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Primary plasma cell leukemia in the era of novel agents for myeloma - a multicenter retrospective analysis of outcome

机译:骨髓瘤新型剂时代的主要血浆细胞白血病 - 结果的多中心回顾性分析

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摘要

Primary plasma cell leukemia (PPCL) is a rare form of multiple myeloma with a dismal prognosis. This retrospective multi-center study examines the national experience of PPCL in the era of novel agents. During 2002-2016, thirty-nine patients with PPCL were identified in 11 Israeli centers. One-fifth of them died in the first 2 months after diagnosis. The overall survival (OS) of those who survived the first 3 months was 22.5 months. About 70% of patients received at least one type of immunomodulatory drug (IMiD) and similarly proteasome inhibitor (PI) during treatment. There was a survival advantage for those who received IMiD but not for those who received PI or other type of standard dose chemotherapy. In multivariate analysis, low performance status and increased uric acid were also associated with shorter OS. In conclusion, this study demonstrates favorable impact of treatment with IMiDs and hematopoietic cell transplantation on the survival of PPCL patients.
机译:初级血浆细胞白血病(PPCL)是一种罕见的多种骨髓瘤,预后令人沮丧。 这个回顾性的多中心研究探讨了PPCL在新型代理商时代的国家经验。 在2002 - 2016年期间,11名以色列中心鉴定了39例PPCL患者。 其中五分之一的五分之一在诊断后的前2个月死亡。 在前3个月幸存下来的人的整体生存(OS)是22.5个月。 在治疗期间,大约70%的患者接受了至少一种免疫调节药物(IMID)和类似的蛋白酶体抑制剂(PI)。 对于那些接受IMID的人来说,还有生存优势,但不是那些接受PI或其他类型的标准剂量化疗的人。 在多变量分析中,低性能状态和尿酸增加也与较短的OS相关。 总之,本研究表明,在PPCL患者的存活下,对胰蛋白酶和造血细胞移植治疗的有利影响。

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