Delforge M, Michiels A, Doyen C, Kentos A, Van Droogenbroeck J, Offner F, Bries G, Demuynck H, Vekemans M C, Meuleman N, Mineur P O, Ravoet C, Depryck B, Van de Velde A, Pierre P, Wu K L, Schots R
Afdeling Hematologie, UZ Gasthuisberg, Leuven.
Acta Clin Belg. 2011 Sep-Oct;66(5):371-5. doi: 10.2143/ACB.66.5.2062589.
The prognosis of multiple myeloma patients has significantly improved since the introduction of the novel agents thalidomide, bortezomib and lenalidomide. We report the data of a medical need programme with lenalidomide plus dexamethasone, conducted in Belgium between August 2007 and March 2008, and including 98 relapsed refractory multiple myeloma patients. In addition to chemotherapy and steroids, all patients had received prior treatment with bortezomib, and 84% of them had been exposed to thalidomide. In 52 patients response data could be retrieved by post-hoc analysis. A partial remission or better was achieved in 52% (49% partial and 3% complete response) of patients, despite a median of 5 previous anti-myeloma treatment lines. Responses were rapid while the majority of patients received lenalidomide with once weekly (also called low-dose) dexamethasone. Treatment with lenalidomide plus dexamethasone did prolong overall survival by nearly half a year in this population with end-stage myeloma. Overall response and quality of response were independent of previous response to thalidomide and bortezomib, although the time to progression tended to be shorter in thalidomide- and bortezomib-refractory patients. It can be concluded that lenalidomide plus dexamethasone is an effective and safe treatment regimen in highly refractory multiple myeloma patients, and that these responses are irrespective of previous exposure or sensitivity to thalidomide and bortezomib.
自新型药物沙利度胺、硼替佐米和来那度胺问世以来,多发性骨髓瘤患者的预后有了显著改善。我们报告了一项于2007年8月至2008年3月在比利时开展的来那度胺联合地塞米松医疗需求项目的数据,该项目纳入了98例复发难治性多发性骨髓瘤患者。除化疗和类固醇外,所有患者之前均接受过硼替佐米治疗,其中84%的患者曾使用过沙利度胺。通过事后分析可获取52例患者的缓解数据。尽管患者之前接受过中位数为5线的抗骨髓瘤治疗,但仍有52%(49%部分缓解和3%完全缓解)的患者实现了部分缓解或更好的缓解。缓解出现迅速,大多数患者接受来那度胺联合每周一次(也称为低剂量)地塞米松治疗。在这个晚期骨髓瘤患者群体中,来那度胺联合地塞米松治疗确实将总生存期延长了近半年。总体缓解率和缓解质量与之前对沙利度胺和硼替佐米的反应无关,尽管沙利度胺和硼替佐米难治性患者的疾病进展时间往往较短。可以得出结论,来那度胺联合地塞米松是治疗高度难治性多发性骨髓瘤患者的一种有效且安全的治疗方案,而且这些缓解与之前是否接触过沙利度胺和硼替佐米或对其是否敏感无关。