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ORIGINAL RESEARCH article

Front. Pharmacol.

Sec. Pharmacology of Anti-Cancer Drugs

Volume 16 - 2025 | doi: 10.3389/fphar.2025.1665484

Clinical characteristics and management of dasatinib-induced chylothorax: retrospective analysis based on case reports

Provisionally accepted
Ya  LiuYa Liu1Ying  HuangYing Huang2Jincai  GuoJincai Guo3Yixiang  HuYixiang Hu1*Xiang  LiuXiang Liu1*
  • 1Xiangtan Central Hospital, Xiangtan, China
  • 2Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, China
  • 3Changsha Stomatological Hospital, Changsha, China

The final, formatted version of the article will be published soon.

Background: Dasatinib-induced chylothorax is a rare but potentially serious complication, and its clinical features remain poorly defined. This study aimed to systematically evaluate its clinical characteristics, therapeutic approaches, and patient outcomes to provide practical guidance for clinical management. Methods: We conducted a retrospective analysis by systematically retrieving case reports of dasatinib-induced chylothorax from relevant databases up to May 31, 2025, to achieve a comprehensive assessment. Results: A total of 24 patients from 22 published case reports and case series were included in this analysis. The median age was 50 years (range 5, 79), and the median time to onset of chylothorax following dasatinib initiation was 41 months (range 1, 168). The most frequently reported clinical symptom was dyspnea (62.5%), followed by fever (25.0%), cough (16.7%), abdominal pain (8.3%), and chest pain (4.2%). Pleural fluid was typically described as white and milky in appearance (87.5%). Biochemical analysis revealed a median pleural fluid triglyceride concentration of 547.4 mg/dL and an albumin level of 4.4 g/dL. Dasatinib therapy was discontinued in 83.3% of patients. Alternative tyrosine kinase inhibitors were prescribed in selected cases, including nilotinib (33.3%), imatinib (20.8%), and bosutinib (16.7%). Supportive treatments consisted primarily of corticosteroids (45.8%), diuretics (45.8%), and thoracentesis (29.2%). Clinical improvement was observed in 91.7% of patients, with a median time to recovery of 12.2 weeks (range 1, 52). Among the four patients who underwent dasatinib rechallenge, three experienced recurrence of chylothorax. Conclusion: Dasatinib-induced chylothorax is rare but often reversible. Early diagnosis, drug discontinuation, and appropriate supportive care are key to recovery. Rechallenge should be undertaken cautiously due to a high risk of recurrence.

Keywords: Dasatinib, Chylothorax, Chronic myeloid leukemia, Pleural Effusion, diagnosis

Received: 14 Jul 2025; Accepted: 15 Sep 2025.

Copyright: © 2025 Liu, Huang, Guo, Hu and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Yixiang Hu, yixianghu@hnu.edu.cn
Xiang Liu, liuxiang876@163.com

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