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Risk factors for hepatic veno-occlusive disease: a retrospective unicentric study in 116 children autografted after a
A Cacchione1, A LeMaitre, D Valteau Couanet
1Department of Pediatrics, Institut Gustave Roussy, Villejuif, France. antonellacacchione@katamail.com
Insights
Previous carboplatin therapy increases the risk of hepatic veno-occlusive disease (HVOD) in pediatric brain tumor patients undergoing autologous hematopoietic stem cell transplant (AHSCT) with a BU-thiotepa (BU-TTP) regimen. This finding aids in identifying high-risk patients.
Area of Science:
- Pediatric Hematology-Oncology
- Stem Cell Transplantation
- Clinical Research
Background:
- Hepatic veno-occlusive disease (HVOD) incidence is rising in pediatric patients receiving BU-thiotepa (BU-TTP) conditioning.
- Understanding risk factors for HVOD is crucial for improving transplant outcomes.
Purpose of the Study:
- To identify risk factors contributing to the increased incidence of HVOD.
- To analyze demographic, clinical, biological, and therapeutic parameters associated with HVOD.
Main Methods:
- Retrospective analysis of 116 pediatric patients treated with BU-TTP and AHSCT.
- Evaluation of risk factors using uni- and multivariate analyses.
- Diagnosis of HVOD based on McDonald's clinical criteria.
Main Results:
- HVOD was diagnosed in 31% of the studied pediatric patients.
- Previous carboplatin therapy (P=0.028) and etoposide (P=0.048) significantly correlated with increased HVOD risk.
- HVOD was associated with a higher risk of post-transplant death due to organ failure (P=0.029).
Conclusions:
- Prior carboplatin administration in conventional chemotherapy is a significant risk factor for developing HVOD.
- This risk is particularly relevant for brain tumor patients undergoing BU-TTP consolidation and AHSCT.
- Identifying these risk factors can inform preventative strategies and patient management.
Abstract:
At our Institute, during the last decade, the incidence of hepatic veno-occlusive disease (HVOD) appears to be on the increase among pediatric patients treated with BU-thiotepa (BU-TTP)-conditioning regimen. We thus performed a retrospective analysis to identify the risk factors for HVOD, which could explain such a change. In total, 116 patients treated at Institut Gustave Roussy, between May 1998 and December 2005 were eligible for this study having received BU-TTP as their first high-dose chemotherapy regimen, followed by autologous hematopoietic SCT (AHSCT). According to McDonald's clinical criteria, HVOD was diagnosed in 31% of these children. Demographic, clinical, biological and therapeutic parameters were evaluated in uni- and multivariate analyses that showed a significant correlation between previous carboplatin therapy and risk of developing post transplant HVOD (P=0.028). Comparable results were found for etoposide (P=0.048). In addition, a correlation between HVOD and risk of post transplant death was linked to its association with other types of organ failure (P=0.029). This study demonstrates that previous VPCARBO administration in conventional chemotherapy significantly increases the risk of HVOD among brain tumor patients later consolidated with BU-TTP followed by AHSCT.
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