Consensus recommendations for the prevention of vomiting and nausea following high-emetic-risk chemotherapy. Review uri icon

Overview

abstract

  • 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-HT(3)) 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-HT(3) 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.

authors

  • Kris, Mark Gregory
  • Tonato, Maurizio
  • Bria, Emilio
  • Ballatori, Enzo
  • Espersen, Birgitte
  • Herrstedt, Jørn
  • Rittenberg, Cynthia
  • Einhorn, Lawrence H
  • Grunberg, Steven
  • Saito, Mitsue
  • Morrow, Gary
  • Hesketh, Paul

publication date

  • August 28, 2010

Research

keywords

  • Antiemetics
  • Antineoplastic Agents
  • Nausea
  • Vomiting

Identity

Scopus Document Identifier

  • 79953297050

Digital Object Identifier (DOI)

  • 10.1007/s00520-010-0976-9

PubMed ID

  • 20803039

Additional Document Info

volume

  • 19 Suppl 1