Abstract
This economic analysis aimed to determine, from the perspective of a Canadian provincial government payer, the cost-effectiveness of docetaxel (Taxotere: Sanofi-Aventis, Laval, QC) in combination with doxorubicin and cyclophosphamide (TAC) compared with 5-fluorouracil, doxorubicin, and cyclophosphamide (FAC) following primary surgery for breast cancer in women with operable, axillary lymph node-positive breast cancer. A Markov model looking at two time phases-5-year treatment and long-term follow-up-was constructed. Clinical events included clinical response (based on disease-free survival and overall survival) and rates of febrile neutropenia, stomatitis, diarrhea, and infections. Health states were "no recurrence," "locoregional recurrence," "distant recurrence," and "death." Costs were based on published sources and are presented in 2006 Canadian dollars. Model inputs included chemotherapy drug acquisition costs, chemotherapy administration costs, relapse and follow-up costs, costs for management of adverse events, and costs for granulocyte colony-stimulating factor (G-CSF) prophylaxis. A 5% discount rate was applied to costs and outcomes alike. Health utilities were obtained from published sources. For TAC as compared with fac, the incremental cost was $6921 per life-year (LY) gained and $6,848 per quality-adjusted life-year (QALY) gained. The model was robust to changes in input variables (for example, febrile neutropenia rate, utility). When G-CSF and antibiotics were given prophylactically before every cycle, the incremental ratios increased to $13,183 and $13,044 respectively. Compared with FAC, TAC offered improved response at a higher cost. The cost-effectiveness ratios were low, indicating good economic value in the adjuvant setting of node-positive breast cancer patients.
Highlights
The multicentre phase iii randomized Breast Cancer International Research Group 001 trial (“tac– fac”) showed that efficacy with docetaxel (Taxotere: Sanofi–Aventis, Laval, QC) in combination with doxorubicin and cyclophosphamide was improved over that with the standard protocol of 5-fluorouracil, doxorubicin, cyclophosphamide for the adjuvant treatment of patients with operable node-positive breast cancer
The model was robust to changes in input variables
The base-case analysis used in this model applied a 5% discount rate, the Canadian costs for chemotherapies recommended by cco guidelines 10, and febrile neutropenia rates based on the available tac–fac study results 17
Summary
The multicentre phase iii randomized Breast Cancer International Research Group (bcirg) 001 trial (“tac– fac”) showed that efficacy with docetaxel (Taxotere: Sanofi–Aventis, Laval, QC) in combination with doxorubicin and cyclophosphamide (tac protocol) was improved over that with the standard protocol of 5-fluorouracil, doxorubicin, cyclophosphamide (fac) for the adjuvant treatment of patients with operable node-positive breast cancer. Recurrences avoided by the use of tac will have an effect in terms of years of life saved and may generate cost savings attributable to the reduction in disease recurrence This economic analysis aimed to determine, from the perspective of a Canadian provincial government payer, the cost-effectiveness of docetaxel (Taxotere: Sanofi–Aventis, Laval, QC) in combination with doxorubicin and cyclophosphamide (tac) compared with 5-fluorouracil, doxorubicin, and cyclophosphamide (fac) following primary surgery for breast cancer in women with operable, axillary lymph node–positive breast cancer
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