Background In this trial of the treatment of newly diagnosedmultiple myeloma, we compared a protocol that entailed a hematopoieticstem-cell autograft followed by an allograft from an HLA-identicalsibling with a protocol of tandem autografts.
Methods We enrolled 162 consecutive patients with newly diagnosedmyeloma who were 65 years of age or younger and who had at leastone sibling. All patients were initially treated with vincristine,doxorubicin, and dexamethasone, followed by melphalan and autologousstem-cell rescue. Patients with an HLA-identical sibling thenreceived nonmyeloablative total-body irradiation and stem cellsfrom the sibling. Patients without an HLA-identical siblingreceived two consecutive myeloablative doses of melphalan, eachof which was followed by autologous stem-cell rescue. The primaryend points were overall survival and event-free survival.
Results After a median follow-up of 45 months (range, 21 to90), the median overall survival and event-free survival werelonger in the 80 patients with HLA-identical siblings than inthe 82 patients without HLA-identical siblings (80 months vs.54 months, P=0.01; and 35 months vs. 29 months, P=0.02, respectively).Among patients who completed their assigned treatment protocols,treatment-related mortality did not differ significantly betweenthe double-autologous-transplant group (46 patients) and theautograft–allograft group (58 patients, P=0.09), but disease-relatedmortality was significantly higher in the double-autologous-transplantgroup (43% vs. 7%, P<0.001). The cumulative incidence ratesof grades II, III, and IV graft-versus-host disease (GVHD) combinedand of grade IV GVHD in the autograft–allograft groupwere 43% and 4%, respectively. Overall, 21 of 58 patients (36%)were in complete remission after a median follow-up of 38 months(range, 10 to 72) after allografting. Of the 46 patients whoreceived two autografts, 25 (54%) died.
Conclusions Among patients with newly diagnosed myeloma, survivalin recipients of a hematopoietic stem-cell autograft followedby a stem-cell allograft from an HLA-identical sibling is superiorto that in recipients of tandem stem-cell autografts. (ClinicalTrials.govnumber, NCT00415987
[ClinicalTrials.gov]
.)
Source Information
From San Giovanni Battista Hospital, University of Turin, Turin (B.B., M.R., L.G., R. Sorasio, P.O., S.B., M.M., A.P., M.B.); the University of Udine, Udine (F.P., R.F.); Santa Croce e Carle Hospital, Cuneo (N.M., A.G.); Santi Antonio e Biagio Hospital, Alessandria (B.A., A.L.); the Institute for Cancer Research and Treatment, Candiolo (F.C.-S., M.A.); and San Giovanni Battista Hospital and Centro Prevenzione Oncologica Regione Piemonte, Turin (I.B., G.C.) — all in Italy; and the Fred Hutchinson Cancer Research Center, University of Washington, Seattle (R. Storb).
Address reprint requests to Dr. Bruno at the Divisione Universitaria di Ematologia, Azienda Ospedaliera San Giovanni Battista, Via Genova 3, Turin 10126, Italy, or at benedetto.bruno{at}unito.it.
Allografting or Autografting for Myeloma
van Rhee F., Crowley J., Barlogie B., Rajkumar S. V., Kyle R. A., Moreau P., Harousseau J.-L., Attal M., Bruno B., Ciccone G., Boccadoro M.
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N Engl J Med 2007;
356:2646-2648, Jun 21, 2007.
Correspondence
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