Predictors of hematologic malignancy relapse in patients with advanced chronic graft-versus-host disease

被引:0
作者
Claire L. Ruben
Filip Pirsl
Seth M. Steinberg
Noa G. Holtzman
Laura Parsons-Wandell
Judy Baruffaldi
Lauren M. Curtis
Sandra A. Mitchell
Ana Zelic Kerep
Edward W. Cowen
Ann Berger
Galen O. Joe
Manuel B. Datiles
Jacqueline W. Mays
Steven Z. Pavletic
机构
[1] National Institutes of Health,Immune Deficiency Cellular Therapy Program, Center for Cancer Research, National Cancer Institute
[2] National Institutes of Health,Biostatistics and Data Management Section, National Cancer Institute
[3] National Institutes of Health,Outcomes Research Branch, Division of Cancer Control and Population Sciences, National Cancer Institute
[4] National Institutes of Health,Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases
[5] National Institutes of Health,Pain and Palliative Care Service, National Institutes of Health Clinical Center
[6] National Institutes of Health,Rehabilitation Medicine Department, National Institutes of Health Clinical Center
[7] National Institutes of Health,National Eye Institute
[8] National Institutes of Health,Oral Immunobiology Unit, National Institute of Dental and Craniofacial Research
来源
Bone Marrow Transplantation | 2021年 / 56卷
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摘要
Malignancy relapse remains a major barrier to treatment success in patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Chronic graft-versus-host disease (cGVHD) markedly reduces hematologic malignancy relapse risk, but relapses still occur in these patients. Patients (n = 275) with moderate or severe cGVHD were enrolled on the National Cancer Institute (NCI) prospective cross-sectional natural history study (NCT00092235). Subjects were median 36 months after allo-HSCT and were followed subsequently for malignancy relapse and survival. Seventeen patients experienced relapse. In a multivariable model including time-dependent influences on relapse, risk factors associated with increased risk of relapse included shorter time from transplant to cGVHD evaluation (HR 0.279, 95% CI 0.078–0.995) and lower number of prior lines of systemic immunosuppressive therapy for cGVHD (HR 0.260, 95% CI 0.094–0.719). In a model excluding time-dependent influences on relapse risk, lower number of prior lines of systemic immunosuppressive therapy for cGVHD (HR 0.288, 95% CI 0.103–0.804), lower C4 complement level (HR 0.346, 95% CI 0.129–0.923), and higher body mass index (HR 3.222, 95% CI 1.156–8.974), were all associated with increased relapse risk. Parameters indicating cGVHD severity and activity are associated with risk of malignancy relapse. Classical predictors of relapse after allo-HSCT do not seem to be prognostic.
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页码:1584 / 1592
页数:8
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