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接受阿来替尼治疗间变性淋巴瘤激酶阳性非小细胞肺癌患者的高胆红素血症:一种组织学特征
Authors Zhang Q , Yan L, Bao Y, Yuan X, Yin D, Xu J
Received 8 August 2024
Accepted for publication 3 December 2024
Published 11 December 2024 Volume 2024:17 Pages 1189—1193
DOI https://doi.org/10.2147/OTT.S486860
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Sanjay Singh
Qian Zhang, Lei Yan, Yujie Bao, Xiaoling Yuan, Donglin Yin,* Jie Xu*
Department of Infectious Disease, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Jie Xu; Donglin Yin, Department of Infectious Disease, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, No. 280 Mohe Road, Baoshan District, Shanghai, 201999, People’s Republic of China, Email xujie@shsmu.edu.cn; 1240441503@qq.com
Background: Alectinib is a second generation of anaplastic lymphoma kinase (ALK) inhibitor that has been approved for the treatment of advanced non-small-cell lung cancer (NSCLC) with ALK rearrangements. Hepatotoxicity is the most common adverse drug reaction. However, there is currently no published report on the pathologic findings of alectinib-induced hyperbilirubinemia.
Case Presentation: Here, we report a case of a patient with NSCLC and chronic hepatitis B (CHB) who was treated with alectinib and developed grade 4 hyperbilirubinemia after 3 years on therapy. Alectinib was discontinued, and an artificial liver support system (ALSS) was used to decline blood bilirubin levels. The pathological manifestations from a liver biopsy showed the hepatocytes with scattered focal necrosis, bile stasis, and vesicular steatosis, bile emboli in capillaries, and star-shaped fibers proliferation in the portal area.
Conclusion: This is the first report of alectinib-induced hyperbilirubinemia which was confirmed by liver histopathology and successfully relieved by ALSS treatment and drug discontinuation.
Keywords: alectinib, ALK, hyperbilirubinemia, NSCLC, ALSS