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伊马替尼辅助治疗胃肠间质瘤患者:患者选择、风险评估和分子反应监测的建议。

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

机构信息

Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, Roentgena 5, 02-781, Warsaw, Poland.

出版信息

Mol Diagn Ther. 2013 Feb;17(1):9-19. doi: 10.1007/s40291-013-0018-7.

Abstract

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.

摘要

基于最近发表的一项比较伊马替尼辅助治疗胃肠道间质瘤(GIST) 12 个月和 36 个月的临床试验结果,该试验显示更长时间的伊马替尼治疗在延迟复发和提高总生存方面具有临床获益,美国食品和药物管理局和欧洲药品管理局都已更新其建议,并批准在手术切除原发性肿瘤后复发风险高的 v-kit Hardy-Zuckerman 4 猫肉瘤病毒致癌基因同源物(KIT)阳性 GIST (也称为 CD117 阳性 GIST)患者中使用伊马替尼治疗 36 个月。本文讨论了伊马替尼辅助治疗的扩展选择标准、不同的复发风险分类以及对治疗反应的评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128a/3565084/5ed8f9bb73fa/40291_2013_18_Fig1_HTML.jpg

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