Budd G T, Fleming T R, Bukowski R M, McCracken J D, Rivkin S E, O'Bryan R M, Balcerzak S P, Macdonald J S
J Clin Oncol. 1987 Feb;5(2):272-7. doi: 10.1200/JCO.1987.5.2.272.
In order to determine the clinical applicability of the in vitro observation of enhanced cytotoxicity of 5-fluorouracil (5-FU) in the presence of excess reduced folates, the Southwest Oncology Group (SWOG) performed a randomized trial evaluating two dose schedules of 5-FU and folinic acid (FA) in 128 patients with metastatic colorectal cancer. Of 125 eligible patients, 62 were randomized to receive bolus FA (200 mg/m2 days 1 through 4) in addition to 5-FU (1,000 mg/m2 days 1 through 4) by continuous four-day infusion (infusion arm), while 63 were randomized to receive bolus FA (200 mg/m2 days 1 through 5) in addition to 5-FU (325 mg/m2 days 1 through 5) by bolus injection (bolus arm). The toxicities of the two schedules differed, with stomatitis being more severe in the infusion arm and leukopenia being more severe in the bolus arm. The response rates and survival data for the two arms are nearly identical. The median survival of patients on the infusion arm is 11.0 months and of patients on the bolus arm, 10.3 months. The infusion arm produced one complete response (CR) and 12 partial responses (PRs), for a major response rate of 21% of eligible patients. The bolus arm produced three CRs and 11 PRs, for a major response rate of 22% of eligible patients. The response rate produced is minimally superior to recent cooperative group studies of colorectal cancer, but the response rate and survival experience are within the range of experience for treatment with 5-FU alone.
为了确定体外观察到的在存在过量还原型叶酸的情况下5-氟尿嘧啶(5-FU)细胞毒性增强的临床适用性,西南肿瘤学组(SWOG)进行了一项随机试验,评估128例转移性结直肠癌患者的两种5-FU和亚叶酸(FA)给药方案。在125例符合条件的患者中,62例被随机分配接受在连续4天输注5-FU(1000mg/m²,第1至4天)基础上推注FA(200mg/m²,第1至4天)(输注组),而63例被随机分配接受在推注5-FU(325mg/m²,第1至5天)基础上推注FA(200mg/m²,第1至5天)(推注组)。两种方案的毒性有所不同,输注组的口腔炎更严重,推注组的白细胞减少更严重。两组的缓解率和生存数据几乎相同。输注组患者的中位生存期为11.0个月,推注组患者为10.3个月。输注组产生1例完全缓解(CR)和12例部分缓解(PR),符合条件患者的主要缓解率为21%。推注组产生3例CR和11例PR,符合条件患者的主要缓解率为22%。所产生的缓解率略优于近期结直肠癌协作组研究,但缓解率和生存情况在单独使用5-FU治疗的经验范围内。