Anal cancer targets changed substantially during chemoradiotherapy despite standard PTV margins
Across 212 CBCTs, 36.8% showed target extensions >10 mm beyond the planning PTV despite progressive overall CTV shrinkage.
Across 212 CBCTs, 36.8% showed target extensions >10 mm beyond the planning PTV despite progressive overall CTV shrinkage.
Across 32 years of T1 anal cancer treatment, five-year colostomy-free survival reached 85.3%, with no treatment-related colostomies.
PACTUS 40 Gy/10 produced 30-month median survival in 28 selected frail patients, but incomplete response and toxicity data limit efficacy conclusions.
Patients aged ≥70 had similar recurrence outcomes after definitive chemoradiotherapy despite inferior overall survival and greater competing mortality.
An explainable model separated three-year local relapse rates of 11% versus 39%, but lacks independent external validation.
Twelve trials used 14 immunotherapy regimens with major differences in eligibility, radiotherapy, chemotherapy, endpoints, and translational analysis.
Most treatment-related deficits improved by six months, although bowel and sexual problems persisted in several standard-dose and locally advanced groups.
Simultaneous integrated boost radiotherapy was associated with 96% two-year disease-free survival versus 70% with sequential boost in anal cancer.
Bone marrow-sparing planning reduced pelvic marrow dose, but heterogeneous evidence did not confirm a consistent reduction in hematologic toxicity.
Patients reported persistently worse quality of life and functioning approximately two years after chemoradiotherapy than matched individuals without cancer.