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用于结肠癌辅助治疗的靶向药物。

Targeted agents for adjuvant therapy of colon cancer.

作者信息

Saif Mohammad Wasif

机构信息

Yale Cancer Center, New Haven, CT 06520, USA

出版信息

Clin Colorectal Cancer. 2006 May;6(1):46-51. doi: 10.3816/CCC.2006.n.020.

DOI:10.3816/CCC.2006.n.020
PMID:16796791
Abstract

Among patients with colorectal cancer (CRC) diagnosed in the United States, 37.2% are diagnosed with stage III and 27.9% with stage II disease. In locoregionally advanced CRC, surgery is the primary treatment modality and has a curative intent. The survival depends on the pathologic stage and varies from 30%-60% for stage III to 60%-80% for stage II. However, as much as 40%-50% of patients will relapse and require additional treatment of the disease. Clinical failure after resection of CRC is predominantly secondary to the clinical progression of previously undetected distant metastatic disease. Until very recently, the absolute benefit for survival obtained with adjuvant therapy compared with control was about 6%. Introduction of oxaliplatin in the adjuvant setting has shown a reduction of 23% in the risk of relapse when compared with 5-fluorouracil alone (MOSAIC). Recent phase III studies have shown that targeted agents improved survival in patients with advanced-stage CRC. Bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, is the first antiangiogenic drug to show improved efficacy when used in combination with irinotecan and oxaliplatin for first- and second-line treatment of CRC. Cetuximab, another monoclonal antibody targeting epidermal growth factor receptor, has shown efficacy in third-line therapy and promising results in first-line phase II studies. There is great interest in whether the biologic agents bevacizumab and cetuximab can improve survival in the adjuvant-therapy setting. This article reviews the adjuvant therapy for colon cancer and discusses the potential role and current trials involving the targeted agents.

摘要

在美国诊断出的结直肠癌(CRC)患者中,37.2%被诊断为III期,27.9%为II期疾病。在局部晚期CRC中,手术是主要的治疗方式,具有治愈目的。生存率取决于病理分期,III期为30%-60%,II期为60%-80%。然而,多达40%-50%的患者会复发并需要对该疾病进行额外治疗。CRC切除术后的临床失败主要是由于先前未检测到的远处转移性疾病的临床进展。直到最近,与对照组相比,辅助治疗在生存方面获得的绝对益处约为6%。在辅助治疗中引入奥沙利铂后,与单独使用5-氟尿嘧啶相比,复发风险降低了23%(MOSAIC研究)。最近的III期研究表明,靶向药物可提高晚期CRC患者的生存率。贝伐单抗是一种靶向血管内皮生长因子的单克隆抗体,是第一种在与伊立替康和奥沙利铂联合用于CRC一线和二线治疗时显示出疗效提高的抗血管生成药物。西妥昔单抗是另一种靶向表皮生长因子受体的单克隆抗体,已在三线治疗中显示出疗效,并在一线II期研究中取得了有前景的结果。人们对生物制剂贝伐单抗和西妥昔单抗在辅助治疗环境中是否能提高生存率非常感兴趣。本文回顾了结肠癌的辅助治疗,并讨论了靶向药物的潜在作用和当前试验。

相似文献

1
Targeted agents for adjuvant therapy of colon cancer.用于结肠癌辅助治疗的靶向药物。
Clin Colorectal Cancer. 2006 May;6(1):46-51. doi: 10.3816/CCC.2006.n.020.
2
[Adjuvant and palliative anticancer treatment of colon carcinoma in 2004].[2004年结肠癌的辅助性和姑息性抗癌治疗]
Praxis (Bern 1994). 2004 Sep 29;93(40):1633-44. doi: 10.1024/0369-8394.93.40.1633.
3
Targeted therapy in colorectal cancer.结直肠癌的靶向治疗
Clin Adv Hematol Oncol. 2006 Feb;4(2):124-32.
4
The future development of bevacizumab in colorectal cancer.贝伐单抗在结直肠癌中的未来发展。
Oncology. 2005;69 Suppl 3:34-45. doi: 10.1159/000088482. Epub 2005 Nov 21.
5
Why do targeted agents not work in the adjuvant setting in colon cancer?为什么靶向药物在结肠癌的辅助治疗环境中不起作用?
Expert Rev Anticancer Ther. 2012 Oct;12(10):1337-45. doi: 10.1586/era.12.111.
6
Targeted drugs in metastatic colorectal cancer with special emphasis on guidelines for the use of bevacizumab and cetuximab: an Acta Oncologica expert report.转移性结直肠癌的靶向药物,特别强调贝伐单抗和西妥昔单抗的使用指南:一篇《肿瘤学学报》专家报告
Acta Oncol. 2005;44(3):203-17. doi: 10.1080/02841860510029798.
7
Chemotherapy of metastatic colorectal cancer.转移性结直肠癌的化疗
Prescrire Int. 2010 Oct;19(109):219-24.
8
Antiangiogenesis agents in colorectal cancer.结直肠癌的抗血管生成药物。
Curr Opin Oncol. 2010 Jul;22(4):374-80. doi: 10.1097/CCO.0b013e328339524e.
9
Bevacizumab: an angiogenesis inhibitor for the treatment of solid malignancies.贝伐单抗:一种用于治疗实体恶性肿瘤的血管生成抑制剂。
Clin Ther. 2006 Nov;28(11):1779-802. doi: 10.1016/j.clinthera.2006.11.015.
10
Liver resection for metastatic colorectal cancer in the age of neoadjuvant chemotherapy and bevacizumab.新辅助化疗和贝伐单抗时代下转移性结直肠癌的肝切除术
Clin Colorectal Cancer. 2006 Sep;6(3):202-7. doi: 10.3816/CCC.2006.n.036.

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