5-氟尿嘧啶(5FU)加或不加亚叶酸(LV)治疗人结直肠癌?文献的多元荟萃分析。

D Brohée
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引用次数: 6

摘要

本荟萃分析基于77项临床研究对5-氟尿嘧啶(5FU)加或不加亚叶酸素(LV)治疗转移性结直肠癌的106项评价。总的来说,在初诊患者中,LV的中位缓解率为31%,而单独使用5FU的中位缓解率为12%。使用前向逐步多元线性回归分析,结果表明,在初治患者报告的应答率中,多达44%的方差可由治疗相关变量解释(P < 0.001)。显著性参数为LV附着度(部分R = 0.636)、累计5FU总剂量(R = 0.344)和每周5FU计划(R = 0.246)。在预处理患者中,后一个参数是唯一显著的参数(R = 0.443)。出乎意料的是,LV管理就像一个全有或全无的管理者,没有任何明显的剂量效应关系。持续5FU输注数周的平均累积给药量是单丸方案的3倍(21.3 vs 7.02 g -2, P < 0.001),可能是影响5FU相关变量的最佳临床方法。因此,建议5FU长期滴注,滴注至最高耐受剂量,并用低剂量亚叶酸加强,可能是5FU治疗结直肠癌最有效的方法。这一假设及其对生存的最终影响应该在随机试验中进行检验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
5-Fluorouracil (5FU) with or without folinic acid (LV) in human colorectal cancer? Multivariate meta-analysis of the literature.

This meta-analysis is based on 106 evaluations of response from 77 clinical studies about 5-fluorouracil (5FU) treatment with or without leucovorin (LV) in metastatic colorectal carcinoma. Overall, in naive patients, LV is associated with a median response rate of 31% as compared with a 12% figure with 5FU alone. Using a forward stepwise multilinear regression analysis, it is shown that as much as 44% of the variance in the reported response rates in naive patients can be accounted for by treatment-related variables (P less than 0.001). The significant parameters are LV adjunction (partial R = 0.636), cumulative total 5FU dose (R = 0.344), and 5FU weekly schedule (R = 0.246). In pretreated patients, the latter parameter is the only significant one (R = 0.443). Unexpectedly, LV administration behaves like an all-or-nothing governor, without any obvious dose-effect relationship. Protracted 5FU infusion over weeks allows a mean cumulative drug delivery, 3 times higher than bolus regimens (21.3 vs 7.02 g m-2, P less than 0.001) and may represent the best clinical approach to influence the 5FU-related variables. Accordingly, it is suggested that 5FU protracted infusion, titrated to the highest tolerable doses and potentiated with low doses of leucovorin, could represent the most efficacious way for using 5FU in colorectal disseminated cancer. This hypothesis and its eventual impact on survival should be tested in randomized trials.

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