Outcomes after auto-SCT in African Americans with multiple myeloma

被引:3
作者
Khaled, Y. [1 ]
Abidi, M. H. [2 ]
Janakiraman, N. [3 ]
Kato, K.
Levine, J. E.
Reddy, P.
Medina, M.
Peres, E.
Hanbali, A. [3 ]
Mineishi, S.
机构
[1] Univ Michigan, Ctr Comprehens Canc, Blood & Marrow Transplantat Program, Ann Arbor, MI 48109 USA
[2] Karmanos Canc Inst, Detroit, MI USA
[3] Henry Ford Hosp, Detroit, MI 48202 USA
关键词
multiple myeloma; auto-SCT; African Americans; STEM-CELL TRANSPLANTATION; SINGLE-CENTER EXPERIENCE; HIGH-DOSE THERAPY; AUTOLOGOUS TRANSPLANTATION; PROGNOSTIC-FACTORS; INTENSIVE THERAPY; RANDOMIZED-TRIAL; SURVIVAL; CHEMOTHERAPY; IMPACT;
D O I
10.1038/bmt.2008.401
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To study the impact of auto-SCT on the outcomes in African Americans (AA) with multiple myeloma (MM), we evaluated 101 consecutive AA patients who underwent auto-SCT. The median PFS and OS were 15.6 and 50.8 months, respectively. The median OS from diagnosis was 60 months. Traditional pre and post transplant prognostic variables earlier examined in Caucasian Americans (CA), including beta-2 microglobulin (B2M), chromosome 13 deletion, CR status after auto-SCT, gender, stage, Ig subtype, time to transplant, number of prior regimens and presence of lytic lesions, were not predictive of improved PFS or OS on univariate analysis. Age, lower CD34 cell dose infused, history of palliative radiation therapy (XRT) prior to auto-SCT and refractory disease at the time of auto-SCT were predictive of inferior PFS. History of palliative XRT was the only predictive factor of inferior PFS and OS after auto-SCT on multivariate analysis. In conclusion, MM in AA tends to relapse early after auto-SCT. It is unclear whether early relapses impact OS. Common prognostic peritransplant variables known in CA with MM may not be applicable to AA with MM. Bone Marrow Transplantation (2009) 43, 845-851; doi: 10.1038/bmt.2008.401; published online 12 January 2009
引用
收藏
页码:845 / 851
页数:7
相关论文
共 28 条
[1]  
Abou-Jawde RM, 2006, HAEMATOLOGICA, V91, P1410
[2]   Clinical outcomes with intensive therapy for patients with primary resistant multiple myeloma [J].
Alexanian, R ;
Weber, D ;
Delasalle, K ;
Handy, B ;
Champlin, R ;
Giralt, S .
BONE MARROW TRANSPLANTATION, 2004, 34 (03) :229-234
[3]   Graft outcome - Impact of complete remission with intensive therapy in patients with responsive multiple myeloma [J].
Alexanian, R ;
Weber, D ;
Giralt, S ;
Dimopoulos, M ;
Delasalle, K ;
Smith, T ;
Champlin, R .
BONE MARROW TRANSPLANTATION, 2001, 27 (10) :1037-1043
[4]  
[Anonymous], Seer Data
[5]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[6]   High-dose therapy intensification compared with continued standard chemotherapy in multiple myeloma patients responding to the initial chemotherapy:: long-term results from a prospective randomized trial from the Spanish cooperative group PETHEMA [J].
Bladé, J ;
Rosiñol, L ;
Sureda, A ;
Ribera, JM ;
Díaz-Mediavilla, J ;
García-Laraña, J ;
Mateos, MV ;
Palomera, L ;
Fernández-Calvo, J ;
Martí, JM ;
Giraldo, P ;
Carbonell, F ;
Callís, M ;
Trujillo, J ;
Gardella, S ;
Moro, MJ ;
Barez, A ;
Soler, A ;
Font, L ;
Fontanillas, M ;
San Miguel, J .
BLOOD, 2005, 106 (12) :3755-3759
[7]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[8]   Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults [J].
Calle, EE ;
Rodriguez, C ;
Walker-Thurmond, K ;
Thun, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (17) :1625-1638
[9]   High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma [J].
Child, JA ;
Morgan, GJ ;
Davies, FE ;
Owen, RG ;
Bell, SE ;
Hawkins, K ;
Brown, J ;
Drayson, MT ;
Selby, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (19) :1875-1883
[10]  
Fonseca Rafael, 2004, Cancer Research, V64, P1546, DOI 10.1158/0008-5472.CAN-03-2876