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甲磺酸伊马替尼治疗晚期胃间质瘤后的病理完全缓解:一例报告

Pathological complete response in advanced gastric stromal tumor after imatinib mesylate therapy: a case report.

作者信息

El Mesbahi Omar, Brahmi Sami Aziz, Akasbi Yousra, El Mrabet Fatima Zahra, Touyar Anas, Ossaden Abdelmalek, Znati Kaoutar, Maazaz Khalid, Amarti Affaf, Tizniti Siham, Taleb Khalid Ait, Ibrahimi Adil

机构信息

Medical Oncology Department, Hassan II University Hospital, Fez, Morocco.

出版信息

J Med Case Rep. 2011 May 21;5:197. doi: 10.1186/1752-1947-5-197.

DOI:10.1186/1752-1947-5-197
PMID:21600007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3124421/
Abstract

INTRODUCTION

Gastrointestinal stromal tumors are a rare neoplasm exhibiting, in most cases, mutations of c-kit. Imatinib mesylate is the standard treatment for patients who have advanced gastrointestinal stromal tumors. Although the response rate in patients treated with imatinib mesylate in prospective clinical studies is above 50%, a complete response is very rare. We report the case of a patient with a gastric gastrointestinal stromal tumor who had a pathological complete response after neoadjuvant treatment with imatinib mesylate.

CASE PRESENTATION

We report the case of a 54-year-old Arab woman with a gastrointestinal stromal tumor who had a pathological complete response after neoadjuvant treatment with imatinib mesylate.

CONCLUSION

The pathological examination of our patient documented a complete pathological response after imatinib therapy. Recently, it has been confirmed that the kinase genotype of KIT and platelet-derived growth factor receptor α can accurately predict a good response to imatinib mesylate therapy. We propose that this patient had a mutation conferring high sensitivity to imatinib mesylate.

摘要

引言

胃肠道间质瘤是一种罕见的肿瘤,在大多数情况下表现为c-kit基因突变。甲磺酸伊马替尼是晚期胃肠道间质瘤患者的标准治疗药物。尽管在前瞻性临床研究中接受甲磺酸伊马替尼治疗的患者缓解率超过50%,但完全缓解非常罕见。我们报告了1例胃胃肠道间质瘤患者,在接受甲磺酸伊马替尼新辅助治疗后获得病理完全缓解的病例。

病例报告

我们报告1例54岁患有胃肠道间质瘤的阿拉伯女性患者,在接受甲磺酸伊马替尼新辅助治疗后获得病理完全缓解。

结论

对我们患者的病理检查记录了伊马替尼治疗后的完全病理缓解。最近,已证实KIT和血小板衍生生长因子受体α的激酶基因型可准确预测对甲磺酸伊马替尼治疗的良好反应。我们认为该患者存在对甲磺酸伊马替尼高度敏感的突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/93f1970f56d0/1752-1947-5-197-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/375e46fab692/1752-1947-5-197-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/f61ed1b11fcc/1752-1947-5-197-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/f9c21ee69fd8/1752-1947-5-197-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/93f1970f56d0/1752-1947-5-197-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/375e46fab692/1752-1947-5-197-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/f61ed1b11fcc/1752-1947-5-197-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/f9c21ee69fd8/1752-1947-5-197-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/3124421/93f1970f56d0/1752-1947-5-197-4.jpg

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Imatinib plasma levels are correlated with clinical benefit in patients with unresectable/metastatic gastrointestinal stromal tumors.伊马替尼的血浆水平与不可切除/转移性胃肠道间质瘤患者的临床获益相关。
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Preoperative imatinib mesylate for unresectable or locally advanced primary gastrointestinal stromal tumors (GIST).
术前使用甲磺酸伊马替尼治疗不可切除或局部晚期原发性胃肠道间质瘤(GIST)。
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