Treatment in advanced colorectal cancer: what, when and how?

被引:82
作者
Chau, I. [1 ,2 ]
Cunningham, D. [1 ,2 ]
机构
[1] Royal Marsden Hosp, Dept Med, London SW3 6JJ, England
[2] Royal Marsden Hosp, Dept Med, Surrey, England
关键词
colorectal cancer; oxaliplatin; irinotecan; capecitabine; bevacizumab; cetuximab; GROWTH-FACTOR RECEPTOR; RANDOMIZED PHASE-II; GENE COPY NUMBER; FLUOROURACIL PLUS OXALIPLATIN; TYROSINE KINASE INHIBITOR; 1ST-LINE TREATMENT; LIVER METASTASES; ADJUVANT TREATMENT; POOLED ANALYSIS; 5-FLUOROURACIL/FOLINIC ACID;
D O I
10.1038/sj.bjc.6605061
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Treatment of advanced colorectal cancer (CRC) increasingly requires a multidisciplinary approach and multiple treatment options add to the complexity of clinical decision-making. Recently novel targeted therapy against angiogenesis and epidermal growth factor receptor completed a plethora of phase III studies. The addition of bevacizumab to chemotherapy improved the efficacy over chemotherapy alone in both first and second line settings, although the magnitude of benefit may not be as great when a more optimal chemotherapy platform is used. Studies performed thus far did not address conclusively whether bevacizumab should be continued in subsequent lines of treatment. Anti-angiogenesis tyrosine kinase inhibitors have not shown any additional benefit over chemotherapy alone so far. Although some benefits were seen with cetuximab in all settings of treating advanced CRC, K-ras mutation status provides an important determinant of who would not benefit from such a treatment. Caution should be exercised in combining anti-angiogenesis with anti-EGFR strategy until further randomised data become available. In this review, we have focused on the implications of these trial results on the everyday management decisions of treating advanced CRC. British Journal of Cancer (2009) 100, 1704-1719. doi: 10.1038/sj.bjc.6605061 www.bjcancer.com Published online 12 May 2009 (C) 2009 Cancer Research UK
引用
收藏
页码:1704 / 1719
页数:16
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