Hematopoietic cell transplantation comorbidity index predicts transplantation outcomes in pediatric patients

被引:64
作者
Smith, Angela R. [1 ]
Majhail, Navneet S. [1 ]
MacMillan, Margaret L. [1 ]
DeFor, Todd E. [1 ]
Jodele, Sonata [2 ]
Lehmann, Leslie E. [3 ]
Krance, Robert [4 ]
Davies, Stella M. [2 ]
机构
[1] Univ Minnesota, Blood & Marrow Transplant Program, Minneapolis, MN 55455 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Bone Marrow Transplant & Immune Deficiency, Cincinnati, OH USA
[3] Childrens Hosp, Dana Farber Canc Inst, Pediat Stem Cell Transplant Program, Boston, MA 02115 USA
[4] Texas Childrens Canc Ctr, Pediat Stem Cell Transplant Program, Houston, TX USA
关键词
HCT-CI; REDUCED-INTENSITY; MORBIDITY; MORTALITY; RISK; VALIDATION; LYMPHOMA; MYELOMA; MODELS;
D O I
10.1182/blood-2010-08-303263
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Quantifying the risk of hematopoietic cell transplantation (HCT)-related mortality for pediatric patients is challenging. The HCT-specific comorbidity index (HCT-CI) has been confirmed as a useful tool in adults, but has not yet been validated in children. We conducted a retrospective cohort study of 252 pediatric patients undergoing their first allogeneic HCT between January 2008 and May 2009. Pretransplantation comorbidities were scored prospectively using the HCT-CI. Median age at transplantation was 6 years (range, 0.1-20) and median follow-up was 343 days (range, 110-624). HCT-CI scores were distributed as follows: 0, n = 139; 1-2, n = 52; and 3+, n = 61. The 1-year cumulative incidence of nonrelapse mortality (NRM) increased (10%, 14%, and 28%, respectively; P < .01) and overall survival (OS) decreased (88%, 67%, and 62%, respectively; P < .01) with increasing HCT-CI score. Multivariate analysis showed that compared with score 0, those with scores of 1-2 and 3+ had relative risks of NRM of 1.5 (95% confidence interval, 0.5-4.3, P = .48) and 4.5 (95% confidence interval, 1.7-12.1, P < .01), respectively. These results indicate that the HCT-CI score predicts NRM and OS in pediatric patients undergoing HCT and is a useful tool to assess risk, guide counseling in the pre-transplantation setting, and devise innovative therapies for the highest risk groups. (Blood. 2011; 117(9): 2728-2734)
引用
收藏
页码:2728 / 2734
页数:7
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