Harousseau Jean-Luc, Moreau Philippe
Department of Hematology, University Hospital Hotel-Dieu, 1 Place Alexis Ricordeau, 44035 Nantes, France.
Clin Lymphoma Myeloma. 2005 Sep;6(2):89-95. doi: 10.3816/CLM.2005.n.034.
Autologous stem cell transplantation (ASCT) is currently considered the standard of care for younger patients with newly diagnosed multiple myeloma based on 3 randomized trials that have shown it is superior to conventional chemotherapy. However, the introduction of novel agents like thalidomide, bortezomib, or lenalidomide may improve the results of standard-dose therapy. For instance, in combination, melphalan/prednisone/thalidomide yields complete response rates comparable with those achieved with ASCT. Different strategies have been proposed to improve the results of ASCT. A randomized trial has shown that tandem ASCT is superior to single ASCT in terms of event-free survival (EFS) and overall survival. Four other randomized trials have produced results in favor of tandem ASCT. However, the benefit remains marginal and patients with poor initial characteristics still have poor outcomes. Further intensification has been tested with encouraging results in patients with high b2-microglobulin levels and chromosome 13 deletion. "Total Therapy II" with intensified induction and post-ASCT chemotherapy also appears to improve outcomes. Another possibility is the use of novel agents in combination with ASCT as part of induction therapy or as maintenance therapy after ASCT. Preliminary results of a French Intergroup study show a significant prolongation of EFS in patients receiving maintenance therapy with thalidomide. Results achieved with allogeneic stem cell transplantation remain disappointing. Although initial results of ASCT followed by reduced-intensity allogeneic stem cell transplantation were promising, with more follow-up, relapses and chronic graft-versus-host disease have limited the enthusiasm. Allogeneic stem cell transplantation should be proposed only in the context of a clinical trial.
自体干细胞移植(ASCT)目前被认为是新诊断的年轻多发性骨髓瘤患者的标准治疗方法,基于3项随机试验表明其优于传统化疗。然而,沙利度胺、硼替佐米或来那度胺等新型药物的引入可能会改善标准剂量治疗的效果。例如,美法仑/泼尼松/沙利度胺联合使用可产生与ASCT相当的完全缓解率。已提出不同策略来改善ASCT的效果。一项随机试验表明,在无事件生存期(EFS)和总生存期方面,串联ASCT优于单次ASCT。其他4项随机试验也得出了支持串联ASCT的结果。然而,获益仍然有限,初始特征较差的患者预后仍然不佳。在高β2-微球蛋白水平和13号染色体缺失的患者中进行了进一步强化治疗测试,结果令人鼓舞。强化诱导和ASCT后化疗的“Total Therapy II”似乎也能改善预后。另一种可能性是将新型药物与ASCT联合使用,作为诱导治疗的一部分或ASCT后的维持治疗。一项法国多中心研究的初步结果显示,接受沙利度胺维持治疗的患者EFS显著延长。异基因干细胞移植的结果仍然令人失望。尽管ASCT后进行减低强度异基因干细胞移植的初步结果很有前景,但随着随访时间的延长,复发和慢性移植物抗宿主病限制了人们的热情。异基因干细胞移植仅应在临床试验的背景下提出。