Department of Hematology, Hospital Clínic de Barcelona, Barcelona, Spain.
Department of Hematology, Hospital Germans Trias I Pujol, Badalona, Spain.
Leukemia. 2017 Sep;31(9):1922-1927. doi: 10.1038/leu.2017.35. Epub 2017 Jan 23.
The phase III trial GEM05MENOS65 randomized 390 patients 65 years old or younger with newly diagnosed symptomatic multiple myeloma (MM) to receive induction with thalidomide/dexamethasone, bortezomib/thalidomide/dexamethasone and Vincristine, BCNU, melphalan, cyclophosphamide, prednisone/vincristine, BCNU, doxorubicin, dexamethasone bortezomib (VBMCP/VBAD/B) followed by autologous stem cell transplantation (ASCT) with MEL-200. After ASCT, a second randomization was performed to compare thalidomide/bortezomib (TV), thalidomide (T) and alfa-2b interferon (alfa2-IFN). Maintenance treatment consisted of TV (thalidomide 100 mg daily plus one cycle of intravenous bortezomib at 1.3 mg/m on days 1, 4, 8 and 11 every 3 months) versus T (100 mg daily) versus alfa2-IFN (3 MU three times per week) for up to 3 years. A total of 271 patients were randomized (TV: 91; T: 88; alfa2-IFN: 92). The complete response (CR) rate with maintenance was improved by 21% with TV, 11% with T and 17% with alfa2-IFN (P, not significant). After a median follow-up of 58.6 months, the progression-free survival (PFS) was significantly longer with TV compared with T and alfa2-IFN (50.6 vs 40.3 vs 32.5 months, P=0.03). Overall survival was not significantly different among the three arms. Grade 2-3 peripheral neuropathy was observed in 48.8%, 34.4% and 1% of patients treated with TV, T and alfa2-IFN, respectively. In conclusion, bortezomib and thalidomide maintenance resulted in a significantly longer PFS when compared with thalidomide or alfa2-IFN. (no. EUDRA 2005-001110-41).
该 III 期试验 GEM05MENOS65 将 390 名年龄在 65 岁或以下的新诊断为有症状的多发性骨髓瘤(MM)患者随机分为三组:接受来那度胺/地塞米松、硼替佐米/来那度胺/地塞米松和长春新碱、卡氮芥、苯丁酸氮芥、环磷酰胺、泼尼松/长春新碱、卡氮芥、阿霉素、地塞米松硼替佐米(VBMCP/VBAD/B)诱导治疗,随后进行自体干细胞移植(ASCT),采用 MEL-200。ASCT 后,进行第二次随机分组,比较来那度胺/硼替佐米(TV)、来那度胺(T)和 α-2b 干扰素(alfa2-IFN)。维持治疗包括 TV(来那度胺 100mg 每日一次,每 3 个月静脉注射硼替佐米 1.3mg/m2,第 1、4、8 和 11 天各一次)、T(100mg 每日一次)和 alfa2-IFN(3MU,每周三次),持续 3 年。共有 271 名患者被随机分组(TV:91;T:88;alfa2-IFN:92)。维持治疗的完全缓解(CR)率 TV 组提高了 21%,T 组提高了 11%,alfa2-IFN 组提高了 17%(P,无显著差异)。中位随访 58.6 个月后,与 T 和 alfa2-IFN 相比,TV 组的无进展生存期(PFS)显著延长(50.6 个月 vs 40.3 个月 vs 32.5 个月,P=0.03)。三组的总生存期无显著差异。接受 TV、T 和 alfa2-IFN 治疗的患者中,分别有 48.8%、34.4%和 1%出现 2-3 级周围神经病变。总之,与来那度胺或 alfa2-IFN 相比,硼替佐米和来那度胺维持治疗可显著延长 PFS。(注册号 EUDRA 2005-001110-41)。