Department of Medicine I, Center for Oncology and Hematology, Wilhelminenspital, Vienna, Austria.
Blood. 2012 Mar 29;119(13):3003-15. doi: 10.1182/blood-2011-11-374249. Epub 2012 Jan 23.
Maintaining results of successful induction therapy is an important goal in multiple myeloma. Here, members of the International Myeloma Working Group review the relevant data. Thalidomide maintenance therapy after autologous stem cell transplantation improved the quality of response and increased progression-free survival (PFS) significantly in all 6 studies and overall survival (OS) in 3 of them. In elderly patients, 2 trials showed a significant prolongation of PFS, but no improvement in OS. A meta-analysis revealed a significant risk reduction for PFS/event-free survival and death. The role of thalidomide maintenance after melphalan, prednisone, and thalidomide is not well established. Two trials with lenalidomide maintenance treatment after autologous stem cell transplantation and one study after conventional melphalan, prednisone, and lenalidomide induction therapy showed a significant risk reduction for PFS and an increase in OS in one of the transplant trials. Maintenance therapy with single-agent bortezomib or in combination with thalidomide or prednisone has been studied. One trial revealed a significantly increased OS with a bortezomib-based induction and bortezomib maintenance therapy compared with conventional induction and thalidomide maintenance treatment. Maintenance treatment can be associated with significant side effects, and none of the drugs evaluated is approved for maintenance therapy. Treatment decisions for individual patients must balance potential benefits and risks carefully, as a widely agreed-on standard is not established.
维持多发性骨髓瘤成功诱导治疗的疗效是一个重要目标。在这里,国际骨髓瘤工作组的成员回顾了相关数据。在所有 6 项研究中,自体干细胞移植后沙利度胺维持治疗显著改善了反应质量,并显著延长了无进展生存期(PFS),其中 3 项研究还延长了总生存期(OS)。在老年患者中,2 项试验显示 PFS 显著延长,但 OS 无改善。一项荟萃分析显示,PFS/无事件生存和死亡的风险显著降低。马法兰、泼尼松和沙利度胺后沙利度胺维持治疗的作用尚未得到充分证实。2 项自体干细胞移植后来那度胺维持治疗试验和 1 项常规马法兰、泼尼松和来那度胺诱导治疗后研究显示,PFS 风险显著降低,其中 1 项移植试验 OS 增加。单药硼替佐米或联合沙利度胺或泼尼松维持治疗已进行了研究。一项试验显示,与常规诱导和沙利度胺维持治疗相比,硼替佐米为基础的诱导和硼替佐米维持治疗的 OS 显著增加。维持治疗可能会引起严重的副作用,而且没有一种评估药物被批准用于维持治疗。对于个体患者的治疗决策必须仔细权衡潜在的益处和风险,因为尚未建立广泛认可的标准。