Early identification of patients at risk of death due to infections, hemorrhage, or graft failure after allogeneic bone marrow transplantation on the basis of the leukocyte counts

被引:29
作者
Mehta, J
Powles, R
Singhal, S
Horton, C
Middleton, G
Eisen, T
Meller, S
Pinkerton, CR
Treleaven, J
机构
[1] Leukaemia Unit, Royal Marsden Hospital, Surrey
[2] Leukaemia Unit, Royal Marsden Hospital, Sutton
关键词
graft failure; growth factors; hemorrhage; infections; leukocyte count; leukopenia;
D O I
10.1038/sj.bmt.1700657
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Allograft recipients are often unwell with significant dysfunction by the time delayed or failed engraftment is diagnosed, We attempted to identify factors associated with graft failure, or death due to infection, hemorrhage or graft failure in 712 undergoing allogeneic BMT, Low leukocyte between days 12 and 22 were strongly associated with subsequent graft failure or death, In multivariate analysis, a leukocyte count of less than or equal to 0.2 x 10(9)/l on day 16 was the most powerful predictor of graft failure or death, Transplants from HLA-mismatched and unrelated donors were also associated with increased risk of both, and T cell depletion with increased risk of graft failure, On the basis of these findings, it may be possible to define graft failure in functional terms as early as 2 weeks after BMT rather than at 3 or 4 weeks, The use of growth factors can then be limited to patients most likely to benefit from them, and it may be possible to salvage patients at risk of complications of low counts early before their clinical condition deteriorates, We suggest that patients with leukocyte counts of 0.2 x 10(9)/l or less 14-16 days after BMT should be started on G-CSF or GM-CSF even if they are clinically well, and consideration should be given to a second infusion of cells.
引用
收藏
页码:349 / 355
页数:7
相关论文
共 31 条
[1]   EFFECT OF HLA COMPATIBILITY ON ENGRAFTMENT OF BONE-MARROW TRANSPLANTS IN PATIENTS WITH LEUKEMIA OR LYMPHOMA [J].
ANASETTI, C ;
AMOS, D ;
BEATTY, PG ;
APPELBAUM, FR ;
BENSINGER, W ;
BUCKNER, CD ;
CLIFT, R ;
DONEY, K ;
MARTIN, PJ ;
MICKELSON, E ;
NISPEROS, B ;
OQUIGLEY, J ;
RAMBERG, R ;
SANDERS, JE ;
STEWART, P ;
STORB, R ;
SULLIVAN, KM ;
WITHERSPOON, RP ;
THOMAS, ED ;
HANSEN, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (04) :197-204
[2]  
ANASETTI C, 1993, BLOOD, V82, pA454
[3]   GM-CSF AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION - ACCELERATED RECOVERY OF NEUTROPHILS, MONOCYTES AND LYMPHOCYTES [J].
ATKINSON, K ;
BIGGS, JC ;
DOWNS, K ;
JUTTNER, C ;
BRADSTOCK, K ;
LOWENTHAL, RM ;
DALE, B ;
SZER, J .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1991, 21 (05) :686-692
[4]  
BOLGER GB, 1986, BONE MARROW TRANSPL, V1, P21
[5]  
BUNJES D, 1990, BONE MARROW TRANSPL, V6, P309
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]  
DAVIES SM, 1994, BONE MARROW TRANSPL, V14, P73
[8]  
DAVIES SM, 1994, BONE MARROW TRANSPL, V13, P51
[9]  
HALE G, 1994, BONE MARROW TRANSPL, V13, P597
[10]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481