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Risk Factors Associated with Kidney Injury and the Impact of Kidney Injury on Overall Survival in Pediatric Recipients Following Allogeneic Stem Cell Transplant
被引:27
|作者:
Satwani, Prakash
[1
]
Bavishi, Sejal
Jin, Zhezhen
[2
]
Jacobson, Judith S.
[3
]
Baker, Courtney
Duffy, Deirdre
Lowe, Leora
Morris, Erin
Cairos, Mitchell S.
[4
,5
]
机构:
[1] Columbia Univ, Div Pediat Blood & Marrow Transplantat, New York Presbyterian Morgan Stanley Childrens Ho, Dept Pediat,Mailman Sch Publ Hlth, New York, NY 10032 USA
[2] Columbia Univ, Dept Biostat, Mailman Sch Publ Hlth, New York Presbyterian Morgan Stanley Childrens Ho, New York, NY 10032 USA
[3] Columbia Univ, Dept Epidemiol, Mailman Sch Publ Hlth, New York Presbyterian Morgan Stanley Childrens Ho, New York, NY 10032 USA
[4] Columbia Univ, Dept Med, New York Presbyterian Morgan Stanley Childrens Ho, New York, NY 10032 USA
[5] Columbia Univ, Dept Pathol & Cell Biol, New York Presbyterian Morgan Stanley Childrens Ho, New York, NY 10032 USA
关键词:
Pediatrics;
Kidney injury;
Reduced toxicity and myeloablative conditioning;
Allogeneic stem cell transplant;
BONE-MARROW-TRANSPLANTATION;
ACUTE-RENAL-FAILURE;
LONG-TERM SURVIVORS;
GLOMERULAR-FILTRATION-RATE;
MYCOPHENOLATE-MOFETIL;
NONMALIGNANT DISEASES;
HOST-DISEASE;
CHILDREN;
PROPHYLAXIS;
CREATININE;
D O I:
10.1016/j.bbmt.2011.02.006
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Pediatric allogeneic stem cell transplant (AlloSCT) patients are at substantial risk of developing kidney injury (KI), and KI contributes to transplant-related morbidity and mortality. We compared the estimated creatinine clearance (eCrCl) at 1, 3, 6, 9, and 12 months post-AlloSCT in 170 patients following reduced toxicity conditioning (RTC) versus myeloablative conditioning (MAC) to baseline. eCrCl was calculated using the Schwartz equation. Patients with >= 50% drop in eCrCl from the baseline were considered to have KI. Patients received tacrolimus and mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis. The logistic regression model was used for assessing risk factors for KI. Seventy-six patients (median age = 10.6 years) received RTC AlloSCT; 94 patients (median age = 8.5 years) received MAC AlloSCT. The incidence of KI at 1 month post-AlloSCT was significantly higher in MAC versus RTC AlloSCT (43/94 [45.7%] versus 13/76 [17.1%] P < .0001). There was no statistical difference in KI at 3, 6, 9, and 12 months post-AlloSCT between the 2 conditioning groups. On multivariate analysis, only MAC was a significant risk factor for KI (odds radio [OR] 3.44, 95% confidence interval [Cl] 1.59-7.42, P = .002). In multivariate analysis for risk factors affecting overall survival (OS), the following were statistically significant: MAC versus RTC (hazard ratio [HR] 2.66, P = .0008), average versus poor-risk disease status (HR 2.09, P = .004), matched sibling donor (MSD) and matched unrelated donor (MUD) versus umbilical cord blood (UCB) (HR 2.31, P = .013), no KI versus KI (HR 2.00, P = .005). In children, MAC is associated with significant risk of KI in the first month after transplant, and KI in the first month post-AlloSCT is associated with a significantly decreased OS. Biol Blood Marrow Transplant 17: 1472-1480 (2011) (C) 2011 American Society for Blood and Marrow Transplantation
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页码:1472 / 1480
页数:9
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