Allogeneic hematopoietic stem cell transplantation in infants is associated with significant morbidity and mortality
Christina Oikonomopoulou1, Anna Paisiou1, Eleni-Dikaia Ioannidou1
1Stem Cell Transplant Unit, Agia Sofia Children's Hospital, Athens, Greece.
Insights
Hematopoietic stem cell transplantation (HSCT) in infants leads to significant mortality and morbidity. Infants face higher risks of toxicity, infection, and graft-versus-host disease (GvHD) due to organ immaturity and immune deficiencies.
Area of Science:
- Pediatric Hematology
- Transplantation Immunology
- Oncology
Background:
- Infants undergo hematopoietic stem cell transplantation (HSCT) for various malignant and non-malignant conditions.
- Limited data exist on outcomes and complications specific to infants undergoing HSCT.
- This study addresses the impact of infancy on HSCT outcomes, toxicity, and complications.
Purpose of the Study:
- To evaluate the outcomes of HSCT in infants.
- To assess transplantation-related mortality (TRM) and complications in this age group.
- To identify factors influencing HSCT success in infants.
Main Methods:
- Retrospective analysis of 55 infants undergoing HSCT.
- Data collected from May 1997 to February 2020.
- Focus on overall survival (OS) and cumulative incidence (CI) of TRM and complications.
Main Results:
- Overall survival (OS) probability was 61%.
- Cumulative incidence (CI) of TRM at 1 year was 30%.
- High CI for graft failure (18%), acute graft-versus-host disease (GvHD) (44%), and infections (39%) were observed.
Conclusions:
- Infancy is associated with significant mortality and morbidity after HSCT.
- Organ immaturity and immune deficiencies increase risks of toxicity and infection in infants.
- Graft-versus-host disease (GvHD) exacerbates infection risk; chemotherapy pharmacokinetics remain a challenge.
Background:
Infants are subjected to hematopoietic stem cell transplantation (HSCT) due to malignant and non-malignant diseases. However, specific data concerning the outcome and transplantation-related complications in infants, as a separate age group, are limited. Our aim was to evaluate the impact of infancy on the outcome, toxicity, and complications after HSCT.
Methods:
We retrospectively analyzed data of 55 infants that underwent HSCT in our unit from May 1997 until February 2020, emphasizing on the probability of overall survival (OS) and the cumulative incidence (CI) of transplantation-related mortality (TRM) and complications.
Results:
We report a probability of OS of 61%, a CI of TRM at day 100 and 365 post transplantation of 22% and 30%, respectively, and additionally a CI of graft failure, acute graft-versus-host disease (GvHD), and infectious complications, 18%, 44%, and 39%, respectively. No statistically significant association was detected between the above mentioned parameters and diagnosis, the use of myeloablative or non-myeloablative/reduced toxicity conditioning regimens or the type of donor.
Conclusions:
We conclude that HSCT in infancy is associated with significant mortality and morbidity. This is possibly attributed to endogenous, age-related factors. More specifically, infants may be at a higher risk of toxicities due to the immaturity of developing vital organs and the deficiency of the newly adopted immune system that predisposes them to infectious complications. The development of GvHD further augments the danger of infections, in a potential vice-versa relationship. Moreover, there are few data on pharmacokinetics of chemotherapy agents, making safe and efficacious drug administration hard.
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