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继发性C-kit突变是胃肠道间质瘤对伊马替尼产生获得性耐药的原因之一。

Secondary C-kit mutation is a cause of acquired resistance to imatinib in gastrointestinal stromal tumor.

作者信息

Zheng Song, Pan Yue-Long, Tao De-You, Wang Jiao-Li, Huang Ke-Er

机构信息

Department of Oncology, Hangzhou First People's Hospital of Zhejiang Province, Hangzhou, China.

出版信息

Scand J Gastroenterol. 2009;44(6):760-3. doi: 10.1080/00365520802647459.

DOI:10.1080/00365520802647459
PMID:19096980
Abstract

C-kit gene gain of function mutations are important in the pathogenesis of gastrointestinal stromal tumors (GISTs). Imatinib is a selective tyrosine kinase inhibitor of KIT and achieves a partial response or stable disease in most patients with metastatic GIST, but there is increasing evidence of acquired resistance. We report a case of GIST with acquired resistance to imatinib during therapy and secondary c-kit mutation besides the primary mutation.

摘要

C-kit基因功能获得性突变在胃肠道间质瘤(GISTs)的发病机制中具有重要作用。伊马替尼是一种KIT选择性酪氨酸激酶抑制剂,在大多数转移性GIST患者中可实现部分缓解或病情稳定,但越来越多的证据表明存在获得性耐药。我们报告了1例GIST患者,在治疗期间对伊马替尼产生获得性耐药,且除原发性突变外还出现了继发性c-kit突变。

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Secondary C-kit mutation is a cause of acquired resistance to imatinib in gastrointestinal stromal tumor.继发性C-kit突变是胃肠道间质瘤对伊马替尼产生获得性耐药的原因之一。
Scand J Gastroenterol. 2009;44(6):760-3. doi: 10.1080/00365520802647459.
2
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A missense mutation in KIT kinase domain 1 correlates with imatinib resistance in gastrointestinal stromal tumors.KIT激酶结构域1中的错义突变与胃肠道间质瘤中的伊马替尼耐药性相关。
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Surgical management after neoadjuvant imatinib therapy in gastrointestinal stromal tumours (GISTs) with respect to imatinib resistance caused by secondary KIT mutations.关于继发KIT突变导致伊马替尼耐药的胃肠道间质瘤(GISTs)新辅助伊马替尼治疗后的外科处理
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Oncol Rep. 2006 Jul;16(1):97-101.

引用本文的文献

1
Prognostic value of KIT/PDGFRA mutations in gastrointestinal stromal tumors: a meta-analysis.KIT/PDGFRA突变在胃肠道间质瘤中的预后价值:一项荟萃分析。
World J Surg Oncol. 2014 Mar 28;12:71. doi: 10.1186/1477-7819-12-71.