CYTARABINE AND CISPLATIN AS SALVAGE THERAPY IN PATIENTS WITH METASTATIC COLORECTAL-CANCER WHO FAILED 5-FLUOROURACIL PLUS FOLINIC ACID REGIMEN

被引:6
作者
ADENIS, A
CARLIER, D
DARLOY, F
PION, JM
BONNETERRE, J
DEMAILLE, A
机构
[1] Centre Oscar Lambret, 59020 Lille Cedex
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 1995年 / 18卷 / 02期
关键词
5-FLUOROURACIL; CDDP; ARA-C; COLORECTAL CANCER;
D O I
10.1097/00000421-199504000-00013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The combination of CDDP and ARA-C has shown some clinical efficiency as first-line therapy in advanced colorectal cancer. Our study was aimed to evaluate the therapeutic activity of this combination in advanced colorectal cancer who failed 5-fluorouracil (FU) and folinic acid (LV) regimen. Seventeen patients with measurable metastatic colorectal cancer who failed 5FU-LV therapy as first line (n = 14) or second line treatment (n = 3), entered the study. Three patients who recurred during adjuvant treatment with 5FU and levamisol, were also included. Median age was 59.5 (40-69). Performance status was as follows: 0 (n = 5), 1 (n = 11), 2 (n = 3), 3 (n = 1). Site of metastases included liver (n = 16), lung (n = 7), abdomen (n = 2), pelvic recurrences (n = 2), cutaneous (n = 1). Seven patients had 2 metastatic sites and two 3. The treatment was given as follows: ARA-C 75 mg/m(2)/day, days 1-3, followed 1 hour later by CDDP 30 mg/m(2)/day, days 1-3, every 28 days. The median number of cycles was 3 (range: 1-6 cycles). All patients but one were evaluable for both response and toxicity. Of these patients, 50% experienced severe hematologic toxicity and nonhematologic toxicity mainly consisted of fatigue and/or vomiting. No objective response was observed, but there were 3 stabilizations and 16 progressive diseases. Median time to progression was 10 weeks. Thus, the CDDP/ARA-C regimen is not of clinical value as salvage therapy in advanced colorectal cancer because of its toxicity and its lack of efficiency.
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页码:158 / 160
页数:3
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