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Therapeutic Activity of Lenalidomide in Mantle Cell Lymphoma and Indolent Non-Hodgkins Lymphomas

机译:来那度胺对套细胞淋巴瘤和惰性非霍奇金淋巴瘤的治疗活性

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摘要

Mantle cell lymphoma (MCL) comprises 3–10% of NHL, with survival times ranging from 3 and 5 years. Indolent lymphomas represent approximately 30% of all NHLs with patient survival largely dependent on validated prognostic scores. High response rates are typically achieved in these patients with current first-line chemoimmunotherapy. However, most patients will eventually relapse and become chemorefractory with poor outcome. Alternative chemoimmunotherapy regimens are often used as salvage strategy and stem cell transplant remains an option for selected patients. However, novel approaches are urgently needed for patients no longer responding to conventional chemotherapy. Lenalidomide is an immunomodulatory drug with activity in multiple myeloma, myelodisplastic syndrome and chronic lymphoproliferative disorders. In phase II studies of indolent NHL and MCL lenalidomide has shown activity with encouraging response rates, both as a single agent and in combination with other drugs. Some of these responses may be durable. Optimal dose of lenalidomide has not been defined yet. The role of lenalidomide in the therapeutic armamentarium of patients with indolent NHL or MCL will be discussed in the present paper.
机译:套细胞淋巴瘤(MCL)占NHL的3-10%,生存时间为3至5年。惰性淋巴瘤约占所有NHL的30%,患者生存率在很大程度上取决于有效的预后评分。在目前采用一线化学免疫治疗的这些患者中,通常可以实现高应答率。但是,大多数患者最终将复发并变成化学难治性患者,预后不良。替代性化学免疫疗法通常被用作挽救策略,而干细胞移植仍然是部分患者的选择。然而,对于不再对常规化学疗法有反应的患者,迫切需要新颖的方法。来那度胺是一种免疫调节药,在多发性骨髓瘤,骨髓增生异常综合征和慢性淋巴细胞增生性疾病中具有活性。在惰性NHL和MCL来那度胺的II期研究中,无论是单一药物还是与其他药物联合使用,均显示出令人鼓舞的反应率。其中一些响应可能是持久的。来那度胺的最佳剂量尚未确定。本文将讨论来那度胺在惰性NHL或MCL患者的治疗装备中的作用。

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