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Updated: Jun 9, 2025

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Published on: March 17, 2020
Multidisciplinary Management of Morbidities Associated with Chronic Graft-Versus-Host Disease
Rahul Shah1,2, Danielle Murphy3, Melissa Logue3
1Division of Cancer Medicine The University of Texas MD Anderson Cancer Center.
Insights
Chronic graft-versus-host disease (cGVHD) significantly impacts HSCT survivors, causing organ damage and affecting quality of life. This review details cGVHD
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Chronic graft-versus-host disease (cGVHD) is a frequent complication of allogeneic hematopoietic stem cell transplantation (HSCT).
- It is a leading cause of non-relapse mortality and significantly impacts survivors' quality of life.
- Traditional treatment relies on systemic immunosuppression, primarily glucocorticoids, which contribute to iatrogenic morbidity.
Purpose of the Study:
- To review the multifaceted impacts of cGVHD beyond established criteria.
- To highlight iatrogenic complications from long-term immunosuppression.
- To outline a framework for comprehensive multidisciplinary management of cGVHD.
Main Methods:
- Literature review of cGVHD impacts and management strategies.
- Analysis of traditional and emerging treatments for steroid-refractory cGVHD.
- Discussion of systemic effects and quality-of-life implications.
Main Results:
- cGVHD affects nearly all organs and extends beyond NIH Consensus Criteria.
- Emerging oral agents (ibrutinib, ruxolitinib, belumosudil) offer new treatment options for steroid-refractory cGVHD.
- Long-term immunosuppression leads to significant iatrogenic complications.
Conclusions:
- cGVHD poses a substantial burden on HSCT survivors, affecting multiple organ systems and overall health.
- Comprehensive management must address both cGVHD and its treatment-related toxicities.
- A multidisciplinary approach is crucial for optimizing patient outcomes and quality of life.
Abstract:
Chronic graft-versus-host disease (cGVHD) represents a common long-term complication after allogeneic hematopoietic stem cell transplantation (HSCT). It imposes a significant morbidity burden and is the leading cause of non-relapse mortality among long-term HSCT survivors. cGVHD can manifest in nearly any organ, severely affecting the quality of life of a transplant survivor. While the mainstay of treatment has remained systemic immunosuppression with glucocorticoids, progress has been made within the last few years with approvals of three oral agents to treat steroid-refractory cGVHD: ibrutinib, ruxolitinib, and belumosudil. Iatrogenesis contributes a significant portion of the morbidity experienced by patients with cGVHD, primarily from glucocorticoids. This review highlights the myriad impacts of cGVHD, including and beyond the traditional organ systems captured by the National Institutes of Health Consensus Criteria, including iatrogenic complications of long-term immunosuppression. It presents the implications of cGVHD and its treatment on cardiovascular and metabolic health, bone density, endocrine function, sexual health, and ocular and pulmonary disease and outlines a framework around the comprehensive multidisciplinary approach for its evaluation and management.
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