THE OPTIMIZATION OF CARBOPLATIN DOSE IN CARBOPLATIN, ETOPOSIDE AND BLEOMYCIN COMBINATION CHEMOTHERAPY FOR GOOD PROGNOSIS METASTATIC NONSEMINOMATOUS GERM-CELL TUMORS OF THE TESTIS

被引:36
作者
CHILDS, WJ
NICHOLLS, EJ
HORWICH, A
机构
[1] INST CANC RES,DOWNS RD,SUTTON SM2 5PT,SURREY,ENGLAND
[2] ROYAL MARSDEN HOSP,SUTTON SM2 5PT,SURREY,ENGLAND
关键词
GERM CELL TUMOR; NONSEMINOMA; TESTIS CARBOPLATIN; PHARMACOKINETICS; CHEMOTHERAPY;
D O I
10.1093/oxfordjournals.annonc.a058182
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
An analysis of carboplatin dose response was performed in 121 patients with good prognosis metastatic nonseminomatous germ cell tumours (NSGCT) of the testis, referred to the Royal Marsden Hospital since 1984, who had been given combination carboplatin, etoposide and bleomycin (CEB) chemotherapy. With a median follow-up of 40 months (range: 7 to 85 months) nine patients (7%) have failed CEB. Carboplatin dose was analysed in all patients using body surface area (BSA) to derive a carboplatin dose per metre squared (mg/m2) and by calculation of a predicted serum concentration chi-time (AUC: area under the curve) derived from the glomerular filtration rate (GFR), using the formula; Dose = AUC(GFR + 25). At a carboplatin dose of 400 mg/m2 or greater 2 out of 58 patients (3.4%) failed treatment while 7 out of 63 patients (11%) who received a dose less than this failed (p > 0.1). At an AUC of 5.0 mg.min/ml or greater, 2 out of 74 patients (2.7%) failed while 7 out of 47 patients (14.9%) who had an AUC less than this failed (p < 0.05). There was evidence for a dose/response relationship at relatively low doses and the failure rate rose to 26% for doses less than 4.5 mg.min/ml (p < 0.001) or 15.6% for doses less than 350 mg/m2 (p > 0.1). In view of the more precise determination of toxicity and efficacy it is recommended that carboplatin dose be based on the GFR.
引用
收藏
页码:291 / 296
页数:6
相关论文
共 31 条
  • [1] ALSARRAF M, 1990, CARBOPLATIN JM 8 CUR, P221
  • [2] BAJORIN DF, 1991, P AM SOC CLIN ONCOL, V10, P535
  • [3] BAJORIN DF, 1991, P AN M AM SOC CLIN, V10, P168
  • [4] A NOVEL PHARMACODYNAMICALLY BASED APPROACH TO DOSE OPTIMIZATION OF CARBOPLATIN WHEN USED IN COMBINATION WITH ETOPOSIDE
    BELANI, CP
    EGORIN, MJ
    ABRAMS, JS
    HIPONIA, D
    EISENBERGER, M
    AISNER, J
    VANECHO, DA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (12) : 1896 - 1902
  • [5] BELANI CP, 1990, CARBOPLATIN JM 8 CUR, P53
  • [6] EARLY CLINICAL-STUDIES WITH CIS-DIAMMINE-1,1-CYCLOBUTANE DICARBOXYLATE PLATINUM-II
    CALVERT, AH
    HARLAND, SJ
    NEWELL, DR
    SIDDIK, ZH
    JONES, AC
    MCELWAIN, TJ
    RAJU, S
    WILTSHAW, E
    SMITH, IE
    BAKER, JM
    PECKHAM, MJ
    HARRAP, KR
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1982, 9 (03) : 140 - 147
  • [7] CARBOPLATIN DOSAGE - PROSPECTIVE EVALUATION OF A SIMPLE FORMULA BASED ON RENAL-FUNCTION
    CALVERT, AH
    NEWELL, DR
    GUMBRELL, LA
    OREILLY, S
    BURNELL, M
    BOXALL, FE
    SIDDIK, ZH
    JUDSON, IR
    GORE, ME
    WILTSHAW, E
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (11) : 1748 - 1756
  • [8] PHASE-I STUDIES WITH CARBOPLATIN AT THE ROYAL-MARSDEN-HOSPITAL
    CALVERT, AH
    HARLAND, SJ
    NEWELL, DR
    SIDDIK, ZH
    HARRAP, KR
    [J]. CANCER TREATMENT REVIEWS, 1985, 12 : 51 - 57
  • [9] CALVERT AH, 1987, P AN M AM SOC CLIN, V6, P45
  • [10] CHANTLER C, 1969, CLIN SCI, V37, P169