Chemotherapy with Targeted Agents for the Treatment of Metastatic Colorectal Cancer

被引:79
|
作者
Koehne, Claus-Henning [1 ]
Lenz, Heinz-Josef [2 ]
机构
[1] Klinikum Oldenburg, Klin Onkol Hamatol, D-26133 Oldenburg, Germany
[2] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Keck Sch Med, Los Angeles, CA 90033 USA
来源
ONCOLOGIST | 2009年 / 14卷 / 05期
关键词
Bevacizumab; Cetuximab; Colorectal cancer; Irinotecan; Panitumumab; CETUXIMAB PLUS IRINOTECAN; ENDOTHELIAL GROWTH-FACTOR; PHASE-III TRIAL; 1ST-LINE TREATMENT; ORAL FLUOROPYRIMIDINES; CUTANEOUS TOXICITIES; TUMOR-GROWTH; COLON-CANCER; RECEPTOR; FLUOROURACIL;
D O I
10.1634/theoncologist.2008-0202
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The introduction of novel agents targeted to specific molecular features of cancer cells promises more options and marked improvements in efficacy for treatment of colon cancer. This overview of clinical studies describes the effects of administering the targeted agents bevacizumab, cetuximab, and panitumumab, also known as monoclonal antibodies, to treat metastatic colorectal cancer (mCRC) patients. All three targeted agents have been approved for use by the U. S. Food and Drug Administration and the European Agency for the Evaluation of Medicinal Products. Bevacizumab has been shown to extend survival when used in combination with irinotecan and 5-fluorouracil-based chemotherapy, and the addition of cetuximab to irinotecan and 5-fluorouracil-based chemotherapy overcomes irinotecan resistance. Cetuximab and panitumumab are both efficacious among refractory mCRC patients with wildtype KRAS tumors. Other targeted agents, for example, the tyrosine kinase inhibitors erlotinib, gefitinib, sunitinib, and vatalanib (PTK787/ZK 222584), are currently in various stages of clinical development. The Oncologist 2009;14:478-488
引用
收藏
页码:478 / 488
页数:11
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