk factors of OXA-induced HSRs among Chinese CRC patients, using data from the China Hospital Pharmacovigilance System (CHPS).
Methods: This retrospective study analyzed adverse drug reaction reports related to OXA from the CHPS, focusing on patients treated for CRC between 2018 and 2022. The incidence rates of HSRs were assessed, and the demographic, clinical, and risk factors associated with HSRs were explored.
Results: This study analyzed the records of 383 CRC patients who were treated with OXA-based regimens. A total of 124 (32.37%) HSRs related to OXA were reported, the majority of which were cutaneous reactions. Severe reactions, including anaphylaxis, occurred in 8% of the HSR cases. In this study, male gender, the eosinophil count, and serum albumin levels were risk factors associated with the occurrence of OXA-induced HSRs.
Conclusions: OXA-induced HSRs are a significant adverse effect in the treatment of CRC. This study emphasizes the importance of identifying the risk factors associated with the occurrence of OXA-induced HSRs to optimize patient safety and treatment efficacy.
Keywords: China; Oxaliplatin (OXA); colorectal cancer (CRC); hypersensitivity reactions (HSRs); pharmacovigilance.
Copyright © 2025 AME Publishing Company. All rights reserved.
Conflict of interest statement
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://jgo.amegroups.com/article/view/10.21037/jgo-2025-312/coif). The authors have no conflicts of interest to declare.
Similar articles
-
Independent risk and protective factors for oxaliplatin-induced hypersensitivity reactions: a retrospective study.Front Pharmacol. 2025 Jul 8;16:1624322. doi: 10.3389/fphar.2025.1624322. eCollection 2025. Front Pharmacol. 2025. PMID: 40697651 Free PMC article.
-
Rapid drug desensitization with chemotherapy: when should omalizumab be considered?Allergol Immunopathol (Madr). 2025 Jul 1;53(4):21-30. doi: 10.15586/aei.v53i4.1349. eCollection 2025. Allergol Immunopathol (Madr). 2025. PMID: 40682225
-
A rapid and systematic review of the clinical effectiveness and cost-effectiveness of paclitaxel, docetaxel, gemcitabine and vinorelbine in non-small-cell lung cancer.Health Technol Assess. 2001;5(32):1-195. doi: 10.3310/hta5320. Health Technol Assess. 2001. PMID: 12065068
-
A rapid and systematic review of the clinical effectiveness and cost-effectiveness of topotecan for ovarian cancer.Health Technol Assess. 2001;5(28):1-110. doi: 10.3310/hta5280. Health Technol Assess. 2001. PMID: 11701100
-
The use of irinotecan, oxaliplatin and raltitrexed for the treatment of advanced colorectal cancer: systematic review and economic evaluation.Health Technol Assess. 2008 May;12(15):iii-ix, xi-162. doi: 10.3310/hta12150. Health Technol Assess. 2008. PMID: 18462574
References
-
- O'Dowd PD, Sutcliffe DF, Griffith DM. Oxaliplatin and its derivatives–An overview. Coordination Chemistry Reviews 2023;497:215439. 10.1016/j.ccr.2023.215439 - DOI
LinkOut - more resources
Full Text Sources