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来那度胺:在滤泡性淋巴瘤治疗中的评价。

Lenalidomide: A Review in Previously Treated Follicular Lymphoma.

机构信息

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

出版信息

Drugs. 2020 Sep;80(13):1337-1344. doi: 10.1007/s40265-020-01381-1.

Abstract

Lenalidomide (Revlimid) is a targeted immunomodulatory drug with multiple mechanisms of action. In the USA and the EU, oral lenalidomide is indicated in combination with rituximab or a rituximab product for the treatment of patients with previously treated follicular lymphoma. In the pivotal, phase III AUGMENT trial, lenalidomide + rituximab significantly prolonged progression-free survival (PFS; primary endpoint) relative to placebo + rituximab in patients with relapsed or refractory indolent non-Hodgkin lymphoma, with the PFS benefit appearing to be specific to patients with follicular lymphoma and extending to elderly patients with this subtype. Lenalidomide + rituximab also demonstrated activity in an interim analysis of the phase III MAGNIFY trial in patients with relapsed or refractory indolent non-Hodgkin lymphoma, including those with rituximab-refractory disease. Lenalidomide had an acceptable tolerability profile. Although grade 3 or 4 neutropenia occurred more frequently with lenalidomide + rituximab than with placebo + rituximab, this was generally well managed with dosage adjustments and growth factor support. In conclusion, lenalidomide in combination with rituximab represents an important new treatment option for previously treated follicular lymphoma, including patients whose disease has become refractory to rituximab.

摘要

来那度胺(瑞复美)是一种具有多种作用机制的靶向免疫调节药物。在美国和欧盟,来那度胺联合利妥昔单抗或利妥昔单抗产品用于治疗先前接受过治疗的滤泡性淋巴瘤患者。在关键性、III 期 AUGMENT 试验中,与安慰剂联合利妥昔单抗相比,来那度胺联合利妥昔单抗显著延长了复发或难治性惰性非霍奇金淋巴瘤患者的无进展生存期(PFS;主要终点),PFS 获益似乎仅限于滤泡性淋巴瘤患者,并扩展至该亚型的老年患者。在复发或难治性惰性非霍奇金淋巴瘤患者的 III 期 MAGNIFY 试验的中期分析中,来那度胺联合利妥昔单抗也显示出活性,包括那些对利妥昔单抗难治的疾病患者。来那度胺具有可接受的耐受性特征。尽管来那度胺联合利妥昔单抗比安慰剂联合利妥昔单抗更常发生 3 级或 4 级中性粒细胞减少症,但通过剂量调整和生长因子支持,通常可以很好地管理。总之,来那度胺联合利妥昔单抗代表了先前治疗的滤泡性淋巴瘤的一种重要的新治疗选择,包括对利妥昔单抗耐药的患者。

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