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来那度胺:对不适用于干细胞移植的新诊断多发性骨髓瘤患者持续使用该药的综述

Lenalidomide: a review of its continuous use in patients with newly diagnosed multiple myeloma not eligible for stem-cell transplantation.

作者信息

McCormack Paul L

机构信息

Springer, Private Bag 65901, Mairangi Bay 0754, Auckland, New Zealand,

出版信息

Drugs Aging. 2015 May;32(5):409-18. doi: 10.1007/s40266-015-0269-6.

Abstract

Lenalidomide (Revlimid(®)) is a second-generation immunomodulatory drug structurally related to thalidomide, with improved efficacy and tolerability, for which the label in the EU was recently expanded to include continuous therapy in patients with previously untreated multiple myeloma not eligible for stem-cell transplantation. In randomized, controlled clinical trials, continuous lenalidomide therapy, either in combination with dexamethasone (FIRST trial) or as maintenance monotherapy following induction with melphalan/prednisone/lenalidomide (MM-015 trial), significantly improved progression-free survival (PFS) compared with induction therapy alone (with non-lenalidomide- or lenalidomide-containing regimens) in patients with newly diagnosed multiple myeloma not eligible for stem-cell transplantation. The improvements in PFS with continuous lenalidomide were reflected in improved health-related quality-of-life measures. An overall survival benefit was observed in the FIRST trial, but not in the MM-015 trial. Continuous lenalidomide and continuous thalidomide regimens displayed similar efficacy, but lenalidomide was associated with significantly less toxicity than thalidomide. Continuous use of lenalidomide did not appear to negatively impact on the drug's tolerability and did not increase the incidence of neutropenia or second primary malignancy compared with shorter-term use. The incidence of most adverse events began to reduce after about 18 months of therapy. In conclusion, continuous lenalidomide regimens provide an effective longer-term treatment option in patients with newly diagnosed multiple myeloma ineligible for stem-cell transplantation.

摘要

来那度胺(瑞复美(Revlimid®))是一种与沙利度胺结构相关的第二代免疫调节药物,疗效和耐受性有所提高,欧盟近期扩大了其适应证范围,将其用于不适于干细胞移植的初治多发性骨髓瘤患者的持续治疗。在随机对照临床试验中,对于不适于干细胞移植的新诊断多发性骨髓瘤患者,来那度胺持续治疗,无论是与地塞米松联合使用(FIRST试验),还是在美法仑/泼尼松/来那度胺诱导治疗后作为维持单药治疗(MM - 015试验),与单独诱导治疗(采用不含来那度胺或含来那度胺的方案)相比,均显著改善了无进展生存期(PFS)。来那度胺持续治疗使PFS得到改善,这也反映在健康相关生活质量指标的改善上。FIRST试验观察到总生存获益,但MM - 015试验未观察到。来那度胺持续治疗方案和沙利度胺持续治疗方案疗效相似,但来那度胺的毒性明显低于沙利度胺。与短期使用相比,持续使用来那度胺似乎对药物耐受性无负面影响,也未增加中性粒细胞减少或第二原发性恶性肿瘤的发生率。大多数不良事件的发生率在治疗约18个月后开始降低。总之,来那度胺持续治疗方案为不适于干细胞移植的新诊断多发性骨髓瘤患者提供了一种有效的长期治疗选择。

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