COST-EFFECTIVENESS OF BRENTUXIMAB VEDOTIN IN RELAPSED OR REFRACTORY SYSTEMIC ANAPLASTIC LARGE CELL LYMPHOMA IN TAIWAN
Author(s)
Zou D1, Kendall R1, Lin Q2, Huang Y2, Tieng J3, Tseng J3, Sajosi P4
1ICON plc, Vancouver, BC, Canada, 2Kantar Health, Taipei, Taiwan, 3Takeda Pharmaceuticals Taiwan, Taipei, Taiwan, 4Takeda Pharmaceuticals International AG, Zurich, Switzerland
OBJECTIVES: To evaluate the cost-effectiveness in Taiwan of brentuximab vedotin (BV) compared with conventional chemotherapy in patients with relapsed or refractory systemic anaplastic large cell lymphoma (R/R sALCL). METHODS: A lifetime partitioned survival model was developed with three health states: progression-free/post-progression/death. An indirect comparison of the survival outcomes was made between 58 patients with R/R sALCL in a phase II, single-arm BV trial and 40 sALCL patients from a Canadian cancer registry who received conventional chemotherapy during 1980-2012 and were followed for up to 20 years. Extrapolation of BV survival after the trial period assumed the same rate of change as for conventional chemotherapy. Resource use was modelled adopting a Taiwanese National Health Insurance Administration perspective. Costs (2015 New Taiwan dollars [NT$]) considered drug acquisition and administration, adverse events management, and standard care for pre- and post-progression. Utility values elicited by response and by progression, and disutilities associated with adverse events were applied to estimate quality-adjusted life years (QALYs). Uncertainty around incremental cost/QALY gained was explored through deterministic and probabilistic sensitivity analyses. RESULTS: Over patients’ modelled lifetime, BV provided an additional 2.35 years in progression-free state and an overall survival advantage of 3.26 years. After applying utilities and discounting, the benefits translated into 1.60 and 1.87 QALYs gained, respectively. The incremental cost/QALY was NT$781,300. At a willingness-to-pay of NT$2,184,300 (triple value of Taiwan GDP), the probability that BV is cost-effective is 99%. Deterministic sensitivity analyses suggested BV’s cost-effectiveness was most sensitive to shorter time horizon, inclusion vial wastage for BV, and cost of post-progression, but was largely insensitive to alternative scenarios regarding survival functions and utilities. CONCLUSIONS: The current economic evaluation demonstrates that BV, which has demonstrated high objective response rates and is approved for R/R sALCL, may also be a cost-effective option for this patient population in Taiwan.
Conference/Value in Health Info
2016-09, ISPOR Asia Pacific 2016, Singapore
Value in Health, Vol. 19, No. 7 (November 2016)
Code
CE2
Topic
Economic Evaluation
Topic Subcategory
Cost-comparison, Effectiveness, Utility, Benefit Analysis
Disease
Oncology