| Literature DB >> 21261498 |
Lionel Karlin1, Jean Soulier, Olivia Chandesris, Sylvain Choquet, Karim Belhadj, Margaret Macro, Didier Bouscary, Raphael Porcher, David Ghez, Marion Malphettes, Bouchra Asli, Jean Claude Brouet, Jean Christophe Bories, Olivier Hermine, Jean Paul Fermand, Bertrand Arnulf.
Abstract
The t(4;14) translocation, found in 15% of multiple myeloma (MM), indicates a poor prognosis. Clinico-biological features associated with this severe outcome and the impact of novel agents are unknown. We report a series of 102 consecutive patients with t(4;14) MM. The median age was 56 years. The isotype was IgA in 42%, and the median serum β(2)-microglobulin was 2.3 mg/L. FGFR3 expression was lacking in 20 (19%) cases. Monoclonal gammopathy of undetermined significance (MGUS) or smoldering MM (sMM) was found in 26 patients (25%). Seven (27%) became symptomatic in a median time of 9 months. Fifty-six of 76 patients with symptomatic MM received high-dose therapy (HDT). The overall response rate (ORR) was 93% (22% CR, 44% VGPR), and the median progression-free survival (PFS) was 12 months. Twenty-four (37%) patients experienced aggressive relapse. Post-second-line ORR was 51% and the median PFS was 7 months, with a trend for longer PFS in patients treated with a bortezomib-based regimen. Median overall survival after HDT was 31 months. t(4;14) is detected in patients with MGUS/sMM and this does not require immediate chemotherapy. Patients with t(4;14) MM have a high ORR after HDT, contrasting with a short PFS and aggressive relapses, and, despite novel agents, still have a poor prognosis.Entities:
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Year: 2011 PMID: 21261498 DOI: 10.3109/10428194.2010.537795
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022