Re-irradiation in progressive diffuse infiltrative pontine glioma in children and young adults.

in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] by Alper Kahvecioglu, Mustafa Cengiz, Guzide Burca Aydin, Mustafa Tezer Kutluk, Gokcen Coban Cifci, Gozde Yazici

TLDR

  • Re-irradiation after initial radiotherapy provides a 3-month OS benefit and clinical improvement for children and young adults with progressive DIPG, with minimal toxicity.

Abstract

This study aims to assess oncological outcomes in children and young adults with diffuse infiltrative pontine glioma (DIPG) who have progressed after initial radiotherapy (RT), with an emphasis on the role of re-irradiation. Data from 33 patients aged 25 years or younger with progressive disease after initial RT were retrospectively analyzed. The median age at diagnosis was 8 years (range 4-24 years), and the median initial RT dose was 54 Gy (range 39-54 Gy). The median time between initial RT and progression was 8 months (range 3-40 months). In addition to systemic therapy, 15 patients (46%) received re-irradiation due to progression, with a median dose of 23.4 Gy (range 19.8-36 Gy), while 18 patients (54%) were treated with systemic therapy alone. In patients who received re-irradiation after progression, the 1‑year post-progression overall survival (OS) was significantly higher compared to those treated with systemic therapy alone (27% vs. 0%, p = 0.01). Among the 15 re-irradiated patients, 9 out of 12 with available data (75%) showed improvement in neurological symptoms following re-irradiation. No patient exhibited acute or late RT-related ≥ grade 3 toxicity. Palliative re-irradiation in children and young adults with progressive DIPG after initial RT provides an approximately 3‑month OS benefit and clinical improvement without significant toxicity and should be considered as a standard-of-care approach.

Overview

  • The study assesses oncological outcomes in children and young adults with diffuse infiltrative pontine glioma (DIPG) who have progressed after initial radiotherapy (RT), with an emphasis on the role of re-irradiation.
  • Data from 33 patients aged 25 years or younger with progressive disease after initial RT were retrospectively analyzed.
  • The study aims to determine the effectiveness of re-irradiation as a treatment option for progressive DIPG after initial RT.

Comparative Analysis & Findings

  • The study found that patients who received re-irradiation after progression had a significantly higher 1-year post-progression overall survival (OS) compared to those treated with systemic therapy alone (27% vs. 0%, p = 0.01).
  • Among the 15 re-irradiated patients, 9 out of 12 with available data (75%) showed improvement in neurological symptoms following re-irradiation.
  • No patient exhibited acute or late RT-related ≥ grade 3 toxicity.

Implications and Future Directions

  • Palliative re-irradiation in children and young adults with progressive DIPG after initial RT provides an approximately 3-month OS benefit and clinical improvement without significant toxicity.
  • This treatment approach should be considered as a standard-of-care option for patients with progressive DIPG after initial RT.
  • Future studies could explore the optimal dose and timing of re-irradiation, as well as its combination with systemic therapy, to improve outcomes for patients with progressive DIPG.