Mayo Clinic, Rochester, Minnesota, USA.
Lancet Oncol. 2010 Jan;11(1):29-37. doi: 10.1016/S1470-2045(09)70284-0. Epub 2009 Oct 21.
High-dose dexamethasone is a mainstay of therapy for multiple myeloma. We studied whether low-dose dexamethasone in combination with lenalidomide is non-inferior to and has lower toxicity than high-dose dexamethasone plus lenalidomide.
Patients with untreated symptomatic myeloma were randomly assigned in this open-label non-inferiority trial to lenalidomide 25 mg on days 1-21 plus dexamethasone 40 mg on days 1-4, 9-12, and 17-20 of a 28-day cycle (high dose), or lenalidomide given on the same schedule with dexamethasone 40 mg on days 1, 8, 15, and 22 of a 28-day cycle (low dose). After four cycles, patients could discontinue therapy to pursue stem-cell transplantation or continue treatment until disease progression. The primary endpoint was response rate after four cycles assessed with European Group for Blood and Bone Marrow Transplant criteria. The non-inferiority margin was an absolute difference of 15% in response rate. Analysis was by modified intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00098475.
445 patients were randomly assigned: 223 to high-dose and 222 to low-dose regimens. 169 (79%) of 214 patients receiving high-dose therapy and 142 (68%) of 205 patients on low-dose therapy had complete or partial response within four cycles (odds ratio 1.75, 80% CI 1.30-2.32; p=0.008). However, at the second interim analysis at 1 year, overall survival was 96% (95% CI 94-99) in the low-dose dexamethasone group compared with 87% (82-92) in the high-dose group (p=0.0002). As a result, the trial was stopped and patients on high-dose therapy were crossed over to low-dose therapy. 117 patients (52%) on the high-dose regimen had grade three or worse toxic effects in the first 4 months, compared with 76 (35%) of the 220 on the low-dose regimen for whom toxicity data were available (p=0.0001), 12 of 222 on high dose and one of 220 on low-dose dexamethasone died in the first 4 months (p=0.003). The three most common grade three or higher toxicities were deep-vein thrombosis, 57 (26%) of 223 versus 27 (12%) of 220 (p=0.0003); infections including pneumonia, 35 (16%) of 223 versus 20 (9%) of 220 (p=0.04), and fatigue 33 (15%) of 223 versus 20 (9%) of 220 (p=0.08), respectively.
Lenalidomide plus low-dose dexamethasone is associated with better short-term overall survival and with lower toxicity than lenalidomide plus high-dose dexamethasone in patients with newly diagnosed myeloma.
National Cancer Institute, Rockville, MD, USA.
高剂量地塞米松是多发性骨髓瘤治疗的主要方法。我们研究了低剂量地塞米松联合来那度胺是否不如高剂量地塞米松联合来那度胺,且毒性更低。
在这项开放标签非劣效性试验中,未经治疗的有症状骨髓瘤患者被随机分配,接受 25 毫克来那度胺,在 28 天周期的第 1-21 天,加 40 毫克地塞米松,在第 1-4、9-12 和 17-20 天(高剂量),或接受相同方案的来那度胺,在第 1、8、15 和 22 天(低剂量)加 40 毫克地塞米松。在四个周期后,患者可以停止治疗以进行干细胞移植,或继续治疗直至疾病进展。主要终点是根据欧洲血液和骨髓移植标准评估的四个周期后的反应率。非劣效性边界为反应率的绝对差异 15%。分析采用改良意向治疗。该试验在 ClinicalTrials.gov 上注册,编号为 NCT00098475。
445 名患者被随机分配:223 名接受高剂量治疗,222 名接受低剂量治疗。在接受高剂量治疗的 214 名患者中,有 169 名(79%)和接受低剂量治疗的 205 名患者中有 142 名(68%)在四个周期内有完全或部分反应(比值比 1.75,80%CI 1.30-2.32;p=0.008)。然而,在一年时的第二次中期分析中,低剂量地塞米松组的总生存率为 96%(95%CI 94-99),而高剂量组为 87%(82-92)(p=0.0002)。因此,试验停止,高剂量治疗组的患者交叉到低剂量治疗组。在接受高剂量方案的 117 名患者(52%)中,在头 4 个月有 3 级或更高级别的毒性作用,而在可获得毒性数据的 220 名接受低剂量方案的患者中,有 76 名(35%)(p=0.0001),222 名接受高剂量地塞米松的患者中有 12 人(10%)和 220 名接受低剂量地塞米松的患者中有 1 人(0.5%)在头 4 个月死亡(p=0.003)。最常见的 3 级或更高毒性是深静脉血栓形成,223 名患者中有 57 名(26%),220 名患者中有 27 名(12%)(p=0.0003);感染包括肺炎,223 名患者中有 35 名(16%),220 名患者中有 20 名(9%)(p=0.04),疲劳 223 名患者中有 33 名(15%),220 名患者中有 20 名(9%)(p=0.08)。
在新诊断的骨髓瘤患者中,来那度胺联合低剂量地塞米松与来那度胺联合高剂量地塞米松相比,可获得更好的短期总生存率和更低的毒性。
美国马里兰州罗克维尔国家癌症研究所。