IDARUBICIN - A PHARMACOECONOMIC EVALUATION OF ITS USE IN ADULT PATIENTS WITH ACUTE MYELOID-LEUKEMIA

被引:2
作者
WHITTINGTON, R
GOA, KL
机构
[1] Adis International Limited, Auckland, 41 Centorian Drive, Private Bag 65901, Mairangi Bay
关键词
D O I
10.2165/00019053-199304040-00007
中图分类号
F [经济];
学科分类号
02 ;
摘要
Idarubicin is an effective agent in the treatment of acute myeloid leukaemia (AML), inducing complete remission in 39 to 80% of newly diagnosed patients. Although it also demonstrates efficacy as monotherapy, and is of use in relapsed or refractory disease, most comparative clinical trials have administered idarubicin intravenously in combination with cytarabine in newly diagnosed patients. These trials indicate that improved survival and response rates, and rapid achievement of remission, are more likely with idarubicin than with daunorubicin, when both agents are given in combination with cytarabine. In elderly patients, however, response rates are lower than in younger patients, and there is less disparity in efficacy between idarubicin and daunorubicin induction therapy. Although AML is an expensive disease to treat, the majority of costs are associated with the length of hospitalisation. with the acquisition cost of the chemotherapy agents contributing < 10% to overall expenditure. Idarubicin combined with cytarabine therapy achieved higher response rates with the first cycle of therapy than daunorubicin. thereby reducing the requirements for a second cycle of therapy and further hospitalisation. Compared with daunorubicin plus cytarabine induction treatment, idarubicin plus cytarabine reduced the costs of achieving a complete response by between 22 and 39% in patients with a median age < 60 years, In patients with a median age of 62 years, who are more representative of the AML population, costs of achieving a complete response were reduced by 3 to 6%. Thus, idarubicin is more cost effective than daunorubicin as induction therapy in combination with cytarabine, in adult patients with AML. The pharmacoeconomic position of idarubicin in postinduction therapy remains to be established.
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页码:287 / 307
页数:21
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