Ludwig Heinz, Kainz Sarah, Schreder Martin, Zojer Niklas, Hinke Axel
Wilhelminen Cancer Research Institute, c/o First Department of Medicine, Clinic Ottakring, Vienna, Austria.
First Department of Medicine, Center for Oncology, Hematology, and Palliative Care, Clinic Ottakring, Vienna, Austria.
EClinicalMedicine. 2023 Mar 20;58:101910. doi: 10.1016/j.eclinm.2023.101910. eCollection 2023 Apr.
Biomarker-defined patients with smoldering multiple myeloma (SMM) were included in the diagnostic category of multiple myeloma (MM) by the International Myeloma Working Group (IMWG) in 2014. This includes ≥60% bone marrow plasma cells (BMPCs), free light chain ratio (FLCratio) ≥100, and >1 MRI-defined ≥5 mm focal lesion, also called SLiM CRAB MM. We examined whether the risk of progression of SLiM CRAB MM patients to CRAB positive MM described in recent studies differs from that reported in earlier studies published before the introduction of the new diagnostic criteria.
We conducted a systematic review with meta-analysis, and included studies on Embase and PubMed (01/01/2010-01/11/2022), selecting studies with digitizable progression curves. Inconsistent studies were excluded. We created forest plots using random effects models from digitized and published data and Kaplan-Meier curves. Main outcomes were median time to progression (TTP), 2-year progression risk, and odds ratios (ORs) comparing 2-year progression risks.
Our meta-analysis including 11 studies with 3482 patients found an approximately 3-fold longer TTP and 50% lower 2-year progression risk of SliM CRAB MM patients in recent (published after 2014) compared with earlier studies. Median TTP in patients with ≥60% BMPCs was 30.31 months [18.71-62.93] in recent compared with 9.20 months [6.02-15.56] in earlier studies; the 2-year progression risk was 45.45% [20.12-62.75] compared with 86.21% [65.74-94.45] in the respective time periods. In patients with a FLCratio ≥ 100, the median TTP was 48.06 months [40.51-64.91] vs. 15.33 months [9.38-19.10], and the 2-year progression risk was 31.61% [25.30-37.39] vs. 73.00% [62.39-80.62] in recent and earlier studies, respectively. Tests for heterogeneity showed that the two time periods differed significantly in their ORs when comparing patients who met the high-and low risk criteria. No appropriate recent studies on focal lesions have been published.
Recent studies show significantly improved prognosis of biomarker-defined MM with ≥60% BMPCs and FLCratio ≥ 100. This warrants careful evaluation for signs of progression before treatment initiation.
Funding was provided by the Austrian Forum against Cancer.
2014年,国际骨髓瘤工作组(IMWG)将生物标志物定义的冒烟型多发性骨髓瘤(SMM)患者纳入多发性骨髓瘤(MM)的诊断类别。这包括≥60%的骨髓浆细胞(BMPC)、游离轻链比值(FLCratio)≥100,以及>1个磁共振成像(MRI)定义的≥5mm局灶性病变,也称为SLiM CRAB MM。我们研究了近期研究中描述的SLiM CRAB MM患者进展为CRAB阳性MM的风险是否与新诊断标准引入之前发表的早期研究报告的风险不同。
我们进行了一项系统评价和荟萃分析,纳入了Embase和PubMed上的研究(2010年1月1日至2022年11月1日),选择具有可数字化进展曲线的研究。排除不一致的研究。我们使用来自数字化和已发表数据的随机效应模型创建森林图和Kaplan-Meier曲线。主要结局为中位进展时间(TTP)、2年进展风险,以及比较2年进展风险的比值比(OR)。
我们的荟萃分析纳入了11项研究,共3482例患者,发现与早期研究相比,近期(2014年后发表)SLiM CRAB MM患者的TTP长约3倍,2年进展风险低50%。≥60%BMPC患者的中位TTP在近期研究中为30.31个月[18.71 - 62.93],而在早期研究中为9.20个月[6.02 - 15.56];相应时间段内的2年进展风险分别为45.45%[20.12 - 62.75]和86.21%[65.74 - 94.45]。对于FLCratio≥100的患者,近期和早期研究中的中位TTP分别为48.06个月[40.51 - 64.91]和15.33个月[9.38 - 19.10],2年进展风险分别为31.61%[25.30 - 37.39]和73.00%[62.39 - 80.62]。异质性检验表明,在比较符合高风险和低风险标准的患者时,两个时间段的OR存在显著差异。近期没有关于局灶性病变的合适研究发表。
近期研究表明,生物标志物定义的≥60%BMPC且FLCratio≥100的MM患者预后显著改善。这需要在开始治疗前仔细评估进展迹象。
资金由奥地利抗癌论坛提供。