A phase II study of continuous-infusion 5-fluorouracil with cisplatin and epirubicin in inoperable pancreatic cancer

被引:54
作者
Evans, TRJ
Lofts, FJ
Mansi, JL
Glees, JP
Dalgleish, AG
Knight, MJ
机构
[1] ST GEORGE HOSP,SCH MED,DEPT SURG,LONDON SW17 0RE,ENGLAND
[2] ST GEORGE HOSP,SCH MED,DEPT RADIOTHERAPY,LONDON SW17 0RE,ENGLAND
关键词
epirubicin; cisplatin; 5-fluorouracil;
D O I
10.1038/bjc.1996.241
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinomas of the exocrine pancreas respond poorly to most chemotherapy regimens. Recently continuous infusional 5-fluorouracil (200 mg m(-2)day(-1)) with 3 weekly cisplatin (60 mg m(-2)) and epirubicin (50 mg m(-2)) (the ECF regimen) has proven to be an active regimen in gastric and breast cancer and consequently worthy of further study in pancreatic cancer. Thirty-five patients were treated with the ECF regimen as above. of whom 29 were evaluable for response and 32 were evaluable for toxicity. The mean age was 59 years (range 37-75). Sixteen patients had locally advanced disease at presentation and 19 had metastases. Objective tumour responses were documented in five (17.3%) patients who achieved a partial response: in 18 (62%) patients there was no change and six (20.7%) patients progressed on therapy, Patients with either stable disease or partial response had a significantly improved overall survival (median = 253 days) compared with patients who progressed (median = 170 days; P=0.01). Grade 3/4 (WHO) toxicity (all cycles) included alopecia in 18 (56%) patients, nausea/vomiting in eight (25%) stomatitis in three (9%) and diarrhoea in seven (22%) patients. with rhinorrhoea and excessive lacrimation in one patient each. Neutropenic sepsis occurred in 13 cycles in ten patients. and there was one toxic death due to sepsis. There were eight other episodes of non-neutropenic sepsis requiring hospital admission. Fourteen patients (40%) experienced complications with their Hickman lines. including thrombotic episodes (six patients) or their line Falling out (live patients). ECF fan prolong survival in patients with locally advanced or metastatic pancreatic cancer who demonstrate a response or stabilisation of their disease. However, this is associated with considerable toxicity.
引用
收藏
页码:1260 / 1264
页数:5
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