The impact of pre-transplantation diabetes and obesity on acute graft-versus-host disease, relapse and death after allogeneic hematopoietic cell transplantation: a study from the EBMT Transplant Complications Working Party - Scorecard - MDSpire
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The impact of pre-transplantation diabetes and obesity on acute graft-versus-host disease, relapse and death after allogeneic hematopoietic cell transplantation: a study from the EBMT Transplant Complications Working Party
Clinical Scorecard: Influence of Pre-Transplant Diabetes and Obesity on Acute Graft-Versus-Host Disease, Relapse Rates, and Mortality Following Allogeneic Hematopoietic Cell Transplantation: Insights from the EBMT Transplant Complications Working Party
At a Glance
Category
Detail
Condition
Impact of pre-transplant diabetes and obesity on acute graft-versus-host disease (GvHD), relapse, and mortality after allogeneic hematopoietic cell transplantation (HCT)
Key Mechanisms
Metabolic changes from obesity and diabetes induce chronic low-grade inflammation and immune modulation, potentially increasing pro-inflammatory cytokines and dysregulating gut microbiome and immunological signaling
Target Population
Adult patients undergoing first allogeneic HCT for hematological malignancies
Care Setting
Allogeneic hematopoietic cell transplantation centers participating in the EBMT registry
Key Highlights
Pre-transplant obesity (BMI ≥ 30 kg/m2) and diabetes (requiring pharmacologic treatment) are associated with metabolic and inflammatory changes that may influence acute GvHD severity.
Registry studies show inconsistent associations between obesity or diabetes and acute GvHD incidence, but obesity is more consistently linked to increased non-relapse mortality.
Recent EBMT data (2016–2020) provide updated insights on the prevalence and impact of pre-transplant diabetes and obesity on transplant outcomes in a large adult cohort.
Guideline-Based Recommendations
Diagnosis
Assess pre-transplant diabetes status using treatment requirements (insulin or oral hypoglycemics, excluding diet alone).
Calculate BMI from pre-transplant height and weight to identify obesity (BMI ≥ 30 kg/m2).
Grade acute GvHD according to Keystone criteria; classify chronic GvHD as limited or extensive per established criteria.
Management
Consider pre-transplant diabetes and obesity as comorbidities potentially influencing transplant outcomes.
Monitor and manage metabolic and inflammatory status pre- and post-transplant to potentially mitigate GvHD risk.
Use reduced intensity/non-myeloablative conditioning regimens increasingly in older or comorbid patients, including those with diabetes or obesity.
Monitoring & Follow-up
Monitor for acute GvHD development and grade post-transplant, especially in patients with pre-existing diabetes or obesity.
Track overall survival, relapse incidence, and non-relapse mortality with attention to comorbidity status.
Perform landmark analyses for survival after grade II–IV acute GvHD occurrence.
Risks
Pre-transplant obesity and diabetes may increase risk of non-relapse mortality.
Pre-transplant diabetes may be associated with higher GvHD-related mortality despite unclear impact on acute GvHD incidence.
Metabolic comorbidities can exacerbate inflammatory responses, potentially worsening transplant complications.
Patient & Prescribing Data
Adults undergoing first allogeneic HCT for hematological malignancies with documented pre-transplant diabetes or obesity
Prevalence of pre-transplant diabetes was 4.4% and obesity 3.9% (BMI ≥ 35 kg/m2) in the EBMT cohort; treatment regimens and donor types were adjusted for in outcome analyses to assess impact on GvHD and mortality
Clinical Best Practices
Incorporate comprehensive pre-transplant assessment of metabolic comorbidities including diabetes and obesity.
Use standardized criteria for GvHD diagnosis and grading to enable consistent outcome evaluation.
Adjust transplant conditioning intensity based on patient comorbidities to optimize outcomes.
Employ multivariable risk modeling including diabetes and obesity status to inform prognosis and patient counseling.
Ensure informed consent includes discussion of potential increased risks related to metabolic comorbidities.
by Lars Klingen Gjærde, Tapani Ruutu, Christophe Peczynski, William Boreland, Nicolaus Kröger, Didier Blaise, Thomas Schroeder, Régis Peffault de Latour, Tobias Gedde-Dahl, Aleksandr Kulagin, Henrik Sengeløv, Ibrahim Yakoub-Agha, Jürgen Finke, Matthias Eder, Grzegorz Basak, Ivan Moiseev, Hélène Schoemans, Christian Koenecke, Olaf Penack, Zinaida Perić