Int. Journal of Clinical Pharmacology and Therapeutics, Volume 63 (2025) - January (30 - 37)

Aplastic anemia associated with osimertinib: Analysis of the FDA adverse event reporting system

Katsuhiro Ohyama1, Seiichiro Katagiri2, Satoshi Takahashi3, Hideaki Ayuhara4, Hironori Takeuchi4, Daigo Akahane2, Akihiko Gotoh2, Yusuke Hori1
1 Center for Experiential Pharmacy Practice, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji, 2 Department of Hematology, 3 Department of Thoracic Surgery, and 4 Hospital Pharmacy, Tokyo Medical University Hospital, Shinjuku-ku, Tokyo, Japan

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DOI 10.5414/CP204627

Abstract

Objective: Aplastic anemia (AA) is a life-threatening disease, and drug-induced AA is rare. Recently, studies on cases that possibly developed AA following osimertinib treatment have been conducted. This study evaluated the association of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs), including osimertinib, with AA and characterized such registered patients using a large spontaneous adverse event reporting database.
Materials and methods: Data from the Food and Drug Administration’s Adverse Event Reporting System spanning from the first quarter of 2015 to the second quarter of 2023 were used. Disproportionality analyses with reporting odds ratio (ROR) and information component (IC) were performed for signal detection. Furthermore, we described a case series of patients who experienced AA during osimertinib treatment.
Results: A signal was detected with osimertinib (ROR: 4.16, 95% confidence interval (CI): 2.54 – 6.80; IC: 1.80, 95% CI: 1.10 – 2.51); however, no signals were detected with other EGFR-TKIs. 16 individuals treated with osimertinib had AA, of whom 14 (87.5%) were registered as suspected drugs. The median age of these individuals was 70.5 years (interquartile range (IQR), 64.8 – 78.3 years), with varying time to onset (IQR, 4 – 210 days) and outcomes, including 3 (18.8%) deaths.
Conclusion: Our analyses generated a safety signal for the association between osimertinib and AA. Further studies are required to understand and confirm the role of osimertinib administration in the development of AA.

Author Details

Authors

Departments

  • 1 Center for Experiential Pharmacy Practice, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji,
  • 2 Department of Hematology,
  • 3 Department of Thoracic Surgery, and
  • 4 Hospital Pharmacy, Tokyo Medical University Hospital, Shinjuku-ku, Tokyo, Japan

Address

Katsuhiro Ohyama, PhD
Center for Experiential Pharmacy Practice
School of Pharmacy
Tokyo University of Pharmacy and Life Sciences
1432-1 Horinouchi, Hachioji,
Tokyo 192-0392, Japan
Email: [email protected]

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Citation

Katsuhiro Ohyama, Seiichiro Katagiri, Satoshi Takahashi, Hideaki Ayuhara, Hironori Takeuchi, Daigo Akahane, Akihiko Gotoh, Yusuke Hori.Aplastic anemia associated with osimertinib: Analysis of the FDA adverse event reporting system
. Int J Clin Pharmacol Ther. 2025; 63: 30-37. doi: 10.5414/CP204627. Pubmed: https://pubmed.ncbi.nlm.nih.gov/39565078/; PMID: 39565078.

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