Prospective, Randomized Study of Single Compared With Double Autologous Stem-Cell Transplantation for Multiple Myeloma: Bologna 96 Clinical Study

Author:

Cavo Michele1,Tosi Patrizia1,Zamagni Elena1,Cellini Claudia1,Tacchetti Paola1,Patriarca Francesca1,Di Raimondo Francesco1,Volpe Ettore1,Ronconi Sonia1,Cangini Delia1,Narni Franco1,Carubelli Affra1,Masini Luciano1,Catalano Lucio1,Fiacchini Mauro1,de Vivo Antonio1,Gozzetti Alessandro1,Lazzaro Antonio1,Tura Sante1,Baccarani Michele1

Affiliation:

1. From the Istituto di Ematologia ed Oncologia Medica [Seràgnoli], Università di Bologna, Bologna; Clinica Ematologia, Università di Udine, Udine; Cattedra di Ematologia, Università di Catania, Catania; Servizio di Ematologia, Avellino; Sezione di Ematologia, Università di Modena, Modena; Unità Operativa di Ematologia, Cagliari; Servizio di Ematologia, Reggio Emilia; Divisione di Ematologia, Università Federico II, Napoli; Divisione di Ematologia e Trapianti, Università di Siena, Siena; and Oncologia...

Abstract

Purpose We performed a prospective, randomized study of single (arm A) versus double (arm B) autologous stem-cell transplantation (ASCT) for younger patients with newly diagnosed multiple myeloma (MM). Patients and Methods A total of 321 patients were enrolled onto the study and were randomly assigned to receive either a single course of high-dose melphalan at 200 mg/m2 (arm A) or melphalan at 200 mg/m2 followed, after 3 to 6 months, by melphalan at 120 mg/m2 and busulfan at 12 mg/kilogram (arm B). Results As compared with assignment to the single-transplantation group (n = 163 patients), random assignment to receive double ASCT (n = 158 patients) significantly increased the probability to attain at least a near complete response (nCR; 33% v 47%, respectively; P = .008), prolonged relapse-free survival (RFS) duration of 18 months (median, 24 v 42 months, respectively; P < .001), and significantly extended event-free survival (EFS; median, 23 v 35 months, respectively; P = .001). Administration of a second transplantation and of novel agents for treating sequential relapses in up to 50% of patients randomly assigned to receive a single ASCT likely contributed to prolong the survival duration of the whole group, whose 7-year rate (46%) was similar to that of the double-transplantation group (43%; P = .90). Transplantation-related mortality was 3% in arm A and 4% in arm B (P = .70). Conclusion In comparison with a single ASCT as up-front therapy for newly diagnosed MM, double ASCT effected superior CR or nCR rate, RFS, and EFS, but failed to significantly prolong overall survival. Benefits offered by double ASCT were particularly evident among patients who failed at least nCR after one autotransplantation.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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