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Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report

PURPOSE: Long-term continuous imatinib is recommended for adult patients with unresectable and/or metastatic KIT+ gastrointestinal stromal tumors (GIST) as long as the patient continues to benefit. In the adjuvant setting, recent findings indicate that patients at considerable risk of recurrence sho...

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Autor principal: Blay, Jean-Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547745/
https://www.ncbi.nlm.nih.gov/pubmed/23206868
http://dx.doi.org/10.1186/2045-3329-2-23
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author Blay, Jean-Yves
author_facet Blay, Jean-Yves
author_sort Blay, Jean-Yves
collection PubMed
description PURPOSE: Long-term continuous imatinib is recommended for adult patients with unresectable and/or metastatic KIT+ gastrointestinal stromal tumors (GIST) as long as the patient continues to benefit. In the adjuvant setting, recent findings indicate that patients at considerable risk of recurrence should receive at least 3 years of imatinib. Because imatinib is often administered for prolonged periods, proper management of imatinib-associated adverse events is crucial. CASE REPORT: We report a 56-year-old man with metastatic KIT+ GIST of the liver who had Grade 3 imatinib intolerance (skin rash) when treatment was started. The rash was managed with antihistamine treatment (Dexchlorpheniramine maleate 4 mg per day) and several temporary (up to 2 weeks) dose interruptions. The patient’s skin rash partially improved, and he tolerated gradual reintroduction of imatinib over several months. The patient maintained imatinib 400 mg/d, and tolerated it during the 2 years when he was on antihistamine treatment. After 2 years, the patient continued imatinib therapy without having to take antihistamines. The patient responded according to RECIST 1.1 and Choi to imatinib treatment for his metastatic GIST (partial response). As of September, 2012, the patient has been on imatinib therapy for 131 months and remains progression free. CONCLUSIONS: The results of this case report demonstrated that a patient with metastatic KIT+ GIST who was initially intolerant to imatinib maintained, and responded to imatinib therapy after treatment of an imatinib-associated adverse effect. These results suggest that initial intolerance to imatinib should not necessarily result in treatment discontinuation, as these adverse effects, when managed properly, may be tolerated and may decrease over time.
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spelling pubmed-35477452013-01-23 Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report Blay, Jean-Yves Clin Sarcoma Res Case Report PURPOSE: Long-term continuous imatinib is recommended for adult patients with unresectable and/or metastatic KIT+ gastrointestinal stromal tumors (GIST) as long as the patient continues to benefit. In the adjuvant setting, recent findings indicate that patients at considerable risk of recurrence should receive at least 3 years of imatinib. Because imatinib is often administered for prolonged periods, proper management of imatinib-associated adverse events is crucial. CASE REPORT: We report a 56-year-old man with metastatic KIT+ GIST of the liver who had Grade 3 imatinib intolerance (skin rash) when treatment was started. The rash was managed with antihistamine treatment (Dexchlorpheniramine maleate 4 mg per day) and several temporary (up to 2 weeks) dose interruptions. The patient’s skin rash partially improved, and he tolerated gradual reintroduction of imatinib over several months. The patient maintained imatinib 400 mg/d, and tolerated it during the 2 years when he was on antihistamine treatment. After 2 years, the patient continued imatinib therapy without having to take antihistamines. The patient responded according to RECIST 1.1 and Choi to imatinib treatment for his metastatic GIST (partial response). As of September, 2012, the patient has been on imatinib therapy for 131 months and remains progression free. CONCLUSIONS: The results of this case report demonstrated that a patient with metastatic KIT+ GIST who was initially intolerant to imatinib maintained, and responded to imatinib therapy after treatment of an imatinib-associated adverse effect. These results suggest that initial intolerance to imatinib should not necessarily result in treatment discontinuation, as these adverse effects, when managed properly, may be tolerated and may decrease over time. BioMed Central 2012-12-04 /pmc/articles/PMC3547745/ /pubmed/23206868 http://dx.doi.org/10.1186/2045-3329-2-23 Text en Copyright ©2012 Blay; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Blay, Jean-Yves
Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title_full Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title_fullStr Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title_full_unstemmed Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title_short Management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
title_sort management of imatinib-associated skin rash in a patient with metastatic gastrointestinal stromal tumor: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547745/
https://www.ncbi.nlm.nih.gov/pubmed/23206868
http://dx.doi.org/10.1186/2045-3329-2-23
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