Publication
Trends in Utilization and Outcomes of Autologous Transplantation as Early Therapy for Multiple Myeloma
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- Persistent URL
- Last modified
- 05/21/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2013-11-01
- Publisher
- Elsevier: 12 months
- Publication Version
- Copyright Statement
- © 2013 American Society for Blood and Marrow Transplantation.
- License
- Final Published Version (URL)
- Title of Journal or Parent Work
- ISSN
- 1083-8791
- Volume
- 19
- Issue
- 11
- Start Page
- 1615
- End Page
- 1624
- Grant/Funding Information
- See article for more funding information.
- The CIBMTR is supported by the Public Health Service (grant/cooperative agreement U24-CA76518) from the National Cancer Institute (NCI) , the National Heart, Lung, and Blood Institute (NHLBI) , and the National Institute of Allergy and Infectious Diseases (NIAID) ; NHLBI and NCI (grant/cooperative agreement 5U01HL069294); Health Resources and Services Administration (HRSA/DHHS; contract HHSH234200637015C); the Office of Naval Research (grants N00014-06-1-0704 and N00014-08-1-0058 )
- Abstract
- The impact of novel drugs for treating multiple myeloma (MM) on the utilization and outcomes of autologous hematopoietic progenitor cell transplantation (AHPCT) is unknown. We reviewed characteristics and outcomes of 20,278 patients who underwent AHPCT within 12months of diagnosis of MM in the United States and Canada and registered at the Center for International Blood and Marrow Transplant Research (CIBMTR) in 3 time cohorts reflecting the increasing availability of novel drugs: 1995 to 1999 (n=2226), 2000 to 2004 (n=6408), and 2005 to 2010 (n=11,644). In the United States, the number of AHPCTs performed increased at a greater rate than new MM cases. Patients in recent cohorts were older, less likely to have stage 3MM, and more likely to have received previous thalidomide, lenalidomide, or bortezomib. On multivariate analysis, AHPCT in the 2000 to 2004 cohort (HR=0.77) or in the 2005 to 2010 cohort (HR=0.68) were associated with lower risk of death. Survival at 60months post-AHPCT improved from 47% in 1995 to 1999 to 55% in 2000 to 2004 and to 57% in 2005 to 2010, owing less to improvement in progression-free survival (50% versus 55% versus 57% at 24months) than to postrelapse/progression survival (58% versus 65% versus 72% at 24months). AHPCT and new biological agents are complementary, nonredundant therapies and should be combined in the management of MM in suitable patients.
- Author Notes
- Keywords
- SUPERIOR
- Autologous stem cell transplantation
- LONG-TERM SURVIVAL
- PLUS DEXAMETHASONE
- Hematology
- INTERNATIONAL STAGING SYSTEM
- CONSOLIDATION THERAPY
- Survival
- Multiple myeloma
- Transplantation
- Immunology
- BORTEZOMIB
- Population study
- Life Sciences & Biomedicine
- INDUCTION
- IMPROVEMENT
- Science & Technology
- STEM-CELL TRANSPLANTATION
- THALIDOMIDE
- Research Categories
- Health Sciences, Oncology
- Health Sciences, Public Health
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