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首页> 外文期刊>Blood cancer journal. >Gain of Chromosome 1q is associated with early progression in multiple myeloma patients treated with lenalidomide, bortezomib, and dexamethasone
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Gain of Chromosome 1q is associated with early progression in multiple myeloma patients treated with lenalidomide, bortezomib, and dexamethasone

机译:染色体1Q的增益与用Lenalidomide,Bortezomib和地塞米松治疗的多发性骨髓瘤患者的早期进展相关

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Gain of chromosome 1q (+1q) is commonly identified in multiple myeloma and has been associated with inferior outcomes. However, the prognostic implication of +1q has not been evaluated in the setting of standard triplet regimens. We retrospectively analyzed 201 consecutive patients with newly diagnosed myeloma who received induction with lenalidomide, bortezomib, and dexamethasone (RVD) and were tested for +1q at diagnosis by fluorescent in-situ hybridization. Patients with +1q (n?=?94), compared to those without +1q (n?=?107), had shorter median progression-free survival (PFS) (41.9 months vs 65.1 months, p?=?0.002, HR?=?1.90) and overall survival (median not reached (NR) for either arm, p?=?0.003, HR 2.69). In subgroup analyses, patients with co-occurring +1q and t(4;14), t(14;16) or del(17p) or with 4 or more copies of 1q had significantly worse PFS (25.1 months and 34.6 months, p??0.001 and p?=?0.0063, respectively), whereas patients with three copies and no other high-risk cytogenetic abnormalities had no significant difference in PFS. These data suggest that when treated with RVD induction, patients with +1q should be considered at very high risk for early progression in multiple myeloma when ≥4 copies are detected or in the context of other high-risk cytogenetic abnormalities.
机译:染色体1Q(+ 1Q)的增益通常在多发性骨髓瘤中鉴定,并且已经与劣质结果有关。然而,在标准三重态方案的设置中尚未评估+ 1Q的预后意义。我们回顾性地分析了201的新诊断的新诊断骨髓瘤,他们接受了Lenalidomide,Bortezomib和地塞米松(RVD)的诱导,并通过荧光原位杂交在诊断中进行+ 1Q进行测试。与没有+ 1q的人(n?= 107)相比,患者+ 1q(n?=?94),较短的中位进展生存(PFS)(41.9个月与65.1个月,p?= 0.002,人力资源?=?1.90)和整体生存(中位数未到达(NR)用于任一臂,p?= 0.003,HR 2.69)。在亚组分析中,共发生+ 1Q和T(4; 14),T(14; 16)或Del(17P)或1Q或以上拷贝的患者显着差,PFS(25.1个月和34.6个月,P ?<?0.001和p?= 0.0063分别),而三份患者和没有其他高危细胞发生异常的患者在PFS中没有显着差异。这些数据表明,当用RVD诱导治疗时,+ 1Q的患者应在许多骨髓瘤的早期进展的情况下考虑,当检测到≥4份或在其他高危细胞发生异常的背景下进行多种骨髓瘤。

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