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

Author:

Rosiñol Laura1,Oriol Albert2,Teruel Ana Isabel3,Hernández Dolores4,López-Jiménez Javier5,de la Rubia Javier6,Granell Miquel7,Besalduch Joan8,Palomera Luis9,González Yolanda10,Etxebeste Mª Asunción11,Díaz-Mediavilla Joaquín12,Hernández Miguel T.13,de Arriba Felipe14,Gutiérrez Norma C.15,Martín-Ramos Mª Luisa16,Cibeira Mª Teresa1,Mateos Mª Victoria15,Martínez Joaquín16,Alegre Adrián17,Lahuerta Juan José16,San Miguel Jesús15,Bladé Joan1

Affiliation:

1. Hospital Clínic de Barcelona, Barcelona, Spain;

2. Hospital Germans Trias i Pujol, Badalona, Spain;

3. Hospital Clínico Universitario de Valencia, Valencia, Spain;

4. Hospital Universitário La Paz, Madrid, Spain;

5. Hospital Ramón y Cajal, Madrid, Spain;

6. Hospital La Fe, Valencia, Spain;

7. Hospital Sant Pau, Barcelona, Spain;

8. Hospital Son Espases, Palma de Mallorca, Spain;

9. Hospital Clínico Univesitario Lozano Blesa, Zaragoza, Spain;

10. Hospital Universitari Dr Josep Trueta, Giorna, Spain;

11. Hospital de Donostia, Donostia, Spain;

12. Hospital Clínico San Carlos, Madrid, Spain;

13. Hospital Universitario de Canarias, La Laguna, Spain;

14. Hospital Morales Messeguer, Murcia, Spain;

15. Hospital Clínico Universitario de Salamanca, Salamanca, Spain;

16. Hospital Universitario Doce de Octubre, Madrid, Spain; and

17. Hospital Universitario La Princesa, Madrid, Spain

Abstract

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).

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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