Literature DB >> 29315478

Prognostic indicators in primary plasma cell leukaemia: a multicentre retrospective study of 117 patients.

Artur Jurczyszyn1, Jakub Radocha2, Julio Davila3, Mark A Fiala4, Alessandro Gozzetti5, Norbert Grząśko6,7, Paweł Robak8, Iwona Hus9, Anna Waszczuk-Gajda10, Renata Guzicka-Kazimierczak11, Erden Atilla12, Giuseppe Mele13, Waldemar Sawicki14, David S Jayabalan15, Grzegorz Charliński16, Agoston G Szabo17, Roman Hajek18, Michel Delforge19, Agnieszka Kopacz20, Dorotea Fantl21, Anders Waage22, Irit Avivi23, Marek Rodzaj24, Xavier Leleu25, Valentine Richez26, Wanda Knopińska-Posłuszny26, Anna Masternak27, Andrew J Yee28, Agnieszka Barchnicka29, Agnieszka Druzd-Sitek30, Thomas Guerrero-Garcia31, Jieqi Liu32, David H Vesole33, Jorge J Castillo34.   

Abstract

We report a multicentre retrospective study that analysed clinical characteristics and outcomes in 117 patients with primary plasma cell leukaemia (pPCL) treated at the participating institutions between January 2006 and December 2016. The median age at the time of pPCL diagnosis was 61 years. Ninety-eight patients were treated with novel agents, with an overall response rate of 78%. Fifty-five patients (64%) patients underwent upfront autologous stem cell transplantation (ASCT). The median follow-up time was 50 months (95% confidence interval [CI] 33; 76), with a median overall survival (OS) for the entire group of 23 months (95% CI 15; 34). The median OS time in patients who underwent upfront ASCT was 35 months (95% CI 24·3; 46) as compared to 13 months (95% CI 6·3; 35·8) in patients who did not receive ASCT (P = 0·001). Multivariate analyses identified age ≥60 years, platelet count ≤100 × 109 /l and peripheral blood plasma cell count ≥20 × 109 /l as independent predictors of worse survival. The median OS in patients with 0, 1 or 2-3 of these risk factors was 46, 27 and 12 months, respectively (P < 0·001). Our findings support the use of novel agents and ASCT as frontline treatment in patients with pPCL. The constructed prognostic score should be independently validated.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  myeloma; plasma cell leukaemia; prognosis; survival; therapeutic response

Mesh:

Year:  2018        PMID: 29315478     DOI: 10.1111/bjh.15092

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


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