Acute emesis: moderately emetogenic chemotherapy

被引:26
作者
Herrstedt, J [1 ]
Koeller, JM
Roila, F
Hesketh, PJ
Warr, D
Rittenberg, C
Dicato, M
机构
[1] Copenhagen Univ Hosp, Dept Oncol 54 B1, DK-2730 Herlev, Denmark
[2] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
[3] Policlin Hosp, Perugia, Italy
[4] Caritas St Elizabeths Med Ctr Boston, Boston, MA USA
[5] Univ Toronto, Princess Margaret Hosp, Toronto, ON, Canada
[6] Rittenberg Oncol Consulting, Metairie, LA USA
[7] Luxembourg Med Ctr, Luxembourg, Luxembourg
关键词
serotonin antagonists; dexamethasone; anthracycline; cyclophosphamide; chemotherapy;
D O I
10.1007/s00520-004-0701-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This paper is a review of the recommendations for the prophylaxis of acute emesis induced by moderately emetogenic chemotherapy as concluded at the Perugia Consensus Conference, which took place at the end of March 2004. The review focuses on new studies appearing since the last consensus conference in 1997. The following issues are addressed: dose and schedule of antiemetics, different groups of antiemetics such as corticosteroids, serotonin (5-HT3)- receptor antagonists, dopamine D-2 receptor antagonists, and neurokinin (NK1) receptor antagonists. Antiemetic prophylaxis in patients receiving multiple cycles of moderately emetogenic chemotherapy is also reviewed. Consensus statements are given, including optimal dose and schedule of 5-HT3-receptor antagonists and of dexamethasone. The new 5-HT3-receptor antagonist, palonosetron, is a reasonable alternative to the well-established agents of this class-on-dansetron, granisetron, tropisetron and dolasetron. It is concluded that the best prophylaxis in patients receiving moderately emetogenic chemotherapy is still the combination of one of the 5-HT3-receptor antagonists and dexamethasone. The results of studies adding a NK1-receptor antagonist to this combination are awaited and might change future recommendations.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 32 条
[1]   TROPISETRON ALONE OR IN COMBINATION WITH DEXAMETHASONE FOR THE PREVENTION AND TREATMENT OF EMESIS INDUCED BY NON-CISPLATIN CHEMOTHERAPY - A RANDOMIZED TRIAL [J].
ADAMS, M ;
SOUKOP, M ;
BARLEY, V ;
YOSEF, H ;
ANDERSON, N ;
BOESEN, E ;
TRASK, CW ;
RUFENACHT, E ;
DEBRUIJN, KM .
ANTI-CANCER DRUGS, 1995, 6 (04) :514-521
[2]  
[Anonymous], 1999, AM J HEALTH-SYST PH, V56, P729
[3]   Oral ondansetron 8 mg twice daily is as effective as 8 mg three times daily in the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy [J].
Beck, TM ;
York, M ;
Chang, A ;
Navari, R ;
Harvey, WH ;
Meshad, M ;
Griffin, D ;
Wentz, A .
CANCER INVESTIGATION, 1997, 15 (04) :297-303
[4]   Comparison of an orally disintegrating ondansetron tablet with the conventional ondansetron tablet for cyclophosphamide-induced emesis in cancer patients: A multicenter, double-masked study [J].
Davidson, N ;
Rapoport, B ;
Erikstein, B ;
L'Esperance, B ;
Ruff, P ;
Paska, W ;
Miller, I ;
Curtis, P .
CLINICAL THERAPEUTICS, 1999, 21 (03) :492-502
[5]  
Davidson NGP, 1997, ONCOLOGY, V54, P380
[6]   Analysis of cumulative probabilities shows that the efficacy of 5HT(3) antagonist prophylaxis is not maintained [J].
deWit, R ;
Schmitz, PIM ;
Verweij, J ;
deBoerDennert, M ;
deMulder, PHM ;
Planting, AST ;
vanderBurg, MEL ;
Stoter, G .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (02) :644-651
[7]  
duBois A, 1997, ONCOLOGY, V54, P7
[8]   Improved prevention of moderately emetogenic chemotherapy-induced nausea and vomiting with palonosetron, a pharmacologically novel 5-HT3 receptor antagonist -: Results of a phase III, single-dose trial versus dolasetron [J].
Eisenberg, P ;
Figueroa-Vadillo, J ;
Zamora, R ;
Charu, V ;
Hajdenberg, J ;
Cartmell, A ;
Macciocchi, A ;
Grunberg, S .
CANCER, 2003, 98 (11) :2473-2482
[9]  
Fujii M, 2000, Gan To Kagaku Ryoho, V27, P1557
[10]   Comparison of oral itasetron with oral ondansetron: Results of a double-blind, active-controlled phase II study in chemotherapy-naive patients receiving moderately emetogenic chemotherapy [J].
Goldschmidt, H ;
Salwender, H ;
Egerer, G ;
Kempe, R ;
Voigt, T .
ANTI-CANCER DRUGS, 1997, 8 (05) :436-444