Literature DB >> 17965891

Cost-effectiveness analysis of aprepitant in the prevention of chemotherapy-induced nausea and vomiting in Belgium.

Lieven Annemans1, Daniëlle Strens, Erica Lox, Christine Petit, Hughes Malonne.   

Abstract

OBJECTIVES: Chemotherapy-induced nausea and vomiting (CINV) remains a major adverse effect of cancer chemotherapy which may increase morbidity, reduce quality of life and threaten the success of cancer therapy. Aprepitant is effective in preventing CINV, achieving higher complete response (no emesis and no rescue therapy) compared to standard prevention, in patients receiving either highly (HEC) or moderately emetogenic chemotherapy (MEC; absolute reduction = 11 and 13%, respectively). We assessed the cost effectiveness of aprepitant-based vs standard prevention in these indications in Belgium.
MATERIALS AND METHODS: A decision analytical model was developed in MS Excel (Fig. 1). To estimate resource use, two approaches were used. The first is based on the preventive regimens applied in randomized controlled trials comparing aprepitant-based CINV prevention (for HEC: aprepitant days 1-3, ondansetron 32 mg i.v. day 1, oral placebo twice daily days 2-4, oral dexamethasone days 1-4; for MEC: aprepitant days 1-3, ondansetron 16 mg p.o. day 1, placebo on days 2-3, oral dexamethasone day 1), vs a standard regimen (for HEC: oral placebo days 1-3, ondansetron 32 mg i.v. day 1 and 16 mg p.o. days 2-4, oral dexamethasone days 1-4; for MEC: oral placebo, ondansetron 16 mg p.o. days 1-3, dexamethasone day 1) The second analysis is based on current real-world resource use in the Belgian setting in the prevention of CINV using a longitudinal Hospital Database. CINV-specific utility values were used to calculate quality-adjusted life years (QALYs). Drug costs were obtained from official reimbursement listings. Treatment costs for CINV were obtained from a German study and adapted to Belgium.
RESULTS: The aprepitant-based regimen is associated with 0.003 and 0.014 more QALYs in HEC and MEC, respectively and with per patient savings of <euro>66.84 (trial based) and <euro>74.62 (real-life based) for HEC and <euro>17.95 (trial based) and <euro>21.70 (real-life based) for MEC. Hence, aprepitant is both more effective and less expensive (=dominant). One-way sensitivity analyses were performed on treatment cost of emesis, the clinical benefit of aprepitant and the cost of ondansetron and showed that the results were robust on the first two parameters but sensitive on the decrease in cost of ondansetron for the moderately emetogenic chemotherapy regimens.
CONCLUSIONS: In both approaches, the aprepitant-based strategy is more effective and less expensive compared to standard care.

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Year:  2007        PMID: 17965891     DOI: 10.1007/s00520-007-0349-1

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


  25 in total

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Journal:  Eur J Cancer       Date:  2000-08       Impact factor: 9.162

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Journal:  J Clin Oncol       Date:  2006-05-22       Impact factor: 44.544

4.  Prevention of chemotherapy- and radiotherapy-induced emesis: results of the 2004 Perugia International Antiemetic Consensus Conference.

Authors:  F Roila; P J Hesketh; J Herrstedt
Journal:  Ann Oncol       Date:  2005-11-28       Impact factor: 32.976

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Journal:  Eur J Cancer       Date:  2004-02       Impact factor: 9.162

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Journal:  Br J Cancer       Date:  1992-07       Impact factor: 7.640

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  16 in total

Review 1.  Aprepitant: a review of its use in the prevention of nausea and vomiting.

Authors:  Monique P Curran; Dean M Robinson
Journal:  Drugs       Date:  2009       Impact factor: 9.546

2.  Cost-utility analysis of aprepitant for patients who truly need it in Japan.

Authors:  Ikuto Tsukiyama; Masahiko Ando; Sumiyo Tsukiyama; Masayuki Takeuchi; Masayuki Ejiri; Yusuke Kurose; Hiroko Saito; Ichiro Arakawa; Tadao Inoue; Etsuro Yamaguchi; Akihito Kubo
Journal:  Support Care Cancer       Date:  2019-02-01       Impact factor: 3.603

3.  A cost-utility analysis of risk model-guided versus physician's choice antiemetic prophylaxis in patients receiving chemotherapy for early-stage breast cancer: a net benefit regression approach.

Authors:  Kednapa Thavorn; Doug Coyle; Jeffrey S Hoch; Lisa Vandermeer; Sasha Mazzarello; Zhou Wang; George Dranitsaris; Dean Fergusson; Mark Clemons
Journal:  Support Care Cancer       Date:  2017-03-09       Impact factor: 3.603

4.  Phase II open label pilot trial of aprepitant and palonosetron for the prevention of chemotherapy-induced nausea and vomiting (CINV) in patients receiving moderately emetogenic FOLFOX chemotherapy for the treatment of colorectal cancer.

Authors:  Joseph S Bubalo; Jon D Herrington; Marc Takemoto; Patricia Willman; Michael S Edwards; Casey Williams; Alan Fisher; Alison Palumbo; Eric Chen; Charles Blanke; Charles D Lopez
Journal:  Support Care Cancer       Date:  2017-10-31       Impact factor: 3.603

5.  Cost-effectiveness analysis of NEPA, a fixed-dose combination of netupitant and palonosetron, for the prevention of highly emetogenic chemotherapy-induced nausea and vomiting: an international perspective.

Authors:  Jonas Nilsson; Vittoria Piovesana; Marco Turini; Claudio Lezzi; Jennifer Eriksson; Matti Aapro
Journal:  Support Care Cancer       Date:  2022-09-08       Impact factor: 3.359

6.  Fosaprepitant and aprepitant: an update of the evidence for their place in the prevention of chemotherapy-induced nausea and vomiting.

Authors:  Patrick Langford; Paul Chrisp
Journal:  Core Evid       Date:  2010-10-21

7.  Therapeutic and preventive antiemetic effect of aprepitant in Japanese patients with thoracic malignancies who truly need it.

Authors:  Sumiyo Ito; Ikuto Tsukiyama; Masahiko Ando; Masayo Katakami; Rie Hamanaka; Kenshi Kosaka; Ayako Matsubara; Masaki Nishimura; Hiroyuki Tanaka; Nobuhiro Asai; Norihito Yokoe; Ayumu Takahashi; Kenji Baba; Katsuhiko Matsuura; Etsuro Yamaguchi; Akihito Kubo
Journal:  Support Care Cancer       Date:  2014-09-17       Impact factor: 3.603

8.  Antiemetic prophylaxis with temozolomide: an audit from a tertiary care center.

Authors:  Vijay M Patil; Arun Chandrasekharan; Dilip Harindran Vallathol; Mridul Malhotra; Ram Abhinav; Priti Agarwal; Anu Rajpurohit; Raees Tonse; Atanu Bhattacharjee; Rakesh Jalali
Journal:  Neurooncol Pract       Date:  2019-04-19

9.  Safety, efficacy, and patient acceptability of single-dose fosaprepitant regimen for the prevention of chemotherapy-induced nausea and vomiting.

Authors:  Luigi Celio; Francesca Ricchini; Filippo De Braud
Journal:  Patient Prefer Adherence       Date:  2013-05-07       Impact factor: 2.711

10.  Ultra-low doses of the transient receptor potential vanilloid 1 agonist, resiniferatoxin, prevents vomiting evoked by diverse emetogens in the least shrew (Cryptotis parva).

Authors:  Nissar A Darmani; Denise A Henry; Weixia Zhong; Seetha Chebolu
Journal:  Behav Pharmacol       Date:  2020-02       Impact factor: 2.277

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