Voxel-based analysis identifies new functional subregions predictive of xerostomia after head and neck cancer radiotherapy.
[BACKGROUND AND PURPOSE] Xerostomia is a common and debilitating toxicity following head and neck cancer (HNC) radiotherapy (RT).
APA
Cubero L, Acosta O, et al. (2026). Voxel-based analysis identifies new functional subregions predictive of xerostomia after head and neck cancer radiotherapy.. International journal of radiation oncology, biology, physics. https://doi.org/10.1016/j.ijrobp.2026.01.040
MLA
Cubero L, et al.. "Voxel-based analysis identifies new functional subregions predictive of xerostomia after head and neck cancer radiotherapy.." International journal of radiation oncology, biology, physics, 2026.
PMID
41707993
Abstract
[BACKGROUND AND PURPOSE] Xerostomia is a common and debilitating toxicity following head and neck cancer (HNC) radiotherapy (RT). Although adaptive radiotherapy (ART) strategies can reduce mean parotid gland (PG) dose, clinical trials have shown limited benefit in reducing xerostomia, suggesting global dose metrics may be insufficient. Voxel-based analysis (VBA) enables assessing local dose-toxicity relationships and may identify symptom-related subregions (SRS) more predictive of toxicity. This study aimed to identify xerostomia-associated SRS using VBA and assess their relevance using a functional salivary atlas.
[MATERIALS AND METHODS] Sixty patients with locally advanced oropharyngeal cancer treated with chemoradiotherapy were randomized to receive standard RT or weekly ART. Xerostomia was assessed at 12 months post-treatment using stimulated salivary flow (SSF), with values ≤ 500 mg/min indicating xerostomia. A customized VBA was applied to identify subregions from voxel-wise dose differences between patients with and without xerostomia using a permutation test (planned dose in standard arm and accumulated dose in ART arm). To assess clinical relevance, a functional salivary atlas was generated from PSMA-PET/CT scans of 13 prostate cancer patients and compared with the subregions. A dosimetric analysis evaluated the predictive value of dose in overlapping regions.
[RESULTS] VBA identified a subregion (300.2 cc) with significantly higher doses in xerostomia patients, located contralaterally near the nasopharynx. Overlap with the functional PSMA-PET atlas revealed two clinically relevant subregions in the contralateral PG (SRS, 6.8cc) and tubarial gland (SRS, 12.7 cc), with doses > 11.5 Gy higher in xerostomia patients. Logistic regression models yielded high predictive performance, with maximum AUCs of 0.88 for SRS and 0.88 for SRS.
[CONCLUSION] VBA revealed two predictive subregions-within the contralateral PG and tubarial glands-strongly associated with xerostomia at 12 months post-RT. Our findings offer a plausible explanation for the persistence of xerostomia despite PG sparing and support incorporating subregional dose metrics and tubarial gland sparing into RT planning.
[MATERIALS AND METHODS] Sixty patients with locally advanced oropharyngeal cancer treated with chemoradiotherapy were randomized to receive standard RT or weekly ART. Xerostomia was assessed at 12 months post-treatment using stimulated salivary flow (SSF), with values ≤ 500 mg/min indicating xerostomia. A customized VBA was applied to identify subregions from voxel-wise dose differences between patients with and without xerostomia using a permutation test (planned dose in standard arm and accumulated dose in ART arm). To assess clinical relevance, a functional salivary atlas was generated from PSMA-PET/CT scans of 13 prostate cancer patients and compared with the subregions. A dosimetric analysis evaluated the predictive value of dose in overlapping regions.
[RESULTS] VBA identified a subregion (300.2 cc) with significantly higher doses in xerostomia patients, located contralaterally near the nasopharynx. Overlap with the functional PSMA-PET atlas revealed two clinically relevant subregions in the contralateral PG (SRS, 6.8cc) and tubarial gland (SRS, 12.7 cc), with doses > 11.5 Gy higher in xerostomia patients. Logistic regression models yielded high predictive performance, with maximum AUCs of 0.88 for SRS and 0.88 for SRS.
[CONCLUSION] VBA revealed two predictive subregions-within the contralateral PG and tubarial glands-strongly associated with xerostomia at 12 months post-RT. Our findings offer a plausible explanation for the persistence of xerostomia despite PG sparing and support incorporating subregional dose metrics and tubarial gland sparing into RT planning.