TY - JOUR
T1 - Cost-effectiveness of sorafenib treatment in field practice for patients with hepatocellular carcinoma
AU - Cammà, Calogero
AU - Cabibbo, Giuseppe
AU - Petta, Salvatore
AU - Enea, Marco
AU - Iavarone, Massimo
AU - Grieco, Antonio
AU - Gasbarrini, Antonio
AU - Villa, Erica
AU - Zavaglia, Claudio
AU - Bruno, Raffaele
AU - Colombo, Massimo
AU - Craxì, Antonio
PY - 2013
Y1 - 2013
N2 - The purpose was to assess the cost-effectiveness of sorafenib in the treatment of hepatocellular carcinoma (HCC) patients incorporating current prices and the results of the recent published field practice SOraFenib Italian Assessment (SOFIA) study. We created a Markov Decision Model to evaluate, in a hypothetical cohort of Caucasian male patients, aged 67 years with Barcelona Clinic Liver Cancer (BCLC) C HCC, or BCLC B HCC who were unfit or failed to respond to locoregional therapies, well compensated cirrhosis, and with performance status 0-1 according to Eastern Cooperative Oncology Group (ECOG), the cost-effectiveness of the following strategies: (1) full or dose-adjusted sorafenib for BCLC B and C patients together; (2) full or dose-adjusted sorafenib for BCLC B patients; (3) full or dose-adjusted sorafenib for BCLC C patients. Outcomes include quality-adjusted life years (QALYs), costs, and incremental cost-effectiveness ratio (ICER). In the base-case analysis dose-adjusted sorafenib was the most effective of the evaluated strategies. For dose-adjusted sorafenib, QALY was 0.44 for BCLC B and C patients together, 0.44 for BCLC C patients, and 0.38 for BCLC B patients. The ICER of dose-adjusted sorafenib compared with BSC was €34,534 per QALY gained for BCLC B and C patients together, €27,916 per QALY gained for BCLC C patients, and €54,881 per QALY gained for BCLC B patients. Results were sensitive to BSC survival rate, and sorafenib treatment duration.
AB - The purpose was to assess the cost-effectiveness of sorafenib in the treatment of hepatocellular carcinoma (HCC) patients incorporating current prices and the results of the recent published field practice SOraFenib Italian Assessment (SOFIA) study. We created a Markov Decision Model to evaluate, in a hypothetical cohort of Caucasian male patients, aged 67 years with Barcelona Clinic Liver Cancer (BCLC) C HCC, or BCLC B HCC who were unfit or failed to respond to locoregional therapies, well compensated cirrhosis, and with performance status 0-1 according to Eastern Cooperative Oncology Group (ECOG), the cost-effectiveness of the following strategies: (1) full or dose-adjusted sorafenib for BCLC B and C patients together; (2) full or dose-adjusted sorafenib for BCLC B patients; (3) full or dose-adjusted sorafenib for BCLC C patients. Outcomes include quality-adjusted life years (QALYs), costs, and incremental cost-effectiveness ratio (ICER). In the base-case analysis dose-adjusted sorafenib was the most effective of the evaluated strategies. For dose-adjusted sorafenib, QALY was 0.44 for BCLC B and C patients together, 0.44 for BCLC C patients, and 0.38 for BCLC B patients. The ICER of dose-adjusted sorafenib compared with BSC was €34,534 per QALY gained for BCLC B and C patients together, €27,916 per QALY gained for BCLC C patients, and €54,881 per QALY gained for BCLC B patients. Results were sensitive to BSC survival rate, and sorafenib treatment duration.
KW - Aged
KW - Antineoplastic Agents
KW - Carcinoma, Hepatocellular
KW - Cost-Benefit Analysis
KW - Drug Costs
KW - Humans
KW - Kaplan-Meier Estimate
KW - Liver Neoplasms
KW - Male
KW - Markov Chains
KW - Multivariate Analysis
KW - Niacinamide
KW - Phenylurea Compounds
KW - Prospective Studies
KW - Quality-Adjusted Life Years
KW - Aged
KW - Antineoplastic Agents
KW - Carcinoma, Hepatocellular
KW - Cost-Benefit Analysis
KW - Drug Costs
KW - Humans
KW - Kaplan-Meier Estimate
KW - Liver Neoplasms
KW - Male
KW - Markov Chains
KW - Multivariate Analysis
KW - Niacinamide
KW - Phenylurea Compounds
KW - Prospective Studies
KW - Quality-Adjusted Life Years
UR - http://hdl.handle.net/10807/52279
U2 - 10.1002/hep.26221
DO - 10.1002/hep.26221
M3 - Article
SN - 0270-9139
VL - 57
SP - 1046
EP - 1054
JO - Hepatology
JF - Hepatology
ER -