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急性白血病患者缓解后强化治疗的成本效益

Cost-effectiveness of postremission intensive therapy in patients with acute leukemia.

作者信息

Yu Y-B, Gau J-P, You J-Y, Chern H-H, Chau W-K, Tzeng C-H, Ho C-H, Hsu H-C

机构信息

Division of Hematology and Oncology, Department of Medicine, Taipei-Veterans General Hospital, Taiwan 11217, Republic of China.

出版信息

Ann Oncol. 2007 Mar;18(3):529-34. doi: 10.1093/annonc/mdl420. Epub 2006 Dec 12.

Abstract

BACKGROUND

We assessed the cost-effectiveness of high-dose arabinoside (HiDAC)-based and allogeneic stem-cell transplantation (alloSCT)-based therapy in patients with acute leukemia.

PATIENTS AND METHODS

We analyzed the outcome, cost and cost-effectiveness of 106 patients treated from January 1994 to January 2002 [94 acute myelogenous leukemia (AML)/12 acute lymphoblastic leukemia (ALL)]. Forty-two young patients at either intermediate or unknown cytogenetic risk received postremission intensive therapy (24 HiDAC-based/18 alloSCT-based therapy).

RESULTS

After a median follow-up of 50 months, the estimated 7-year overall survival for the HiDAC-based group showed a tendency to be higher than the alloSCT-based group (48% versus 28%, P = 0.1452). The HiDAC-based group spent a significantly lower total cost ($US51,857 versus 75,474, P = 0.004) than the alloSCT-based group. Cost-effectiveness analysis showed that the mean cost per year of life saved for the HiDAC-based group is considerably less expensive than the alloSCT-based group ($US11,224 versus 21,564). The reduced total cost for the HiDAC-based group originated from lower cost in room fees, medication, laboratory and procedure, but not in blood transfusion and professional manpower fees.

CONCLUSION

For the postremission therapy in young AML patients at either intermediate or unknown cytogenetic risk, cost-effectiveness of HiDAC-based therapy compares favorably with that of alloSCT-based therapy, which deserves further clinical trials.

摘要

背景

我们评估了以大剂量阿糖胞苷(HiDAC)为基础和以异基因干细胞移植(alloSCT)为基础的疗法对急性白血病患者的成本效益。

患者与方法

我们分析了1994年1月至2002年1月期间接受治疗的106例患者的结局、成本及成本效益[94例急性髓系白血病(AML)/12例急性淋巴细胞白血病(ALL)]。42例处于中等或细胞遗传学风险未知的年轻患者接受缓解后强化治疗(24例接受以HiDAC为基础的治疗/18例接受以alloSCT为基础的治疗)。

结果

中位随访50个月后,以HiDAC为基础的治疗组估计7年总生存率有高于以alloSCT为基础的治疗组的趋势(48%对28%,P = 0.1452)。以HiDAC为基础的治疗组的总花费显著低于以alloSCT为基础的治疗组(51,857美元对75,474美元, P = 0.004)。成本效益分析显示,以HiDAC为基础的治疗组每挽救一年生命的平均成本比以alloSCT为基础的治疗组低得多(11,224美元对21,564美元)。以HiDAC为基础的治疗组总花费降低源于病房费用、药物、实验室及操作费用较低,但输血及专业人力费用并非如此。

结论

对于处于中等或细胞遗传学风险未知的年轻AML患者的缓解后治疗,以HiDAC为基础的治疗的成本效益优于以alloSCT为基础的治疗,值得进一步进行临床试验。

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