Literature DB >> 9629876

Consensus proposal for 5HT3 antagonists in the prevention of acute emesis related to highly emetogenic chemotherapy. Dose, schedule, and route of administration.

D R Gandara1, F Roila, D Warr, M J Edelman, E A Perez, R J Gralla.   

Abstract

Selective antagonists to the Type 3 serotonin receptor (5HT3) in combination with corticosteroids are now considered the standard of care for the prevention of emesis from moderately to highly emetogenic chemotherapy. Here we address issues of optimal dose, schedule and route of administration of four currently available selectable 5HT3 antagonists. This paper utilizes an evidence based medicine approach to the literature regarding this class of drugs, emphasizing the results large, randomized, controlled trials to make formal recommendations concerning optimal use of this important new class of anti-emetic agents. We conclude that for each drug there is a plateau in therapeutic efficacy at a definable dose level above which further dose escalation does not improve outcome. Furthermore, a single dose is as effective as multiple doses or continuous infusion, and finally, emerging data demonstrate that the oral route is equally efficacious as the intravenous route of administration, even with highly emetogenic chemotherapy.

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Year:  1998        PMID: 9629876     DOI: 10.1007/s005200050160

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  13 in total

Review 1.  Stratified administration of serotonin 5-HT3 receptor antagonists (setrons) for chemotherapy-induced emesis. Economic implications.

Authors:  L A Sanchez; M Holdsworth; S B Bartel
Journal:  Pharmacoeconomics       Date:  2000-12       Impact factor: 4.981

2.  A double-blind, crossover, randomized dose-comparison trial of granisetron for the prevention of acute and delayed nausea and emesis in children receiving moderately emetogenic carboplatin-based chemotherapy.

Authors:  Su G Berrak; Nihal Ozdemir; Nadi Bakirci; Emine Turkkan; Cengiz Canpolat; Bahar Beker; Asim Yoruk
Journal:  Support Care Cancer       Date:  2007-03-20       Impact factor: 3.603

Review 3.  State of the Art Antiemetic Therapy for Cancer Patients.

Authors:  Thomas K H Lau; Claudia H W Yip; Winnie Yeo
Journal:  Curr Oncol Rep       Date:  2016-01       Impact factor: 5.075

Review 4.  Anti-emetics for cancer chemotherapy-induced emesis: Potential of alternative delivery systems.

Authors:  L Kraut; A A Fauser
Journal:  Drugs       Date:  2001       Impact factor: 9.546

Review 5.  Consensus proposals for the prevention of acute and delayed vomiting and nausea following high-emetic-risk chemotherapy.

Authors:  Mark G Kris; Paul J Hesketh; Jorn Herrstedt; Cynthia Rittenberg; Lawrence H Einhorn; Steven Grunberg; Jim Koeller; Ian Olver; Sussanne Borjeson; Enzo Ballatori
Journal:  Support Care Cancer       Date:  2004-11-23       Impact factor: 3.603

6.  A multinational study to measure the value that patients with cancer place on improved emesis control following cisplatin chemotherapy.

Authors:  G Dranitsaris; P Leung; R Ciotti; A Ortega; M Spinthouri; L Liaropoulos; R Labianca; A Quadri
Journal:  Pharmacoeconomics       Date:  2001       Impact factor: 4.981

7.  Oral ondansetron is highly active as rescue antiemetic treatment for moderately emetogenic chemotherapy: results of a randomized phase II study.

Authors:  Alessandra Fabi; Mariangela Ciccarese; Giulio Metro; Antonella Savarese; Diana Giannarelli; Carmen M Nuzzo; Michelangelo Russillo; Isabella Sperduti; Ilaria Carbone; Emilio Bria; Francesco Cognetti
Journal:  Support Care Cancer       Date:  2008-05-14       Impact factor: 3.603

Review 8.  Does pharmacogenomics account for variability in control of acute chemotherapy-induced nausea and vomiting with 5-hydroxytryptamine type 3 receptor antagonists?

Authors:  Morgan Trammel; Mary Roederer; Jai Patel; Howard McLeod
Journal:  Curr Oncol Rep       Date:  2013-06       Impact factor: 5.075

9.  Current position of 5HT3 antagonists and the additional value of NK1 antagonists; a new class of antiemetics.

Authors:  R de Wit
Journal:  Br J Cancer       Date:  2003-06-16       Impact factor: 7.640

10.  Granisetron vs ondansetron: is it a question of duration of 5-HT3 receptor blockade?

Authors:  P Blower; M Aapro
Journal:  Br J Cancer       Date:  2002-05-20       Impact factor: 7.640

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