The Chronic Graft-versus-Host Disease Failure-Free Survival (cGVHD-FFS) Index

被引:6
作者
Pidala, Joseph A. [1 ]
Hamilton, Betty K. [2 ]
Martin, Paul J. [3 ,4 ]
Onstad, Lynn [3 ]
Storer, Barry E. [3 ]
Palmer, Jeanne [5 ]
Alousi, Amin [6 ]
Cutler, Corey [7 ]
Jagasia, Madan H. [8 ]
Chen, George L. [9 ]
Arora, Mukta [10 ]
Flowers, Mary E. [3 ,4 ]
Lee, Stephanie J. [3 ,4 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[2] Cleveland Clin, Taussig Canc Inst, Dept Hematol & Med Oncol, Blood & Marrow Transplantat, Cleveland, OH 44106 USA
[3] Fred Hutchinson Canc Ctr, Clin Res Div, Seattle, WA USA
[4] Univ Washington, Dept Med, Seattle, WA USA
[5] Mayo Clin, Phoenix, AZ USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplant & Cellular Therapy, Houston, TX 77030 USA
[7] Dana Farber Canc Inst, Div Hematol Malignancies, Dept Med Oncol, Boston, MA 02115 USA
[8] Vanderbilt Ingram Canc Ctr, Div Hematol Oncol, Nashville, TN USA
[9] Roswell Pk Canc Inst, Dept Med, Buffalo, NY USA
[10] Univ Minnesota, Hematol Oncol & Transplantat, Minneapolis, MN USA
关键词
Chronic graft-versus-host disease; Failure-free survival; Prognostic model; CONSENSUS DEVELOPMENT PROJECT; MEASURING THERAPEUTIC RESPONSE; CLINICAL-TRIALS; CRITERIA; DIAGNOSIS;
D O I
10.1016/j.bbmt.2019.07.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In clinical trials of chronic graft-versus-host disease (cGVHD), the need to start a new systemic treatment is considered a treatment failure. A composite endpoint called "failure-free survival"" (FFS), where events are initiation of a new systemic cGVHD treatment, recurrent malignancy, and death, has been suggested as a possible long-term indicator of success. The goal of the current study was to identify changes in cGVHD manifestations from baseline to 6 months that could accurately predict subsequent longer-term FFS, thereby making it possible to assess outcomes earlier than would otherwise be possible. We used data from 2 prospective, multicenter, observational studies to develop the cGVHD-FFS index. The cGVHD-FFS index was calculated at 6 months, a typical time point for assessment of the primary endpoint of phase II cGVHD trials. Subsequent FFS was only 45% within the next 2 years. We found that changes in the scores for the eyes, joint/fascia, and mouth ulcers from baseline to 6 months were associated with subsequent FFS, but the prognostic accuracy of these changes was not adequate for use in trials. Biomarker studies might help to identify criteria that improve prediction of long-term clinical outcomes in patients with cGVHD. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc..
引用
收藏
页码:2468 / 2473
页数:6
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