Literature DB >> 26334220

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

Yuzo Yamamoto1, Isamu Okamoto2,3, Kohei Otsubo1, Eiji Iwama1,4, Naoki Hamada1, Taishi Harada1, Koichi Takayama1, Yoichi Nakanishi1,5.   

Abstract

Alectinib, the second generation anaplastic lymphoma kinase (ALK) inhibitor, has significant potency in patients with ALK rearrangement positive non-small cell lung cancer (NSCLC), and its toxicity is generally well tolerable. We report a patient who developed severe acute interstitial lung disease after alectinib treatment. An 86-year-old woman with stage IV lung adenocarcinoma positive for rearrangement of ALK gene was treated with alectinib. On the 215th day after initiation of alectinib administration, she was admitted to our hospital with the symptom of progressive dyspnea. Computed tomography (CT) revealed diffuse ground glass opacities and consolidations in both lungs, and analysis of bronchoalveolar lavage fluid revealed pronounced lymphocytosis. There was no evidence of infection or other specific causes of her condition, and she was therefore diagnosed with interstitial lung disease induced by alectinib. Her CT findings and respiratory condition improved after steroid pulse therapy. As far as we are aware, this is the first reported case of alectinib-induced severe interstitial lung disease (ILD). We should be aware of the possibility of such a severe adverse event and should therefore carefully monitor patients treated with this drug.

Entities:  

Keywords:  ALK-rearrangement; Alectinib; Crizotinib; Interstitial lung disease; Non-small cell lung cancer

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Substances:

Year:  2015        PMID: 26334220     DOI: 10.1007/s10637-015-0284-9

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  9 in total

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

Authors:  Satoshi Ikeda; Hiroshige Yoshioka; Machiko Arita; Takahiro Sakai; Naoyuki Sone; Akihiro Nishiyama; Takashi Niwa; Machiko Hotta; Tomohiro Tanaka; Tadashi Ishida
Journal:  Jpn J Clin Oncol       Date:  2014-11-14       Impact factor: 3.019

2.  Safety and activity of alectinib against systemic disease and brain metastases in patients with crizotinib-resistant ALK-rearranged non-small-cell lung cancer (AF-002JG): results from the dose-finding portion of a phase 1/2 study.

Authors:  Shirish M Gadgeel; Leena Gandhi; Gregory J Riely; Alberto A Chiappori; Howard L West; Michele C Azada; Peter N Morcos; Ruey-Min Lee; Linta Garcia; Li Yu; Frederic Boisserie; Laura Di Laurenzio; Sophie Golding; Jotaro Sato; Shumpei Yokoyama; Tomohiro Tanaka; Sai-Hong Ignatius Ou
Journal:  Lancet Oncol       Date:  2014-08-18       Impact factor: 41.316

3.  Severe acute interstitial lung disease after crizotinib therapy in a patient with EML4-ALK-positive non-small-cell lung cancer.

Authors:  Akihiro Tamiya; Isamu Okamoto; Masaki Miyazaki; Shigeki Shimizu; Masanori Kitaichi; Kazuhiko Nakagawa
Journal:  J Clin Oncol       Date:  2012-11-19       Impact factor: 44.544

4.  First-line crizotinib versus chemotherapy in ALK-positive lung cancer.

Authors:  Benjamin J Solomon; Tony Mok; Dong-Wan Kim; Yi-Long Wu; Kazuhiko Nakagawa; Tarek Mekhail; Enriqueta Felip; Federico Cappuzzo; Jolanda Paolini; Tiziana Usari; Shrividya Iyer; Arlene Reisman; Keith D Wilner; Jennifer Tursi; Fiona Blackhall
Journal:  N Engl J Med       Date:  2014-12-04       Impact factor: 91.245

5.  Crizotinib reduces the rate of dark adaptation in the rat retina independent of ALK inhibition.

Authors:  Chang-Ning Liu; Nagappan Mathialagan; Patrick Lappin; Jay Fortner; Chris Somps; Gary Seitis; Theodore R Johnson; Wenyue Hu; Diane Matsumoto
Journal:  Toxicol Sci       Date:  2014-10-16       Impact factor: 4.849

6.  Crizotinib versus chemotherapy in advanced ALK-positive lung cancer.

Authors:  Alice T Shaw; Dong-Wan Kim; Kazuhiko Nakagawa; Takashi Seto; Lucio Crinó; Myung-Ju Ahn; Tommaso De Pas; Benjamin Besse; Benjamin J Solomon; Fiona Blackhall; Yi-Long Wu; Michael Thomas; Kenneth J O'Byrne; Denis Moro-Sibilot; D Ross Camidge; Tony Mok; Vera Hirsh; Gregory J Riely; Shrividya Iyer; Vanessa Tassell; Anna Polli; Keith D Wilner; Pasi A Jänne
Journal:  N Engl J Med       Date:  2013-06-01       Impact factor: 91.245

7.  Crizotinib-induced acute interstitial lung disease in a patient with EML4-ALK positive non-small cell lung cancer and chronic interstitial pneumonia.

Authors:  Naohiro Watanabe; Yoshio Nakahara; Hiroyuki Taniguchi; Tomoki Kimura; Yasuhiro Kondoh; Kensuke Kataoka; Koji Sakamoto
Journal:  Acta Oncol       Date:  2013-06-11       Impact factor: 4.089

8.  CH5424802 (RO5424802) for patients with ALK-rearranged advanced non-small-cell lung cancer (AF-001JP study): a single-arm, open-label, phase 1-2 study.

Authors:  Takashi Seto; Katsuyuki Kiura; Makoto Nishio; Kazuhiko Nakagawa; Makoto Maemondo; Akira Inoue; Toyoaki Hida; Nobuyuki Yamamoto; Hiroshige Yoshioka; Masao Harada; Yuichiro Ohe; Naoyuki Nogami; Kengo Takeuchi; Tadashi Shimada; Tomohiro Tanaka; Tomohide Tamura
Journal:  Lancet Oncol       Date:  2013-04-30       Impact factor: 41.316

Review 9.  Development of anaplastic lymphoma kinase (ALK) inhibitors and molecular diagnosis in ALK rearrangement-positive lung cancer.

Authors:  Eiji Iwama; Isamu Okamoto; Taishi Harada; Koichi Takayama; Yoichi Nakanishi
Journal:  Onco Targets Ther       Date:  2014-03-05       Impact factor: 4.147

  9 in total
  6 in total

Review 1.  Infectious Complications of Biological and Small Molecule Targeted Immunomodulatory Therapies.

Authors:  Joshua S Davis; David Ferreira; Emma Paige; Craig Gedye; Michael Boyle
Journal:  Clin Microbiol Rev       Date:  2020-06-10       Impact factor: 26.132

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.  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

4.  HMGB1 induces lung fibroblast to myofibroblast differentiation through NF‑κB‑mediated TGF‑β1 release.

Authors:  Qiong Wang; Jun Wang; Junfang Wang; Shanchao Hong; Feifei Han; Jingyu Chen; Guoqian Chen
Journal:  Mol Med Rep       Date:  2017-03-23       Impact factor: 2.952

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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