IMATINIB IS COST-EFFECTIVE THAN INTERFERON-ALPHA (IFN) FOR PATIENTS WITH NEWLY DIAGNOSED CHRONIC PHASE CHRONIC MYELOID LEUKEMIA FROM THE CHINESE PUBLIC HEALTH CARE SYSTEM PERSPECTIVE

Author(s)

Z. Chen, MD, PhD, Professor1, C. Wang, MD, Professor2, Weiwei Feng, PhD, Associate Director, Health Economics31Shanghai Fudan University Affiliated Huashan Hospital, Shanghai, Shanghai, China; 2 Shanghai Jiaotong University Affiliated First Hospital, Shanghai, Shanghai, China; 3 Novartis Pharmaceuticals, Florhem Park, NJ, USA

OBJECTIVES: Imatinib, a break-through oral molecular targeted therapy, has demonstrated impressive and durable responses as well as significant survival advantage compared to IFN based treatment in newly diagnosed CP CML. However, imatinib has not been registered on the Chinese National Reimbursement Drug List (RDL) whereas IFN has, solely based on the drug price. Although IFN plus Ara-C has been shown to be more effective than IFN alone, IFN is normally used alone to treat CP CML in China. The objective of this study was to compare imatinib with IFN in newly diagnosed CP CML from the Chinese public health care system’s perspective.  METHODS:  The 60-month data from the International Randomized Interferon versus STI571 Study (IRIS) was used to estimate survival for imatinib and utility values for survival.  Since most patients randomized to receive IFN crossed over to the alternate treatment imatinib in IRIS, historical data from the literature was used to estimate survival for IFN. Survival estimates were based on published survival curves for patients who achieved and those who did not achieve a complete cytogenetic response after treatment with IFN. Lifetime costs of treatment containing drug costs, office visits, lab tests, and hospitalizations were estimated based on treatment protocols from tier 3 hospitals in China.  Incremental cost-effectiveness ratio (ICER), which is the difference in costs divided by the difference in quality adjusted life years (QALY) between imatinib and IFN, was calculated.  All costs and outcomes were discounted at a rate of 3.5% per annum following the UK Health Technology Assessment recommendation. RESULTS:  Total survival was estimated to be 19 and 9 for patients treated with imatinib and IFN, respectively.  The discounted QALYs were 11.83 with imatinib and 5.41 with IFN.  The discounted lifetime costs of treatment were RMB1169,661 with imatinib and RMB715,983 with IFN.  The ICER for imatinib comparing with IFN was RMB70,510 per QALY. CONCLUSIONS:  The World Health Organization (WHO) considered a cost-effectiveness ratio (CER) of less than three times the GDP per capita as cost effective in developing countries.  Based on the 2006 GDP per capita for China US$7,700, the WHO CER for China would be RMB175,167.  The ICER for imatinib over IFN was RMB70,510 which is less than half of the WHO CER threshold.  Therefore, imatinib is cost-effective comparing with IFN in newly diagnosed CP CML from the Chinese public health care system’s perspective.

Conference/Value in Health Info

2008-09, ISPOR Asia Pacific 2008, Seoul, South Korea

Value in Health, Vol. 11, No. 6 (November 2008)

Code

CN4

Topic

Economic Evaluation

Topic Subcategory

Cost-comparison, Effectiveness, Utility, Benefit Analysis

Disease

Oncology

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