Gunnellini Marco, Falchi Lorenzo
S. C. Oncohematology, Perugia University, S. Maria, 05100 Terni, Italy.
Adv Hematol. 2012;2012:523842. doi: 10.1155/2012/523842. Epub 2012 Jun 14.
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.
套细胞淋巴瘤(MCL)占非霍奇金淋巴瘤(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%,患者的生存很大程度上取决于经过验证的预后评分。目前一线化疗免疫疗法通常能使这些患者获得较高的缓解率。然而,大多数患者最终会复发并对化疗产生耐药,预后较差。替代化疗免疫疗法方案常被用作挽救策略,干细胞移植仍是部分患者的选择。然而,对于不再对传统化疗有反应的患者,迫切需要新的治疗方法。来那度胺是一种免疫调节药物,对多发性骨髓瘤、骨髓增生异常综合征和慢性淋巴细胞增殖性疾病有活性。在惰性NHL和MCL的II期研究中,来那度胺已显示出活性,无论是作为单一药物还是与其他药物联合使用,缓解率都令人鼓舞。其中一些反应可能是持久的。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患者治疗方案中的作用。