双药vs单药高剂量melphalan 200mg /m2和自体干细胞移植治疗多发性骨髓瘤:北欧地区484例患者的区域研究

B. Björkstrand, T. Klausen, K. Remes, A. Gruber, L. Knudsen, O. Bergmann, S. Lenhoff, H. Johnsen
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引用次数: 3

摘要

自体干细胞移植仍然被认为是年轻多发性骨髓瘤(MM)患者的标准治疗方法。这种疾病是由造血干细胞移植支持的高剂量治疗(HDT)的最常见适应症,许多数据支持该手术的益处。随机研究的结果支持串联自体移植,尽管对总生存率的影响尚不清楚。基于北欧地区的顺序注册试验,我们旨在评估常规单次或双次HDT的结果。在1994-2000年期间,我们共登记了484名诊断时年龄小于60岁的未接受治疗的患者,他们在地区基础上最初接受单一[试验NMSG #5/94和#7/98 (N=383)]或双重[试验Huddinge Karolinska Turku Herlev (N=101)]高剂量melphalan (200mg /m2)治疗,并支持自体干细胞移植。单次移植组40%的患者和两次移植组60%的患者获得完全或非常好的部分缓解(p=0.0006)。诊断后5年无进展生存的概率在单移植组为25% (95% CL 18-32%),在双移植组为46% (95% CL 33-55%) (p=0.0014)。单次移植组的5年生存率为60%,双次移植组为64% (p=0.9)。在多变量分析中,包括单次与双次移植、β2微球蛋白水平、年龄、性别和疾病分期,只有β2微球蛋白水平可预测总生存期(p>0.0001)和无进展生存期(p=0.001)。根据这些结果,双次和单次移植之间的1:1病例对照匹配比较未发现总生存率和无进展生存率的显着差异。在这项回顾性分析中,在北欧地区患者中,与单次移植相比,双次移植(200 mg/m2)似乎并没有改善最终结果。这些数据与博洛尼亚96试验的最新出版物一致,表明不应首先推荐第二次移植作为标准治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Double versus single high-dose melphalan 200 mg/m2 and autologous stem cell transplantation for multiple myeloma: a region-based study in 484 patients from the Nordic area
Autologous stem cell transplantation is still considered the standard of care in young patients with multiple myeloma (MM). This disease is the most common indication for high-dose therapy (HDT) supported by hematopoietic stem cell transplantation and much data support the benefit of this procedure. Results of randomized studies are in favor of tandem autologous transplantation although the effect on overall survival is unclear. Based on sequential registration trials in the Nordic area, we aimed to evaluate the outcome of conventional single or double HDT. During 1994–2000 we registered a total of 484 previously untreated patients under the age of 60 years at diagnosis who on a regional basis initially were treated with single [Trial NMSG #5/94 and #7/98 (N=383)] or double [Trial Huddinge Karolinska Turku Herlev (N=101)] high-dose melphalan (200 mg/m2) therapy supported by autologous stem cell transplantation. A complete or very good partial response was achieved by 40% of patients in the single transplant group and 60% of patients in the double transplant group (p=0.0006). The probability of surviving progression free for five years after the diagnosis was 25% (95% CL 18–32%) in the singletransplant group and 46% (95% CL 33–55%) in the double transplant group (p=0.0014). The estimated overall five-year survival rate was 60% in the single transplant group and 64% in the doubletransplant (p=0.9). In a multivariate analysis of variables, including single versus double transplantation, β2 microglobulin level, age, sex and disease stage, only β2 microglobulin level was predictive for overall survival (p>0.0001) and progression free survival (p=0.001). In accordance with these results, a 1:1 case-control matched comparison between double and single transplantation did not identify significant differences in overall and progression free survival. In this retrospective analysis up front double transplantation with melphalan (200 mg/m2) as compared to single transplantation did not seem to improve the final outcome among patients in the Nordic area. These data are in accordance with recent publications from the Bologna 96 trial indicating that a second transplant should not be recommended up front as standard care.
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