ESTRO ACROP and SIOPE recommendations for myeloablative Total Body Irradiation in children

Bianca A W Hoeben1, Montserrat Pazos2, Enrica Seravalli3

  • 1Dept. of Radiation Oncology, University Medical Center Utrecht, The Netherlands; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Insights

Standardized recommendations for myeloablative Total Body Irradiation (TBI) in children undergoing hematopoietic stem cell transplantation (HSCT) are crucial. These guidelines aim to improve outcomes and reduce late adverse effects in pediatric patients with high-risk leukemia.

Area of Science:

  • Pediatric Oncology
  • Radiation Oncology
  • Hematopoietic Stem Cell Transplantation

Background:

  • Myeloablative Total Body Irradiation (TBI) is a key conditioning regimen for allogeneic HSCT, particularly in pediatric high-risk acute lymphoblastic leukemia (ALL).
  • Current TBI practices exhibit significant heterogeneity and institutional variability.
  • TBI is associated with substantial late adverse effects, necessitating standardization to optimize the benefit-to-toxicity ratio in children.

Purpose of the Study:

  • To develop consensus recommendations for myeloablative TBI techniques and toxicity management in pediatric HSCT.
  • To provide guidance for standardizing TBI practices across institutions.
  • To improve treatment outcomes and reduce long-term toxicities in children undergoing HSCT.

Main Methods:

  • A literature search and evaluation of myeloablative TBI techniques and toxicities in pediatric populations were conducted.
  • Expert consensus was established through bimonthly virtual meetings by the European Society for Paediatric Oncology (SIOPE) Radiotherapy TBI Working Group and ESTRO experts.
  • Evidence levels from retrospective studies (III-IV) were considered.

Main Results:

  • Myeloablative TBI is primarily used for high-risk ALL and relapsed hematologic malignancies in children, with caution advised for those younger than 3-4 years due to toxicity risks.
  • Recommended TBI dose is 12-14.4 Gy in 1.6-2 Gy fractions b.i.d., with specific dose reductions for organs at risk: lungs (<8 Gy), kidneys (≤10 Gy), and lenses (<12 Gy) at dose rates ≥6 cGy/min.
  • Advanced techniques like TomoTherapy, VMAT TBI, and Total Marrow (and/or Lymphoid) Irradiation show promise for improved dose homogeneity and organ sparing and warrant further study.

Conclusions:

  • ESTRO ACROP SIOPE have established expert consensus recommendations for myeloablative TBI in pediatric HSCT.
  • These recommendations cover both conventional and advanced conformal TBI techniques.
  • The guidelines aim to standardize TBI practices and improve the management of toxicities in children undergoing HSCT.
Abstract