Race and outcomes of autologous hematopoietic cell transplantation for multiple myeloma.

Publication Type:

Journal Article

Source:

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, Volume 16, Issue 3, p.395-402 (2010)

Keywords:

2010, Adult, African Americans, Age Factors, Aged, Aged, 80 and over, Center-Authored Paper, Clinical Research Division, Continental Population Groups, DISEASE PROGRESSION, Disease-Free Survival, Drug Therapy, European Continental Ancestry Group, Female, hematopoietic stem cell transplantation, Humans, Kaplan-Meier Estimate, Karnofsky Performance Status, Male, Middle Aged, Multiple Myeloma, RECURRENCE, Transplantation, Autologous, Treatment Outcome

Abstract:

Blacks are twice as likely to develop and die from multiple myeloma (MM), and are less likely to receive an autologous hematopoietic-cell transplant (AHCT) for MM compared to Whites. The influence of race on outcomes of AHCT for MM is not well described. We compared the probability of overall survival (OS), progression-free survival (PFS), disease progression, and nonrelapse mortality (NRM) among Black (N=303) and White (N=1892) recipients of AHCT for MM, who were reported to the Center for International Blood and Marrow Transplant Research (CIBMTR) from 1995 to 2005. The Black cohort was more likely to be female, and had better Karnofsky performance scores, but lower hemoglobin and albumin levels at diagnosis. Black recipients were younger and more likely to be transplanted later in their disease course. Disease stage and treatment characteristics prior to AHCT were similar between the 2 groups. Black and White recipients had similar probabilities of 5-year OS (52% versus 47%, P=.19) and PFS (19% versus 21%, P=.64) as well as cumulative incidences of disease progression (72% versus 72%, P=.97) and NRM (9% versus 8%, P=.52). In multivariate analyses, race was not associated with any of these endpoints. Black recipients of AHCT for MM have similar outcomes compared to Whites, suggesting that the reasons underlying lower rates of AHCT in Blacks need to be studied further to ensure equal access to effective therapy.