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Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation

Inflammatory myofibroblastic tumor (IMT), a rare sarcoma, is primarily treated via resection of the mass. However, in cases of recurrence or unresectable tumors, no standard care exists. While crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor, is only approved for non-small-cell lung cancer...

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Autores principales: Ogata, Misato, Hatachi, Yukimasa, Ogata, Takatsugu, Satake, Hironaga, Imai, Yukihiro, Yasui, Hisateru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478978/
https://www.ncbi.nlm.nih.gov/pubmed/30449794
http://dx.doi.org/10.2169/internalmedicine.1640-18
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author Ogata, Misato
Hatachi, Yukimasa
Ogata, Takatsugu
Satake, Hironaga
Imai, Yukihiro
Yasui, Hisateru
author_facet Ogata, Misato
Hatachi, Yukimasa
Ogata, Takatsugu
Satake, Hironaga
Imai, Yukihiro
Yasui, Hisateru
author_sort Ogata, Misato
collection PubMed
description Inflammatory myofibroblastic tumor (IMT), a rare sarcoma, is primarily treated via resection of the mass. However, in cases of recurrence or unresectable tumors, no standard care exists. While crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor, is only approved for non-small-cell lung cancer with ALK mutation, it is reportedly effective for other malignant tumors with ALK mutation. We herein report a case involving a 37-year-old woman with retroperitoneal IMT with ALK mutation, who experienced recurrence after complete resection, in whom crizotinib treatment resulted in complete response. ALK-inhibitor efficacy against malignancies with ALK mutations should be investigated in future.
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spelling pubmed-64789782019-04-24 Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation Ogata, Misato Hatachi, Yukimasa Ogata, Takatsugu Satake, Hironaga Imai, Yukihiro Yasui, Hisateru Intern Med Case Report Inflammatory myofibroblastic tumor (IMT), a rare sarcoma, is primarily treated via resection of the mass. However, in cases of recurrence or unresectable tumors, no standard care exists. While crizotinib, an anaplastic lymphoma kinase (ALK) inhibitor, is only approved for non-small-cell lung cancer with ALK mutation, it is reportedly effective for other malignant tumors with ALK mutation. We herein report a case involving a 37-year-old woman with retroperitoneal IMT with ALK mutation, who experienced recurrence after complete resection, in whom crizotinib treatment resulted in complete response. ALK-inhibitor efficacy against malignancies with ALK mutations should be investigated in future. The Japanese Society of Internal Medicine 2018-11-19 2019-04-01 /pmc/articles/PMC6478978/ /pubmed/30449794 http://dx.doi.org/10.2169/internalmedicine.1640-18 Text en Copyright © 2019 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ogata, Misato
Hatachi, Yukimasa
Ogata, Takatsugu
Satake, Hironaga
Imai, Yukihiro
Yasui, Hisateru
Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title_full Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title_fullStr Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title_full_unstemmed Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title_short Effectiveness of Crizotinib for Inflammatory Myofibroblastic Tumor with ALK mutation
title_sort effectiveness of crizotinib for inflammatory myofibroblastic tumor with alk mutation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478978/
https://www.ncbi.nlm.nih.gov/pubmed/30449794
http://dx.doi.org/10.2169/internalmedicine.1640-18
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