PHASE I-II INTRAPERITONEAL MITOXANTRONE IN ADVANCED PRETREATED OVARIAN-CANCER

被引:14
作者
NICOLETTO, MO
PADRINI, R
FERRAZZI, E
NASCIMBEN, O
VISONA, E
TUMOLO, S
PALUMBO, M
COSTA, L
VINANTE, O
MONFARDINI, S
FIORENTINO, MV
机构
[1] PADOVA GEN HOSP,DIV MED ONCOL,I-35100 PADUA,ITALY
[2] USSL 21,I-35100 PADUA,ITALY
[3] UNIV PADUA,DEPT PHARMACOL,I-35100 PADUA,ITALY
[4] MED ONCOL DIV,ROVIGO,ITALY
[5] RADIOTHERAPY DIV,MESTRE,ITALY
[6] CANC INST,AVIANO,ITALY
[7] UNIV PADUA,FAC CHEM,I-35100 PADUA,ITALY
[8] PADOVA GEN HOSP,CARDIOL SERV,NOALE,ITALY
[9] MED ONCOL DIV,NOALE,ITALY
关键词
D O I
10.1016/0959-8049(93)90065-N
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
36 previously treated patients (25 with anthracyclines) with advanced epithetial ovarian cancer have been treated with intraperitoneal (i.p.) mitoxantrone (M) at increasing doses. The response was evaluated through repeated laparoscopy with multiple biopsies and serial measurement of Ovarian Cancer Antigen 125 (CA 125); 11/36 patients had a complete (6 patients) or partial (5 patients) response. Toxicity (both local and general) was observed starting from 25 mg/M2 of M per cycle. The amount of drug reaching systemic circulation was monitored by measuring M plasma value after i.p. treatment. This study showed wide variations in serum levels obtained after i.p. doses ranging from 23 to 36 Mg/M2 . The area under the curve (AUC) of mitoxantrone plasma samples, did not correlate with the i.p. administered dose. Conversely, a correlation seems to exist between the plasma AUC and the responder status. Patients who showed clinical responses to i.p. treatment with mitoxantrone had AUCs and plasma peak levels of the drug that were significantly higher than those in non-responders (P = 0.03, Fisher's exact test).
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收藏
页码:1242 / 1248
页数:7
相关论文
共 29 条
[1]  
ALBERTS DS, 1988, CANCER RES, V48, P5874
[2]  
ALBERTS DS, 1985, SEMIN ONCOL, V12, P38
[3]  
ALBERTS DS, 1985, INVEST NEW DRUG, V3, P101
[4]   A RADIOIMMUNOASSAY USING A MONOCLONAL-ANTIBODY TO MONITOR THE COURSE OF EPITHELIAL OVARIAN-CANCER [J].
BAST, RC ;
KLUG, TL ;
STJOHN, E ;
JENISON, E ;
NILOFF, JM ;
LAZARUS, H ;
BERKOWITZ, RS ;
LEAVITT, T ;
GRIFFITHS, CT ;
PARKER, L ;
ZURAWSKI, VR ;
KNAPP, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (15) :883-887
[5]   ESCALATING DOSE REGIMEN OF INTRAPERITONEAL MITOXANTRONE - PHASE-I STUDY - CLINICAL AND PHARMACOKINETIC EVALUATION [J].
BLOCHLDAUM, B ;
EICHLER, HG ;
RAINER, H ;
JAKESZ, R ;
SALZER, H ;
STEGER, G ;
SCHULLER, J ;
GUNTHER, E ;
PROKSCH, B ;
EHNINGER, G .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (07) :1133-1138
[6]  
DEDRICK RL, 1978, CANCER TREAT REP, V62, P1
[7]   MITOXANTRONE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC POTENTIAL IN THE CHEMOTHERAPY OF CANCER [J].
FAULDS, D ;
BALFOUR, JA ;
CHRISP, P ;
LANGTRY, HD .
DRUGS, 1991, 41 (03) :400-449
[8]  
FIGO Cancer Committee, 1986, GYNECOL ONCOL, V25, P383
[9]  
FIORENTINO MV, 1988, 6TH P MED C CHEM TAO, P504
[10]  
FIORENTINO MV, 1989, P AM SOC CLIN ONCOL, V8, P646