Achievement of VGPR to induction therapy is an important prognostic factor for longer PFS in the IFM 2005-01 trial.


Autoria(s): Moreau P.; Attal M.; Pégourié B.; Planche L.; Hulin C.; Facon T.; Stoppa A.M.; Fuzibet J.G.; Grosbois B.; Doyen C.; Ketterer N.; Sebban C.; Kolb B.; Chaleteix C.; Dib M.; Voillat L.; Fontan J.; Garderet L.; Jaubert J.; Mathiot C.; Esseltine D.; Avet-Loiseau H.; Harousseau J.L.; IFM 2005-01 study investigators
Data(s)

2011

Resumo

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).

Identificador

https://serval.unil.ch/?id=serval:BIB_8B4B5AC3FE33

isbn:1528-0020 (Electronic)

pmid:21098740

doi:10.1182/blood-2010-08-300863

isiid:000288496300013

Idioma(s)

en

Fonte

Blood, vol. 117, no. 11, pp. 3041-3044

Tipo

info:eu-repo/semantics/article

article