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Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer

BACKGROUND: Alectinib is an oral drug developed for the treatment of patients with fusion gene encoding echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK)-rearranged non-small cell lung cancer (NSCLC). Here, we present the case of a patient treated with alectinib...

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Autores principales: Kimura, Tatsuo, Sowa-Osako, Junko, Nakai, Toshiyuki, Ohyama, Ayako, Kawaguchi, Tomoya, Tsuruta, Daisuke, Ohsawa, Masahiko, Hirata, Kazuto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216233/
https://www.ncbi.nlm.nih.gov/pubmed/28101031
http://dx.doi.org/10.1159/000453314
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author Kimura, Tatsuo
Sowa-Osako, Junko
Nakai, Toshiyuki
Ohyama, Ayako
Kawaguchi, Tomoya
Tsuruta, Daisuke
Ohsawa, Masahiko
Hirata, Kazuto
author_facet Kimura, Tatsuo
Sowa-Osako, Junko
Nakai, Toshiyuki
Ohyama, Ayako
Kawaguchi, Tomoya
Tsuruta, Daisuke
Ohsawa, Masahiko
Hirata, Kazuto
author_sort Kimura, Tatsuo
collection PubMed
description BACKGROUND: Alectinib is an oral drug developed for the treatment of patients with fusion gene encoding echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK)-rearranged non-small cell lung cancer (NSCLC). Here, we present the case of a patient treated with alectinib who developed a hypersensitivity reaction with successful rechallenge treatment. CASE PRESENTATION: A 39-year-old woman who was a passive smoker was referred to Osaka City University Hospital for the evaluation of a skin event caused by treatment for NSCLC with the fusion gene EML4-ALK. The skin reaction was observed on the anterior chest, upper arms, and ear auricles on day 11 of treatment with oral alectinib. The skin event presented as widely distributed erythematous macules that were confluent, indicating a severe and life-threatening form. The skin lesions started to resolve after the initiation of treatment with 40 mg prednisolone. After regrowth of the tumor, she received a rechallenge program for alectinib for 2 weeks; thereafter, alectinib treatment was successfully reinitiated. CONCLUSION: To the best of our knowledge, we present the first case in which alectinib, which binds to the adenosine triphosphate site of EML4-ALK, induced erythema multiforme. Moreover, successful readministration of alectinib through our rechallenge program has not been reported so far.
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spelling pubmed-52162332017-01-18 Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer Kimura, Tatsuo Sowa-Osako, Junko Nakai, Toshiyuki Ohyama, Ayako Kawaguchi, Tomoya Tsuruta, Daisuke Ohsawa, Masahiko Hirata, Kazuto Case Rep Oncol Case Report BACKGROUND: Alectinib is an oral drug developed for the treatment of patients with fusion gene encoding echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK)-rearranged non-small cell lung cancer (NSCLC). Here, we present the case of a patient treated with alectinib who developed a hypersensitivity reaction with successful rechallenge treatment. CASE PRESENTATION: A 39-year-old woman who was a passive smoker was referred to Osaka City University Hospital for the evaluation of a skin event caused by treatment for NSCLC with the fusion gene EML4-ALK. The skin reaction was observed on the anterior chest, upper arms, and ear auricles on day 11 of treatment with oral alectinib. The skin event presented as widely distributed erythematous macules that were confluent, indicating a severe and life-threatening form. The skin lesions started to resolve after the initiation of treatment with 40 mg prednisolone. After regrowth of the tumor, she received a rechallenge program for alectinib for 2 weeks; thereafter, alectinib treatment was successfully reinitiated. CONCLUSION: To the best of our knowledge, we present the first case in which alectinib, which binds to the adenosine triphosphate site of EML4-ALK, induced erythema multiforme. Moreover, successful readministration of alectinib through our rechallenge program has not been reported so far. S. Karger AG 2016-12-08 /pmc/articles/PMC5216233/ /pubmed/28101031 http://dx.doi.org/10.1159/000453314 Text en Copyright © 2016 the Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Kimura, Tatsuo
Sowa-Osako, Junko
Nakai, Toshiyuki
Ohyama, Ayako
Kawaguchi, Tomoya
Tsuruta, Daisuke
Ohsawa, Masahiko
Hirata, Kazuto
Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title_full Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title_fullStr Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title_full_unstemmed Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title_short Alectinib-Induced Erythema Multiforme and Successful Rechallenge with Alectinib in a Patient with Anaplastic Lymphoma Kinase-Rearranged Lung Cancer
title_sort alectinib-induced erythema multiforme and successful rechallenge with alectinib in a patient with anaplastic lymphoma kinase-rearranged lung cancer
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216233/
https://www.ncbi.nlm.nih.gov/pubmed/28101031
http://dx.doi.org/10.1159/000453314
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