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

Leuk Res. 2018 May:68:9-14. doi: 10.1016/j.leukres.2018.02.010. Epub 2018 Mar 2.

Abstract

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.

Keywords: Immunomodulatory drugs (IMiDs); Multiple myeloma; Novel agents; Primary plasma cell leukemia.

Publication types

  • Multicenter Study

MeSH terms

  • Adjuvants, Immunologic / therapeutic use*
  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents / therapeutic use*
  • Combined Modality Therapy
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Israel
  • Leukemia, Plasma Cell / drug therapy*
  • Leukemia, Plasma Cell / therapy
  • Male
  • Middle Aged
  • Multiple Myeloma / drug therapy
  • Multivariate Analysis
  • Prognosis
  • Proteasome Inhibitors / therapeutic use*
  • Retrospective Studies
  • Survival Analysis
  • Treatment Outcome

Substances

  • Adjuvants, Immunologic
  • Antineoplastic Agents
  • Proteasome Inhibitors