Doroshow J H, Bertrand M, Newman E, Multhauf P, Leong L, Blayney D, Goldberg D, Margolin K, Carr B, Akman S
Department of Medical Oncology and Therapeutics Research, City of Hope National Medical Center, Duarte, CA 91010.
NCI Monogr. 1987(5):171-4.
In this study, 50 patients were randomly assigned to treatment with 5-fluorouracil (FUra) or FUra plus high-dose continuous-infusion folinic acid. Five of 27 evaluable patients in the FUra group versus 10 of 21 patients in the FUra plus folinic acid arm of the study had objective partial remissions, P = 0.02. Time to progression was 3.9 months for FUra and 8.0 months for FUra and folinic acid, P = 0.006; however, median survivals (11.9 versus 14.5 months) were not different in this crossover study. Toxicity in both treatment arms was mild, although patients receiving FUra plus folinic acid experienced significantly more stomatitis than patients treated with FUra alone. This study suggests that high-dose, continuous-infusion folinic acid, which produces a steady-state level of biologically active folates of 10 microM, significantly increases the therapeutic activity of FUra.
在本研究中,50例患者被随机分配接受5-氟尿嘧啶(FUra)治疗或FUra加用大剂量持续输注亚叶酸治疗。FUra组27例可评估患者中有5例出现客观部分缓解,而在研究中FUra加亚叶酸组的21例患者中有10例出现客观部分缓解,P = 0.02。FUra组的疾病进展时间为3.9个月,FUra加亚叶酸组为8.0个月,P = 0.006;然而,在这项交叉研究中,两组的中位生存期(分别为11.9个月和14.5个月)并无差异。尽管接受FUra加亚叶酸治疗的患者发生口腔炎的情况明显多于仅接受FUra治疗的患者,但两个治疗组的毒性均较轻。本研究表明,能产生10微摩尔生物活性叶酸稳态水平的大剂量持续输注亚叶酸可显著提高FUra的治疗活性。