Thymidylate synthase inhibition by an oral regimen consisting of tegafur-uracil (UFT) and low-dose leucovorin for patients with gastric cancer

被引:11
作者
Ichikura, T
Tomimatsu, S
Okusa, Y
Yahara, T
Uefuji, K
Tamakuma, S
机构
[1] First Department of Surgery, National Defense Medical College, Tokorozawa, 3-2, Namiki
关键词
gastric cancer; 5-fluorouracil; leucovorin; biochemical modulation; thymidylate synthase;
D O I
10.1007/s002800050503
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:401 / 405
页数:5
相关论文
共 29 条
[1]  
[Anonymous], 1995, JAP CLASS GASTR CARC
[2]   A PHASE-II TRIAL OF 5-FLUOROURACIL AND HIGH-DOSE INTRAVENOUS LEUCOVORIN IN GASTRIC-CARCINOMA [J].
ARBUCK, SG ;
DOUGLASS, HO ;
TRAVE, F ;
MILLIRON, S ;
BARONI, M ;
NAVA, H ;
EMRICH, LJ ;
RUSTUM, YM .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (08) :1150-1156
[3]   PROSPECTIVE RANDOMIZED COMPARISON OF FLUOROURACIL VERSUS FLUOROURACIL AND HIGH-DOSE CONTINUOUS INFUSION LEUCOVORIN CALCIUM FOR THE TREATMENT OF ADVANCED MEASURABLE COLORECTAL-CANCER IN PATIENTS PREVIOUSLY UNEXPOSED TO CHEMOTHERAPY [J].
DOROSHOW, JH ;
MULTHAUF, P ;
LEONG, L ;
MARGOLIN, K ;
LITCHFIELD, T ;
AKMAN, S ;
CARR, B ;
BERTRAND, M ;
GOLDBERG, D ;
BLAYNEY, D ;
ODUJINRIN, O ;
DELAP, R ;
SHUSTER, J ;
NEWMAN, E .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (03) :491-501
[4]   A RANDOMIZED TRIAL OF FLUOROURACIL AND FOLINIC ACID IN PATIENTS WITH METASTATIC COLORECTAL-CARCINOMA [J].
ERLICHMAN, C ;
FINE, S ;
WONG, A ;
ELHAKIM, T .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (03) :469-475
[5]  
EVANS RM, 1980, CANCER RES, V40, P4113
[6]  
IKENAKA K, 1983, JPN J CANC CHEMOTHER, V10, P227
[7]  
KAJIYAMA Y, 1993, JPN J CANC CHEMOTHER, V20, P1797
[8]  
KONISHI T, 1990, JPN J GATROENTEROL S, V23, P2024
[9]   ANTITUMOR-ACTIVITY OF FLUOROPYRIMIDINES AND THYMIDYLATE SYNTHETASE INHIBITION [J].
KUBOTA, T ;
FUJITA, S ;
KODAIRA, S ;
YAMAMOTO, T ;
JOSUI, K ;
ARISAWA, Y ;
SUTO, A ;
ISHIBIKI, K ;
ABE, O ;
MABUCHI, K ;
FUSE, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1991, 82 (04) :476-482
[10]   HIGH-DOSE FOLINIC ACID, 5-FLUOROURACIL BOLUS AND CONTINUOUS INFUSION IN POOR-PROGNOSIS PATIENTS WITH ADVANCED MEASURABLE GASTRIC-CANCER [J].
LOUVET, C ;
DEGRAMONT, A ;
DEMUYNCK, B ;
NORDLINGER, B ;
MAISANI, JE ;
LAGADEC, B ;
DELFAU, S ;
VARETTE, C ;
GONZALEZCANALI, G ;
KRULIK, M .
ANNALS OF ONCOLOGY, 1991, 2 (03) :229-230