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Extended adjuvant therapy with imatinib in patients with gastrointestinal stromal tumors: Recommendations for patient selection, risk assessment, and molecular response monitoring

机译:伊马替尼在胃肠道间质瘤患者中扩大辅助治疗:有关患者选择,风险评估和分子反应监测的建议

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摘要

On the basis of the recently published results of a clinical trial comparing 12 and 36 months of imatinib in adjuvant therapy for gastrointestinal stromal tumors (GISTs), which demonstrated clinical benefit of longer imatinib treatment in terms of delaying recurrences and improving overall survival, both the US Food and Drug Administration and the European Medicines Agency have updated their recommendations and approved 36 months of imatinib treatment in patients with v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog (KIT)-positive GISTs (also known as CD117-positive GISTs) at high risk of recurrence after surgical resection of a primary tumor. This article discusses patient selection criteria for extended adjuvant therapy with imatinib, different classifications of risk of recurrence, and assessment of the response to therapy.
机译:根据最近发表的一项临床试验结果比较了伊马替尼在胃肠道间质瘤(GIST)辅助治疗中的12个月和36个月的比较,这表明更长的伊马替尼治疗在延缓复发和改善总体生存方面具有临床益处,美国食品药品监督管理局和欧洲药品管理局已经更新了他们的建议,并批准了v-kit Hardy-Zuckerman 4猫肉瘤病毒癌基因同源(KIT)阳性GIST(也称为CD117阳性GIST)患者的伊马替尼治疗36个月)原发肿瘤手术切除后复发风险高。本文讨论了使用伊马替尼进行辅助治疗的患者选择标准,复发风险的不同分类以及对治疗反应的评估。

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