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http://dx.doi.org/10.7314/APJCP.2013.14.12.7701

Cost-Effectiveness Analysis of Granisetron-Based versus Standard Antiemetic Regimens in Low-Emetogenic Chemotherapy: A Hospital-based Perspective from Malaysia  

Keat, Chan Huan (Department of Pharmacy, Sultanah Bahiyah Hospital)
Ghani, Norazila Abdul (Department of Pharmacy, Sultanah Bahiyah Hospital)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.14, no.12, 2013 , pp. 7701-7706 More about this Journal
Abstract
Background: In a prospective cohort study of antiemetic therapy conducted in Malaysia, a total of 94 patients received low emetogenic chemotherapy (LEC) with or without granisetron injections as the primary prophylaxis for chemotherapy-induced nausea and vomiting (CINV). This study is a retrospective cost analysis of two antiemetic regimens from the payer perspective. Materials and Methods: This cost evaluation refers to 2011, the year in which the observation was conducted. Direct costs incurred by hospitals including the drug acquisition, materials and time spent for clinical activities from prescribing to dispensing of home medications were evaluated (MYR 1=$0.32 USD). As reported to be significantly different between two regimens (96.1% vs 81.0%; p=0.017), the complete response rate of acute emesis which was defined as a patient successfully treated without any emesis episode within 24 hours after LEC was used as the main indicator for effectiveness. Results: Antiemetic drug acquisition cost per patient was 40.7 times higher for the granisetron-based regimen than for the standard regimen (MYR 64.3 vs 1.58). When both the costs for materials and clinical activities were included, the total cost per patient was 8.68 times higher for the granisetron-based regimen (MYR 73.5 vs 8.47). Considering the complete response rates, the mean cost per successfully treated patient in granisetron group was 7.31 times higher (MYR 76.5 vs 10.5). The incremental cost-effectiveness ratio (ICER) with granisetron-based regimen, relative to the standard regimen, was MYR 430.7. It was found to be most sensitive to the change of antiemetic effects of granisetron-based regimen. Conclusions: While providing a better efficacy in acute emesis control, the low incidence of acute emesis and high ICER makes use of granisetron as primary prophylaxis in LEC controversial.
Keywords
Granisetron; CINV; low emetogenic; cost-effectiveness; Malaysia;
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1 Aleyasin A, Hanafi S, Saffarieh E, et al (2012). Efficacy of generic granisetron vs $Kytril^{(R)}$ for PONV in major gynecological operations: a randomized, double-blind clinical trial. Iranian J Pharm Res, 11, 1059-64.
2 Almazron S and Alnaim L (2012). Evaluation of adherence to chemotherapy-induced nausea and vomiting guidelines. An observational study. J Cancer Therapy, 3, 613-20.   DOI
3 Annemans L, Strens D, Lox E, et al (2008). Cost-effectiveness analysis of aprepitant in the prevention of chemotherapyinduced nausea and vomiting in Belgium. Support Care Cancer, 16, 905-15.   DOI
4 Ballatori E, Roila F, Berto P, et al (1994). Cost and costeffectiveness analysis of ondansetron versus metoclopramide regimens: a hospital perspective from Italy. Pharmacoeconomics, 5, 227-37.   DOI   ScienceOn
5 Burmeister H, Achi S, Studer C, et al (2012). Adherence to ESMO clinical recommendations for prophylaxis of chemotherapy-induced nausea and vomiting. Supp Care Cancer, 20, 141-7.   DOI
6 Chan HK, Phua G, Kassim MS, et al (2013). Can granisetron injection used as primary prophylaxis improve the control of nausea and vomiting with low-emetogenic chemotherapy? Asian Pac J Cancer Prev, 14, 469-73.   과학기술학회마을   DOI   ScienceOn
7 Colayco DC and Hay J (2010). Cost-effectiveness of serotonintype 3 receptor antagonists for chemotherapy-induced emesis in non-small cell lung cancer patients receiving cisplatinbased chemotherapy. Value Health, 13, 41.
8 Cox F and Hirsch J (1993). Ondansetron: a cost-effective advance in anti-emetic therapy. Oncol, 50, 186-90.   DOI   ScienceOn
9 Cunningham D, Gore M, Davidson N, et al (1993). The real costs of emesis - an economic analysis of ondansetron versus metoclopramide in controlling emesis in patients receiving chemotherapy for cancer. Eur J Cancer, 29, 303-6.
10 Erntoft S (2011). Pharmaceutical priority setting and the use of health economic evaluations: a systematic literature review. Value Health, 14, 587-99.   DOI   ScienceOn
11 Ismail F, Mohamed AK, Lim KH, et al (2011). Systemic therapy of cancer, 2nd edition. Ministry of Health, Kuala Lumpur, 75-8.
12 Ettinger DS, Armstrong DK, Barbour S, et al (2012). Antiemesis. JNCCN, 10, 456-85.
13 Hassali MA, Thambyappa J, Nambiar S, et al (2013). TRIPS, Free Trade Agreements and the Pharmaceutical Industry in Malaysia. In "The New Political Economy of Pharmaceuticals: Production, Innnovation and TRIPS in the Global South", Eds Lofgren H and Williams OD. Palgrave Macmillan, Basingstoke pp 152-66.
14 Humphreys S, Pellissier J, Jones A (2013). Cost-effectiveness of an aprepitant regimen for prevention of chemotherapyinduced nausea and vomiting in patients with breast cancer in the UK. Cancer Manag Res, 5, 215-24.
15 Jordan K, Hinke A, Grothey A et al (2007). A meta-analysis comparing the efficacy of four 5-HT3-receptor antagonists for acute chemotherapy-induced emesis. Support Care Cancer, 15, 1023-33.   DOI   ScienceOn
16 Jordan K, Schmoll HJ, Aapro MS (2007). Comparative activity of antiemetic drugs. Oncol Hemato, 61, 162-75.
17 Koeller JM, Aapro MS, Gralla RJ, et al (2002). Antiemetic guidelines: creating a more practical treatment approach. Supp Care Cancer, 10, 519-22.   DOI   ScienceOn
18 Kris MG, Hesketh PJ, Herrstedt J, et al (2005). Consensus proposals for the prevention of acute and delayed vomiting and nausea following high-emetic-risk chemotherapy. Supp Care Cancer, 13, 85-96.   DOI
19 Lordick F, Ehlken B, Ihbe-Heffinger A, et al (2007). Health outcomes and cost-effectiveness of aprepitant in outpatients receiving antiemetic prophylaxis for highly emetogenic chemotherapy in Germany. Eur J Cancer, 43, 299-307.   DOI   ScienceOn
20 Lopes G, Burke T, Pellissier J, et al (2012). Aprepitant for patients receiving highly-emetogenic chemotherapy: an economic analysis for Singapore. Value Health Regional Iss, 1, 66-74.   DOI   ScienceOn
21 Marshall DA and Hux M (2009). Design and analysis issues for economic analysis alongside clinical trials. Med Care, 47, 14-20.   DOI   ScienceOn
22 Moore S, Tumeh J, Wojtanowski S, et al (2007). Cost-effectiveness of aprepitant for the prevention of chemotherapy-induced nausea and vomiting associated with highly emetogenic chemotherapy. Value Health, 10, 23-31.   DOI   ScienceOn
23 Pharmacy Services Division Malaysia (2011). Drug Formulary. Ministry of Health, Kuala Lumpur pp 37.
24 Rothermel C (2013). What is health economics and outcome research? A primer for medical writers. Am Med Writers Assoc J, 28, 98-104.
25 Uyl-de Groot CA, Wait S, Buijt I (2000). Economics and healthrelated quality of life in antiemetic therapy: recommendations for trial design. Eur j Cancer, 36, 1522-35.   DOI   ScienceOn
26 Yonemura M, Katsumata N, Hashimoto H, et al (2009). Randomized controlled study comparing two doses of intravenous granisetron (1 and 3 mg) for acute chemotherapy-induced nausea and vomiting in cancer patients: a non-inferiority trial. Jpn J Clin Oncol, 39, 443-8.   DOI   ScienceOn