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Comorbidity as a prognostic variable in multiple myeloma: comparative evaluation of common comorbidity scores and use of a novel MM–comorbidity score

机译:合并症作为多发性骨髓瘤的预后变量:常见合并症评分的比较评估和新型MM合并症评分的使用

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摘要

Comorbidities have been demonstrated to affect progression-free survival (PFS) and overall survival (OS), although their impact in multiple myeloma (MM) patients is as yet unsettled. We (1) assessed various comorbidities, (2) compared established comorbidity indices (CIs; Charlson comorbidity index (CCI), hematopoietic cell transplantation-specific comorbidity index (HCT-CI)), Kaplan Feinstein (KF) and Satariano index (SI) and (3) developed a MM-CI (Freiburger comorbidity index, FCI) in 127 MM patients. Univariate analysis determined moderate or severe pulmonary disease (hazard ratio (HR): 3.5, P<0.0001), renal impairment (via estimated glomerular filtration rate (eGFR); HR: 3.4, P=0.0018), decreased Karnofsky Performance Status (KPS, HR: 2.7, P=0.0004) and age (HR: 2, P=0.0114) as most important variables for diminished OS. Through multivariate analysis, the eGFR ⩽30 ml/min/1.73m2, impaired lung function and KPS ⩽70% were significant for decreased OS, with HRs of 2.9, 2.8 and 2.2, respectively. Combination of these risk factors within the FCI identified significantly different median OS rates of 118, 53 and 25 months with 0, 1 and 2 or 3 risk factors, respectively, (P<0.005). In light of our study, comorbidities are critical prognostic determinants for diminished PFS and OS. Moreover, comorbidity scores are important treatment decision tools and will be valuable to implement into future analyses and clinical trials in MM.
机译:尽管合并症对多发性骨髓瘤(MM)患者的影响尚不明确,但已证明可影响无进展生存期(PFS)和总生存期(OS)。我们(1)评估了各种合并症,(2)比较了已建立的合并症指数(CIs; Charlson合并症指数(CCI),造血细胞移植特异性合并症指数(HCT-CI)),Kaplan Feinstein(KF)和Satariano指数(SI) (3)在127例MM患者中发展了MM-CI(弗莱堡合并症)。单因素分析确定中度或重度肺部疾病(危险比(HR):3.5,P <0.0001),肾功能不全(通过估计的肾小球滤过率(eGFR); HR:3.4,P = 0.0018),卡诺夫斯基机能状态(KPS, HR:2.7,P = 0.0004)和年龄(HR:2,P = 0.0114)是降低OS的最重要变量。通过多变量分析,eGFR⩽30ml / min / 1.73m 2 ,肺功能受损和KPS⩽70%对OS降低具有显着意义,HR分别为2.9、2.8和2.2。这些风险因素在FCI中的组合确定OS发生率中位数显着不同,分别为118、53和25个月,分别为0、1、2或3个风险因素(P <0.005)。根据我们的研究,合并症是PFS和OS降低的重要预后决定因素。此外,合并症评分是重要的治疗决策工具,对于在MM的未来分析和临床试验中实施具有重要价值。

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