Munshi Nikhil C, Avet-Loiseau Herve, Rawstron Andy C, Owen Roger G, Child J Anthony, Thakurta Anjan, Sherrington Paul, Samur Mehmet Kemal, Georgieva Anna, Anderson Kenneth C, Gregory Walter M
Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Unit for Genomics in Myeloma, Institut Universitaire du Cancer, Toulouse, France.
JAMA Oncol. 2017 Jan 1;3(1):28-35. doi: 10.1001/jamaoncol.2016.3160.
Numerous studies have evaluated the prognostic value of minimal residual disease (MRD) in patients with multiple myeloma (MM). Most studies were small and varied in terms of patient population, treatment, and MRD assessment methods.
To evaluate the utility of MRD detection in patients with newly diagnosed MM.
A Medline search was conducted for articles published in English between January 1990 and January 2016.
Eligible studies reported MRD status and progression-free survival (PFS) or overall survival (OS) in 20 or more patients following treatment. Among 405 articles identified, 21 met the initial eligibility criteria and were included in the analysis.
Information on patient characteristics, treatment, MRD assessment, and outcomes were extracted using a standard form.
The impact of MRD status on PFS and OS was assessed by pooling data from relevant trials. Data were adjusted to allow for different proportions of patients with MRD in different studies, and analyzed using the Peto method. Forest plots were created based on Cox model analysis. Other prespecified research questions were addressed qualitatively.
Fourteen studies (n = 1273) provided data on the impact of MRD on PFS, and 12 studies (n = 1100) on OS. Results were reported specifically in patients who had achieved conventional complete response (CR) in 5 studies for PFS (n = 574) and 6 studies for OS (n = 616). An MRD-negative status was associated with significantly better PFS overall (hazard ratio [HR], 0.41; 95% CI, 0.36-0.48; P < .001) and in studies specifically looking at CR patients (HR, 0.44; 95% CI, 0.34-0.56; P < .001). Overall survival was also favorable in MRD-negative patients overall (HR, 0.57; 95% CI, 0.46-0.71; P < .001) and in CR patients (HR, 0.47; 95% CI, 0.33-0.67; P < .001). Tests of heterogeneity found no significant differences among the studies for PFS and OS.
Minimal residual disease-negative status after treatment for newly diagnosed MM is associated with long-term survival. These findings provide quantitative evidence to support the integration of MRD assessment as an end point in clinical trials of MM.
众多研究评估了微小残留病(MRD)在多发性骨髓瘤(MM)患者中的预后价值。大多数研究规模较小,在患者群体、治疗方法和MRD评估方法方面存在差异。
评估MRD检测在新诊断MM患者中的效用。
对1990年1月至2016年1月期间发表的英文文章进行了Medline检索。
符合条件的研究报告了20例或更多患者治疗后的MRD状态和无进展生存期(PFS)或总生存期(OS)。在识别出的405篇文章中,21篇符合初始纳入标准并纳入分析。
使用标准表格提取有关患者特征、治疗、MRD评估和结果的信息。
通过汇总相关试验的数据,评估MRD状态对PFS和OS的影响。对数据进行调整,以考虑不同研究中MRD患者的不同比例,并使用Peto方法进行分析。基于Cox模型分析创建森林图。对其他预先设定的研究问题进行定性分析。
14项研究(n = 1273)提供了关于MRD对PFS影响的数据,12项研究(n = 1100)提供了关于OS影响的数据。在5项关于PFS的研究(n = 574)和6项关于OS的研究(n = 616)中,具体报告了达到传统完全缓解(CR)的患者的结果。总体而言,MRD阴性状态与显著更好的PFS相关(风险比[HR],0.41;95%置信区间[CI],0.36 - 0.48;P <.001),在专门针对CR患者的研究中也是如此(HR,0.44;95% CI,0.34 - 0.56;P <.001)。总体而言,MRD阴性患者的总生存期也较好(HR,0.57;95% CI,0.46 - 0.71;P <.001),在CR患者中也是如此(HR,0.47;95% CI,0.33 - 0.67;P <.001)。异质性检验发现,各研究在PFS和OS方面无显著差异。
新诊断MM治疗后微小残留病阴性状态与长期生存相关。这些发现提供了定量证据,支持将MRD评估作为MM临床试验的一个终点。