| Literature DB >> 29501828 |
Chezi Ganzel1, Ory Rouvio2, Irit Avivi3, Hila Magen4, Osnat Jarchowsky5, Katrin Herzog6, Yossi Cohen7, Tamar Tadmor8, Netanel A Horwitz9, Merav Leiba10, Arnon Nagler10, Yael Cohen3, Shlomo Bulvik6, Aaron Polliack11, Jacob M Rowe12, Moshe E Gatt11.
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.Entities:
Keywords: Immunomodulatory drugs (IMiDs); Multiple myeloma; Novel agents; Primary plasma cell leukemia
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Year: 2018 PMID: 29501828 DOI: 10.1016/j.leukres.2018.02.010
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156