Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, 4301 West Markham #816, Little Rock, AR 72205, USA.
Ann Hematol. 2011 Apr;90(4):423-8. doi: 10.1007/s00277-010-1130-y. Epub 2010 Dec 14.
Multiple myeloma (MM) survival plots usually display steeper initial and shallower subsequent slopes reflecting differences in disease biology and likely prognostic factors (PF). S9321 trial was selected to determine PF operative at baseline and subsequent 3, 4, 5, and 7-year landmarks (LM-0, LM-3, LM-4, LM-5, and LM-7). With a median follow-up of 8.2 years, survival was similar in transplant and standard therapy arms, justifying data pooling. Median survival for 775 eligible patients is 48 months. According to proportional hazards models, seven of 12 investigated baseline variables retained independent significance for LM-0, of which only two (beta-2-microglobulin and age) extended out to LM-7; the remaining five comprised features of disease aggressiveness (lactate dehydrogenase, calcium, platelet count, C-reactive protein) and host co-morbidity (performance status). Our observations of LM dependency of PF can be exploited toward advancing myeloma therapy by stratifying patients according to whether early or late portions of the survival history are being targeted.
多发性骨髓瘤(MM)生存曲线通常显示初始斜率较陡,后续斜率较浅,反映了疾病生物学和可能的预后因素(PF)的差异。选择 S9321 试验来确定基线和随后的 3、4、5 和 7 年里程碑(LM-0、LM-3、LM-4、LM-5 和 LM-7)时的 PF 操作。中位随访 8.2 年后,移植组和标准治疗组的生存情况相似,因此可以对数据进行汇总。775 名合格患者的中位生存时间为 48 个月。根据比例风险模型,12 个基线变量中有 7 个在 LM-0 时具有独立意义,其中只有 2 个(β-2-微球蛋白和年龄)扩展到 LM-7;其余 5 个包括疾病侵袭性(乳酸脱氢酶、钙、血小板计数、C 反应蛋白)和宿主合并症(表现状态)的特征。我们观察到 PF 对 LM 的依赖性可以通过根据生存史的早期或晚期部分是否作为目标来分层患者,从而推进骨髓瘤治疗。