Role of genomic markers in colorectal cancer treatment

被引:44
作者
Allen, WL [1 ]
Johnston, PG [1 ]
机构
[1] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Dept Oncol, Drug Resistance Grp, Belfast BT9 7AB, Antrim, North Ireland
关键词
D O I
10.1200/JCO.2005.19.752
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For the last four decades, fluorouracil (FU) has been the main treatment of choice in colorectal cancer (CRC) in both the advanced and adjuvant settings. In the advanced setting, FU monotherapy produces response rates of only 10% to 20%. Furthermore, in resected stage III CRC, FU monotherapy has increased overall survival by only 20%. The combination of FU with newer therapies such as oxaliplatin and irinotecan has significantly improved response rates to 40% to 50%. Despite these improvements, more than half of advanced CRC patients derive no benefit from treatment; this is due to either acquired or inherent drug resistance. This review aims to highlight the current prognostic and predictive markers that have been identified for CRC to date. The limited use of these predictive markers underscores the importance of and need for multiple marker testing in order to improve response rates and decrease toxicity. This review will also focus on high throughput methods to identify panels of predictive markers for CRC, which ultimately aim to tailor treatment according to an individual patient and tumor profile. (c) 2005 by American Society of Clinical Oncology.
引用
收藏
页码:4545 / 4552
页数:8
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