医学
内科学
多发性骨髓瘤
比例危险模型
危险系数
多元分析
胃肠病学
骨髓
单变量分析
外科
置信区间
作者
Abdullah S. Al Saleh,Harsh Parmar,Alissa Visram,Eli Muchtar,Francis K. Buadi,Ronald S. Go,Angela Dispenzieri,Prashant Kapoor,Rahma Warsame,Martha Q. Lacy,David Dingli,Nelson Leung,Wilson I. Gonsalves,Taxiarchis Kourelis,Morie A. Gertz,Robert A. Kyle,S. Vincent Rajkumar,Shaji Kumar
标识
DOI:10.1016/j.clml.2020.03.012
摘要
Background Previous reports have suggested that a higher bone marrow plasma-cell percentage (BMPC%) is associated with worse outcomes. However, it is unknown whether BMPC% is an independent predictor because genetic information was not available at that time. Currently the impact of BMPC% at diagnosis of multiple myeloma (MM) is not well described. Patients and Methods We evaluated the prognostic impact of BMPC% ≥ 60% versus < 60% in 1426 newly diagnosed MM patients. All patients had an estimation of their BMPC% at diagnosis, and the highest percentage was used. Progression-free survival (PFS) and overall survival (OS) analyses were performed by the Kaplan-Meier method. Univariate and multivariate analyses for PFS and OS using the Cox proportional hazards model were performed for age, Revised International Staging System (R-ISS) score, creatinine level, and BMPC%. Results BMPC% ≥ 60% was found in 562 patients (39%), and the median PFS was shorter for these patients compared to BMPC% < 60% (22.6 vs. 32.1 months; P < .0001). Also, for OS, the median was shorter for the higher BMPC% group (53.4 vs. 75.4 months; P < .0001). On the multivariate analysis for PFS, age ≥ 65 years (hazard ratio [HR], 1.46; P < .0001), R-ISS (1-2 vs. 3) (HR, 0.49; P < .0001), and BMPC% ≥ 60% (HR, 1.23; P = .015) were predictive. On the multivariate analysis for OS, age ≥ 65 years (HR, 2.23; P < .001), R-ISS (1-2 vs. 3) (HR, 0.41; P < .0001), and BMPC% ≥ 60% (HR, 1.24; P = .02) were also predictive. Conclusion BMPC% ≥ 60% at diagnosis is predictive for PFS and OS, even in a multivariate analysis that included known prognostic factors for MM.
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