Literature DB >> 25398579

Interstitial lung disease induced by alectinib (CH5424802/RO5424802).

Satoshi Ikeda1, Hiroshige Yoshioka2, Machiko Arita2, Takahiro Sakai2, Naoyuki Sone2, Akihiro Nishiyama2, Takashi Niwa2, Machiko Hotta3, Tomohiro Tanaka4, Tadashi Ishida2.   

Abstract

A 75-year-old woman with anaplastic lymphoma kinase (ALK)-rearranged Stage IV lung adenocarcinoma was administered the selective anaplastic lymphoma kinase inhibitor, alectinib, as a third-line treatment in a Phase 1-2 study. On the 102nd day, chest computed tomography showed diffuse ground glass opacities. Laboratory data revealed high serum levels of KL-6, SP-D and lactate dehydrogenase without any clinical symptoms. There was no evidence of infection. Marked lymphocytosis was seen in bronchoalveolar lavage fluid analysis, and transbronchial lung biopsy showed mild thickening of alveolar septa and lymphocyte infiltration. Interstitial lung disease was judged to be related to alectinib based on improvements in imaging findings and serum biomarkers after discontinuation of alectinib. To our knowledge, this is the first reported case of alectinib-induced interstitial lung disease. Alectinib is a promising drug for ALK-rearranged non-small cell lung cancer. Clinical trials of this selective anaplastic lymphoma kinase inhibitor will facilitate the meticulous elucidation of its long-term safety profile.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  adverse event; alectinib; anaplastic lymphoma kinase; interstitial lung disease; non-small cell lung cancer

Mesh:

Substances:

Year:  2014        PMID: 25398579     DOI: 10.1093/jjco/hyu183

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  6 in total

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Authors:  Joshua S Davis; David Ferreira; Emma Paige; Craig Gedye; Michael Boyle
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Review 2.  Tyrosine Kinase Inhibitor-Induced Interstitial Lung Disease: Clinical Features, Diagnostic Challenges, and Therapeutic Dilemmas.

Authors:  Rashmi R Shah
Journal:  Drug Saf       Date:  2016-11       Impact factor: 5.606

3.  Severe acute interstitial lung disease in a patient with anaplastic lymphoma kinase rearrangement-positive non-small cell lung cancer treated with alectinib.

Authors:  Yuzo Yamamoto; Isamu Okamoto; Kohei Otsubo; Eiji Iwama; Naoki Hamada; Taishi Harada; Koichi Takayama; Yoichi Nakanishi
Journal:  Invest New Drugs       Date:  2015-09-04       Impact factor: 3.850

4.  Case report: continued treatment with alectinib is possible for patients with lung adenocarcinoma with drug-induced interstitial lung disease.

Authors:  Tatsuya Nitawaki; Yoshihiko Sakata; Kodai Kawamura; Kazuya Ichikado
Journal:  BMC Pulm Med       Date:  2017-12-06       Impact factor: 3.317

5.  Pulmonary Adenocarcinoma, Harboring Both an EGFR Mutation and ALK Rearrangement, Presenting a Stable Disease to Erlotinib and a Partial Response to Alectinib.

Authors:  Akira Yokoyama; Atsuhisa Tamura; Kazuko Miyakawa; Kei Kusaka; Masahiro Shimada; Takashi Hirose; Hirotoshi Matsui; Masashi Kitani; Akira Hebisawa; Ken Ohta
Journal:  Intern Med       Date:  2018-03-09       Impact factor: 1.271

6.  The safety and serious adverse events of approved ALK inhibitors in malignancies: a meta-analysis.

Authors:  Helei Hou; Dantong Sun; Kewei Liu; Man Jiang; Dong Liu; Jingjuan Zhu; Na Zhou; Jing Cong; Xiaochun Zhang
Journal:  Cancer Manag Res       Date:  2019-05-07       Impact factor: 3.989

  6 in total

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