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

被引:2902
作者
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
机构
[1] Univ Cincinnati, Childrens Hosp, Div Hematol Oncol, Cincinnati, OH 45229 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] Natl Canc Inst, NIH, Bethesda, MD USA
[4] Hop St Louis, Paris, France
[5] Univ Florida, Shands Cans Ctr, Gainesville, FL USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] Univ Washington, Sch Med, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[8] Univ Tennessee, Memphis, TN 38163 USA
[9] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[10] US FDA, Rockville, MD 20857 USA
[11] Naval Med Res Ctr, CW Bill Young Dept Def Marrow Donor Recruitment &, Silver Spring, MD USA
[12] NHLBI, NIH, Bethesda, MD 20892 USA
[13] Northwestern Univ, Childrens Mem Hosp, Sch Med, Chicago, IL 60614 USA
[14] NIAMSD, NIH, Bethesda, MD 20892 USA
[15] Med Coll Wisconsin, Ctr Int Blood & Marrow Transplant Res, Milwaukee, WI 53226 USA
[16] NEI, NIH, Bethesda, MD 20892 USA
[17] Univ British Columbia, British Columbia Childrens Hosp, Vancouver, BC V5Z 1M9, Canada
[18] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
chronic graft-versus-host disease; allogeneic hematopoietic cell transplantation; consensus; diagnosis; staging;
D O I
10.1016/j.bbmt.2005.09.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This consensus document is intended to serve 3 functions. First, it standardizes the criteria for diagnosis of chronic graft-versus-host disease (GVHD). Second, it proposes a new clinical scoring system (0-3) that describes the extent and severity of chronic GVHD for each organ or site at any given time, taking functional impact into account. Third, it proposes new guidelines for global assessment of chronic GVHD severity that are based on the number of organs or sites involved and the degree of involvement in affected organs (mild, moderate, or severe). Diagnosis of chronic GVHD requires the presence of at least 1 diagnostic clinical sign of chronic GVHD (e.g., poikiloderma or esophageal web) or the presence of at least I distinctive manifestation (e.g., keratoconjunctivitis sicca) confirmed by pertinent biopsy or other relevant tests (e.g., Schirmer test) in the same or another organ. Furthermore, other possible diagnoses for clinical symptoms must be excluded. No time limit is set for the diagnosis of chronic GVHD. The Working Group recognized 2 main categories of GVHD, each with 2 subcategories. The acute GVHD category is defined in the absence of diagnostic or distinctive features of chronic GVHD and includes (1) classic acute GVHD occurring within 100 days after transplantation and (2) persistent, recurrent, or late acute GVHD (features of acute GVHD occurring beyond 100 days, often during withdrawal of immune suppression). The broad category of chronic GVHD includes (1) classic chronic GVHD (without features or characteristics of acute GVHD) and (2) an overlap syndrome in which diagnostic or distinctive features of chronic GVHD and acute GVHD appear together. It is currently recommended that systemic therapy he considered for patients who meet criteria for chronic GVHD of moderate to severe global severity. (c) 2005 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:945 / 956
页数:12
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