Brain Dose–Volume Thresholds and Survival in Dogs With Intracranial Tumours Treated With the 10 × 4 Gy Radiotherapy Schedule: A Combined Analysis of Two Trials

Dogs with intracranial tumours routinely receive radiotherapy, yet species‐specific dose–volume constraints for normal brain tissue remain undefined. In human radiation oncology, exceeding certain brain dose–volume thresholds markedly increases the risk of radiation‐induced injury (e.g., radionecrosis). Current veterinary practice often extrapolates human guidelines without validation in discrete species, creating a gap in evidence‐based planning. This study aimed to identify brain dose–volume thresholds associated with overall survival (OS) in canine brain‐tumour patients. We pooled data from two prospective randomised trials ( n = 105 dogs) treated with 10 daily fractions of 4 Gy (total 40 Gy) for intracranial tumours at a single institution. Semi‐automated scripting extracted multiple dose–volume metrics, including generalised equivalent uniform dose (gEUD), for the whole brain and brain minus gross tumour volume (Brain–GTV). An iterative Kaplan–Meier and Cox proportional hazards approach identified optimal dosimetric cutoffs, which were then adjusted for tumour volume and body weight via a regression residual method. A brain‐volume‐adjusted gEUD threshold was also derived to account for variation in brain size. Exposure to normal brain to doses around 30–40 Gy emerged as the strongest predictor of OS. Brain–GTV V32 Gy ≤ 13 cm $^{3}$ was associated with longer OS (covariate‐adjusted cutoff 13.4 cm $^{3}$ , HR = 1.74; p = 0.022, unadjusted optimal split 11.5 cm $^{3}$ , HR = 2.08; p = 0.001). Whole‐brain gEUD > 30 Gy similarly predicted poorer survival (HR = 1.72; p = 0.034). Implementing a personalised gEUD ceiling increased 2‐year sensitivity from 31% to 38% with only a three‐point drop in specificity. In a 10 × 4 Gy canine intracranial radiotherapy model, limiting Brain–GTV V32 Gy to ≤ 13 cm $^{3}$ and whole‐brain gEUD to ≤ 30 Gy was associated with longer overall survival. A brain‐volume‐adjusted gEUD ceiling further refined risk prediction. These evidence‐based thresholds provide actionable guidance for veterinary treatment planning, with the potential to improve outcomes in canine brain tumour therapy.

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Publication Details

Journal
Universität Zürich, ZORA
Published
2025-12-19
DOI
https://doi.org/10.5167/uzh-282965
Primary Topic
Veterinary Oncology Research
Type
article
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article

Brain Dose–Volume Thresholds and Survival in Dogs With Intracranial Tumours Treated With the 10 × 4 Gy Radiotherapy Schedule: A Combined Analysis of Two Trials

Sergejs Unterkirhers, Valeria Sabina Meier, Carla Rohrer Bley
Universität Zürich, ZORA
Veterinary Oncology Research
article

Brain Dose–Volume Thresholds and Survival in Dogs With Intracranial Tumours Treated With the 10 × 4 Gy Radiotherapy Schedule: A Combined Analysis of Two Trials

Sergejs Unterkirhers, Valeria Sabina Meier, Carla Rohrer Bley
article en

Abstract

Dogs with intracranial tumours routinely receive radiotherapy, yet species‐specific dose–volume constraints for normal brain tissue remain undefined. In human radiation oncology, exceeding certain brain dose–volume thresholds markedly increases the risk of radiation‐induced injury (e.g., radionecrosis). Current veterinary practice often extrapolates human guidelines without validation in discrete species, creating a gap in evidence‐based planning. This study aimed to identify brain dose–volume thresholds associated with overall survival (OS) in canine brain‐tumour patients. We pooled data from two prospective randomised trials ( n = 105 dogs) treated with 10 daily fractions of 4 Gy (total 40 Gy) for intracranial tumours at a single institution. Semi‐automated scripting extracted multiple dose–volume metrics, including generalised equivalent uniform dose (gEUD), for the whole brain and brain minus gross tumour volume (Brain–GTV). An iterative Kaplan–Meier and Cox proportional hazards approach identified optimal dosimetric cutoffs, which were then adjusted for tumour volume and body weight via a regression residual method. A brain‐volume‐adjusted gEUD threshold was also derived to account for variation in brain size. Exposure to normal brain to doses around 30–40 Gy emerged as the strongest predictor of OS. Brain–GTV V32 Gy ≤ 13 cm $^{3}$ was associated with longer OS (covariate‐adjusted cutoff 13.4 cm $^{3}$ , HR = 1.74; p = 0.022, unadjusted optimal split 11.5 cm $^{3}$ , HR = 2.08; p = 0.001). Whole‐brain gEUD > 30 Gy similarly predicted poorer survival (HR = 1.72; p = 0.034). Implementing a personalised gEUD ceiling increased 2‐year sensitivity from 31% to 38% with only a three‐point drop in specificity. In a 10 × 4 Gy canine intracranial radiotherapy model, limiting Brain–GTV V32 Gy to ≤ 13 cm $^{3}$ and whole‐brain gEUD to ≤ 30 Gy was associated with longer overall survival. A brain‐volume‐adjusted gEUD ceiling further refined risk prediction. These evidence‐based thresholds provide actionable guidance for veterinary treatment planning, with the potential to improve outcomes in canine brain tumour therapy.

Universität Zürich, ZORA
Openalex Percentile: Top 26%
Veterinary Oncology Research
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Brain Dose–Volume Thresholds and Survival in Dogs With Intracranial Tumours Treated With the 10 × 4 Gy Radiotherapy Schedule: A Combined Analysis of Two Trials — Sergejs Unterkirhers, Valeria Sabina Meier, et al. · Universität Zürich, ZORA (2025) | TGRS Research Map | TGRS