Clinical laboratory markers of inflammation as determinants of chronic graft-versus-host disease activity and NIH global severity

被引:48
作者
Grkovic, L. [1 ,2 ]
Baird, K. [3 ]
Steinberg, S. M. [4 ]
Williams, K. M. [1 ]
Pulanic, D. [2 ]
Cowen, E. W. [5 ]
Mitchell, S. A. [6 ]
Hakim, F. T. [1 ]
Martires, K. J. [5 ]
Avila, D. N. [1 ]
Taylor, T. N. [1 ]
Salit, R. B. [1 ]
Rowley, S. D. [7 ]
Zhang, D. [4 ]
Fowler, D. H. [1 ]
Bishop, M. R. [1 ]
Gress, R. E. [1 ]
Pavletic, S. Z. [1 ]
机构
[1] NCI, Graft Versus Host & Autoimmun Unit, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA
[2] Clin Hosp Ctr Zagreb, Dept Internal Med, Div Hematol, Zagreb, Croatia
[3] NCI, Pediat Oncol Branch, NIH, Bethesda, MD 20892 USA
[4] NCI, Biostat & Data Management Sect, Off Clin Director, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
[5] NCI, Dermatol Branch, NIH, Bethesda, MD 20892 USA
[6] NCI, Div Canc Control & Populat Sci, NIH, Bethesda, MD 20892 USA
[7] Hackensack Univ, Med Ctr, John Theurer Canc Ctr, Hackensack, NJ USA
基金
美国国家卫生研究院;
关键词
chronic graft-versus-host disease; inflammation; activity; CRP; platelets; C-REACTIVE PROTEIN; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; CONSENSUS DEVELOPMENT PROJECT; WORKING GROUP-REPORT; NEPHROTIC SYNDROME; RHEUMATOID-ARTHRITIS; SYSTEMIC-SCLEROSIS; CHRONIC GVHD; INTERLEUKIN-6;
D O I
10.1038/leu.2011.254
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic graft-versus-host disease (cGVHD) remains a major cause of non-relapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Currently there are no accepted measures of cGVHD activity to aid in clinical management and disease staging. We analyzed clinical markers of inflammation in the sera of patients with established cGVHD and correlated those with definitions of disease activity. In all, 189 adults with cGVHD (33% moderate and 66% severe according to National Institutes of Health (NIH) global scoring) were consecutively enrolled onto a cross-sectional prospective cGVHD natural history study. At the time of evaluation, 80% were receiving systemic immunosuppression and failed a median of four prior systemic therapies (PST) for their cGVHD. Lower albumin (P < 0.0001), higher C-reactive protein (P = 0.043), higher platelets (P = 0.030) and higher number of PST (P < 0.0001) were associated with active disease defined as clinician's intention to intensify or alter systemic therapy due to the lack of response. Higher platelet count (P = 0.021) and higher number of PST (P < 0.0001) were associated with more severe diseased defined by NIH global score. This study identified common laboratory indicators of inflammation that can serve as markers of cGVHD activity and severity. Leukemia (2012) 26, 633-643; doi:10.1038/leu.2011.254; published online 18 October 2011
引用
收藏
页码:633 / 643
页数:11
相关论文
共 52 条
[1]   Clinical grading in chronic graft-versus-host disease: Is it time for change? [J].
Akpek, G .
LEUKEMIA & LYMPHOMA, 2002, 43 (06) :1211-1220
[2]  
[Anonymous], NONPARAMETRIC STAT M
[3]   TRANSFORMING GROWTH-FACTOR-BETA AS A PREDICTOR OF LIVER AND LUNG FIBROSIS AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOR ADVANCED BREAST-CANCER [J].
ANSCHER, MS ;
PETERS, WP ;
REISENBICHLER, H ;
PETROS, WP ;
JIRTLE, RL .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (22) :1592-1598
[4]   CYTOKINE DYSREGULATION IN CHRONIC GRAFT-VERSUS-HOST DISEASE [J].
BARAK, V ;
LEVISCHAFFER, F ;
NISMAN, B ;
NAGLER, A .
LEUKEMIA & LYMPHOMA, 1995, 17 (1-2) :169-173
[5]   Feasibility of NIH consensus criteria for chronic graft-versus-host disease [J].
Cho, B-S ;
Min, C-K ;
Eom, K-S ;
Kim, Y-J ;
Kim, H-J ;
Lee, S. ;
Cho, S-G ;
Kim, D-W ;
Lee, J-W ;
Min, W-S ;
Kim, C-C .
LEUKEMIA, 2009, 23 (01) :78-84
[6]   Nephrotic syndrome after allogeneic hematopoietic stem cell transplantation as a late complication of chronic graft-versus-host disease [J].
Colombo, AA ;
Rusconi, C ;
Esposito, C ;
Bernasconi, P ;
Caldera, D ;
Lazzarino, M ;
Alessandrino, EP .
TRANSPLANTATION, 2006, 81 (08) :1087-1092
[7]   National Institutes of Health consensus development project on criteria for clinical trials in chronic graft-versus-host disease: I. Diagnosis and staging working group report [J].
Filipovich, AH ;
Weisdorf, D ;
Pavletic, S ;
Socie, G ;
Wingard, JR ;
Lee, SJ ;
Martin, P ;
Chien, J ;
Przepiorka, D ;
Couriel, D ;
Cowen, EW ;
Dinndorf, P ;
Farrell, A ;
Hartzman, R ;
Henslee-Downey, J ;
Jacobsohn, D ;
McDonald, G ;
Mittleman, B ;
Rizzo, JD ;
Robinson, M ;
Schubert, M ;
Schultz, K ;
Shulman, H ;
Turner, M ;
Vogelsang, G ;
Flowers, MED .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (12) :945-956
[8]   Treatment Change as a Predictor of Outcome among Patients with Classic Chronic Graft-versus-Host Disease [J].
Flowers, Mary E. D. ;
Storer, Barry ;
Carpenter, Paul ;
Rezvoni, Andrew R. ;
Vigorito, Afonso C. ;
Campregher, Paulo V. ;
Moravec, Carina ;
Kiem, Hans-Peter ;
Fero, Matthew ;
Georges, George ;
Warren, Edus ;
Lee, Stephanie ;
Sanders, Jean E. ;
Appelbaum, Fred ;
Martin, Paul J. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2008, 14 (12) :1380-1384
[9]  
Flowers MED, 2009, CHRONIC GRAFT VERSUS HOST DISEASE: INTERDISCIPLINARY MANAGEMENT, P56, DOI 10.1017/CBO9780511576751.007
[10]   Biomarkers in newly diagnosed pediatric-extensive chronic graft-versus-host disease: a report from the Children's Oncology Group [J].
Fujii, Hisaki ;
Cuvelier, Geoff ;
She, Kevin ;
Aslanian, Soudabeh ;
Shimizu, Hiromi ;
Kariminia, Amina ;
Krailo, Mark ;
Chen, Zhengjia ;
McMaster, Rob ;
Bergman, Axel ;
Goldman, Frederick ;
Grupp, Stephen A. ;
Wall, Donna A. ;
Gilman, Andrew L. ;
Schultz, Kirk R. .
BLOOD, 2008, 111 (06) :3276-3285