Alaterre Elina, Raimbault Sebastien, Goldschmidt Hartmut, Bouhya Salahedine, Requirand Guilhem, Robert Nicolas, Boireau Stéphanie, Seckinger Anja, Hose Dirk, Klein Bernard, Moreaux Jérôme
HORIBA Medical, Parc Euromédecine, Montpellier, France.
Institute of Human Genetics, CNRS-UM UMR9002, Montpellier, France.
Oncotarget. 2017 Oct 30;8(58):98931-98944. doi: 10.18632/oncotarget.22131. eCollection 2017 Nov 17.
Multiple myeloma (MM) is a B cell neoplasia characterized by clonal plasma cell (PC) proliferation. Minimal residual disease monitoring by multi-parameter flow cytometry is a powerful tool for predicting treatment efficacy and MM outcome. In this study, we compared CD antigens expression between normal and malignant plasma cells to identify new potential markers to discriminate normal from malignant plasma cells, new potential therapeutic targets for monoclonal-based treatments and new prognostic factors. Nine genes were significantly overexpressed and 16 were significantly downregulated in MMC compared with BMPC (ratio ≥2; FDR , , and ) was associated with a prognostic value in two independent cohorts of patients with MM (HM cohort and TT2 cohort, n=345). The expression level of these four genes was then used to develop a CD gene risk score that classified patients in two groups with different survival ( = 2.06E-6) in the HM training cohort. The prognostic value of the CD gene risk score was validated in two independent cohorts of patients with MM (TT2 cohort and HOVON65/GMMGHD4 cohort, n=282 patients). The CD gene risk score remained a prognostic factor that separated patients in two groups with significantly different overall survival also when using publicly available data from a cohort of relapsing patients treated with bortezomib (n=188). In conclusion, the CD gene risk score allows identifying high risk patients with MM based on , , and expression and could represent a powerful tool for simple outcome prediction in MM.
多发性骨髓瘤(MM)是一种以克隆性浆细胞(PC)增殖为特征的B细胞肿瘤。通过多参数流式细胞术监测微小残留病是预测治疗效果和MM预后的有力工具。在本研究中,我们比较了正常浆细胞和恶性浆细胞之间的CD抗原表达,以鉴定区分正常与恶性浆细胞的新潜在标志物、基于单克隆治疗的新潜在治疗靶点以及新的预后因素。与骨髓单个核细胞(BMPC)相比,MMC中有9个基因显著过表达,16个基因显著下调(比值≥2;FDR<0.05)。在两个独立的MM患者队列(HM队列和TT2队列,n = 345)中,该比值与预后价值相关。然后,利用这四个基因的表达水平建立了一个CD基因风险评分,该评分在HM训练队列中将患者分为两组,两组患者的生存率不同(P = 2.06E - 6)。CD基因风险评分的预后价值在两个独立的MM患者队列(TT2队列和HOVON65/GMMG HD4队列,n = 282例患者)中得到验证。当使用来自接受硼替佐米治疗的复发患者队列的公开可用数据(n = 188)时,CD基因风险评分仍然是一个预后因素,可将患者分为两组,两组患者的总生存期有显著差异。总之,CD基因风险评分能够基于[具体基因名称1]、[具体基因名称2]、[具体基因名称3]和[具体基因名称4]的表达来识别MM高危患者,并且可能成为MM中简单预后预测的有力工具。