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Superiority of bortezomib, thalidomide, and dexamethasone (VTD) as induction pretransplantation therapy in multiple myeloma: a randomized phase 3 PETHEMA/GEM study

Authors :
Javier López-Jiménez
Maria-Victoria Mateos
Joaquín Parra Martínez
Albert Oriol
Javier de la Rubia
D. Hernández
Joan Besalduch
Adrian Alegre
María Teresa Cibeira
Jesús F. San Miguel
Laura Rosiñol
Yolanda González
Miquel Granell
Norma C. Gutiérrez
Miguel T. Hernandez
Joaquín Díaz-Mediavilla
Luis Palomera
Maria Luisa Martin-Ramos
Juan José Lahuerta
Joan Bladé
Ana Isabel Teruel
Felipe de Arriba
Grupo Español de Mieloma
Maria Asunción Etxebeste
Source :
Blood, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe, instname
Publication Year :
2012
Publisher :
AMER SOC HEMATOLOGY, 2012.

Abstract

The Spanish Myeloma Group conducted a trial to compare bortezomib/thalidomide/dexamethasone (VTD) versus thalidomide/dexamethasone (TD) versus vincristine, BCNU, melphalan, cyclophosphamide, prednisone/vincristine, BCNU, doxorubicin, dexamethasone/bortezomib (VBMCP/VBAD/B) in patients aged 65 years or younger with multiple myeloma. The primary endpoint was complete response (CR) rate postinduction and post–autologous stem cell transplantation (ASCT). Three hundred eighty-six patients were allocated to VTD (130), TD (127), or VBMCP/VBAD/B (129). The CR rate was significantly higher with VTD than with TD (35% vs 14%, P = .001) or with VBMCP/VBAD/B (35% vs 21%, P = .01). The median progression-free survival (PFS) was significantly longer with VTD (56.2 vs 28.2 vs 35.5 months, P = .01). In an intention-to-treat analysis, the post-ASCT CR rate was higher with VTD than with TD (46% vs 24%, P = .004) or with VBMCP/VBAD/B (46% vs 38%, P = .1). Patients with high-risk cytogenetics had a shorter PFS and overall survival in the overall series and in all treatment groups. In conclusion, VTD resulted in a higher pre- and posttransplantation CR rate and in a significantly longer PFS although it was not able to overcome the poor prognosis of high-risk cytogenetics. Our results support the use of VTD as a highly effective induction regimen prior to ASCT. The study was registered with http://www.clinicaltrials.gov (NCT00461747) and Eudra CT (no. 2005-001110-41).

Details

ISSN :
00064971
Database :
OpenAIRE
Journal :
Blood, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe, instname
Accession number :
edsair.doi.dedup.....4237bb2c6e7a37d9be0c0a663210462f