PREVENTION OF EMESIS BY ICS 205-930 IN CHILDREN RECEIVING CYTOTOXIC CHEMOTHERAPY

被引:19
作者
HACHIMIIDRISSI, S
DESCHEPPER, J
MAURUS, R
OTTEN, J
机构
关键词
D O I
10.1016/S0959-8049(05)80423-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nausea and vomiting are among the most frequent and severe acute side-effects of cytotoxic therapy and are not optimally controlled by conventional antiemetics. This situation warrants the evaluation of new classes of antiemetic agents such as the 5-HT3 receptor antagonists. 19 children with a median age of 9 years (range 2-16 years), treated with cytotoxic drug combinations that had previously caused nausea and vomiting refractory to conventional antiemetics, were given the selective 5-HT3 receptor antagonist ICS 205-930. The drug was given intravenously (i.v.) at 0.2 mg/kg (maximum 5 mg) during the chemotherapy infusion period and was continued orally for up to 5 days in chemotherapy courses containing cisplatin. The number of emetic episodes was recorded and the response was scored according to following scale: grade 1 = no nausea, no emetic episode; grade 2 = up to four episodes of vomiting and less than 5 h of nausea; grade 3 = five or more than five emetic episodes and/or nausea for at least 5 h. The 19 patients received a total of 169 various courses of chemotherapy combined with ICS 205-930. A score of 3 was observed during one course only, a score of 2 in 37 out of the 169 courses, including the four courses with cisplatin. The drug was very well tolerated. Side-effects possibly related to ICS 205-930 were mild to moderate headache in 4 patients during seven courses overall and obstipation in 3 patients during 11 courses. The results strongly suggest that ICS 205-930 is a highly effective and safe antiemetic agent in non-naive pediatric patients receiving non-cisplatin cytotoxic chemotherapy and who had failed conventional antiemetic treatment.
引用
收藏
页码:854 / 856
页数:3
相关论文
共 12 条
[1]   METOCLOPRAMIDE - DOSE-RELATED TOXICITY AND PRELIMINARY ANTIEMETIC STUDIES IN CHILDREN RECEIVING CANCER-CHEMOTHERAPY [J].
ALLEN, JC ;
GRALLA, R ;
REILLY, L ;
KELLICK, M ;
YOUNG, C .
JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (08) :1136-1141
[2]   NEUROPHARMACOLOGY OF EMESIS INDUCED BY ANTI-CANCER THERAPY [J].
ANDREWS, PLR ;
RAPEPORT, WG ;
SANGER, GJ .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1988, 9 (09) :334-341
[3]   THE ANTI-EMETIC POTENTIAL OF THE 5-HYDROXYTRYPTAMINE3 RECEPTOR ANTAGONIST BRL-43694 [J].
BERMUDEZ, J ;
BOYLE, EA ;
MINER, WD ;
SANGER, GJ .
BRITISH JOURNAL OF CANCER, 1988, 58 (05) :644-650
[4]   RANDOMIZED TRIAL OF INTRAVENOUS HIGH-DOSE METOCLOPRAMIDE AND INTRAMUSCULAR CHLORPROMAZINE IN CONTROLLING NAUSEA AND VOMITING INDUCED BY CYTO-TOXIC DRUGS [J].
CUNNINGHAM, D ;
SOUKOP, M ;
GILCHRIST, NL ;
FORREST, GJ ;
HEPPLESTONE, A ;
CALDER, IT ;
MCARDLE, CS ;
HUTCHEON, AW ;
KAYE, SB .
BRITISH MEDICAL JOURNAL, 1985, 290 (6468) :604-605
[5]   CHEMOTHERAPY INDUCED EMESIS - MECHANISMS AND TREATMENT - A REVIEW [J].
EDWARDS, CM .
JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 1988, 81 (11) :658-662
[6]   5-HT3 RECEPTOR ANTAGONISTS INJECTED INTO THE AREA POSTREMA INHIBIT CISPLATIN-INDUCED EMESIS IN THE FERRET [J].
HIGGINS, GA ;
KILPATRICK, GJ ;
BUNCE, KT ;
JONES, BJ ;
TYERS, MB .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (01) :247-255
[7]  
LEIBUNDGUT U, 1987, LANCET, V1, P1198
[8]   EFFICACY AND SAFETY OF GRANISETRON IN THE PREVENTION OF CHEMOTHERAPY-INDUCED EMESIS IN PEDIATRIC-PATIENTS [J].
LEMERLE, J ;
AMARAL, D ;
SOUTHALL, DP ;
UPWARD, J ;
MURDOCH, RD .
EUROPEAN JOURNAL OF CANCER, 1991, 27 (09) :1081-1083
[9]   ANTIEMETIC THERAPY FOR CHEMOTHERAPY-INDUCED VOMITING - METOCLOPRAMIDE, BENZTROPINE, DEXAMETHASONE, AND LORAZEPAM REGIMEN COMPARED WITH CHLORPROMAZINE ALONE [J].
MARSHALL, G ;
KERR, S ;
VOWELS, M ;
OGORMANHUGHES, D ;
WHITE, L .
JOURNAL OF PEDIATRICS, 1989, 115 (01) :156-160
[10]   5-HT3 ANTAGONIST ONDANSETRON - AN EFFECTIVE OUTPATIENT ANTIEMETIC IN CANCER-TREATMENT [J].
PINKERTON, CR ;
WILLIAMS, D ;
WOOTTON, C ;
MELLER, ST ;
MCELWAIN, TJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1990, 65 (08) :822-825