Chen Jiezhong, Han Mei, Saif Muhammad Wasif
School of Biomedical Sciences, University of Queensland, St. Lucia, Australia.
Illawarra Health and Medical Research Institute, The University of Wollongong, Wollongong, Australia.
Anticancer Res. 2016 Jan;36(1):21-6.
Colon cancer is a common type of cancer with high mortality. The standard therapy for colon cancer is 5-FU-based regimen, although the current response rate to 5-FU is only 10-15%. Various approaches have been used to improve the efficacy of 5-FU including inhibition of its degradation enzyme dihydropyrimidine dehydrogenase (DPD) such as S1, UTF, use of 5-FU pro-drug capecitabine to exploit thymidine phosphorylase (TP) and supplementation of reduced folate acid to increase cytotoxicity. TAS-102 is a newly-developed anti-folate drug containing the 5-FU analogue trifluridine (TFD) and tipiracil hydrochloride (TPI). TPI is an inhibitor of TFD degradation enzyme thymidine phosphorylase and thus increases the bioavailability of TFD. In the present review, we summarize recent progress with regard to TAS-102, including pre-clinical tests and clinical trials. We further propose several approaches to further improve the efficacy of TAS-102 including combination with targeted therapy and immune therapy.
结肠癌是一种常见的高死亡率癌症。结肠癌的标准治疗方案是以5-氟尿嘧啶(5-FU)为基础的方案,尽管目前5-FU的有效率仅为10%-15%。人们采用了各种方法来提高5-FU的疗效,包括抑制其降解酶二氢嘧啶脱氢酶(DPD),如S1、UTF;使用5-FU前体药物卡培他滨来利用胸苷磷酸化酶(TP);补充还原叶酸以增加细胞毒性。TAS-102是一种新开发的抗叶酸药物,含有5-FU类似物三氟尿苷(TFD)和盐酸替吡嘧啶(TPI)。TPI是TFD降解酶胸苷磷酸化酶的抑制剂,因此可提高TFD的生物利用度。在本综述中,我们总结了TAS-102的最新进展,包括临床前试验和临床试验。我们还提出了几种进一步提高TAS-102疗效的方法,包括与靶向治疗和免疫治疗联合使用。