Ye Xueshi, Li Wanli, Zhang Lifei, Yu Junyao
Department of Hematology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Department of Orthopedics, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Front Oncol. 2022 Feb 18;12:852573. doi: 10.3389/fonc.2022.852573. eCollection 2022.
Circulating cell-free DNA (cfDNA) detection, a non-invasive method, appears promising for genetic analyses as well as quantitative assessment of tumor burden in patients with cancer. Although the analysis of cfDNA for clinical prognosis and monitoring disease burden in multiple myeloma (MM) has been recently studied, the results are unclear. In this meta-analysis, we explored the clinical significance of circulating cfDNA detection in patients with MM. We searched PubMed, Embase, and the Cochrane Library for eligible studies published up until July 25, 2021. Diagnostic accuracy variables were calculated and analyzed using Meta-Disc, and prognostic data were analyzed using Review Manager. Overall, seven studies comprising 235 myeloma patients met our inclusion criteria. The overall sensitivity and specificity of cfDNA to detect minimal residual disease (MRD) were 0.58 and 0.91, respectively. Moreover, higher levels of cfDNA were associated with worse progression-free survival as well as with poor overall survival. Our meta-analysis revealed that ctDNA detection has an obvious advantage in terms of MRD detection specificity, but it showed no superiority over bone marrow assessment in terms of MRD detection sensitivity, and higher levels of cfDNA were indicative of worse prognosis in patients with MM. cfDNA detection is a non-invasive method and thus shows promise as a good alternative to BM biopsies for monitoring clonal evolution and tumor burden so as to guide the treatment of patients with MM.
循环游离DNA(cfDNA)检测是一种非侵入性方法,在癌症患者的基因分析以及肿瘤负荷定量评估方面似乎很有前景。尽管最近已经对cfDNA用于多发性骨髓瘤(MM)临床预后和疾病负担监测的分析进行了研究,但结果尚不清楚。在这项荟萃分析中,我们探讨了循环cfDNA检测在MM患者中的临床意义。我们在PubMed、Embase和Cochrane图书馆中检索了截至2021年7月25日发表的符合条件的研究。使用Meta-Disc计算和分析诊断准确性变量,使用Review Manager分析预后数据。总体而言,七项研究共纳入235例骨髓瘤患者,符合我们的纳入标准。cfDNA检测微小残留病(MRD)的总体敏感性和特异性分别为0.58和0.91。此外,cfDNA水平较高与无进展生存期较差以及总生存期较差相关。我们的荟萃分析表明,ctDNA检测在MRD检测特异性方面具有明显优势,但在MRD检测敏感性方面并不优于骨髓评估,并且较高水平的cfDNA表明MM患者预后较差。cfDNA检测是一种非侵入性方法,因此有望成为骨髓活检的良好替代方法,用于监测克隆进化和肿瘤负荷,从而指导MM患者的治疗。