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Primary immunosuppressive TNI-based conditioning regimens in pediatric patients treated with haploidentical
Insights
A modified total nodal irradiation (TNI) conditioning regimen before haploidentical hematopoietic cell transplantation (HCT) in children showed good engraftment and long-term survival. Late toxicities were manageable, including growth issues and hormonal deficiencies.
Area of Science:
- Pediatric Hematology
- Oncology
- Radiation Oncology
Background:
- Haploidentical hematopoietic cell transplantation (HCT) offers an alternative for patients lacking matched donors.
- Total nodal irradiation (TNI) is a conditioning regimen used prior to HCT.
- Optimizing TNI regimens for pediatric HCT is crucial for improving outcomes.
Purpose of the Study:
- To evaluate the toxicity and efficacy of a modified total nodal irradiation (TNI)-based conditioning regimen.
- To assess outcomes in pediatric patients undergoing haploidentical HCT with this regimen.
Main Methods:
- Retrospective analysis of 7 pediatric patients (2 malignant, 5 non-malignant diseases).
- Patients received a single-dose 7 Gy TNI regimen with systemic agents before haploidentical HCT.
- Long-term follow-up data was collected and analyzed.
Main Results:
- Successful engraftment in 6/7 patients; one required reconditioning.
- Event-free survival (EFS) of 71.4% and overall survival (OS) of 85.7% after a median follow-up of 103.5 months.
- Late toxicities included manageable hormonal deficiencies (3/5), growth failure (2/5 height, 1/5 weight), and acceptable lung function decline (FEV1 71%, VC 78%). No secondary malignancies were reported.
Conclusions:
- A single-dose 7 Gy TNI-based conditioning regimen is effective for pediatric haploidentical HCT.
- The regimen supports sustained engraftment and long-term survival with a tolerable toxicity profile.
- Late toxicities are manageable, supporting the use of this regimen in pediatric HCT.
Purpose:
This retrospective analysis aims to address the toxicity and efficacy of a modified total nodal irradiation (TNI)-based conditioning regimen before haploidentical hematopoietic cell transplantation (HCT) in pediatric patients.
Materials And Methods:
Patient data including long-term follow-up were evaluated of 7 pediatric patients with malignant (n = 2) and non-malignant diseases (n = 5) who were treated by a primary TNI-based conditioning regimen. TNI was performed using anterior/posterior opposing fields. All patients received 7 Gy single-dose TNI combined with systemic agents followed by an infusion of peripheral blood stem cells (n = 7). All children had haploidentical family donors.
Results:
Engraftment was reached in 6/7 children after a median time of 9.5 days; 1 child had primary graft failure but was successfully reconditioned shortly thereafter. After an average follow-up time of 103.5 months (range 8.8-138.5 months), event-free (EFS) and overall survival (OS) rates were 71.4% and 85.7%, respectively. One child with a non-malignant disease died 8.8 months after transplantation due to a relapse and a multiple organ failure. Follow-up data was available for 5/6 long-term survivors with a median follow-up (FU) of 106.2 months (range 54.5-138.5 months). Hypothyroidism and deficiency of sexual hormones was present in 3/5 patients each. Mean forced expiratory volume in 1 s (FEV1) after TNI was 71%; mean vital capacity (VC) was 78%. Growth failure (< 10th percentile) occurred in 2/5 patients (height) and 1/5 patient (weight). No secondary malignancies were reported.
Conclusion:
In this group of patients, a primary single-dose 7 Gy TNI-based conditioning regimen before HCT in pediatric patients allowed sustained engraftment combined with a tolerable toxicity profile leading to long-term OS/EFS. Late toxicity after a median FU of over 9 years includes growth failure, manageable hormonal deficiencies, and acceptable decrease in lung function.
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