A prospective PETHEMA study of tandem autologous transplantation versus autograft followed by reduced-intensity conditioning allogeneic transplantation in newly diagnosed multiple myeloma

Author:

Rosiñol Laura1,Pérez-Simón José Antonio2,Sureda Anna3,de la Rubia Javier4,de Arriba Felipe5,Lahuerta Juan José6,González José David7,Díaz-Mediavilla Joaquín8,Hernández Belén9,García-Frade Javier10,Carrera Dolores11,León Angel12,Hernández Miguel13,Abellán Pascual Fernández14,Bergua Juan Miguel15,San Miguel Jesús2,Bladé Joan1

Affiliation:

1. Hospital Clinic, Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona;

2. Hospital Clínico/Centro de Investigación del Cáncer, Salamanca;

3. Hospital de la Santa Creu i Sant Pau, Barcelona;

4. Hospital La Fe, Valencia;

5. Hospital Morales Messeguer, Murcia;

6. Hospital Doce de Octubre, Madrid;

7. Hospital Materno-Insular, Las Palmas de Gran Canaria;

8. Hospital Clínico San Carlos, Madrid;

9. Hospital General Ciudad Real, Ciudad Real;

10. Hospital Rio Hortega, Valladolid;

11. Hospital de Asturias, Oviedo;

12. Hospital de Jerez de la Frontera, Jerez;

13. Hospital Universitario Canarias, Sta Cruz de Tenerife;

14. Hospital de Alicante, Alicante; and

15. Hospital San Pedro de Alcántara, San Pedro de Alcántara, Spain

Abstract

One hundred ten patients with multiple myeloma (MM) failing to achieve at least near-complete remission (nCR) after a first autologous stem cell transplantation (ASCT) were scheduled to receive a second ASCT (85 patients) or a reduced-intensity-conditioning allograft (allo-RIC; 25 patients), depending on the human leukocyte antigen (HLA)–identical sibling donor availability. There was a higher increase in complete remission (CR) rate (40% vs 11%, P = .001) and a trend toward a longer progression-free survival (PFS; median, 31 months vs not reached, P = .08) in favor of allo-RIC. In contrast, it was associated with a trend toward a higher transplantation-related mortality (16% vs 5%, P = .07), a 66% chance of chronic graft-versus-host disease and no statistical difference in event-free survival and overall survival. Although the PFS plateau observed with allo-RIC is very encouraging, this procedure is associated with high morbidity and mortality, and therefore it should still be considered investigational and restricted to well-designed prospective clinical trials. This trial is registered at ClinicalTrials.gov ID number NCT00560053

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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