Herrmann R, Knuth A, Kleeberg U, Middeke H, Korsten F W, Trux F A, Schmieder A, Evers C
Division of Oncology, Kantonsspital, Basel, Switzerland.
Ann Oncol. 1992 Jul;3(7):539-43. doi: 10.1093/oxfordjournals.annonc.a058256.
Methotrexate (MTX) modulates 5-fluorouracil (FU) in several in vitro and in vivo experimental systems. Results of phase II studies have suggested improved response rates for the sequential application of MTX and FU in colorectal cancer. In a prospective randomized multicenter study we compared sequential MTX (300 mg/m2) and FU (900 mg/m2) using a seven-hour time interval and leucovorin rescue with FU (450 mg/m2/d for five days) in patients with previously untreated metastatic colorectal cancer. Of 172 patients randomized 159 were eligible for survival analysis and 153 for toxicity and response evaluation. Complete or partial response has been seen in 25.3% of patients receiving sequential MTX and FU and in 17.6% of those receiving FU alone (p = 0.11). There have been two long-term survivors, apparently cured by MTX/FU. Overall toxicity was more pronounced with FU alone, but sequential MTX/FU caused four toxic deaths. Median survival and survival rates at one and two years were not significantly different. It is concluded that this schedule of sequential MTX and FU is no more effective than a dose-intensive treatment with FU alone in metastatic colorectal cancer.
在多个体外和体内实验系统中,甲氨蝶呤(MTX)可调节5-氟尿嘧啶(FU)。II期研究结果表明,MTX和FU序贯应用于结直肠癌时缓解率有所提高。在一项前瞻性随机多中心研究中,我们比较了序贯使用MTX(300 mg/m²)和FU(900 mg/m²)(时间间隔7小时,并使用亚叶酸解救)与单独使用FU(450 mg/m²/天,共5天)对既往未接受治疗的转移性结直肠癌患者的疗效。172例随机分组的患者中,159例符合生存分析条件,153例符合毒性和反应评估条件。接受MTX和FU序贯治疗的患者中,25.3%出现完全或部分缓解,单独接受FU治疗的患者中这一比例为17.6%(p = 0.11)。有两名长期存活者,显然经MTX/FU治愈。单独使用FU时总体毒性更明显,但MTX/FU序贯治疗导致4例因毒性死亡。中位生存期以及1年和2年生存率无显著差异。结论是,在转移性结直肠癌中,这种MTX和FU序贯方案并不比单独使用FU的剂量密集治疗更有效。