Predictive Value of Bronchiolitis Obliterans Syndrome Stage 0p in Chronic Graft-versus-Host Disease of the Lung

被引:43
作者
Abedin, Sameem [1 ]
Yanik, Gregory A. [2 ]
Braun, Thomas [2 ]
Pawarode, Attaphol [2 ]
Magenau, John [2 ]
Goldstein, Steven C. [2 ]
Levine, John E. [2 ]
Kitko, Carrie L. [2 ]
Couriel, Daniel R. [2 ]
机构
[1] Northwestern Univ, Div Hematol Oncol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Univ Michigan Hlth Syst, Blood & Marrow Transplant Program, Ann Arbor, MI USA
关键词
Chronic GVHD; Bronchiolitis obliterans syndrome; BOS; 0p; HLA CLASS-I; GENOMIC ANCESTRY; UNRELATED DONORS; POPULATIONS; POLYMORPHISM; ALLELES; COLOR;
D O I
10.1016/j.bbmt.2015.02.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bronchiolitis obliterans syndrome (BOS) is a significant post-transplant complication with low survival. BOS stage 0p (BOS 0p) is a parameter detected on pulmonary function tests (PFTs) after lung transplantation to identify patients at risk to develop BOS. We performed a retrospective study on 442 patients who underwent allogeneic stem cell transplant from 2007 to 2011 to evaluate whether development of BOS 0p is a risk factor in this population for BOS. Patients who met criteria for BOS 0p were significantly more likely to develop BOS (hazard ratio [HR], 3.22; P < .001). BOS 0p was significantly associated with a history of lung disease pre-transplant (HR, 2.48; P = .001) and chronic graft-versus-host disease (GVHD) outside the lung post-transplant (HR, 23; P < .001). Finally, BOS 0p criteria were adequately sensitive in predicting BOS (85%), with a high negative predictive value (98%). Our findings suggest a routine PFT screening strategy with the intent of detecting BOS 0p, especially among patients with prior lung disease and who developed chronic GVHD, could suitably identify an at-risk population for the development of BOS. 2015 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1127 / 1144
页数:18
相关论文
共 35 条
[1]  
Abramson Joseph H, 2011, Epidemiol Perspect Innov, V8, P1, DOI 10.1186/1742-5573-8-1
[2]   Human leukocyte antigen-A, -B, and-DRB1 allele and haplotype frequencies in the Mozambican population: A blood donor-based population study [J].
Assane, Antonio A. A. ;
Fabricio-Silva, Gustavo M. ;
Cardoso-Oliveira, Juliana ;
Mabunda, Nedio E. J. ;
Sousa, Amina M. ;
Jani, Ilesh V. ;
Ferreira, Orlando C., Jr. ;
Porto, Luis C. M. S. .
HUMAN IMMUNOLOGY, 2010, 71 (10) :1027-1032
[3]   IMPACT OF RACIAL GENETIC-POLYMORPHISM ON THE PROBABILITY OF FINDING AN HLA-MATCHED DONOR [J].
BEATTY, PG ;
MORI, M ;
MILFORD, E .
TRANSPLANTATION, 1995, 60 (08) :778-783
[4]  
Brasil. Ministerio da Saude. Instituto Nacional de Cancer, REDOME REG NAC DOAD
[5]   Assessment of the Relationship between Self-Declared Ethnicity, Mitochondrial Haplogroups and Genomic Ancestry in Brazilian Individuals [J].
Cardena, Mari M. S. G. ;
Ribeiro-dos-Santos, Andrea ;
Santos, Sidney ;
Mansur, Alfredo J. ;
Pereira, Alexandre C. ;
Fridman, Cintia .
PLOS ONE, 2013, 8 (04)
[6]   Evaluation of computational methods for the reconstruction of HLA haplotypes [J].
Castelli, E. C. ;
Mendes-Junior, C. T. ;
Veiga-Castelli, L. C. ;
Pereira, N. F. ;
Petzl-Erler, M. L. ;
Donadi, E. A. .
TISSUE ANTIGENS, 2010, 76 (06) :459-466
[7]   Association of Genetic Variants with Self-Assessed Color Categories in Brazilians [J].
Durso, Danielle Fernandes ;
Bydlowski, Sergio Paulo ;
Hutz, Mara Helena ;
Suarez-Kurtz, Guilherme ;
Magalhaes, Tiago R. ;
Junho Pena, Sergio Danilo .
PLOS ONE, 2014, 9 (01)
[8]   Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows [J].
Excoffier, Laurent ;
Lischer, Heidi E. L. .
MOLECULAR ECOLOGY RESOURCES, 2010, 10 (03) :564-567
[9]  
Flores M, 1996, HIST DO RIO GRANDE D
[10]   Allele frequency net: a database and online repository for immune gene frequencies in worldwide populations [J].
Gonzalez-Galarza, Faviel F. ;
Christmas, Stephen ;
Middleton, Derek ;
Jones, Andrew R. .
NUCLEIC ACIDS RESEARCH, 2011, 39 :D913-D919