Poon M A, O'Connell M J, Moertel C G, Wieand H S, Cullinan S A, Everson L K, Krook J E, Mailliard J A, Laurie J A, Tschetter L K
North Central Cancer Treatment Group, Saskatchewan Cancer Foundation, Regina, Canada.
J Clin Oncol. 1989 Oct;7(10):1407-18. doi: 10.1200/JCO.1989.7.10.1407.
The purpose of this study was to evaluate the effectiveness of several new approaches designed to enhance the activity of fluorouracil (5-FU) in the management of advanced colorectal cancer. A total of 429 patients were randomized to one of the following regimens: single-agent 5-FU, given by standard 5-day, intensive-course intravenous bolus technique; 5-FU plus high-dose folinic acid (leucovorin) or 5-FU plus low-dose leucovorin; 5-FU plus high-dose methotrexate (MTX) with oral leucovorin rescue; 5-FU plus low-dose MTX; and 5-FU plus cisplatin (CDDP). The median survival for patients receiving 5-FU alone was 7.7 months. The high- and low-dose leucovorin plus 5-FU regimens had median survivals of 12.2 and 12.0 months, respectively, and offered a significant survival advantage over 5-FU alone with one-sided P values of .037 and .050, respectively (P = .051 for each treatment after correction for prognostic variables). The only other regimen possibly associated with improved survival was high-dose MTX plus 5-FU, with a median survival of 10.5 months (P = .21, P = .076 corrected). In addition, both high- and low-dose leucovorin plus 5-FU regimens were associated with significantly improved tumor response rates (P = .04 and .001) and significantly improved interval-to-tumor-progression rates (P = .015 and .007) when compared with 5-FU alone. Only the low-dose leucovorin plus 5-FU regimen was associated with significant (P less than .05) superiority in each of the following parameters of quality of life: performance status, weight gain, and symptomatic relief. The overall most therapeutically favorable regimen in this trial was 5-FU given with low-dose leucovorin; fortuitously, this regimen is associated with very low drug cost. Whereas this is the first study to demonstrate both improved palliation and survival for any regimen compared with 5-FU given by rapid intravenous (IV) injection for 5 consecutive days at a dose of 500 mg/m2/d in patients with advanced colorectal cancer, the magnitude of the gain is still relatively small. Our low-dose leucovorin plus 5-FU regimen is currently being studied in a national trial with the hope that this increased advanced disease activity may produce more substantive gains in the surgical adjuvant setting.
本研究的目的是评估几种旨在增强氟尿嘧啶(5-FU)活性以用于晚期结直肠癌治疗的新方法的有效性。总共429例患者被随机分配至以下治疗方案之一:单药5-FU,采用标准的5日强化疗程静脉推注技术给药;5-FU加用高剂量甲酰四氢叶酸(亚叶酸钙)或5-FU加用低剂量亚叶酸钙;5-FU加用高剂量甲氨蝶呤(MTX)并口服亚叶酸钙解救;5-FU加用低剂量MTX;以及5-FU加用顺铂(CDDP)。接受单纯5-FU治疗的患者的中位生存期为7.7个月。高剂量和低剂量亚叶酸钙加5-FU方案的中位生存期分别为12.2个月和12.0个月,与单纯5-FU相比具有显著的生存优势,单侧P值分别为0.037和0.050(校正预后变量后每种治疗的P值均为0.051)。唯一可能与生存期改善相关的其他方案是高剂量MTX加5-FU,中位生存期为10.5个月(校正后P = 0.21,P = 0.076)。此外,与单纯5-FU相比,高剂量和低剂量亚叶酸钙加5-FU方案均与显著改善的肿瘤缓解率(P = 0.04和0.001)以及显著改善的至肿瘤进展时间率(P = 0.015和0.007)相关。只有低剂量亚叶酸钙加5-FU方案在以下生活质量参数中的每一项上均具有显著(P < 0.05)优势:体能状态、体重增加和症状缓解。本试验中总体治疗效果最有利的方案是5-FU与低剂量亚叶酸钙联合使用;巧合的是,该方案的药物成本非常低。虽然这是第一项证明与以500 mg/m²/d的剂量连续5天快速静脉注射5-FU相比,任何方案在晚期结直肠癌患者中均能改善姑息治疗效果和生存期的研究,但获益程度仍然相对较小。我们的低剂量亚叶酸钙加5-FU方案目前正在一项全国性试验中进行研究,希望这种在晚期疾病中的活性增强在手术辅助治疗环境中能产生更实质性的获益。