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用于胃癌个性化医疗的靶向和细胞毒性药物的预测性生物标志物。

Predictive biomarkers for targeted and cytotoxic agents in gastric cancer for personalized medicine.

作者信息

Wang Shalong, Yuan Lianwen

机构信息

Geriatric Surgery Department, Second Xiangya Hospital Affiliated with Central South University.

出版信息

Biosci Trends. 2016 Jul 19;10(3):171-80. doi: 10.5582/bst.2016.01078. Epub 2016 Jun 2.

Abstract

Gastric cancer (GC) is the fourth most common cancer and the second leading cause of cancer. The treatment of GC remains challenging as the outcomes achieved with surgery alone or adjuvant or neoadjuvant chemotherapy and radiotherapy are relatively poor. New treatment strategies are emerging and are being tested in solid tumors including GC. Over the past few years, the treatment of metastatic colorectal cancer (CRC) has made great advances, but strategies to manage GC have improved little. Multiple drug resistance is common in GC chemotherapy and targeted therapy; some patients appear to receive treatment that is suboptimal or even inefficacious. Unfortunately, there are few validated predictive biomarkers to guide the tailored treatment of GC. ToGA and AVAGAST are two phase III trials that tested the efficacy and safety of targeted agents in advanced gastric cancer (AGC), and results clearly indicated that patients need to be selected and that targeted agents are the best hope for better results. This review aims to provide an overview of potential predictive biomarkers for cytotoxic and targeted agents in GC.

摘要

胃癌(GC)是第四大常见癌症,也是癌症的第二大主要死因。由于单纯手术或辅助或新辅助化疗及放疗所取得的治疗效果相对较差,GC的治疗仍然具有挑战性。新的治疗策略不断涌现,并正在包括GC在内的实体瘤中进行试验。在过去几年中,转移性结直肠癌(CRC)的治疗取得了巨大进展,但GC的治疗策略进展甚微。多重耐药在GC化疗和靶向治疗中很常见;一些患者似乎接受了次优甚至无效的治疗。不幸的是,几乎没有经过验证的预测生物标志物来指导GC的个体化治疗。ToGA和AVAGAST是两项测试靶向药物在晚期胃癌(AGC)中的疗效和安全性的III期试验,结果清楚地表明需要对患者进行筛选,靶向药物是取得更好治疗效果的最大希望。本综述旨在概述GC中细胞毒性药物和靶向药物的潜在预测生物标志物。

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