Trigger-based adaptive proton therapy improves coverage and cardiac sparing in esophageal cancer
Adaptive IMPT improved cumulative target coverage and reduced heart dose without increasing lung dose in a 192-patient retrospective cohort.
Adaptive IMPT improved cumulative target coverage and reduced heart dose without increasing lung dose in a 192-patient retrospective cohort.
Five proton centres outline why conventional radiation protection workflows cannot simply be assumed adequate for ultra-high dose-rate FLASH research.
A preclinical proton STAR workflow achieved benchmark-level target coverage, OAR sparing and cardiac gating latency below 30 ms.
Control, predictability, information and relational continuity emerged as key needs for making awake pediatric proton therapy more manageable.
After proton reirradiation for recurrent pediatric ependymoma, 5-year survival was 64% with one grade 3 radiation injury and no grade 4+ toxicity.
A 1.5–3.0 mm foam elevation reduced marker contouring time by 30–37% while keeping average positional error near 1 mm.
ITV underdosage occurred in 21% of distal esophageal IMPT patients, yet no GTV underdosage occurred and tumor response was unchanged.
Interplay-related underdosage largely disappeared after five fractions, although two high-motion plans retained clinically relevant target deficits.
Age ≥75 did not independently predict outcomes after proton therapy for HCC, while CCI ≥3 was associated with more than threefold higher mortality.
In two PDAC cell lines, measured proton RBE remained near 1.0 through the Bragg peak but rose as high as 6.1 distally.
In a prospective proton registry enriched for ultracentral, large, and re-irradiated lung tumors, two-year local control was 77% with no grade ≥3 toxicity.
After two days of local configuration, a pretrained model generated oropharyngeal IMPT plans with overall quality comparable to manual planning.
Across 478 patients, hypofractionated proton re-irradiation showed encouraging site-specific outcomes, but heterogeneous retrospective evidence prevents firm conclusions on efficacy or safety.
Kidney proton SBRT modeling supported 4-mm superior–inferior and 3-mm lateral/anterior–posterior positioning uncertainty with intrafraction repositioning.
A child developed hemorrhagic colitis after only 12.6 Gy(RBE), suggesting preceding intensive systemic therapy may increase bowel vulnerability.