Dipartimento di Medicina Clinica e Sperimentale, Università di Pisa, Via Savi 10, I-56126, Pisa, Italy.
Unità di Farmacologia, Università di Pisa, Via Roma, 55, I-56126, Pisa, Italy.
Invest New Drugs. 2020 Feb;38(1):92-98. doi: 10.1007/s10637-019-00804-5. Epub 2019 Jun 1.
The aim of this study was to investigate possible synergistic effects in vitro of trifluridine/tipiracil (TAS-102) and 5-fluoruracil (5-FU) on fluoropyrimidine-sensitive colon cancer cell lines of different mutational status in order to build a rational basis for the future use of this combination therapy in adjuvant settings or as a first-line treatment for metastatic disease. Proliferation assays were performed on HT-29 (B-raf mutated), SW-620 (ras mutated), and Caco-2 (wild type) colon cancer cell lines exposed to 120-h treatments of 5-FU, TAS-102 and their different combination schedules (simultaneous, sequential and reverse) at equimolar and non-equimolar ratios. The synergistic, additive and antagonistic effects of 5-FU and TAS-102 were determined by the combination index (CI) and dose reduction index (DRI). Our preclinical in vitro results may suggest an apparently counterintuitive but strongly synergistic combination of 5-FU and TAS-102 in fluoropyrimidine-sensitive colon cancer cells allowing a marked theoretical reduction in the administered doses of both drugs. In particular, this association seems to be highly effective in wild-type colon cancer cells, both in sequential and simultaneous schedules. Together, these data may build a rational basis for the future use of TAS-102 combined with 5-FU in adjuvant settings, or as a first-line treatment for metastatic disease.
本研究旨在探讨三氟尿苷/替匹嘧啶(TAS-102)与氟尿嘧啶(5-FU)在不同突变状态的氟嘧啶敏感结肠癌细胞系中的体外协同作用,为该联合治疗方案在辅助治疗或转移性疾病的一线治疗中的未来应用提供合理的依据。在 HT-29(B-raf 突变)、SW-620(ras 突变)和 Caco-2(野生型)结肠癌细胞系中,通过对 120 小时的 5-FU、TAS-102 及其不同联合方案(同时、序贯和逆转)的处理,进行了增殖试验,这些方案采用等摩尔和非等摩尔比例。通过组合指数(CI)和剂量减少指数(DRI)确定 5-FU 和 TAS-102 的协同、相加和拮抗作用。我们的临床前体外结果可能表明,5-FU 和 TAS-102 在氟嘧啶敏感结肠癌细胞中存在明显的反直觉但强烈的协同作用,允许两种药物的给药剂量明显减少。特别是,这种联合治疗在野生型结肠癌细胞中,无论是序贯还是同时治疗,似乎都非常有效。这些数据为 TAS-102 联合 5-FU 在辅助治疗中的未来应用或作为转移性疾病的一线治疗提供了合理的依据。