Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
Jichi Medical University Saitama Medical Center, Saitama, Japan.
Int J Hematol. 2023 May;117(5):660-668. doi: 10.1007/s12185-022-03530-6. Epub 2023 Jan 3.
Allogeneic bone marrow transplantation (BMT) from an HLA-matched sibling donor is recommended as an initial treatment for young patients. However, immunosuppressive therapy (IST) with cyclosporine and anti-thymocyte globulin may be a viable option even when an HLA-identical sibling donor is available.
We constructed a Markov model to simulate the 10-year clinical course of patients aged 21-40 years with newly diagnosed severe aplastic anemia. Immediate BMT and IST were compared as an initial treatment assuming the availability of an HLA-identical sibling donor. Transition probabilities after treatment were determined based on a registry data analysis for BMT and a long-term prospective study for IST.
Quality-adjusted life years (QALYs) after treatment selection were 6.77 for BMT and 6.74 for IST. One-way sensitivity analysis revealed that the utility for being alive without GVHD after BMT, that for being alive with partial response after IST, and the response rate after initial IST strongly affected the results.
BMT and IST produced similar QALY for young patients with severe aplastic anemia. An estimation of the response rate to the initial IST may enable an individualized comparison between BMT and IST.
对于年轻患者,建议采用 HLA 匹配的同胞供者异基因骨髓移植(BMT)作为初始治疗。然而,即使有 HLA 完全匹配的同胞供者,环孢素和抗胸腺细胞球蛋白的免疫抑制治疗(IST)也可能是一种可行的选择。
我们构建了一个马尔可夫模型,以模拟 21-40 岁新诊断的严重再生障碍性贫血患者的 10 年临床病程。假设存在 HLA 完全匹配的同胞供者,将即刻 BMT 和 IST 作为初始治疗进行比较。根据 BMT 的注册数据分析和 IST 的长期前瞻性研究确定治疗后的转移概率。
治疗选择后的质量调整生命年(QALY)分别为 BMT 的 6.77 和 IST 的 6.74。单因素敏感性分析表明,BMT 后无移植物抗宿主病存活的效用、IST 后部分反应存活的效用以及初始 IST 后的反应率强烈影响结果。
BMT 和 IST 为年轻的严重再生障碍性贫血患者带来了相似的 QALY。对初始 IST 反应率的估计可以实现 BMT 和 IST 之间的个体化比较。