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Updated: Jul 15, 2026

Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease
Published on: March 17, 2020
The incidence and risk factors for chronic graft-versus-host-disease
Jerzy Wojnar1, Sebastian Giebel, Aleksandra Holowiecka-Goral
1Dept. of Haematology and Bone Marrow Transplantation, Silesian Medical University, Katowice, Poland. klinhem@slam.katowice.pl
Insights
Chronic graft-versus-host-disease (cGVHD) affects nearly half of patients post-allogeneic hematopoietic cell transplantation (alloHCT). Key risk factors include prior acute GVHD, older recipient age, and unrelated donors, guiding personalized treatment strategies.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Chronic graft-versus-host-disease (cGVHD) significantly impacts survival and quality of life following allogeneic hematopoietic cell transplantation (alloHCT).
- Understanding the incidence and risk factors for cGVHD is crucial for improving patient outcomes.
Purpose of the Study:
- To evaluate the incidence of cGVHD after alloHCT.
- To identify recipient, donor, and procedure-related risk factors associated with cGVHD development.
Main Methods:
- Analysis of 255 patients undergoing myeloablative alloHCT between 1992-2003.
- Inclusion of patients who survived without disease progression.
- Multivariate analysis to determine risk factors for overall and extensive cGVHD.
Main Results:
- The cumulative incidence of overall and extensive cGVHD was 48% and 22%, respectively.
- Risk factors for cGVHD included preceding acute GVHD, recipient age ≥40 years, unrelated donor hematopoietic cell transplantation (URD-HCT), chronic myeloid leukemia (CML) or myelodysplastic syndrome diagnosis, and CD3 cell dose.
- Factors for extensive cGVHD included preceding acute GVHD, URD-HCT, CD3 cell dose >100 x 10^6/kg, and steroid use for acute GVHD prophylaxis.
Conclusions:
- Multiple factors related to the recipient, donor, and transplant procedure influence the risk of cGVHD.
- Individualized treatment approaches and modification of identified risk factors may enhance patient outcomes after alloHCT.
Objectives:
Chronic graft-versus-host-disease (cGVHD) deteriorates survival and quality of life after allogeneic hematopoietic cell transplantation (alloHCT). We evaluated the incidence and risk factors for this complication based on a single-center experience.
Methods:
255 consecutive patients, aged 29 (10-56) years, who survived without disease progression after alloHCT performed between 1992-2003 were included in the analysis. The preparative regimen was myeloablative, donors were either related (n=177) or unrelated volunteers (URD-HCT) (n=78).
Results:
Cumulative incidence of the overall and extensive cGVHD equaled 48% and 22%, respectively. In a multivariate analysis the following factors were associated with increased risk of cGVHD: preceding grade II-IV acute GVHD, recipient age > or =40 years, URD-HCT, the diagnosis of chronic myeloid leukemia (CML) or myelodysplastic syndrome, and CD3 cell dose 50 x 10(6)/kg. Similar factors, excluding recipient age contributed to increased risk of extensive cGVHD, however, the cut-point for CD3 cell dose was 100 x l0(6)/kg and the use of steroids for acute GVHD prophylaxis was found an additional risk factor. In a CML subgroup the risk of cGVHD was increased for patients previously treated with interferon.
Conclusions:
Various recipient-, donor-, and procedure-related factors are related to the risk of cGVHD. Individualized treatment and modification of risk factors may contribute to improved outcome.
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