COMBINATION CHEMOTHERAPY WITH CYCLOPHOSPHAMIDE, FLUOROURACIL, AND EITHER EPIRUBICIN OR MITOXANTRONE - A COMPARATIVE RANDOMIZED MULTICENTER STUDY IN METASTATIC BREAST-CARCINOMA

被引:16
作者
PERITI, P
PANNUTI, F
DELLACUNA, GR
MAZZEI, T
MINI, E
MARTONI, A
PRETI, P
ERCOLINO, L
PAVESI, L
RIBECCO, A
机构
[1] OSP S ORSOLA MALPIGHI,DIV ONCOL,BOLOGNA,ITALY
[2] FDN CLIN LAVORO,DIV ONCOL,PAVIA,ITALY
关键词
D O I
10.3109/07357909109021321
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
From February 1987 to January 1989, 60 patients with advanced breast cancer and no prior chemotherapy for advanced disease were randomized and studied, with 31 treated with fluorouracil, epirubicin, and cyclophosphamide (FEC) and 29 patients with fluorouracil, mitoxantrone, and cyclophosphamide (FNC). Doses were 500 mg/m2 fluorouracil, 500 mg/m2 cyclophosphamide, and 50 mg/m2 epirubicin2 or 10 mg/m mitoxantrone, i.v. Day 1 every 3 weeks. There were no statistically significant differences in pretreatment patient characteristics between the groups. Fifty-six patients were evaluable for response (29 in the FEC arm and 27 in the FNC arm). The response rates were 48.2% for the FEC group (complete response (CR) 10.3% and partial response (PR) 37.9%) and 40.7% for the FNC group (CR 3.7% and PR 37%) (not significantly different, NS). The median response duration was 247 and 267 days, respectively (NS), the median time to progression and time to treatment failure was 244 and 155.5 days for the FEC group and 86 and 98 days for the FNC group, respectively (NS). The incidence of nausea/vomiting was 87.1% in the FEC group and 79.3% in the FNC group, with comparable severity. Alopecia occurred in 80.6% of FEC patients and 44.8% of FNC patients (p < 0.05). The incidences and degrees of severity of leukopenia, anemia, and cardiotoxicity were comparable in the two treatment groups. Efficacy and toxicity of the two regimens were quite similar. FNC can improve the quality of life of patients by providing significantly less alopecia.
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页码:249 / 255
页数:7
相关论文
共 40 条
  • [21] LEVIN M, 1984, CANCER TREAT REP, V68, P1511
  • [22] MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
  • [23] 2-6
  • [24] MULTIDRUG RESISTANCE
    MOSCOW, JA
    COWAN, KH
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (01) : 14 - 20
  • [25] MITOXANTRONE AS 1ST-LINE CHEMOTHERAPY IN ADVANCED BREAST-CANCER - RESULTS OF A COLLABORATIVE EUROPEAN STUDY
    MOURIDSEN, HT
    CORNBLEET, M
    STUARTHARRIS, R
    SMITH, I
    COLEMAN, R
    RUBENS, R
    MCDONALD, M
    RAINER, H
    VANOOSTEROM, A
    SMYTH, J
    [J]. INVESTIGATIONAL NEW DRUGS, 1985, 3 (02) : 139 - 148
  • [26] A COMPARISON OF MITOXANTRONE AND DOXORUBICIN IN BREAST-CANCER
    NEIDHART, JA
    GOCHNOUR, D
    ROACH, R
    HOTH, D
    YOUNG, D
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (05) : 672 - 677
  • [27] PANNUTI F, 1981, 12TH P INT C CHEM FL, P350
  • [28] PERITI P, 1985, INVEST NEW DRUG, V3, P167
  • [29] PERITI P, 1987, INT C S SERIES, V110, P9
  • [30] ROBUSTELLI DG, 1981, 12TH P INT C CHEM FL, P1462