DOUBLE-MODULATION OF 5-FLUOROURACIL IN THE TREATMENT OF ADVANCED COLORECTAL-CARCINOMA - REPORT OF A TRIAL WITH SEQUENTIAL METHOTREXATE, INTRAVENOUS (LOADING DOSE) FOLINIC ACID, 5-FLUOROURACIL, AND A LITERATURE-REVIEW

被引:1
作者
BALABAN, EP
GRAHAM, M
PERKINS, S
SHEEHAN, RG
FRENKEL, EP
ROSS, M
BULL, J
PRUITT, B
PERIMAN, P
RUUD, C
LUCE, J
机构
[1] DEPT VET AFFAIRS MED CTR,DALLAS,TX
[2] HARRIS METHODIST HOSP,FT WORTH,TX
[3] UNIV TEXAS,HLTH SCI CTR,DIV MED ONCOL,HOUSTON,TX
[4] TEXAS TECH UNIV,SCH MED,DIV MED ONCOL,AMARILLO,TX
[5] DON & SYBIL HARRINGTON CANC CTR,AMARILLO,TX
关键词
D O I
10.3109/07357909409021388
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
5-Fluorouracil (5-FU) modulation with either folinic acid (FA) or methotrexate(MTX) has improved 5-FU's potential cytoreductivity. We combined MTX and FA with 5-FU to further augment 5-FU's cytoreductivity. Patients (n = 34) with advanced colorectal carcinoma were first given intravenous MTX (escalated from 30 mg/m(2) to 70 mg/m(2)). FA (100 mg/m(2)) was infused 17-24 hr later, followed by 5-FU (600 mg/m(2)). Oral rescue doses of FA were begun 24 hr after MTX. Patients were treated every 2 weeks. No previously treated patient (n = 6) responded. Eight of the remaining 28 (29%) (95% confidence interval, 15-47%) patients achieved a PR. Median survival was 9.3 months. Toxicity (primarily gastrointestinal) necessitated dosage modification in 10 patients (29%). These results, in addition to a literature review, reveal that the manipulation of 5-FU by two modulating agents does not improve the response rate seen with single-agent modulation.
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页码:12 / 19
页数:8
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