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首页> 外文期刊>The lancet oncology >Bortezomib, melphalan, and prednisone versus bortezomib, thalidomide, and prednisone as induction therapy followed by maintenance treatment with bortezomib and thalidomide versus bortezomib and prednisone in elderly patients with untreated multiple myeloma: a randomised trial.
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Bortezomib, melphalan, and prednisone versus bortezomib, thalidomide, and prednisone as induction therapy followed by maintenance treatment with bortezomib and thalidomide versus bortezomib and prednisone in elderly patients with untreated multiple myeloma: a randomised trial.

机译:对于未经治疗的多发性骨髓瘤老年患者,硼替佐米,美法仑和泼尼松与硼替佐米,沙利度胺和泼尼松作为诱导疗法,然后采用硼替佐米和沙利度胺与硼替佐米和泼尼松维持治疗:一项随机试验。

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BACKGROUND: Bortezomib plus melphalan and prednisone (VMP) is significantly better than melphalan plus prednisone alone for elderly patients with untreated multiple myeloma; however, toxic effects are high. We investigated a novel and less intensive bortezomib-based regimen to maintain efficacy and to reduce toxic effects. METHODS: Between March, 2006, and October, 2008, 260 patients with untreated multiple myeloma, 65 years and older, from 63 Spanish centres, were randomly assigned to receive six cycles of VMP (n=130) or bortezomib plus thalidomide and prednisone (VTP; n=130) as induction therapy, consisting of one cycle of bortezomib twice per week for 6 weeks (1.3 mg/m(2) on days 1, 4, 8, 11, 22, 25, 29, and 32), plus either melphalan (9 mg/m(2) on days 1-4) or daily thalidomide (100 mg), and prednisone (60 mg/m(2) on days 1-4). The first cycle was followed by five cycles of bortezomib once per week for 5 weeks (1.3 mg/m(2) on days 1, 8, 15, and 22) plus the same doses of melphalan plus prednisone and thalidomide plus prednisone. 178 patients completed the six induction cycles and were randomly assigned to maintenance therapy with bortezomib plus prednisone (n=87) or bortezomib plus thalidomide (n=91), consisting of one conventional cycle of bortezomib for 3 weeks (1.3 mg/m(2) on days 1, 4, 8, and 11) every 3 months, plus either prednisone (50 mg every other day) or thalidomide (50 mg per day), for up to 3 years. Treatment codes were generated with a computerised random number generator, and neither participants nor study personnel were masked to treatment. The primary endpoint was response rate in induction and maintenance phases. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00443235. FINDINGS: In the induction phase, 105 (81%) patients in the VTP group and 104 (80%) in the VMP group achieved partial responses or better (p=0.9), including 36 (28%) and 26 (20%) complete remissions, respectively (p=0.2). Treatment with VTP resulted in more serious adverse events (40 [31%] vs 20 [15%], p=0.01) and discontinuations (22 [17%] vs 15 [12%], p=0.03) than did treatment with VMP. The most common toxicities (grade 3 or worse) were infections (one [1%] in the VTP group vs nine [7%] in the VMP group), cardiac events (11 [8%] vs 0), and peripheral neuropathy (nine [7%] vs 12 [9%]). After maintenance therapy, the complete remission rate was 42% (40 [44%] patients in complete remission in the bortezomib plus thalidomide group, 34 [39%] in the bortezomib plus prednisone group). No grade 3 or worse haematological toxicities were recorded during maintenance therapy; two (2%) patients in the bortezomib plus prednisone group and six (7%) in the bortezomib plus thalidomide group developed peripheral neuropathy. INTERPRETATION: Reduced-intensity induction with a bortezomib-based regimen, followed by maintenance, is a safe and effective treatment for elderly patients with multiple myeloma. FUNDING: Pethema (Spanish Program for the Treatment of Hematologic Diseases).
机译:背景:对于未经治疗的多发性骨髓瘤老年患者,硼替佐米联合美法仑和泼尼松(VMP)明显优于单独美法仑加泼尼松。但是,毒性作用很高。我们研究了一种基于硼替佐米的新型且强度较小的方案,以维持疗效并减少毒性作用。方法:在2006年3月至2008年10月之间,来自西班牙63个中心的260名65岁及以上未治疗的多发性骨髓瘤患者被随机分配接受六个周期的VMP(n = 130)或硼替佐米加沙利度胺和泼尼松治疗( VTP; n = 130)作为诱导疗法,包括每周两次硼替佐米治疗,持续6周(第1、4、8、11、22、25、29和32天为1.3 mg / m(2)),加上美法仑(1-4天时为9 mg / m(2))或每日沙利度胺(100 mg)和泼尼松(1-4天时为60 mg / m(2))。第一个周期之后是硼替佐米的五个周期,每周一次,共5周(第1、8、15和22天为1.3 mg / m(2)),再加上相同剂量的美法仑加泼尼松和沙利度胺加泼尼松。 178名患者完成了6个诱导周期,并随机分配使用硼替佐米+泼尼松(n = 87)或硼替佐米+沙利度胺(n = 91)的维持治疗,包括一个常规的硼替佐米周期3周(1.3 mg / m(2) ),每3个月的第1、4、8和11天),加泼尼松(每隔一天50毫克)或沙利度胺(每天50毫克),最多3年。使用计算机化的随机数生成器生成治疗代码,参与者和研究人员都不会被屏蔽。主要终点是诱导和维持阶段的缓解率。分析是按意向进行的。该试验已在ClinicalTrials.gov上注册,编号为NCT00443235。结果:在诱导期,VTP组的105名患者(81%)和VMP组的104名患者(80%)达到了部分缓解或更好(p = 0.9),包括36名(28%)和26名(20%)完全缓解(p = 0.2)。与VMP治疗相比,VTP治疗导致更严重的不良事件(40 [31%] vs 20 [15%],p = 0.01)和停药(22 [17%] vs 15 [12%],p = 0.03) 。最常见的毒性(3级或更严重)是感染(VTP组1 [1%],VMP组9 [7%]),心脏事件(11 [8%] vs 0)和周围神经病变( 9 [7%]和12 [9%])。维持治疗后,完全缓解率为42%(硼替佐米加沙利度胺组完全缓解的患者为40 [44%],硼替佐米加泼尼松组为34 [39%]的患者完全缓解)。维持治疗期间未记录到3级或更严重的血液学毒性;硼替佐米加泼尼松组中有2名(2%)患者和硼替佐米加沙利度胺组中有6名(7%)患者出现周围神经病变。解释:以硼替佐米为基础的方案降低强度诱导,然后维持,对于老年多发性骨髓瘤患者是一种安全有效的治疗方法。资金:Pethema(西班牙血液病治疗计划)。

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