Palonosetron:: a unique 5-HT3-receptor antagonist for the prevention of chemotherapy-induced emesis

被引:39
作者
Grunberg, SM
Koeller, JM
机构
[1] Fletcher Allen Healthcare, Burlington, VT 05401 USA
[2] Univ Vermont, Div Hematol Oncol, Burlington, VT 05405 USA
[3] Univ Texas, Hlth Sci Ctr, Div Pharmacotherapy, San Antonio, TX 78285 USA
[4] Univ Texas, Austin, TX 78712 USA
关键词
5-HT3-receptor antagonist; chemotherapy; emesis; palonosetron;
D O I
10.1517/14656566.4.12.2297
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Palonosetron (Aloxi(TM)) is a 5-HT3-receptor antagonist antiemetic indicated for the prevention of acute and delayed nausea and vomiting following moderately emetogenic chemotherapy and for acute nausea and vomiting following highly emetogenic chemotherapy. Although it is the fourth member of this class to enter the US market, palonosetron is distinguished by distinct pharmacological characteristics. It has a higher binding affinity for the 5-HT3 receptor and a terminal serum half-life at least four times greater than any other available agent of this class (similar to 40 h). The high affinity and long half-life may explain the persistence of antiemetic effect throughout the delayed emesis risk period. The indications for palonosetron are supported by one dose-ranging study and three large, randomised, Phase III studies that all demonstrated at least equivalent activity (and in some cases, superior activity) compared to other 5-HT3-receptor antagonists. In spite of the pharmacological differences, the side effect profile of palonosetron is comparable to that of other 5-HT3-receptor antagonists. Palonosetron may prove valuable in combination therapy for delayed emesis and may be an appropriate agent for clinical settings, such as multiple-day chemotherapy, where acute emesis is repeatedly induced. Palonosetron provides a convenience advantage if multiple-day 5-HT3-receptor antagonist therapy is anticipated and is a unique addition to the antiemetic armamentarium.
引用
收藏
页码:2297 / 2303
页数:7
相关论文
共 22 条
[1]  
AAPRO MS, 2003, SUPPORT CARE CANCER, V11, pA17
[2]   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
[3]  
CARTMELL AD, 2003, P AN M AM SOC CLIN, V22, pA3041
[4]   ON THE RECEIVING END PATIENT PERCEPTION OF THE SIDE-EFFECTS OF CANCER-CHEMOTHERAPY [J].
COATES, A ;
ABRAHAM, S ;
KAYE, SB ;
SOWERBUTTS, T ;
FREWIN, C ;
FOX, RM ;
TATTERSALL, MHN .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (02) :203-208
[5]   Comparison of L-758,298, a prodrug for the selective neurokinin-1 antagonist, L-754,030, with ondansetron for the prevention of cisplatin-induced emesis [J].
Cocquyt, V ;
Van Belie, S ;
Reinhardt, RR ;
Decramer, MLA ;
O'Brien, M ;
Schellens, JHM ;
Borms, M ;
Verbeke, L ;
Van Aelst, F ;
De Smet, M ;
Carides, AD ;
Eldridge, K ;
Gertz, BJ .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (07) :835-842
[6]  
EISENBERG P, 2003, IN PRESS CANCER
[7]   DELAYED EMESIS FOLLOWING HIGH-DOSE CISPLATIN - A DOUBLE-BLIND RANDOMIZED COMPARATIVE TRIAL OF ONDANSETRON (GR-38032F) VERSUS PLACEBO [J].
GANDARA, DR ;
HARVEY, WH ;
MONAGHAN, GG ;
PEREZ, EA ;
HESKETH, PJ .
EUROPEAN JOURNAL OF CANCER, 1993, 29A :S35-S38
[8]   Palonosetron improves prevention of chemotherapy-induced nausea and vomiting following moderately emetogenic chemotherapy: results of a double-blind randomized phase III trial comparing single doses of palonosetron with ondansetron [J].
Gralla, R ;
Lichinitser, M ;
Van der Vegt, S ;
Sleeboom, H ;
Mezger, J ;
Peschel, C ;
Tonini, G ;
Labianca, R ;
Macciocchi, A ;
Aapro, M .
ANNALS OF ONCOLOGY, 2003, 14 (10) :1570-1577
[9]   ANTI-EMETIC EFFICACY OF HIGH-DOSE METOCLOPRAMIDE - RANDOMIZED TRIALS WITH PLACEBO AND PROCHLORPERAZINE IN PATIENTS WITH CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING [J].
GRALLA, RJ ;
ITRI, LM ;
PISKO, SE ;
SQUILLANTE, AE ;
KELSEN, DP ;
BRAUN, DW ;
BORDIN, LA ;
BRAUN, TJ ;
YOUNG, CW .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (16) :905-909
[10]   DOSE RANGING PHASE-I STUDY OF THE SEROTONIN ANTAGONIST GR38032F FOR PREVENTION OF CISPLATIN-INDUCED NAUSEA AND VOMITING [J].
GRUNBERG, SM ;
STEVENSON, LL ;
RUSSELL, CA ;
MCDERMED, JE .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (08) :1137-1141