TY - JOUR
T1 - Consensus recommendations for the prevention of vomiting and nausea following high-emetic-risk chemotherapy
AU - Kris, Mark G.
AU - Tonato, Maurizio
AU - Bria, Emilio
AU - Ballatori, Enzo
AU - Espersen, Birgitte
AU - Herrstedt, Jørn
AU - Rittenberg, Cynthia
AU - Einhorn, Lawrence H.
AU - Grunberg, Steven
AU - Saito, Mitsue
AU - Morrow, Gary
AU - Hesketh, Paul
PY - 2011/3/1
Y1 - 2011/3/1
N2 - In this update of our 2005 document, we used an evidence-based approach whenever possible to formulate recommendations, emphasizing the results of controlled trials concerning the best use of antiemetic agents for the prevention of emesis and nausea following anticancer chemotherapies of high emetic risk. A three-drug combination of a 5-hydroxytryptamine type 3 receptor (5-HT3) receptor antagonist, dexamethasone, and aprepitant beginning before chemotherapy and continuing for up to 4 days remains the standard of care. We address issues of dose, schedule, and route of administration of five selective 5-HT3 receptor antagonists. We conclude that, for each of these five drugs, there is a plateau in therapeutic efficacy above which further dose escalation does not improve outcome. In trials designed to prove the equivalence of palonosetron to ondansetron and granisetron, palonosetron proved superior in emesis prevention, while adverse effects were comparable. Furthermore, for all classes of antiemetic agents, a single dose is as effective as multiple doses or a continuous infusion. The oral route is as efficacious as the intravenous route of administration.
AB - In this update of our 2005 document, we used an evidence-based approach whenever possible to formulate recommendations, emphasizing the results of controlled trials concerning the best use of antiemetic agents for the prevention of emesis and nausea following anticancer chemotherapies of high emetic risk. A three-drug combination of a 5-hydroxytryptamine type 3 receptor (5-HT3) receptor antagonist, dexamethasone, and aprepitant beginning before chemotherapy and continuing for up to 4 days remains the standard of care. We address issues of dose, schedule, and route of administration of five selective 5-HT3 receptor antagonists. We conclude that, for each of these five drugs, there is a plateau in therapeutic efficacy above which further dose escalation does not improve outcome. In trials designed to prove the equivalence of palonosetron to ondansetron and granisetron, palonosetron proved superior in emesis prevention, while adverse effects were comparable. Furthermore, for all classes of antiemetic agents, a single dose is as effective as multiple doses or a continuous infusion. The oral route is as efficacious as the intravenous route of administration.
KW - Antiemetic agents
KW - High-emetic-risk chemotherapy
KW - Nausea
UR - http://www.scopus.com/inward/record.url?scp=79953297050&partnerID=8YFLogxK
U2 - 10.1007/s00520-010-0976-9
DO - 10.1007/s00520-010-0976-9
M3 - Review
C2 - 20803039
AN - SCOPUS:79953297050
SN - 0941-4355
VL - 19
SP - S25-S32
JO - Supportive Care in Cancer
JF - Supportive Care in Cancer
IS - SUPPL. 1
ER -