Lacy Martha Q, Gertz Morie A, Dispenzieri Angela, Hayman Suzanne R, Geyer Susan, Kabat Brian, Zeldenrust Steven R, Kumar Shaji, Greipp Philip R, Fonseca Rafael, Lust John A, Russell Stephen J, Kyle Robert A, Witzig Thomas E, Bergsagel P Leif, Stewart A Keith, Rajkumar S Vincent
Division of Hematology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.
Mayo Clin Proc. 2007 Oct;82(10):1179-84. doi: 10.4065/82.10.1179.
To determine the long-term effects of a combined regimen of lenalidomide and dexamethasone (Rev-Dex) on time to progression, progression-free survival, and overall survival (OS) in patients with multiple myeloma.
From March 2004 through October 2004, 34 patients were registered for the study. They were treated with 25 mg/d of lenalidomide on days 1 through 21 of a 28-day cycle and 40 mg/d of dexamethasone on days 1 through 4, 9 through 12, and 17 through 20 of each cycle. After 4 cycles of therapy, patients were allowed to discontinue treatment to pursue autologous stem cell transplant (SCT). Treatment beyond 4 cycles was permitted at the physician s discretion.
Thirteen patients proceeded to SCT after initial therapy and were censored at that time point for purposes of calculation of response. Thirty-one patients achieved an objective response, defined as a partial response or better (91%; 95% confidence interval, 79%-98%), with a complete response plus very good partial response rate of 56%. The complete response plus very good partial response among the 21 patients who received Rev-Dex without SCT was 67%. The 2-year progression-free survival rates for patients proceeding to SCT and patients remaining on Rev-Dex were 83% and 59%, respectively; the OS rates were 92% and 90% at 2 years and 92% and 85% at 3 years, respectively. The 3-year OS rate for the whole cohort was 88%.
The Rev-Dex regimen is highly active in the treatment of newly diagnosed multiple myeloma. Responses are durable with a low progression rate at 2 years. Randomized trials that incorporate quality-of-life measures are needed to determine if this and other combination regimens are better used early in therapy or should be reserved for later interventions.
确定来那度胺与地塞米松联合方案(Rev-Dex)对多发性骨髓瘤患者疾病进展时间、无进展生存期和总生存期(OS)的长期影响。
2004年3月至2004年10月,34例患者登记参加本研究。他们在28天周期的第1至21天接受25mg/d来那度胺治疗,在每个周期的第1至4天、第9至12天和第17至20天接受40mg/d地塞米松治疗。4个周期的治疗后,允许患者停止治疗以进行自体干细胞移植(SCT)。4个周期后的治疗可由医生酌情决定。
13例患者在初始治疗后进行了SCT,并在该时间点进行截尾以计算缓解情况。31例患者达到客观缓解,定义为部分缓解或更好(91%;95%置信区间,79%-98%),完全缓解加非常好的部分缓解率为56%。在21例未进行SCT而接受Rev-Dex治疗的患者中,完全缓解加非常好的部分缓解率为67%。进行SCT的患者和继续接受Rev-Dex治疗的患者的2年无进展生存率分别为83%和59%;2年时的OS率分别为92%和90%,3年时分别为92%和85%。整个队列的3年OS率为88%。
Rev-Dex方案在新诊断的多发性骨髓瘤治疗中具有高度活性。缓解持久,2年时疾病进展率低。需要纳入生活质量测量的随机试验来确定该方案及其他联合方案是更适合在治疗早期使用还是应留作后期干预。