HIGH-DOSE EPIRUBICIN IS EFFECTIVE IN MEASURABLE METASTATIC PROSTATE-CANCER - A PHASE-II STUDY OF THE EORTC GENITOURINARY GROUP

被引:28
作者
BRAUSI, M
JONES, WG
FOSSA, SD
DEMULDER, PHM
DROZ, JP
LENTZ, MA
VANGLABBEKE, M
PAWINSKI, A
机构
[1] COOKRIDGE HOSP,DEPT CLIN ONCOL,LEEDS LS16 6QB,W YORKSHIRE,ENGLAND
[2] OSPED RAMAZZINI,DEPT UROL SURG,I-41012 MODENA,ITALY
[3] DET NORSKE RADIUMHOSP,DEPT MED ONCOL,N-0310 OSLO 3,NORWAY
[4] DET NORSKE RADIUMHOSP,DEPT RADIOTHERAPY,N-0310 OSLO 3,NORWAY
[5] SINT RADBOUT ZIEKENHUIS,DEPT INTERNAL MED,6500 HB NIJMEGEN,NETHERLANDS
[6] INST GUSTAVE ROUSSY,DEPT ONCOL,F-94805 VILLEJUIF,FRANCE
[7] EORTC DATA CTR,EORTC PHASE UNIT 2,B-1200 BRUSSELS,BELGIUM
关键词
EPIRUBICIN; PROSTATE CANCER; CHEMOTHERAPY; HORMONE RESISTANCE; PHASE II STUDY; PROSTATE SPECIFIC ANTIGEN (PSA);
D O I
10.1016/0959-8049(95)00193-M
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
39 hormone-resistant prostate cancer patients with bidimensionally measurable metastatic lesions were given epirubicin 100 mg/m(2) intravenously every 3 weeks. One patient was ineligible and excluded from analyses. According to WHO criteria, 9 patients (24%) had a partial response, 16 patients (42%) had stable disease (including 3 patients (8%) with a partial response not confirmed 1 month later), 11 patients (29%) had progressive disease, and in 2 patients (5%) response was not evaluated. Toxicity was as expected. Fifty-five per cent of patients had WHO grade 3/4 toxicity for white blood cells, and 3% of patients grade 3 toxicity for platelets. Other toxicities included nausea and vomiting, mucositis and alopecia. 2 patients with pre-existing cardiac disease developed cardiotoxicity (1 grade 2, 1 grade 3). An attempt was made to correlate response with prostate specific antigen (PSA) measurements. A positive trend was seen, but 2 non-responding patients showed a > 50% decrease in value.
引用
收藏
页码:1622 / 1626
页数:5
相关论文
共 15 条
  • [1] BERRY WR, 1979, CANCER, V44, P763, DOI 10.1002/1097-0142(197908)44:2<763::AID-CNCR2820440251>3.0.CO
  • [2] 2-5
  • [3] EISENBERGER M A, 1988, NCI (National Cancer Institute) Monographs, P151
  • [4] LOW-DOSE FORTNIGHTLY METHOTREXATE IN ADVANCED PROSTATE-CANCER
    JONES, WG
    FOSSA, SD
    VERBAEYS, AC
    DROZ, JP
    KLIJN, JGM
    BOVEN, E
    DEPAUW, M
    SYLVESTER, R
    [J]. EUROPEAN JOURNAL OF CANCER, 1990, 26 (05) : 646 - 646
  • [5] JONES WG, 1987, CANCER TREAT REP, V71, P1317
  • [6] MITOMYCIN-C IN THE TREATMENT OF METASTATIC PROSTATE-CANCER - REPORT ON AN EORTC PHASE-II STUDY
    JONES, WG
    FOSSA, SD
    BONO, AV
    CROLES, JJ
    STOTER, G
    DEPAUW, M
    SYLVESTER, R
    [J]. WORLD JOURNAL OF UROLOGY, 1986, 4 (03) : 182 - 185
  • [7] IS THERE A PLACE FOR CHEMOTHERAPY IN ADVANCED PROSTATIC-CANCER
    JONES, WG
    [J]. AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1988, 11 : S98 - S100
  • [8] AN EORTC PHASE-II STUDY OF VINDESINE IN ADVANCED PROSTATE-CANCER
    JONES, WG
    FOSSA, SD
    DENIS, L
    CONINX, P
    GLASHAN, RW
    AKDAS, A
    DEPAUW, M
    [J]. EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (05): : 583 - 588
  • [9] JONES WG, 1991, CURR OPIN UROL, V1, P21
  • [10] LAURIE JA, 1992, CANCER, V69, P1440, DOI 10.1002/1097-0142(19920315)69:6<1440::AID-CNCR2820690622>3.0.CO