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[Clinical characteristics and prognosis of 46 patients with macrofocal multiple myeloma].

医学 多发性骨髓瘤 内科学 胃肠病学 阶段(地层学) 总体生存率 人口 单中心 外科 生物 环境卫生 古生物学
作者
Wenqiang Yan,Huishou Fan,Jingyu Xu,J H Liu,C X Du,Shuhui Deng,W W Sui,Ya Xu,Lihua Qiu,Gary An
出处
期刊:PubMed 卷期号:61 (7): 801-805
标识
DOI:10.3760/cma.j.cn112138-20210908-00626
摘要

The clinical characteristics, laboratory results, response to treatment, and prognosis of 46 macrofocal multiple myeloma(MFMM) patients at our center from January 2013 to December 2019 were analyzed retrospectively. The other 92 patients were selected as matched-controls based on diagnostic period and treatment. Among the 1 137 MM patients, 46 patients met the definition criteria of MFMM (4.0%), with median age 56 years, which was not statistically different from whole MM population (P=0.066). According to the international staging system (ISS) and Revised ISS, the proportion of patients with advanced stage in MFMM group was less common than that of controls (P<0.05). More plasmacytomas in MFMM patients were presented (43.5% vs. 18.5%, P<0.05). Regarding cytogenetic abnormalities, there were minor patients manifesting high-risk features in MFMM group (15.8% vs. 32.2%, P=0.058). Translocation(11;14) could be detected in 32.4% MFMM patients and 9.4% typical myeloma patients (P<0.05). The treatment regimens were comparable. As to the best response of treatment, the complete response (CR) rate in MFMM group was significantly higher than that of controls (78.3% vs. 60.9%, P<0.05). The median follow-up time was 37.9 months. The median progression-free survival in MFMM and control groups were 77.5 vs. 39.8 months, respectively (P<0.05). The overall survival (OS) of MFMM patients was significantly longer (not reached vs. 68.2 months, P<0.05).
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