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Real-world data on prognosis and outcome of primary plasma cell leukemia in the era of novel agents: a multicenter national study by the Greek Myeloma Study Group

机译:新药时代下原发性浆细胞白血病的预后和预后的真实数据:希腊骨髓瘤研究小组进行的多中心国家研究

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We have studied the efficacy and the prognostic impact of novel agents in 50 primary plasma cell leukemia (pPCL) patients registered in our database. Eighty percent of patients were treated upfront with novel agent-based combinations; 40% underwent autologous stem cell transplantation (ASCT). Objective response rate was 76; 38% achieved at least very good partial response (≥vgPR) and this correlated significantly with bortezomib-based therapy plus ASCT. At the time of evaluation, 40 patients had died. Early mortality rate (≤1 month) was 6%. Median progression-free survival (PFS) and overall survival (OS) were 12 months and 18 months respectively, both significantly longer in patients treated with bortezomib-based therapy?+?ASCT vs. others (PFS: 18 vs. 9 months; p?=?0.004, OS: 48 vs. 14 months; p?=?0.007). Bortezomib-based therapy?+?ASCT predicted for OS in univariate analysis. In multivariate analysis, achievement of ≥vgPR and LDH?≥?300?U/L were significant predictors for OS. These real-world data, based on one of the largest reported national multicenter series of pPCL patients treated mostly with novel agents support that, among the currently approved induction therapies, bortezomib-based regimens are highly effective and reduce the rate of early mortality whereas in combination with ASCT consolidation they prolong OS.
机译:我们已经研究了新药对我们数据库中注册的50名原发性浆细胞白血病(pPCL)患者的疗效和预后影响。百分之八十的患者接受了新的基于药物的联合治疗; 40%接受了自体干细胞移植(ASCT)。客观回应率为76; 38%的患者至少达到了很好的局部反应(≥vgPR),这与基于硼替佐米的治疗加ASCT显着相关。在评估时,有40名患者死亡。早期死亡率(≤1个月)为6%。中位数无进展生存期(PFS)和总生存期(OS)分别为12个月和18个月,以硼替佐米为基础的治疗++ ASCT与其他患者相比均明显更长(PFS:18个月对9个月; p ?=?0.004,作业系统:48个月与14个月; p?=?0.007)。在单变量分析中,基于硼替佐米的治疗+?ASCT可以预测OS。在多变量分析中,≥vgPR和LDH≥300?U / L是OS的重要预测指标。这些实际数据基于报告的最大的全国性多中心pPCL患者多中心系列研究之一,这些患者大多接受新型药物治疗,这表明在目前批准的诱导疗法中,以硼替佐米为基础的治疗方案非常有效,并且可以降低早期死亡率。与ASCT整合相结合,可以延长操作系统的运行时间。

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