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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Efficacy and Safety of Raltitrexed Combinations with Uracil-Tegafur or Mitomycin C as Salvage Treatment in Advanced Colorectal Cancer Patients: A Multicenter Study of Anatolian Society of Medical Oncology (ASMO)
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Efficacy and Safety of Raltitrexed Combinations with Uracil-Tegafur or Mitomycin C as Salvage Treatment in Advanced Colorectal Cancer Patients: A Multicenter Study of Anatolian Society of Medical Oncology (ASMO)

机译:乌拉西尔-TEGAFUR或丝裂霉素C的疗效和安全性作为晚期结肠直肠癌患者的救人治疗:Anatolian医学肿瘤学会的多中心研究(ASMO)

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There is no standard treatment for patients with colorectal cancer (CRC) progressing after irinotecan and oxaliplatin treatment. Here we aimed to retrospectively evaluate the efficacy and tolerability of raltitrexed in combination with oral 5-fluoropyrimidine (uracil tegafur-UFT) or mitomycin C as salvage therapy in mCRC patients. A total of 62 patients who had received raltitrexed combined with UFT or mitomycin C were identified between December 2008 and June 2013. They were given raltitrexed 2.6 mg/m2 (max 5 mg) i.v. on day 1 in combination with either oral UFT 500 mg/day on days 1-14 every 3 weeks (group A) or mitomycin C 6 mg/m2 i.v. on day every 3 weeks (group B). Forty-two patients (67.7%) were in group A and 20 (32.2%) in group B. In 15 patients (24%) grade 3/4 toxicity was observed, resulting in dose reduction, and in 13 patients (20.9%) dose delay was necessary. The median progression free survival (PFS) was 3 months (95%CI 2.65-3.34) and median overall survival (OS) was 6 months (95%CI 2.09-9.90) in the whole group. Median PFS was 3 months (95%CI 2.60-3.39) in group A vs 3 months (95%CI 1.64-4.35) in group B (p=0.90). Median OS was 6 months (95%CI 2.47-9.53) in group A vs 12 months (95%CI 2.83-21.1) in group B (p=0.46). The combination of raltitrexed with UFT or mitomycin C seem to be a salvage therapy option due to safety profile and moderate clinical activity in heavily-pretreated mCRC patients.
机译:在伊替康和奥沙利铂治疗后进展结直肠癌(CRC)的患者没有标准治疗方法。在这里,我们的目的是回顾性地评估罗尔特雷德与口腔5-氟嘧啶(Uracil Tegafur-UFT)或丝霉素C组合的疗效和耐受性作为MCRC患者的抢救治疗。 2008年12月至2013年6月在2008年12月至6月期间,共发现了62名已接受罗尔特拉特或丝裂霉素C的患者。他们被授予RaltitRexed 2.6mg / m2(最多5 mg)I.v.在第1天与口腔UFT 500 mg /天组合每3周(a)或丝霉素C 6 mg / m 2 I.v。每天每3周(B组)。四十二名患者(67.7%)在B组和20组(32.2%)中,在B组中。在15名患者中观察到患者3/4级毒性,导致剂量减少,13名患者(20.9%)剂量延迟是必要的。中位进展免费存活(PFS)为3个月(95%CI 2.65-3.34),中位数总存活(OS)为整组组6个月(95%CI 2.09-9.90)。在B组(P = 0.90)中,中位数PFS为3个月(95%CI 1.64-4.35)的3个月(95%CI 1.64-4.35)。在B组(P = 0.46)中,中位OS​​为6个月(95%CI 2.47-9.53)中的VS 12个月(95%CI 2.83-21.1)。由于安全型材和严重预处理的MCRC患者的安全性曲线和中度临床活性,Raltitrexed的组合似乎是挽救疗法选择。

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