Survival after relapse following tandem autotransplants in multiple myeloma patients: the University of Arkansas total therapy I experience

Athanasios Fassas(University of Arkansas for Medical Sciences), Bart Barlogie(University of Arkansas for Medical Sciences), Susan Ward(University of Arkansas for Medical Sciences), Sundar Jagannath(University of Arkansas for Medical Sciences), David H. Vesole(University of Arkansas for Medical Sciences), Sandy Mattox(University of Arkansas for Medical Sciences), David S. Siegel(University of Arkansas for Medical Sciences), Firas Muwalla(University of Arkansas for Medical Sciences), Maurizio Zangari(University of Arkansas for Medical Sciences), Elias Anaissie(University of Arkansas for Medical Sciences), Frits van Rhee(University of Arkansas for Medical Sciences), Raymond Thertulien(University of Arkansas for Medical Sciences), Choon‐Kee Lee(University of Arkansas for Medical Sciences), Raman Desikan(University of Arkansas for Medical Sciences), Varant Arzumanian(University of Arkansas for Medical Sciences), Jason McCoy(University of Arkansas for Medical Sciences), Guido Tricot(University of Arkansas for Medical Sciences)
British Journal of Haematology
October 20, 2003
Cited by 12

Abstract

Despite the superiority of high-dose (compared with standard) treatment in multiple myeloma, relapses still occur. We evaluated relapse patterns, salvage treatments employed and outcome in patients given tandem transplants on our total therapy I protocol. We focused on 146 patients (of 231 enrolled) who received tandem autotransplants < or =12 months apart and survived > or =2 months after the second transplant. With a median follow-up of 9 years after enrollment, 31 (21%) patients remain in complete or stable partial remission. Ninety-five (65%) patients received therapy for relapsing myeloma. The median time from the first transplant to relapse was 2.9 years. The median overall survival from relapse was 2.4 years. In one-quarter (23/95) of cases, the postrelapse interval exceeded the interval from the first transplant to relapse. On multivariate analysis, the presence of any cytogenetic abnormalities [P<0.001, Hazard Ratio (HR): 3.84] and beta-2 microglobulin levels >4 mg/l at relapse (P<0.001, HR: 2.87) were significant for poor survival after relapse. The median survival after relapse was 5.1, 1.3 and 0.7 years in patients with none (44%), one (46%) and two (10%) poor-risk factors, respectively. In conclusion, a sizeable fraction of myeloma patients relapsing after tandem autotransplants without poor-risk features enjoyed meaningful survival prolongation when appropriately treated.


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