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晚期胃癌治疗的新视角:S-1作为一种新型口服5-氟尿嘧啶疗法联合顺铂

New Perspectives in the Treatment of Advanced Gastric Cancer: S-1 as a Novel Oral 5-FU Therapy in Combination with Cisplatin.

作者信息

Mahlberg Rolf, Lorenzen Sylvie, Thuss-Patience Peter, Heinemann Volker, Pfeiffer Per, Möhler Markus

机构信息

First Department of Medicine, Mutterhaus der Borromäerinnen, Trier, Germany.

出版信息

Chemotherapy. 2017;62(1):62-70. doi: 10.1159/000443984. Epub 2016 Sep 20.

Abstract

Oral fluoropyrimidines have been available for more than 10 years. Capecitabine is well established in treating solid tumors in Europe. S-1 (Teysuno®), an oral formulation containing the 5-fluorouracil (5-FU) prodrug tegafur and the two enzyme modulators gimeracil and oteracil, has not been available in non-Asia countries until recently. In Japan, S-1 in combination with cisplatin is the recommended first-line treatment in patients with gastric cancer. In Europe, the first trials with S-1 were disappointing due to high unacceptable incidences of adverse events. Pharmacokinetic studies showed differences in Asian and Caucasian patients; therefore, a new non-Asian study program was initiated, which led to the pivotal phase 3 trial First-Line Advanced Gastric Cancer Study (FLAGS). In FLAGS, 1,053 patients with advanced gastric cancer from 24 non-Asian countries were enrolled. S-1 plus cisplatin showed no overall survival (OS) benefit when compared to 5-FU plus cisplatin. The primary endpoint superior OS was not met but better tolerability was shown. A post hoc noninferiority OS and safety analysis showed that S-1 plus cisplatin has the same efficacy as 5-FU plus cisplatin but a more favorable safety profile. This led to the approval of S-1 in combination with cisplatin in gastric cancer in Europe in 2011. This article reviews the mode of action of S-1, pivotal study results from an EU point of view, and future perspectives.

摘要

口服氟嘧啶类药物已经应用超过10年。卡培他滨在欧洲治疗实体瘤方面已得到广泛应用。S-1(替吉奥®)是一种含有5-氟尿嘧啶(5-FU)前体药物替加氟以及两种酶调节剂吉美嘧啶和奥替拉西的口服制剂,直到最近才在非亚洲国家上市。在日本,S-1联合顺铂是推荐用于胃癌患者的一线治疗方案。在欧洲,最初关于S-1的试验结果令人失望,因为不良事件发生率高得令人难以接受。药代动力学研究表明亚洲患者和白种人患者存在差异;因此,启动了一项新的非亚洲研究项目,该项目促成了关键的3期试验——一线晚期胃癌研究(FLAGS)。在FLAGS试验中,招募了来自24个非亚洲国家的1053例晚期胃癌患者。与5-FU联合顺铂相比,S-1联合顺铂未显示出总生存期(OS)获益。主要终点指标优越的总生存期未达到,但显示出了更好的耐受性。一项事后非劣效性总生存期和安全性分析表明,S-1联合顺铂与5-FU联合顺铂具有相同的疗效,但安全性更好。这使得S-1联合顺铂于2011年在欧洲获批用于胃癌治疗。本文回顾了S-1的作用模式、从欧盟角度来看的关键研究结果以及未来展望。

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