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亚叶酸钙与氟尿嘧啶联合疗法

[Levofolinate and fluorouracil combination therapy].

作者信息

Takeuchi S, Murakami M

机构信息

Nagoya Branch Oncology Group, Wyeth Lederle (Japan), 2-2-13 Nishiki, Naka-ku, Nagoya 460-0003, Japan.

出版信息

Nihon Yakurigaku Zasshi. 2001 Sep;118(3):211-8. doi: 10.1254/fpj.118.211.

DOI:10.1254/fpj.118.211
PMID:11577462
Abstract

Levofolinate and fluorouracil regimen (l-leucovorin and 5 fluorouracil regimen) is a biochemical modulation of 5 fluorouracil (5FU) by leucovorin (LV). In the USA and Europe d,l-LV and 5FU regimen is frequently administered for colorectal cancer treatment and recognized as the standard regimen. In Japan, multi-institutional clinical trials of l-leucovorin (l-LV), a bioactive diastereomer of leucovorin, and 5FU combination were conducted for the treatment of advanced gastrointestinal cancer with comparable results to the US/Europe data. This l-LV and 5FU regimen was approved in August 1999 for the indications of advanced gastric cancer and colorectal cancer. The dosage and administration is referred to the weekly method developed at RPMI. Recently, the irinotecan (CPT-11) or oxariplatin plus LV and 5FU combination showed higher antitumor activities than the LV and 5FU combination with increased progression-free survival. These regimens, however, are not yet properly established because clinical trial results with Japanese patients are not completed for agreement of the dosage and administration schedule. For the l-LV and 5FU regimen diarrhea and leukocytopenia, including grade 3 and higher, were reported as the major adverse events. Administration for eligible patients with periodical monitoring of diagnostic data is necessary.

摘要

亚叶酸钙与氟尿嘧啶方案(左亚叶酸钙与5-氟尿嘧啶方案)是亚叶酸钙(LV)对5-氟尿嘧啶(5FU)的一种生化调节。在美国和欧洲,消旋亚叶酸钙与5FU方案常用于结直肠癌治疗,并被视为标准方案。在日本,针对亚叶酸钙的生物活性非对映异构体左亚叶酸钙(l-LV)与5FU联合治疗晚期胃肠道癌开展了多机构临床试验,结果与美国/欧洲的数据相当。该l-LV与5FU方案于1999年8月获批用于晚期胃癌和结直肠癌的适应症。剂量与给药方法参考了RPMI研发的每周给药法。最近,伊立替康(CPT-11)或奥沙利铂联合LV与5FU方案显示出比LV与5FU方案更高的抗肿瘤活性,无进展生存期延长。然而,这些方案尚未完全确立,因为针对日本患者的临床试验结果尚未完成,无法就剂量和给药方案达成一致。对于l-LV与5FU方案,腹泻和白细胞减少(包括3级及以上)被报告为主要不良事件。有必要对符合条件的患者进行给药,并定期监测诊断数据。

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