Ocular Chronic Graft-versus-Host Disease and Its Relation to Other Organ Manifestations and Outcomes after Allogeneic Hematopoietic Cell Transplantation

被引:5
|
作者
Jeppesen, Helene [1 ,6 ]
Gjaerde, Lars Klingen [2 ]
Lindegaard, Jens [3 ]
Julian, Hanne Olsen [4 ]
Heegaard, Steffen [1 ,5 ]
Sengelov, Henrik [2 ]
机构
[1] Copenhagen Univ Hosp, Dept Ophthalmol, Rigshosp, Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Dept Haematol, Rigshosp, Copenhagen, Denmark
[3] Copenhagen Eye Infirm, Copenhagen, Denmark
[4] Molholm Private Hosp, Dept Ophthalmol, Vejle, Denmark
[5] Univ Copenhagen, Dept Pathol, Eye Pathol Sect, Copenhagen, Denmark
[6] Copenhagen Univ Hosp, Dept Ophthalmol, Rigshosp, Blegdamsvej 9, DK-2100 Copenhagen, Denmark
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2022年 / 28卷 / 12期
关键词
Ocular graft-versus-host disease; Chronic graft-versus-host; disease; Ectoderm; Hematopoietic stem cell; transplantation; Bone marrow transplantation; Dry eye; Keratoconjunctivitis sicca; Ocular surface disease; Germ layer; CONSENSUS DEVELOPMENT PROJECT; BONE-MARROW-TRANSPLANTATION; DRY EYE SYNDROME; CLINICAL-TRIALS; RISK-FACTORS; CRITERIA; GVHD; DIAGNOSIS; ANTIGENS; TARGET;
D O I
10.1016/j.jtct.2022.08.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ocular chronic graft-versus-host disease (cGVHD) has been shown to significantly reduce quality of life after allo-geneic hematopoietic stem cell transplantation (HSCT). To learn more about this bothersome complication, we investigated the relationship between ocular cGVHD and cGVHD in other organs. We also investigated the associ-ations between ocular cGVHD and overall mortality, nonrelapse mortality, and relapse. In this single-center study, we retrospectively included 1221 consecutive adults who underwent allogeneic HSCT. Patients were examined by an ophthalmologist before HSCT and annually for 5 years after HSCT or more frequently if needed. Patients with dry eye disease before HSCT were excluded. The International Chronic Ocular GVHD Consensus Group criteria were used to diagnose ocular cGVHD. Nonocular cGVHD was diagnosed using the National Institute of Health cri -teria. Out of 601 patients who were diagnosed with systemic cGVHD during follow-up, 279 (46%) developed ocu-lar cGVHD. Ocular cGVHD was more frequent in patients with extensive cGVHD compared to those with limited cGVHD (50% versus 29%; P < .0001) and was associated with cGVHD in skin (P < .0001), oral cavity (P = .0024), genitals (P = .0023), and nails (P = .031). The frequency of ocular cGVHD was higher in patients with skin cGVHD with sclerosis compared to those with skin cGVHD without sclerosis (70% versus 49%; P = .0003). In an adjusted time-dependent Cox model, ocular cGVHD was associated with increased nonrelapse mortality (adjusted hazard ratio [HR], 1.61; 95% confidence interval [CI], 1.17 to 2.21; P = .003), whereas there was no support for an associa-tion with relapse (adjusted HR, .85; 95% CI, .53 to 1.36; P = .5). Special attention to eye problems after HSCT should be given to patients with extensive cGVHD and cGVHD in ectodermal-derived organs (skin, mouth, nails, and gen-itals). Furthermore, ocular cGVHD is a potential risk factor for nonrelapse mortality.(c) 2022 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:833.e1 / 833.e7
页数:7
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