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Does the interval from tumour surgery to radiotherapy influence survival in paediatric high grade glioma?
Amedeo A Azizi1, Simon Paur2, Alexandra Kaider3
1Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria. amedeo.azizi@meduniwien.ac.at.
Insights
The interval between surgery and radiotherapy did not impact survival for pediatric high-grade glioma (pHGG) patients. This finding supports molecular testing before treatment initiation in pHGG cases.
Area of Science:
- Pediatric Oncology
- Neuro-oncology
- Radiation Oncology
Background:
- Pediatric high-grade glioma (pHGG) is rare, with radiotherapy being a standard treatment post-surgery.
- The impact of the interval from surgery to radiotherapy (ISRT) on survival in pediatric patients is not well-established.
- Existing data primarily focuses on adult glioblastoma, leaving a gap in pediatric knowledge.
Purpose of the Study:
- To investigate the potential influence of the interval from surgery to radiotherapy (ISRT) on survival outcomes in pediatric high-grade glioma (pHGG) patients.
- To analyze survival data in relation to ISRT in a cohort of children and adolescents diagnosed with non-pontine HGG.
- To provide evidence-based insights for optimizing treatment protocols in pediatric HGG management.
Main Methods:
- Retrospective single-center analysis of pediatric patients (3-19 years) with non-pontine HGG.
- Inclusion of 38 patients with varying grades (3 and 4) and extents of resection (gross total, partial, biopsy only).
- Analysis of overall survival (OS) and progression-free survival (PFS) in relation to ISRT, tumor grade, extent of resection, and chemotherapy regimens.
Main Results:
- ISRT, whether analyzed continuously or dichotomized, did not significantly affect OS or PFS in pediatric HGG patients.
- Higher extent of resection, lower tumor grade, and temozolomide chemotherapy showed a significant positive impact on OS and PFS.
- Patients with grade 4 tumors were more likely to receive radiotherapy sooner after surgery.
Conclusions:
- The interval from surgery to radiotherapy (ISRT) does not appear to influence survival in pediatric high-grade glioma (pHGG).
- The findings suggest that it is safe to conduct molecular analyses within a four-week period before initiating radiotherapy for pHGG.
- This supports the integration of molecular profiling into treatment planning for upcoming targeted therapies in pediatric HGG.
Purpose:
Paediatric high grade glioma (pHGG) are rare. Following maximum safe resection, children >3 years with HGG receive radiotherapy as standard of care. Whether the interval from tumour surgery to radiotherapy (ISRT) influences survival is disputed in adults with glioblastoma, data for children are lacking. This retrospective single-centre analysis investigates a possible impact of ISRT on survival in paediatric patients with HGG.
Methods:
Survival was analysed in patients aged 3-19 years with non-pontine HGG.
Results:
Thirty-eight patients were included (female:male 19:19) with a median age of 11.0 years (3.4-17.7). Seventeen patients had grade 3 and 21 grade 4 glioma. Gross total resection was achieved in 26.3%, partial resection in 36.8% and 36.8% underwent biopsy only. All patients received concomitant and adjuvant chemotherapy. Fifty percent (n = 19) started irradiation ≤17 days (median interval 12 days [range 5-17]), 50% thereafter (median 28 days [range 19-78]). More patients with grade 4 tumours were irradiated shortly after surgery. ISRT (as a continuous variable and dichotomised into two groups by the median ISRT of 18 days) did not significantly influence overall survival (OS) or progression-free survival (PFS). Higher extent of resection (EOR), lower tumour grade as well as chemotherapy with temozolomide had a significant positive impact on OS and PFS in univariate analysis and (except for the effect of temozolomide on PFS) also in multivariable analysis.
Conclusions:
ISRT did not influence survival in pHGG. In view of upcoming targeted treatment options in pHGG the present data suggest that it is safe to perform molecular analyses within a 4-week timeframe before radiotherapy.
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