Medinger M, Steinbild S, Mross K
Klinik für Tumorbiologie, Albert-Ludwigs-Universität Freiburg.
Praxis (Bern 1994). 2004 Sep 29;93(40):1633-44. doi: 10.1024/0369-8394.93.40.1633.
This article reviews the available data regarding the acticity of postoperative adjuvant systemic therapy for colorectal cancer as first and second-line treatment in metastatic disease. The efficacy of adjuvant treatment of patients with stage III colorectal cancer is well established. 5-fluorouracil (5-FU) and folic acid over 6 months (still) represent todays standard and should serve as comparison in randomized studies. The risk of relapse is low in stage II colon carcinoma and consequently the efficacy is relatively small compared to stage III. New investigation indicate, Capecitabene has the potential to replace 5-FU/FS as standard treatment for patients with colon cancer. Efficacy results are expected to be available in 2004. In metastatic disease combination of 5-FU/folic acid plus CPT-11 or OXA are treatment of choice for the first-line therapy of metastatic colorectal carcinoma. FOLFOX is high-dose intensity oxaliplatin added to the simplified bimonthly leucovorin and 5-fluorouracil regimen as second- line therapy for metastatic colorectal cancer. It resulted in prolongation of the median progress free survival from 6,8 to 8,8 months and increased the survival for 4,5 months. New perspectives are novel chemotherapeutic and targeted agents in metastatic colorectal cancer: For the first time, there has been a targeted therapy shown convincingly to prolong survival for patients with unresectable metastatic colorectal cancer in a well-performed Phase III trial. This agent is bevacizumab, a humanised monoclonal antibody targeting the circulating proangiogenic growth factor vascular endothelial growth factor. Results with bevacizumab should lead to rapid expansion of the number of strategies targeting tumour neovasculature. Additionally, an antibody against the epidermal growth factor, cetuximab, has been shown to have both single-agent activity and the potential ability to partially reverse resistance to a chemotherapy drug. These advancements, as well as data on other novel treatment agents that have been studied specifically in patients with colorectal neoplasms, are discussed in detail.
本文综述了有关结直肠癌术后辅助全身治疗作为转移性疾病一线和二线治疗的现有数据。III期结直肠癌患者辅助治疗的疗效已得到充分证实。5-氟尿嘧啶(5-FU)和叶酸治疗6个月(至今)仍是目前的标准治疗方法,应作为随机研究中的对照。II期结肠癌复发风险较低,因此与III期相比疗效相对较小。新的研究表明,卡培他滨有可能取代5-FU/叶酸成为结肠癌患者的标准治疗方法。预计2004年可获得疗效结果。在转移性疾病中,5-FU/叶酸联合CPT-11或奥沙利铂是转移性结直肠癌一线治疗的首选方案。FOLFOX是在简化的每两个月一次的亚叶酸钙和5-氟尿嘧啶方案中加入高剂量强度的奥沙利铂,作为转移性结直肠癌的二线治疗方案。它使无进展生存期的中位数从6.8个月延长至8.8个月,并使生存期延长了4.5个月。转移性结直肠癌的新前景是新型化疗药物和靶向药物:在一项精心设计的III期试验中,首次有靶向治疗令人信服地显示可延长不可切除转移性结直肠癌患者的生存期。这种药物是贝伐单抗,一种靶向循环促血管生成生长因子血管内皮生长因子的人源化单克隆抗体。贝伐单抗的结果应会导致针对肿瘤新生血管的治疗策略数量迅速增加。此外,一种抗表皮生长因子抗体西妥昔单抗已显示出单药活性以及部分逆转对化疗药物耐药性的潜在能力。本文将详细讨论这些进展以及专门针对结直肠肿瘤患者研究的其他新型治疗药物的数据。
Praxis (Bern 1994). 2004-9-29
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