TREATMENT OF ADVANCED PANCREATIC-CANCER WITH 5-FLUOROURACIL, FOLINIC ACID AND INTERFERON ALPHA-2A - RESULTS OF A PHASE-II TRIAL

被引:35
作者
BERNHARD, H
JAGERARAND, E
BERNHARD, G
HEIKE, M
KLEIN, O
RIEMANN, JF
MEYER, KH
DIPPOLD, W
KNUTH, A
机构
[1] KRANKENHAUS NW FRANKFURT,MED KLIN 2,D-60488 FRANKFURT,GERMANY
[2] UNIV MAINZ,MED KLIN & POLIKLIN 1,D-55101 MAINZ,GERMANY
[3] UNIV MAINZ,INST MED STAT & DOKUMENTAT,D-55101 MAINZ,GERMANY
[4] KLINIKUM STADT LUDWIGSHAFEN,MED KLIN C,D-67063 LUDWIGSHAFEN,GERMANY
关键词
PANCREATIC CARCINOMA; 5-FLUOROURACIL; FOLINIC ACID; INTERFERON ALPHA-2A; PHASE II TRIAL;
D O I
10.1038/bjc.1995.20
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Interferon alpha-2a (IFN-alpha) and folinic acid (FA) have been shown to modulate the cytotoxic effects of 5-fluorouracil (5-FU) in the treatment of cancer. A phase II study was initiated to evaluate the effect of a combination of 5-FU/FA/IFN-alpha in patients with advanced pancreatic cancer. Sixty previously untreated patients with advanced adenocarcinoma of the pancreas were treated with 500 mg m(-2) FU via an intravenous bolus 1 h after the initiation of a 2 h infusion of 500 mg m(-2) FA. Before starting the, FA infusion, 6 million units (MU) of IFN-alpha was administered subcutaneously. The treatment was repeated once a week. Of 57 evaluable patients, eight (14%) had a partial response (PR), eight (14%) a minor response (MR) and 28 (49%) no change of disease (NC). Thirteen patients (23%) had progressive disease (PD). The median survival time was 10 months for all patients, 22 months for patients with partial remission and 5 months for patients with progressive disease. Many patients with tumour-related pain whose tumours were affected in terms of PR, MR, NC were free of pain during treatment with this regimen (22/36 patients). The common toxicities observed were fever (56%), nausea (37%) and diarrhoea (33%). These data suggest that biochemical modulation of 5-FU with FA and IFN-alpha has some positive effects in the treatment of pancreatic cancer of moderate toxicity.
引用
收藏
页码:102 / 105
页数:4
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