达拉图穆马
来那度胺
泊马度胺
伊扎莫布
Carfilzomib公司
硼替佐米
多发性骨髓瘤
医学
全景望远镜
肿瘤科
养生
地塞米松
内科学
挽救疗法
化疗
生物
组蛋白脱乙酰基酶
生物化学
基因
组蛋白
作者
Jean Luc Harousseau,Michel Attal
出处
期刊:Blood
[American Society of Hematology]
日期:2017-07-05
卷期号:130 (8): 963-973
被引量:67
标识
DOI:10.1182/blood-2017-03-726703
摘要
Abstract The standard treatment of relapsed multiple myeloma has been either lenalidomide-dexamethasone (RD) or bortezomib-dexamethasone (VD) but it is changing rapidly for 2 reasons. First, lenalidomide and bortezomib are currently used in frontline treatment and many patients become resistant to these agents early in the course of their disease. Second, 6 second-line new agents have been recently developed and offer new possibilities (pomalidomide, carfilzomib and ixazomib, panobinostat, elotuzumab, and daratumumab). Recent randomized studies have shown that triple combinations adding 1 of these new agents (except pomalidomide) to the RD or VD regimens were superior to the double combinations in terms of response rate and progression-free survival (PFS). Their place in the treatment of first relapse is discussed here. Among these agents, daratumumab is clearly a breakthrough and daratumumab-based combinations might become the preferred option in the near future. However, all of these drugs are expensive and are not available or affordable in all countries. We propose a decision algorithm for first relapse in fit patients with the objective of achieving the best PFS. The choice of salvage regimen is based on lenalidomide/bortezomib resistance, daratumumab availability, and cost. Autologous transplantation should be considered in younger patients if not used upfront.
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