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确定意义未明的单克隆丙种球蛋白病的临床意义:一项监测、流行病学和最终结果(SEER)-医疗保险人群分析

Determining the clinical significance of monoclonal gammopathy of undetermined significance: a SEER-Medicare population analysis.

作者信息

Go Ronald S, Gundrum Jacob D, Neuner Joan M

机构信息

Center for Cancer and Blood Disorders, Gundersen Health System, La Crosse, WI.

Department of Medical Research, Gundersen Medical Foundation, La Crosse, WI.

出版信息

Clin Lymphoma Myeloma Leuk. 2015 Mar;15(3):177-186.e4. doi: 10.1016/j.clml.2014.09.004. Epub 2014 Sep 28.

Abstract

BACKGROUND

Clinical guidelines have recommended annual follow-up examinations of most patients with monoclonal gammopathy of undetermined significance (MGUS); however, evidence supporting this practice is lacking. We performed a population-based study to examine the patterns of disease presentation and outcomes of patients with multiple myeloma, Waldenström macroglobulinemia, and lymphoplasmacytic lymphoma (monoclonal gammopathy-associated malignancies) comparing those with or without a previous MGUS follow-up examination.

MATERIALS AND METHODS

Patients with monoclonal gammopathy-associated malignancy from 1994 through 2007 were identified using the Surveillance, Epidemiology, and End Results-Medicare linked database and divided into 2 cohorts: those with follow-up (MGUS follow-up examination preceding the diagnosis) and those with no follow-up (no such follow-up examination). We compared the outcomes, including the rates of major complications at cancer diagnosis (acute kidney injury, cord compression, dialysis use, fracture, and hypercalcemia) and survival using propensity score adjustment and Cox proportional hazard models. All statistical tests were 2-sided.

RESULTS

Of the 17,457 study patients, 6% had undergone MGUS follow-up. After multivariable modeling, the follow-up group had significantly fewer major complications at diagnosis (odds ratio 0.68; 95% confidence interval [CI], 0.57-0.80) and better disease-specific (median, 38 vs. 29 months, P < .001; hazard ratio [HR] 0.85; 95% CI, 0.76-0.94) and overall (median, 23 vs. 19 months, P < .001; HR 0.87; 95% CI, 0.80-0.95) survival.

CONCLUSION

Patients with MGUS follow-up preceding the diagnosis of a monoclonal gammopathy-associated malignancy can experience fewer major complications and have longer survival than those without such follow-up examinations. Future studies replicating our findings in the non-Medicare population and determining the optimal schedule and cost-effectiveness of MGUS follow-up are warranted.

摘要

背景

临床指南建议对大多数意义未明的单克隆丙种球蛋白病(MGUS)患者进行年度随访检查;然而,缺乏支持这一做法的证据。我们开展了一项基于人群的研究,以检查多发性骨髓瘤、华氏巨球蛋白血症和淋巴浆细胞淋巴瘤(单克隆丙种球蛋白病相关恶性肿瘤)患者的疾病表现模式和结局,并比较有或没有进行过MGUS随访检查的患者。

材料与方法

利用监测、流行病学和最终结果-医疗保险链接数据库识别1994年至2007年期间患有单克隆丙种球蛋白病相关恶性肿瘤的患者,并将其分为两组:有随访组(诊断前进行过MGUS随访检查)和无随访组(未进行过此类随访检查)。我们使用倾向评分调整和Cox比例风险模型比较了结局,包括癌症诊断时的主要并发症发生率(急性肾损伤、脊髓压迫、透析使用、骨折和高钙血症)和生存率。所有统计检验均为双侧检验。

结果

在17457例研究患者中,6%接受过MGUS随访。经过多变量建模后,随访组在诊断时的主要并发症显著较少(比值比0.68;95%置信区间[CI],0.57 - 0.80),疾病特异性生存率更高(中位数,38个月对29个月,P <.001;风险比[HR] 0.85;95% CI,0.76 - 0.94),总体生存率也更高(中位数,23个月对19个月,P <.001;HR 0.87;95% CI,0.80 - 0.95)。

结论

与未进行此类随访检查的患者相比,在诊断单克隆丙种球蛋白病相关恶性肿瘤之前进行过MGUS随访的患者主要并发症较少,生存期更长。有必要开展未来研究,在非医疗保险人群中复制我们的研究结果,并确定MGUS随访的最佳时间表和成本效益。

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