Literature DB >> 11227393

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

L A Sanchez1, M Holdsworth, S B Bartel.   

Abstract

The serotonin 5-HT3 receptor antagonists or 'setrons' have become the standard of care for the prevention of chemotherapy-induced emesis (CIE) and are first-line therapy for acute CIE in healthcare organisations worldwide. However, their superior efficacy versus standard antiemetics comes at a significant cost. Currently, 3 agents are available in the US: ondansetron, granisetron and dolasetron. The most important treatment-related factor contributing to CIE is the emetogenicity of chemotherapy. The ability to customise, or stratify, the setron dose to match the emetogenic challenge of the chemotherapy administered has potential benefits, both clinically and economically. In adults, there is an appreciable amount of clinical literature addressing stratified administration; however, the amount of 'hard' economic data is rather limited. Intuitively, if clinical outcomes are equivalent, then stratified administration should be associated with economic benefits, as it generally promotes the use of doses lower than those recommended by the manufacturer. The literature strongly substantiates this for ondansetron, but is not as favourable for granisetron or dolasetron. As the rationale and justification for dose stratification is contained in the clinical literature, the authors have reviewed the pertinent literature supporting the clinical and economic benefits of dose stratification in both adult and paediatric patients. The authors also provide a discussion of various additional strategies that can be employed to ensure the appropriate and cost-effective use of setrons in real-world practice settings. These strategies include the use of lower doses than recommended by manufacturers, use for acute versus delayed phase emesis, enhancing the antiemetic efficacy by the addition of a corticosteroid, use of oral versus injectable formulations (when appropriate) and the implementation and use of local, national and international drug use guidelines.

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Year:  2000        PMID: 11227393     DOI: 10.2165/00019053-200018060-00002

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  85 in total

1.  Costs of treating and preventing nausea and vomiting in patients receiving chemotherapy.

Authors:  D J Stewart; S Dahrouge; D Coyle; W K Evans
Journal:  J Clin Oncol       Date:  1999-01       Impact factor: 44.544

2.  A comparison of two dose levels of granisetron in patients receiving moderately emetogenic cytostatic chemotherapy. The Granisetron Study Group.

Authors:  I E Smith
Journal:  Eur J Cancer       Date:  1990       Impact factor: 9.162

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Authors:  R J Gralla; M G Kris; L B Tyson; R A Clark
Journal:  Recent Results Cancer Res       Date:  1988

4.  Prevention of acute emesis in cancer patients following high-dose cisplatin with the combination of oral dolasetron and dexamethasone.

Authors:  M G Kris; K B Pendergrass; R M Navari; T H Grote; A M Nelson; V Thomas; B B Ferguson; D S Allman; B A Pizzo; T W Baker; I J Fernando; S B Chernoff
Journal:  J Clin Oncol       Date:  1997-05       Impact factor: 44.544

Review 5.  Ondansetron. Therapeutic use as an antiemetic.

Authors:  R J Milne; R C Heel
Journal:  Drugs       Date:  1991-04       Impact factor: 9.546

6.  A comparison of two dose levels of granisetron in patients receiving high-dose cisplatin. The Granisetron Study Group.

Authors:  M Soukop
Journal:  Eur J Cancer       Date:  1990       Impact factor: 9.162

7.  5-HT3 receptor antagonists in the prophylaxis of acute vomiting induced by moderately emetogenic chemotherapy--a randomised study.

Authors:  I T Jantunen; T T Muhonen; V V Kataja; M K Flander; L Teerenhovi
Journal:  Eur J Cancer       Date:  1993       Impact factor: 9.162

8.  Results of a compassionate-use program using intravenous ondansetron to prevent nausea and vomiting in patients receiving emetogenic cancer chemotherapy.

Authors:  W R Berry; K W House; J T Lee; P B Plagge; M W Meshad; R Grapski
Journal:  Semin Oncol       Date:  1992-12       Impact factor: 4.929

9.  Prevention of cisplatin-induced emesis: a double-blind multicenter randomized crossover study comparing ondansetron and ondansetron plus dexamethasone.

Authors:  F Roila; M Tonato; F Cognetti; E Cortesi; G Favalli; M Marangolo; D Amadori; M A Bella; V Gramazio; D Donati
Journal:  J Clin Oncol       Date:  1991-04       Impact factor: 44.544

Review 10.  Granisetron. An update of its therapeutic use in nausea and vomiting induced by antineoplastic therapy.

Authors:  Y E Yarker; D McTavish
Journal:  Drugs       Date:  1994-11       Impact factor: 9.546

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  3 in total

Review 1.  Ondansetron: a review of its use as an antiemetic in children.

Authors:  C R Culy; N Bhana; G L Plosker
Journal:  Paediatr Drugs       Date:  2001       Impact factor: 3.022

2.  Economic evaluation of three two-drug chemotherapy regimens in advanced non-small-cell lung cancer.

Authors:  Niels Neymark; Pilar Lianes; Egbert F Smit; Jan P van Meerbeeck
Journal:  Pharmacoeconomics       Date:  2005       Impact factor: 4.981

Review 3.  Options for the prevention and management of acute chemotherapy-induced nausea and vomiting in children.

Authors:  L Lee Dupuis; Paul C Nathan
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

  3 in total

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