| Literature DB >> 21098740 |
Philippe Moreau1, Michel Attal, Brigitte Pégourié, Lucie Planche, Cyrille Hulin, Thierry Facon, Anne-Marie Stoppa, Jean-Gabriel Fuzibet, Bernard Grosbois, Chantal Doyen, Nicolas Ketterer, Catherine Sebban, Brigitte Kolb, Carine Chaleteix, Mamoun Dib, Laurent Voillat, Jean Fontan, Laurent Garderet, Jérôme Jaubert, Claire Mathiot, Dixie Esseltine, Hervé Avet-Loiseau, Jean-Luc Harousseau.
Abstract
In the 2005-01 trial, we have demonstrated that bortezomib-dexamethasone as induction therapy before autologous stem cell transplantation was superior to vincristine-adriamycin-dexamethasone. We conducted a post-hoc analysis to assess the prognostic impact of initial characteristics as well as response to therapy in patients enrolled in this study. Multivariate analysis showed that ISS stages 2 and 3 and achievement of response less than very good partial response (VGPR) both after induction therapy and after autologous stem cell transplantation were adverse prognostic factors for progression-free survival, the most important one being achievement of response less than VGPR after induction. Progression-free survival was significantly improved with bortezomib-dexamethasone induction therapy in patients with poor-risk cytogenetics and ISS stages 2 and 3 compared with vincristine-adriamycin-dexamethasone. In these 2 groups of patients, achievement of at least VGPR after induction was of major importance. This study is registered with EudraCT (https://eudract.ema.europa.eu; EUDRACT 2005-000537-38) and http://clinicaltrials.gov (NCT00200681).Entities:
Mesh:
Year: 2010 PMID: 21098740 DOI: 10.1182/blood-2010-08-300863
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113