Donor versus no-donor comparison of newly diagnosed myeloma patients included in the HOVON-50 multiple myeloma study

Author:

Lokhorst Henk M.1,van der Holt Bronno2,Cornelissen Jan J.3,Kersten Marie-José4,van Oers Marinus4,Raymakers Reinier1,Minnema Monique C.1,Zweegman Sonja5,Janssen Jeroen J.5,Zijlmans Mark3,Bos Gerard6,Schaap Nicolaas7,Wittebol Shulamiet8,de Weerdt Okke9,Ammerlaan Rianne2,Sonneveld Pieter3

Affiliation:

1. Department of Hematology, University Medical Center Utrecht, Utrecht, The Netherlands;

2. Hovon Data Center, Rotterdam, The Netherlands;

3. Department of Hematology, Erasmus Medical Center, Rotterdam, The Netherlands;

4. Department of Hematology, Academic Medical Center, Amsterdam, The Netherlands;

5. Department of Hematology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands;

6. Department of Hematology, Academic Hospital Maastricht, Maastricht, The Netherlands;

7. Radboud University Nijmegen Hospital, Nijmegen, The Netherlands;

8. Meander Medical Center, Amersfoort, The Netherlands; and

9. Antonius Hospital, Nieuwegein, The Netherlands

Abstract

To prospectively evaluate allogeneic stem cell transplantation (allo-SCT) for myeloma as part of first-line therapy, a donor versus no-donor analysis was performed of patients treated in the HOVON-50 study, a study that was originally designed to examine thalidomide combined with intensive therapy. Two hundred sixty patients having received an autologous-SCT fulfilled the criteria to be included, 138 patients without an HLA-identical sibling donor and 122 patients with a donor. After a median follow-up of 77 months, complete remission, progression-free survival (PFS), and overall survival were not significantly different between the 2 groups. PFS at 6 years was 28% for patients with a donor versus 22% for patients without a donor (P = .19) and overall survival at 6 years from high-dose melphalan was 55%, irrespective of having a donor (P = .68). Cumulative incidence of nonrelapse mortality at 6 years after autologous-SCT was 16% in the donor group versus 3% in the no-donor group (P < .001). However, PFS was significantly prolonged in the 99 patients who actually proceeded to allo-SCT compared with the 115 patients who continued maintenance or received a second high-dose melphalan, but the difference did not translate into a prolonged survival benefit. These results do not support a general application of allo-SCT in all myeloma patients as part of first-line therapy.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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