| Literature DB >> 27378674 |
Christian W Eskelund1, Arne Kolstad2, Mats Jerkeman3, Riikka Räty4, Anna Laurell5, Sandra Eloranta6, Karin E Smedby6, Simon Husby7, Lone B Pedersen7, Niels S Andersen7, Mikael Eriksson3, Eva Kimby8, Hans Bentzen9, Outi Kuittinen10, Grete F Lauritzsen2, Herman Nilsson-Ehle11, Elisabeth Ralfkiaer7, Mats Ehinger12, Christer Sundström13, Jan Delabie14, Marja-Liisa Karjalainen-Lindsberg15, Christopher T Workman16,17, Christian Garde16,17, Erkki Elonen4, Peter Brown7, Kirsten Grønbaek7, Christian H Geisler7.
Abstract
In recent decades, the prognosis of Mantle Cell Lymphoma (MCL) has been significantly improved by intensified first-line regimens containing cytarabine, rituximab and consolidation with high-dose-therapy and autologous stem cell transplantation. One such strategy is the Nordic MCL2 regimen, developed by the Nordic Lymphoma Group. We here present the 15-year updated results of the Nordic MCL2 study after a median follow-up of 11·4 years: For all patients on an intent-to-treat basis, the median overall and progression-free survival was 12·7 and 8·5 years, respectively. The MCL International Prognostic Index (MIPI), biological MIPI, including Ki67 expression (MIPI-B) and the MIPI-B including mIR-18b expression (MIPI-B-miR), in particular, significantly divided patients into distinct risk groups. Despite very long response durations of the low and intermediate risk groups, we observed a continuous pattern of relapse and the survival curves never reached a plateau. In conclusion, despite half of the patients being still alive and 40% in first remission after more than 12 years, we still see an excess disease-related mortality, even among patients experiencing long remissions. Even though we consider the Nordic regimen as a very good choice of regimen, we recommend inclusion in prospective studies to explore the benefit of novel agents in the frontline treatment of MCL.Entities:
Keywords: Mantle Cell Lymphoma; Non-Hodgkin Lymphoma; clinical trials; high dose therapy
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Year: 2016 PMID: 27378674 DOI: 10.1111/bjh.14241
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998