Double-blind, randomized comparison of the antiemetic efficacy of intravenous dolasetron mesylate and intravenous ondansetron in the prevention of acute cisplatin-induced emesis in patients with cancer

被引:111
作者
Hesketh, P
Navari, R
Grote, T
Gralla, R
Hainsworth, J
Kris, M
Anthony, L
Khojasteh, A
Tapazoglou, E
Benedict, C
Hahne, W
机构
[1] BOSTON UNIV, MED CTR, BOSTON, MA USA
[2] SIMON WILLIAMSON CLIN, BIRMINGHAM, AL USA
[3] SALEM RES GRP, WINSTON SALEM, NC USA
[4] ALTON OCHSNER MED FDN & OCHSNER CLIN, NEW ORLEANS, LA 70121 USA
[5] SARAH CANNON CANC CTR, NASHVILLE, TN USA
[6] VANDERBILT UNIV, MED CTR, NASHVILLE, TN USA
[7] MEM SLOAN KETTERING CANC CTR, NEW YORK, NY 10021 USA
[8] COLUMBIA COMPREHENS CANC CTR CLIN, COLUMBIA, MO USA
[9] ST JOHN HOSP & MED CTR, DETROIT, MI USA
[10] UNIV TEXAS, HLTH SCI CTR, HOUSTON, TX USA
[11] HOECHST MARION ROUSSEL, KANSAS CITY, MO USA
关键词
D O I
10.1200/JCO.1996.14.8.2242
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the comparative antiemetic efficacy of single-dose intravenous (IV) dolasetron mesylate and ondansetron in preventing cisplatin-induced nausea and vomiting. Patients and Methods: Cancer patients (n = 609) receiving first-course cisplatin chemotherapy were randomized to one of three treatments: 1.8 or 2.4 mg/kg dolasetron mesylate salt (equivalent to 1.3 and 1.8 mg/kg dolasetron base, respectively) or 32 mg ondansetron. Each treatment was infused over 15 minutes, 30 minutes before cisplatin administration. Patients were stratified to cisplatin doses of <greater than or equal to greater than or equal to 70 and less than 91 mg/m(2) (n = 368) or greater than or equal to 91 mg/m(2) (n = 241), administered over less than or equal to 3 hours, protocol-defined efficacy criteria included complete response (zero emetic episodes and no rescue medication), major response (1 to 2 emetic episodes and no rescue medication), and patients' report of nausea severity and satisfaction recorded on a 100-mm visual analog scale (VAS). Results: The three treatments met protocol-specified criteria for equivalence, Complete response rates for dolasetron mesylate 1.8 mg/kg, 2.4 mg/kg, and ondansetron, respectively, were 49.2%, 45.6%, and 50.4% for patients in the lower cisplatin stratum (mean, 74.7 mg/m(2)) and 36.8%, 31.3%, and 31.8% in the higher cisplatin stratum (mean, 100.6 mg/m(2)). No significant differences were observed in the extent of nausea with either dolasetron dose compared with ondansetron. Less nausea was noted with 1.8 mg/kg dolasetron compared with the 2.4 mg/kg dose (P = .044) All three antiemetic treatments were well tolerated. Asymptomatic electrocardiogram changes were recorded with both dolasetron and ondansetron. Conclusion: A single IV dose of dolasetron mesylate (1.8 or 2.4 mg/kg) has comparable safety and efficacy to a single 32-mg IV dose of ondansetron in patients receiving cisplatin chemotherapy. (C) 1996 by American Society of Clinical Oncology.
引用
收藏
页码:2242 / 2249
页数:8
相关论文
共 35 条
[1]   PHASE-I/II TRIAL OF GRANISETRON - A NOVEL 5-HYDROXYTRYPTAMINE ANTAGONIST FOR THE PREVENTION OF CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING [J].
ADDELMAN, M ;
ERLICHMAN, C ;
FINE, S ;
WARR, D ;
MURRAY, C .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (02) :337-341
[2]  
ANDREWS P L R, 1992, European Journal of Cancer, V28A, pS2, DOI 10.1016/0959-8049(92)90628-F
[3]  
BALTZER L, 1993, P AN M AM SOC CLIN, V12, P462
[4]   STRATIFIED, RANDOMIZED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS ONDANSETRON ADMINISTERED AS A MULTIPLE-DOSE REGIMEN VERSUS 2 SINGLE-DOSE REGIMENS IN THE PREVENTION OF CISPLATIN-INDUCED NAUSEA AND VOMITING [J].
BECK, TM ;
HESKETH, PJ ;
MADAJEWICZ, S ;
NAVARI, RM ;
PENDERGRASS, K ;
LESTER, EP ;
KISH, JA ;
MURPHY, WK ;
HAINSWORTH, JD ;
GANDARA, DR ;
BRICKER, LJ ;
KELLER, AM ;
MORTIMER, J ;
GALVIN, DV ;
HOUSE, KW ;
BRYSON, JC .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (12) :1969-1975
[5]   CHARACTERIZATION OF THE NOVEL 5-HT3 ANTAGONISTS MDL-73147EF (DOLASETRON MESILATE) AND MDL-74156 IN NG108-15 NEUROBLASTOMA X GLIOMA-CELLS [J].
BOEIJINGA, PH ;
GALVAN, M ;
BARON, BM ;
DUDLEY, MW ;
SIEGEL, BW ;
SLONE, AL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 219 (01) :9-13
[6]  
BONNETERRE J, IN PRESS EUR J CANC
[7]   HUMAN DOLASETRON PHARMACOKINETICS .1. DISPOSITION FOLLOWING SINGLE-DOSE INTRAVENOUS ADMINISTRATION TO NORMAL-MALE SUBJECTS [J].
BOXENBAUM, H ;
GILLESPIE, T ;
HECK, K ;
HAHNE, W .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1992, 13 (09) :693-701
[8]  
CLARK R, 1985, ONCOL NURS FORUM S, V12, P96
[9]   ACUTE ANTIEMETIC EFFICACY AND SAFETY OF DOLASETRON MESYLATE, A 5-HT3 ANTAGONISTS, IN CANCER-PATIENTS TREATED WITH CISPLATIN [J].
CONROY, T ;
CAPPELAERE, P ;
FABBRO, M ;
FAUSER, AA ;
SPLINTER, TAW ;
SPIELMANN, M ;
SCHNEIDER, M ;
CHEVALLIER, B ;
GOUPIL, A ;
CHAUVERGNE, J ;
FARGEOT, P ;
PREVOT, G ;
OGRADY, P ;
GREEN, D ;
HARDENBERG, J ;
BOYCE, M .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1994, 17 (02) :97-102
[10]  
COX DR, 1972, J R STAT SOC B, V34, P187