Erythropoietic growth factors for treatment-induced anemia in hepatitis C: A cost-effectiveness analysis

被引:24
作者
Spiegel, BMR
Chen, K
Chiou, CF
Robbins, S
Younossi, ZM
机构
[1] Univ Calif Los Angeles, UCLA VA Ctr Outcomes Res & Educ, David Geffen Sch Med,Div Digest Dis, VA Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA
[2] VA Greater Los Angeles Healthcare Syst, Div Gastroenterol, Los Angeles, CA USA
[3] Cerner Hlth Insights, Beverly Hills, CA USA
[4] Amgen Inc, Global Hlth Econ, Thousand Oaks, CA 91320 USA
[5] Inova Fairfax Hosp, Annandale, VA USA
关键词
D O I
10.1016/S1542-3565(05)00695-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Treatment-induced anemia undermines the efficacy of antiviral therapy in hepatitis C by mandating ribavirin dose reduction and diminishing adherence to therapy. Erythropoietic growth factors (EGFs) may correct treatment-induced anemia, facilitate maintenance of full-dose therapy, and improve rates of sustained virologic response (SVR). We sought to determine the cost effectiveness of adjunctive treatment with an EGF vs standard care in the treatment of hepatitis C. Methods: We used a decision analysis to calculate the cost effectiveness of 2 treatment strategies for a patient cohort with chronic hepatitis C, increased transaminase levels, and no cirrhosis who were receiving pegylated-interferon and ribavirin (RBV): (1) RBV dose-reduction for anemia, followed by discontinuation of therapy if anemia persisted (standard care strategy), (2) adjunctive treatment with EGF therapy for anemia, with RBV dose reduction reserved for persistent anemia despite EGF therapy (EGF strategy). We conducted cost-effectiveness and cost-utility analyses to compare short- and long-term outcomes between the strategies. Results: The percentage achieving SVR was 52.3% in the standard care strategy and 59.5% in the EGF strategy. Compared with standard care, the EGF strategy cost an incremental $36,568 per unadjusted life-year gained and $16,443 per quality-adjusted life-year gained. In a sensitivity analysis, if a third-party payer was willing to pay $50,000 per quality-adjusted life-year gained for the use of an EGF, then 86.1% of patients would be within the budget. Conclusions: Compared with standard care, adjunctive therapy with an EGF for the management of treatment-induced anemia may increase the probability of achieving SVR, increase unadjusted lifespan, and increase quality-adjusted lifespan at an acceptable cost.
引用
收藏
页码:1034 / 1042
页数:9
相关论文
共 50 条
[1]   Epoetin alfa maintains ribavirin dose in HCV-infected patients: A prospective, double-blind, randomized controlled study [J].
Afdhal, NH ;
Dieterich, DT ;
Pockros, PJ ;
Schiff, ER ;
Shiffman, ML ;
Sulkowski, MS ;
Wright, T ;
Younossi, Z ;
Goon, BL ;
Tang, KL ;
Bowers, PJ .
GASTROENTEROLOGY, 2004, 126 (05) :1302-1311
[2]  
*AM MED ASS, 2004, AMA CPT COD BOOK
[3]  
[Anonymous], 2002, Designing and conducting cost-effectiveness analyses in medicine and health care
[4]   Relationship of health-related quality of life to treatment adherence and sustained response in chronic hepatitis C patients [J].
Bernstein, D ;
Kleinman, L ;
Barker, CM ;
Revicki, DA ;
Green, J .
HEPATOLOGY, 2002, 35 (03) :704-708
[5]   A cost-effectiveness analysis of peginterferon alfa-2b plus ribavirin for the treatment of naive patients with chronic hepatitis C [J].
Buti, M ;
Medina, M ;
Casado, MA ;
Wong, JB ;
Fosbrook, L ;
Esteban, R .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (05) :687-694
[6]  
*CDC NAT CTR HLTH, NAT VIT STAT REP
[7]  
Chong CAKY, 2003, AM J GASTROENTEROL, V98, P630, DOI [10.1016/S0002-9270(02)06054-9, 10.1111/j.1572-0241.2003.07332.x]
[8]   Early virologic response to treatment with peginterferon alfa-2b plus ribavirin in patients with chronic hepatitis C [J].
Davis, GL ;
Wong, JB ;
McHutchison, JG ;
Manns, MP ;
Harvey, J ;
Albrecht, J .
HEPATOLOGY, 2003, 38 (03) :645-652
[9]   Hemolytic anemia induced by ribavirin therapy in patients with chronic hepatitis C virus infection: Role of membrane oxidative damage [J].
De Franceschi, L ;
Fattovich, G ;
Turrini, F ;
Ayi, K ;
Brugnara, C ;
Manzato, F ;
Noventa, F ;
Stanzial, AM ;
Solero, P ;
Corrocher, R .
HEPATOLOGY, 2000, 31 (04) :997-1004
[10]  
DEFRANCHIS R, 1988, NEW ENGL J MED, V319, P983