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结直肠癌的预测和预后标志物

Predictive and prognostic markers in colorectal cancer.

作者信息

Wilson Peter M, Ladner Robert D, Lenz Heinz-Josef

机构信息

Department of Pathology, University of Southern California/Norris Comprehensive Cancer Center, Keck School of Medicine, Los Angeles, CA.

出版信息

Gastrointest Cancer Res. 2007 Nov;1(6):237-46.

PMID:19262902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2631215/
Abstract

Colorectal cancer (CRC) is the third most commonly diagnosed cancer in both men and women in the United States, with an estimated 153,760 new cases predicted for 2007. Since the 1960s, 5-fluorouracil (5-FU) has remained the mainstay of therapeutic options in the treatment of advanced CRC, with response rates of 20% to 25%. The introduction of newer agents such as oxaliplatin and irinotecan in combination with 5-FU has increased response rates to 40% to 50% in advanced disease and improved overall survival. The development of monoclonal antibodies targeting the epidermal growth factor receptor or vascular endothelial growth factor has demonstrated additional clinical benefit for patients with metastatic disease. However, many patients succumb to their disease, and a significant proportion will experience severe chemotherapy-associated toxicities while deriving little or no benefit. To improve the treatment of CRC, efforts must be directed toward the identification of patients who are likely to respond to a specific therapy, those who will experience severe toxicities, and those who will benefit from chemotherapy in the adjuvant setting. However, the utility of individual markers of response, toxicity, and disease recurrence remains in question. Efforts are now under way to develop multimarker profiles that can more accurately predict disease response. In this review, we discuss both predictive and prognostic markers identified in the treatment of CRC in terms of their robustness and their ability to assist the clinician in developing the most efficacious and least toxic therapeutic strategy for each patient.

摘要

结直肠癌(CRC)是美国男性和女性中第三大最常被诊断出的癌症,预计2007年有153,760例新发病例。自20世纪60年代以来,5-氟尿嘧啶(5-FU)一直是晚期CRC治疗中治疗选择的主要药物,有效率为20%至25%。奥沙利铂和伊立替康等新型药物与5-FU联合使用,使晚期疾病的有效率提高到40%至50%,并改善了总生存期。靶向表皮生长因子受体或血管内皮生长因子的单克隆抗体的研发已证明对转移性疾病患者有额外的临床益处。然而,许多患者死于该病,相当一部分患者在获益甚微或无获益的情况下会经历严重的化疗相关毒性。为了改善CRC的治疗,必须致力于识别可能对特定疗法有反应的患者、会经历严重毒性的患者以及在辅助治疗中会从化疗中获益的患者。然而,反应、毒性和疾病复发的个体标志物的实用性仍存在疑问。目前正在努力开发能够更准确预测疾病反应的多标志物概况。在本综述中,我们根据其稳健性以及协助临床医生为每位患者制定最有效且毒性最小的治疗策略的能力,讨论在CRC治疗中识别出的预测性和预后性标志物。

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本文引用的文献

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FCGR2A and FCGR3A polymorphisms associated with clinical outcome of epidermal growth factor receptor expressing metastatic colorectal cancer patients treated with single-agent cetuximab.FCGR2A和FCGR3A基因多态性与接受单药西妥昔单抗治疗的表皮生长因子受体表达型转移性结直肠癌患者的临床结局相关。
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ASCO 2006 update of recommendations for the use of tumor markers in gastrointestinal cancer.美国临床肿瘤学会(ASCO)2006年关于肿瘤标志物在胃肠道癌中应用的推荐更新
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Dermatologic side effects associated with the epidermal growth factor receptor inhibitors.与表皮生长因子受体抑制剂相关的皮肤副作用。
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Cancer stem cells--perspectives on current status and future directions: AACR Workshop on cancer stem cells.癌症干细胞——现状与未来方向展望:美国癌症研究协会癌症干细胞研讨会
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