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通过量化循环克隆性浆细胞增强新诊断多发性骨髓瘤的 R-ISS 分类。

Enhancing the R-ISS classification of newly diagnosed multiple myeloma by quantifying circulating clonal plasma cells.

机构信息

Division of Hematology, Mayo Clinic, Rochester, Minnesota.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

出版信息

Am J Hematol. 2020 Mar;95(3):310-315. doi: 10.1002/ajh.25709. Epub 2020 Jan 8.

DOI:10.1002/ajh.25709
PMID:31867775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7724649/
Abstract

Our prior studies identified the prognostic significance of quantifying cPCs by multiparametric flow cytometry (MFC) in newly diagnosed multiple myeloma (NDMM) patients. We evaluated if a similar quantification of cPCs could add prognostic value to the current R-ISS classification of 556 consecutive NDMM patients seen at the Mayo Clinic, Rochester from 2009 to 2017. Those patients that had ≥5 cPCs/μL and either R-ISS stage I or stage II disease were re-classified as R-ISS IIB stage for the purposes of this study. The median time to next therapy (TTNT) and overall survival (OS) for patients with ≥5 cPCs/μL at diagnosis was as follows: R-ISS I (N = 110) - 40 months and not reached; R-ISS II (N = 69) - 30 and 72 months; R-ISS IIB (N = 96) - 21 and 45 months and R-ISS III (N = 281) - 20 and 47 months respectively. Finally, ≥ 5 cPCs/μL retained its adverse prognostic significance in a multivariable model for TTNT and OS. Hence, quantifying cPCs by MFC can potentially enhance the R-ISS classification of a subset of NDMM patients with stage I and II disease by identifying those patients with a worse than expected survival outcome.

摘要

我们之前的研究通过多参数流式细胞术(MFC)定量检测初诊多发性骨髓瘤(NDMM)患者中的循环肿瘤细胞(cPCs),确定了其预后意义。我们评估了在 2009 年至 2017 年期间,Mayo 诊所罗切斯特分部的 556 例连续 NDMM 患者中,是否可以通过类似的 cPCs 定量方法为当前的 R-ISS 分类增加预后价值。为了进行这项研究,将 R-ISS 分期 I 或 II 期且 cPCs≥5/μL 的患者重新分类为 R-ISS IIB 期。诊断时 cPCs≥5/μL 的患者,其下一次治疗的中位时间(TTNT)和总生存期(OS)如下:R-ISS I(N=110)-40 个月和未达到;R-ISS II(N=69)-30 个月和 72 个月;R-ISS IIB(N=96)-21 个月和 45 个月;R-ISS III(N=281)-20 个月和 47 个月。最后,在 TTNT 和 OS 的多变量模型中,cPCs≥5/μL 保留了其不良预后意义。因此,通过 MFC 定量检测 cPCs,可通过识别那些预期生存结果较差的患者,潜在地增强 R-ISS 分类中 I 期和 II 期疾病的部分患者的预后判断。

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