Uyl-de Groot C A, Löwenberg B, Vellenga E, Suciu S, Willemze R, Rutten F F
Institute for Medical Technology Assessment/Department of Health Policy and Management, Erasmus University Rotterdam, The Netherlands.
Br J Haematol. 1998 Mar;100(4):629-36. doi: 10.1046/j.1365-2141.1998.00635.x.
We conducted a prospective, randomized, multicentre clinical trial comparing the effects and costs of GM-CSF as an adjunct to intensive chemotherapy in elderly patients with acute myeloid leukaemia (AML). The patients were randomized to either daunomycin-cytosine arabinoside (control arm: n = 161) or daunomycin-cytosine arabinoside with GM-CSF (GM-CSF arm: n = 157). The primary end-point was the effect of GM-CSF on the percentage of complete remissions (CR). Survival duration, disease-free survival, quality of life and costs were evaluated separately. CR after remission induction treatment was achieved in 55% of the patients in the control group and in 56% of the patients in the GM-CSF group (P = NS). The duration of survival and disease-free survival at 2 years after randomization were estimated at 22% and 19% for the control group and 22% and 14% for the GM-CSF group (P = NS). Considering the short-term quality of life, the administration of GM-CSF resulted in more problems with regard to depressed mood, diarrhoea and rash/eczema. With regard to the long-term quality of life there were no significant differences between the two groups. The average costs of the primary treatment were higher in GM-CSF-treated patients than in the control group, i.e. US$40782 and US$34465, respectively (P < 0.01). The costs during the follow-up period did not differ between the two groups. The results of this randomized clinical trial indicate that daunomycin-cytosine arabinoside plus GM-CSF is not a cost-effective treatment strategy when compared with daunomycin-cytosine arabinoside alone.
我们进行了一项前瞻性、随机、多中心临床试验,比较粒细胞巨噬细胞集落刺激因子(GM-CSF)作为辅助强化化疗手段对老年急性髓细胞白血病(AML)患者的疗效和成本。患者被随机分为两组,一组接受柔红霉素-阿糖胞苷治疗(对照组:n = 161),另一组接受柔红霉素-阿糖胞苷联合GM-CSF治疗(GM-CSF组:n = 157)。主要终点是GM-CSF对完全缓解(CR)率的影响。分别评估了生存期、无病生存期、生活质量和成本。诱导缓解治疗后,对照组55%的患者达到CR,GM-CSF组为56%(P = 无显著性差异)。随机分组后2年的生存期和无病生存期估计,对照组分别为22%和19%,GM-CSF组分别为22%和14%(P = 无显著性差异)。考虑短期生活质量,GM-CSF的使用在情绪低落、腹泻和皮疹/湿疹方面导致了更多问题。关于长期生活质量,两组之间没有显著差异。GM-CSF治疗患者的初始治疗平均成本高于对照组,分别为40782美元和34465美元(P < 0.01)。随访期间两组成本无差异。这项随机临床试验的结果表明,与单独使用柔红霉素-阿糖胞苷相比,柔红霉素-阿糖胞苷加GM-CSF不是一种具有成本效益的治疗策略。