A COMPARATIVE-STUDY WITH 2 ADMINISTRATION SCHEDULES OF LEUCOVORIN AND 5-FLUOROURACIL IN ADVANCED COLORECTAL-CANCER

被引:2
|
作者
TSAVARIS, N
FOUTZILAS, G
MARKANTONAKIS, P
MYLONAKIS, N
BACOYANNIS, C
ZISIADIS, A
BASDANIS, G
KARVOUNIS, N
SOBOLOS, K
KOSMIDIS, P
机构
[1] Second Dept of Medical Oncology, “Metaxa” Cancer Hospital, Piraeus, 185 37
[2] University of Thessaloniki, School of Medicine, First Dept. of Internal Medicine, AHEPA Hospital, Thessaloniki
关键词
LEUCOVORIN; 5-FLUOROURACIL; COLORECTAL CANCER;
D O I
10.1179/joc.1995.7.1.71
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
One hundred and seven previously untreated patients with measurable metastatic colorectal cancer who were treated with 5-fluorouracil (5FU) and leucovorin (LV) in two different maximum doses and schedules were retrospectively analyzed. Group A, 52 pts, was treated with LV 200 mg/m(2)/D IV push, followed by 5FU 700 mg/m(2)/D IV 1 h infusion for 5 D. Cycle was repeated every 21 D. Group B, 55 pts, was treated with LV 500 mg/m(2)/D in a 2 h infusion and 5FU 600 mg/m(2)/D IV bolus at mid-time of LV infusion, repeated every week for 6 wk followed by 2-wk rest period. There was no difference in response (A 8%, B 11%). Median survival for A was 37 (2-131) wk, B was 59 (1-112) wk (P = 0.021), time to progression for A was 20 (0-131) wk, B 30 (0-102) wk (P = 0.021). Administered mean dose intensity of LV was 350.8 mg/m(2)/wk in group A and 405.0 mg/m(2)/wk in group B without any significant difference; that of 5FU was significantly higher in group A as compared to group B (1205.3 vs 468.9 mg/m(2)/wk, respectively) (p < 0.0001). This difference was a consequence of the planned dose intensity for this drug in the two treatment regimens. Toxicity was more frequent and intense in group A for mucositis (P < 0.001), fatigue (P < 0.01), and neurotoxicity (P < 0.05), and in group B for neutropenia (P < 0.001) and nausea-vomiting (P < 0.001). There were one and four iatrogenic deaths in group A and B patients, respectively (NS). Although this study was not prospective and randomized, we can conclude that toxicity was significantly different in the two groups, with a prevalence of mucositis in group A and neutropenia in group B and a higher number of iatrogenic deaths in the latter group. Response rates were the same for the two groups although survival and time to progression were significantly increased for group B patients.
引用
收藏
页码:71 / 77
页数:7
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