Thymidylate synthase inhibition by an oral regimen consisting of tegafur-uracil (UFT) and low-dose leucovorin for patients with gastric cancer |
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Authors: | T. Ichikura S. Tomimatsu Y. Okusa T. Yahara K. Uefuji S. Tamakuma |
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Affiliation: | (1) First Department of Surgery, National Defense Medical College, 3-2, Namiki, Tokorozawa, Japan Tel. 0429-95-1511, ext. 2356; Fax 0429-95-0638, JP |
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Abstract: | Purpose: 5-Fluorouracil (5-FU) remains a standard therapy for patients with advanced gastric cancer. There has been no study using an oral regimen with a combination of tegafur, a masked compound of 5-FU, and leucovorin in gastric cancer. The purpose of this study was to determine whether orally administered low-dose leucovorin enhances thymidylate synthase (TS) inhibition when added to tegafur-uracil (UFT) in patients with gastric cancer. Methods: A group of 26 patients with resectable gastric cancer were assigned to one of two regimens: UFT alone or UFT plus leucovorin. UFT, equivalent to 400 mg/day tegafur, with or without 30 mg/day leucovorin, was administered orally in divided daily doses every 12 h for 3 consecutive days prior to surgery. Tumor specimens were taken immediately following gastrectomy, and the TS inhibition rate (TSIR) was determined using a ligand-binding assay. Results: The TSIR was significantly higher in the UFT plus leucovorin group than in the UFT alone group (P<0.01). The TSIR in the patients treated with UFT alone ranged between 14% and 50%, while six of the eight patients treated with UFT plus leucovorin had a TSIR of 55% or higher. The remaining two patients in the group treated with UFT plus leucovorin, with a TSIR of 31% and 44%, had undifferentiated tumors. Conclusion: Our results suggest that orally administered low-dose leucovorin can add to the efficacy of UFT in patients with gastric cancer, and provide preliminary data for a randomized clinical trial. Received: 27 June 1995/Accepted: 6 December 1995 |
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Keywords: | Gastric cancer 5-Fluorouracil Leucovorin Biochemical modulation Thymidylate synthase |
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