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氟尿嘧啶与氟尿嘧啶及高剂量持续输注亚叶酸钙用于治疗既往未接受过化疗的晚期可测量结直肠癌患者的前瞻性随机对照研究。

Prospective randomized comparison of fluorouracil versus fluorouracil and high-dose continuous infusion leucovorin calcium for the treatment of advanced measurable colorectal cancer in patients previously unexposed to chemotherapy.

作者信息

Doroshow J H, Multhauf P, Leong L, Margolin K, Litchfield T, Akman S, Carr B, Bertrand M, Goldberg D, Blayney D

机构信息

Department of Medical Oncology and Therapeutics Research, City of Hope Cancer Research Center, Duarte, CA 91010.

出版信息

J Clin Oncol. 1990 Mar;8(3):491-501. doi: 10.1200/JCO.1990.8.3.491.

Abstract

Seventy-nine patients with advanced, measurable, metastatic colorectal cancer previously unexposed to chemotherapy were randomly assigned to treatment with either fluorouracil (FUra) administered intravenously at a dose of 370 mg/m2/d for 5 days or the combination of FUra in the same dose and schedule with high-dose continuous infusion leucovorin calcium (500 mg/m2/d) beginning 24 hours before the first dose of FUra and continuing for 12 hours after the completion of FUra therapy. Patients whose disease progressed on treatment with FUra alone were, if eligible, crossed over to receive leucovorin and FUra. Three patients on the FUra plus leucovorin arm of the study were excluded from the analysis because they did not meet eligibility requirements. The treatment arms were well balanced for prognostic criteria including performance status, age, prior radiotherapy, distribution of metastatic sites, and on-study carcinoembryonic antigen (CEA), lactic dehydrogenase, and serum albumin. FUra plus leucovorin was superior to FUra alone for response (P = .0019) and for time to progression or death (log-rank, P = .045). Response rates were 16 of 36 (44%) versus five of 40 (13%), and median time to progression or death was 164 versus 120 days in the two arms of the trial, respectively. Overall survival, however, while longer in the FUra and leucovorin arm was not significantly so. An analysis of the toxicities experienced by the patients in the two treatment groups showed that, except for significantly more stomatitis in the leucovorin arm of the study, the side effects experienced by patients treated with either regimen were comparable. These results suggest that the efficacy of FUra in patients with advanced, measurable, metastatic colorectal cancer can be enhanced significantly by administration of a continuous high-dose infusion of leucovorin calcium.

摘要

79例先前未接受过化疗的晚期、可测量、转移性结直肠癌患者被随机分配接受以下治疗:氟尿嘧啶(FUra)以370mg/m²/d的剂量静脉注射,持续5天;或相同剂量和疗程的FUra联合大剂量持续输注亚叶酸钙(500mg/m²/d),在第一剂FUra前24小时开始,在FUra治疗结束后持续12小时。仅接受FUra治疗病情进展的患者,若符合条件,则交叉接受亚叶酸钙和FUra治疗。该研究中FUra加亚叶酸钙组的3例患者因不符合入选标准而被排除在分析之外。治疗组在预后标准方面,包括体能状态、年龄、既往放疗情况、转移部位分布以及研究期间的癌胚抗原(CEA)、乳酸脱氢酶和血清白蛋白水平,均具有良好的平衡性。FUra加亚叶酸钙在缓解率(P = 0.0019)和疾病进展或死亡时间方面(对数秩检验,P = 0.045)优于单用FUra。缓解率在试验的两组中分别为36例中的16例(44%)和40例中的5例(13%),疾病进展或死亡的中位时间分别为164天和120天。然而,总体生存率虽然在FUra和亚叶酸钙组更长,但差异无统计学意义。对两个治疗组患者所经历的毒性进行分析表明,除研究中亚叶酸钙组的口腔炎明显更多外,两种治疗方案治疗的患者所经历的副作用相当。这些结果表明,通过持续大剂量输注亚叶酸钙,可显著提高FUra对晚期、可测量、转移性结直肠癌患者的疗效。

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