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在生物治疗时代优化转移性结直肠癌的姑息治疗

Optimizing palliative treatment of metastatic colorectal cancer in the era of biologic therapy.

作者信息

Grothey Axel, Marshall John L

机构信息

Division of Medical Oncology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

出版信息

Oncology (Williston Park). 2007 Apr;21(5):553-64, 566; discussion 566-8, 577-8.

Abstract

Over the past decade, new cytotoxic and biologic therapies beyond the old standard-of-care, biomodulated fluorouracil (5-FU), have become available for the treatment of metastatic colorectal cancer (mCRC). The introductions of irinotecan (Camptosar), oxaliplatin (Eloxatin), and bevacizumab (Avastin) have prolonged survival, but the optimal use of these new therapies remains to be determined. Issues remain regarding management of toxicities, treatment of elderly patients or those with poor performance status, and the duration of treatment with front-line therapy. This article reviews recent and ongoing studies of newer therapies in an effort to determine the best use of these drugs in the treatment of mCRC. Current data support the front-line use of bevacizumab added to either 5-FU/leucovorin alone or 5-FU/leucovorin in combination with oxaliplatin (FOLFOX/bevacizumab) or irinotecan (FOLFIRI/bevacizumab). If oxaliplatin is used in first-line therapy, oxaliplatin should be discontinued before the development of severe neurotoxicity and be reintroduced or replaced with irinotecan on disease progression. Definitive conclusions on the sequence and duration of front-line therapy and the most effective strategy to ameliorate toxicity await results of ongoing prospective clinical trials.

摘要

在过去十年中,除了旧的标准治疗药物生物调节氟尿嘧啶(5-氟尿嘧啶,5-FU)之外,新型细胞毒性和生物疗法已可用于治疗转移性结直肠癌(mCRC)。伊立替康(开普拓,Camptosar)、奥沙利铂(乐沙定,Eloxatin)和贝伐单抗(阿瓦斯汀,Avastin)的应用延长了患者生存期,但这些新疗法的最佳使用方式仍有待确定。在毒性管理、老年患者或身体状况较差患者的治疗以及一线治疗的持续时间方面仍存在问题。本文综述了关于这些新疗法的近期及正在进行的研究,以确定这些药物在mCRC治疗中的最佳使用方法。目前的数据支持在一线治疗中使用贝伐单抗,可将其添加至单独使用的5-FU/亚叶酸或5-FU/亚叶酸与奥沙利铂联合方案(FOLFOX/贝伐单抗)或伊立替康联合方案(FOLFIRI/贝伐单抗)中。如果在一线治疗中使用奥沙利铂,应在出现严重神经毒性之前停药,并在疾病进展时重新引入或用伊立替康替代。关于一线治疗的顺序和持续时间以及减轻毒性的最有效策略的明确结论,有待正在进行的前瞻性临床试验的结果。

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