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Blood Cancer J ; 8(3): 31, 2018 03 09.
Article En | MEDLINE | ID: mdl-29523783

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.


Bortezomib/administration & dosage , Leukemia, Plasma Cell/mortality , Leukemia, Plasma Cell/therapy , Stem Cell Transplantation , Adult , Aged , Aged, 80 and over , Autografts , Disease-Free Survival , Female , Greece/epidemiology , Humans , Leukemia, Plasma Cell/pathology , Male , Middle Aged , Retrospective Studies , Survival Rate
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