Radiotherapy may help prime immunotherapy in biologically distinct acral melanoma
Acral melanoma has an immune-cold phenotype and weaker ICI responsiveness; radiotherapy-based immune priming is biologically plausible but clinically unproven.
Acral melanoma has an immune-cold phenotype and weaker ICI responsiveness; radiotherapy-based immune priming is biologically plausible but clinically unproven.
VMAT-based PCI spared additional memory-network structures while maintaining whole-brain coverage in two patients with limited-stage SCLC.
Reported atrial fibrillation occurred in 7.6% after thoracic radiotherapy when cohorts with substantial perioperative confounding were excluded.
Personalized ctDNA was detected in 85% at baseline and remained independently prognostic before treatment, after radiotherapy and after surgery.
HYPOCON will test 40 Gy/20 fractions followed by 15 Gy/3 against 55 Gy/20, both with concurrent cisplatin.
Large cystic Koos III–IV vestibular schwannomas showed greater early shrinkage after SRS, with 100% local control in 15 cystic cases.
AEWS1221 was the first Children's Oncology Group trial to evaluate SBRT, introduced to make treatment of every metastatic site achievable. Preliminary data suggest it reached a minority of eligible patients. That, rather than the local control rate, is the finding that matters.
Double-arc VMAT was slightly more robust, but single-arc planning achieved clinically comparable dosimetry with simulated bilateral hip prostheses.
Stage I SCLC survival was similar whether SBRT preceded chemotherapy or was delivered after chemotherapy had started.
An integrated CT-linac workflow delivered emergency radiotherapy in 24.7 minutes, with symptom relief in nearly 90% of patients.
Each 10-Gy increase in biologically effective dose was associated with 39% higher odds of pathological complete response in esophageal squamous cell carcinoma.
DEGRO supports postoperative radiotherapy within eight weeks while expanding hypofractionated options for frail and selected Merkel cell carcinoma patients.
Adding advanced extranodal extension to N3 modestly improved prognostic discrimination and identified patients with substantially greater distant failure risk.
Jaw-partitioned VMAT improved dose gradients and peak-to-valley separation in GRID and lattice plans, but approximately doubled monitor units.
Model-predicted microscopic glioblastoma spread could be incorporated into clinically deliverable plans, but dose-painting accuracy deteriorated as target complexity increased.