Hypofractionated conformal radiotherapy for pediatric diffuse intrinsic pontine glioma (DIPG): a randomized

Mohamed S Zaghloul1, Eman Eldebawy1, Soha Ahmed1

  • 1Radiation Oncology Department, Children's Cancer Hospital, Egypt (CCHE) and National Cancer Institute, Cairo University, Egypt.

Insights

Hypofractionated radiotherapy for pediatric diffuse intrinsic pontine glioma (DIPG) showed similar survival outcomes to conventional radiotherapy. This approach reduces patient and healthcare burdens, though it did not meet non-inferiority criteria.

Area of Science:

  • Pediatric Oncology
  • Radiation Oncology
  • Neuro-oncology

Background:

  • Pediatric diffuse intrinsic pontine glioma (DIPG) has a poor prognosis despite various treatment strategies.
  • Optimizing radiotherapy is crucial for improving outcomes in pediatric DIPG.

Purpose of the Study:

  • To compare the efficacy and safety of hypofractionated radiotherapy (HF-RT) versus conventional radiotherapy (CF-RT) for pediatric DIPG.
  • To evaluate overall survival (OS) and progression-free survival (PFS) between the two radiotherapy fractionation schedules.

Main Methods:

  • A randomized trial involving 71 newly diagnosed pediatric DIPG patients.
  • Patients were assigned to either hypofractionated (39Gy/13 fractions/2.6 weeks) or conventional (54Gy/30 fractions/6 weeks) radiotherapy arms.
  • Outcomes assessed included OS, PFS, and treatment-related side effects.

Main Results:

  • Median OS was 7.8 months for HF-RT vs. 9.5 months for CF-RT; 1-year OS was 36.4% vs. 26.2%.
  • Median PFS was 6.6 months for HF-RT vs. 7.3 months for CF-RT; 1-year PFS was 22.5% vs. 17.9%.
  • No significant difference in immediate or delayed side effects was observed between the groups.

Conclusions:

  • Hypofractionated radiotherapy for pediatric DIPG offers a reduced treatment burden for patients and healthcare systems.
  • While survival results were comparable, HF-RT did not meet the predefined non-inferiority margin compared to conventional radiotherapy.
  • Further research may explore optimized hypofractionation schedules for DIPG treatment.
Abstract

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