Increased potentiation of 5-fluorouracil induced thymidylate synthase inhibition by 5,10-methylenetetrahydrofolate (arfolitixorin) compared to leucovorin in patients with colorectal liver metastases; The Modelle-001 Trial

在结直肠癌肝转移患者中,与亚叶酸钙相比,5,10-亚甲基四氢叶酸(阿福替沙林)能更显著地增强5-氟尿嘧啶诱导的胸苷酸合成酶抑制作用;Modelle-001试验

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Abstract

BACKGROUND: 5-Fluorouracil (5-FU) is a cornerstone in treatment of colorectal cancer (CRC) and is usually combined with leucovorin (LV) to enhance the antitumour effect by increase thymidylate synthase (TS) inhibition, the key target enzyme for 5-FU. Arfolitixorin (Arfo) is an active form of the reduced folate, [6 R]-5,10-methylenetetrahydrofolate ([6 R]-MeTHF and in contrast to LV, does not need to be metabolized. The Modelle-001 was designed to explore whether a single intravenous bolus injection of Arfo as compared to LV, together with 5-FU increases the inhibition of TS, levels of folate concentrations and polyglutamylation in CRC liver metastases (CRLM) and liver parenchyma. PATIENTS AND METHODS: Thirty patients with CRLM received either LV (60 mg/m(2)) or Arfo (30 mg/m(2) or 120 mg/m(2)) in combination with 5-FU preoperatively. Levels of folates and and TS inhibition were measured. RESULTS: Significantly higher MeTHF levels and higher TS inhibition were measured in the Arfo groups compared to LV60, and there was a difference in folate poly-glutamylation between the groups. CONCLUSION: The Modelle-001 Trial demonstrated significantly higher levels of MeTHF in metastases following Arfo compared to LV. This resulted in a greater increase TS inhibition in metastases although not statistically significant.

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