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Clinical features and treatment outcome in newly diagnosed Chinese patients with multiple myeloma: results of a multicenter analysis

机译:新诊断的中国多发性骨髓瘤患者的临床特征和治疗结果:多中心分析结果

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摘要

The aim of this study was to understand the clinical features and treatment outcome of Chinese patients with multiple myeloma (MM). This retrospective study enrolled 940 newly diagnosed inpatients (median age, 59 years; immunoglobulin (Ig)D isotype, 6.5%) with complete follow-up data at three centers. In all, 85.8% of patients were of Durie-Salmon stage III and 48.3% were of International Staging System (ISS) stage III at diagnosis. Also, 9.6% of patients had extramedullary plasmacytoma. Compared with IgG, IgD-type patients were diagnosed at a younger age, and more patients were of ISS stage III, with hypercalcemia, elevated levels of lactate dehydrogenase, hyperuricemia, renal dysfunction and 1q21 amplification (P=0.03). The overall survival (OS) benefit was more prominent in IgG than in IgD when patients received bortezomib; however, they showed no significant difference when they received older therapies such as melphalan combined with prednisone or vincristine combined with adriamycin and dexamethasone. Fluorescence in situ hybridization (FISH) results showed that 17.6% had 17p13 deletion. Conventional cytogenetics revealed that 13.3% were hypodiploid and those cases had the worst survival, but hyperdiploid cases (9.3%) did not show any survival benefit compared with those with a normal karyotype (77.4%). Median OS and progression-free survival for all patients were 54 and 26 months, respectively. Significant factors for survival by multivariate analysis were gender, ISS stage, number of FISH abnormalities and extramedullary disease. MM in mainland China presents with different features, with patients being of younger age and having higher risk and more survival benefit in IgG patients receiving bortezomib.
机译:这项研究的目的是了解中国多发性骨髓瘤(MM)患者的临床特征和治疗结果。这项回顾性研究纳入了三个中心的940例新诊断的住院患者(中位年龄59岁;免疫球蛋白(Ig)D同型,6.5%)。在诊断时,共有85.8%的患者为Durie-Salmon III期,而48.3%的患者为国际分期系统(ISS)III期。另外,9.6%的患者患有髓外浆细胞瘤。与IgG相比,IgD型患者被诊断为年龄更小,并且进入ISS III期的患者有高钙血症,乳酸脱氢酶水平升高,高尿酸血症,肾功能不全和1q21扩增(P = 0.03)。当患者接受硼替佐米治疗时,IgG的总体生存(OS)获益比IgD的更为显着。然而,当他们接受较旧的疗法,如美法仑联合泼尼松或长春新碱与阿霉素和地塞米松联合时,他们的表现没有显着差异。荧光原位杂交(FISH)结果表明17.6%的人有17p13缺失。传统的细胞遗传学研究显示,次二倍体为13.3%,且存活率最差,但与正常核型相比,超二倍体(9.3%)没有显示任何生存获益。所有患者的中位OS和无进展生存期分别为54个月和26个月。通过多因素分析得出的生存的重要因素是性别,ISS分期,FISH异常数量和髓外疾病。中国大陆的MM具有不同的特征,年龄较小的患者在接受硼替佐米的IgG患者中具有更高的风险和更大的生存获益。

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