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环氧化酶-2抑制剂作为上消化道癌症(食管癌、胃癌和胰腺癌)的放射增敏剂。

COX-2 inhibitors as radiation sensitizers for upper GI tract cancers: esophagus, stomach, and pancreas.

作者信息

Rich Tyvin A, Shepard Robert

机构信息

Department of Radiation Oncology, University of Virginia Health Sciences System, Charlottesville 22901, USA.

出版信息

Am J Clin Oncol. 2003 Aug;26(4):S110-3. doi: 10.1097/01.COC.0000074148.37768.3E.

Abstract

Cancers of the esophagus, stomach, and pancreas have been successfully treated recently with combinations of radiosensitizing chemotherapy and irradiation. New approaches building onto 5-fluorouracil chemoradiation include capecitabine (Xeloda) and irradiation. Capecitabine is an oral 5-fluorouracil (5-FU) prodrug that is more convenient than using infusional 5-FU, appears to have a similar therapeutic profile, and can be combined with daily irradiation. The addition of a cyclooxygenase-2 (COX-2) inhibitor is being investigated in upper gastrointestinal cancer sites because there is a high degree of overexpression of COX-2 in these cancers.

摘要

近期,采用放射增敏化疗与放疗相结合的方法已成功治疗了食管癌、胃癌和胰腺癌。在5-氟尿嘧啶化放疗基础上发展而来的新方法包括卡培他滨(希罗达)与放疗。卡培他滨是一种口服的5-氟尿嘧啶(5-FU)前体药物,比使用静脉输注的5-FU更方便,似乎具有相似的治疗效果,并且可与每日放疗联合使用。由于在上消化道癌部位环氧化酶-2(COX-2)高度过表达,因此正在对添加COX-2抑制剂进行研究。

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