| Literature DB >> 29463854 |
Irit Avivi1, Ariane Boumendil2, Hervé Finel2, Arnon Nagler3, Aïda Botelho de Sousa4, Josep Maria Ribera Santasusana5, Elizabeth Vandenberghe6, Boris Afanasyev7, Dominique Bordessoule8, José Maria Moraleda9, Eulogio Conde Garcia10, David Pohlreich11, Gonzalo Gutiérrez Garcia12, Kirsty Thomson13, Reuven Or14, Dietrich Beelen15, Eliana Zuffa16, Sebastian Giebel17, Christian Berthou18, Gilles Salles19, Angela Melpignano20, Silvia Montoto2,21, Peter Dreger2,22.
Abstract
The purpose of this retrospective registry study was to investigate the outcome of autoSCT for primary mediastinal B-cell lymphoma (PMBCL) in the rituximab era, including the effects of eventual post-transplant radiotherapy (RT) consolidation. Patients with PMBCL aged between 18 and 70 years who were treated with a first autoSCT between 2000 and 2012 and registered with the EBMT were eligible. Eighty-six patients with confirmed PMBCL and the full data set required for this analysis were evaluable. Sixteen patients underwent autoSCT in remission after first-line therapy (CR/PR1), 44 patients were transplanted with chemosensitive relapsed or primary refractory disease (CR/PR >1), and 24 patients were chemorefractory at the time of autoSCT. With a median follow-up of 5 years, 3-year estimates of relapse incidence, progression-free survival, and overall survival were 6%, 94%, and 100% for CR/PR1; 31%, 64%, and 85% for CR/PR >1; and 52%, 39%, and 41% for REF, respectively. Whilst there was no significant benefit of post-transplant RT in the CR/PR >1 group, RT could completely prevent disease recurrence post d100 in the refractory group. In conclusion, autoSCT with or without consolidating RT is associated with excellent outcome in chemoimmunotherapy-sensitive PMBCL, whereas its benefits seem to be limited in chemoimmunotherapy-refractory disease.Entities:
Mesh:
Year: 2018 PMID: 29463854 DOI: 10.1038/s41409-017-0063-7
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483