Perirenal hydrogel spacer reduced bowel dose in simulated kidney SBRT
In one cadaveric RCC plan, stable 1-cm perirenal separation reduced large-bowel Dmax from 34.5 to 22.1 Gy.
In one cadaveric RCC plan, stable 1-cm perirenal separation reduced large-bowel Dmax from 34.5 to 22.1 Gy.
Seven patients completed 60 Gy with no recurrences, grade ≥3 skin toxicity, fibrosis, cartilage necrosis, or nasal contour deformation at early follow-up.
Four patients completed 54 Gy after airway reconstruction without graft-related toxicity or local recurrence during early follow-up.
A child developed hemorrhagic colitis after only 12.6 Gy(RBE), suggesting preceding intensive systemic therapy may increase bowel vulnerability.
All 50 proton SBRT fractions were completed, with online adaptation used in 84% to restore target coverage or resolve OAR violations.
VMAT-based PCI spared additional memory-network structures while maintaining whole-brain coverage in two patients with limited-stage SCLC.
Model-predicted microscopic glioblastoma spread could be incorporated into clinically deliverable plans, but dose-painting accuracy deteriorated as target complexity increased.
A phase I study safely escalated five-fraction stereotactic boosts to 30-35 Gy after recent prior radiotherapy, with 86.5% one-year local control.
A best MRI model reached AUC 0.91, but across 366 configurations radiomics did not consistently outperform a simple clinical model.
Ten-year biochemical control was 64.7% after salvage proton therapy, with 3.2% late grade 3 genitourinary toxicity.
Grade ≥3 mucositis at week 6 occurred in 11.1% with benzydamine versus 70.6% with standard care.
Accumulated gastrointestinal doses were generally lower than planned, while higher small-bowel dose showed exploratory associations with diarrhoea after MR-guided SABR.
MRI radiomics predicted VEGFA expression with validation AUC 0.718, while high VEGFA independently correlated with worse overall survival.
NRF2 directly activated WNT5A, sustaining β-catenin signaling, cancer stemness and radioresistance across esophageal cancer models.
Reduced-volume MR-guided RT caused no grade ≥3 toxicity, but two of ten patients developed in-field recurrence after five-fraction treatment.