Twenty-fraction cervical chemoradiation shortened treatment but raised a late GI toxicity signal
44 Gy in 20 fractions shortened cervical cancer treatment by seven days but showed numerically more severe late GI toxicity.
44 Gy in 20 fractions shortened cervical cancer treatment by seven days but showed numerically more severe late GI toxicity.
After 50 Gy in five fractions, local progression was 15% at one year, while distant progression remained the dominant failure pattern.
In randomized phase II SOFT Preop, five-fraction SBRT better preserved patient-reported quality of life than 28-fraction chemoradiotherapy. Pathological nodal positivity did not differ significantly, but oncologic noninferiority was not established.
NRG-HN009 found no reduction in overall acute grade 3-4 toxicity with weekly versus three-weekly cisplatin during definitive head and neck RT. Toxicity profiles differed, and neither phase II cohort met the criteria to proceed to phase III.
In PACE-A, moderate-to-severe erectile dysfunction at 5 years affected 44% of SBRT respondents vs 89% after prostatectomy. The patient-reported difference was significant, but analyses were as treated and follow-up questionnaires were incomplete.
TRIDENT found no OS benefit from starting TTFields during RT/TMZ rather than at maintenance in newly diagnosed glioblastoma. Median OS was 17.7 vs 17.5 months. A post hoc MGMT-methylated subgroup signal remains exploratory.
Tocilizumab, atezolizumab and 24 Gy/3-fraction FSRT produced only a 3.4% objective response rate in recurrent glioblastoma.
Pain response after reirradiation was 60% in lesions that previously responded to RT versus 15% after primary nonresponse.
In a randomized phase III trial, short-course RT-based TNT produced a numerically higher pCR rate than long-course chemoradiotherapy, but no significant DFS, LRFS, or OS benefit emerged after 28 months of follow-up.
In randomized STELLAR II, adding sintilimab to short-course RT-based TNT increased complete response from 26.8% to 51.9% in pMMR locally advanced rectal cancer, with higher toxicity. Three-year DFS remains pending.
In randomized phase III PACE-A, 5-fraction SBRT and radical prostatectomy both achieved excellent long-term disease control in localized prostate cancer, with no significant efficacy difference after a median 8 years of follow-up.
In phase III NRG-CC009, SRS did not improve neurocognitive failure vs HA-WBRT plus memantine, but median OS was 17.4 vs 8.6 months. Adjusted intracranial control, neurologic mortality, and grade 3-5 toxicity were similar.
In phase III Alliance A071801, postoperative fractionated SRS improved 1-year surgical bed control to 87% vs 81% with single-fraction SRS, without significantly increasing radiation necrosis. Overall survival also favored fSRS.
In randomized phase III NRG-GI003, protons substantially reduced non-tumor liver dose but did not improve OS, PFS, or local progression over photons in advanced HCC. Grade 3+ toxicity was numerically lower.
Ten-year CHN HYPOPMRT results show durable locoregional control and similar survival with 43.5 Gy in 15 fractions vs 50 Gy in 25 fractions after mastectomy, with no emerging severe late-toxicity signal.