30-Second Takeaway
- Dose-reduced preoperative RT (36 Gy) provides excellent local control in myxoid liposarcoma.
- Baseline testosterone may predict who gains mortality benefit from adding docetaxel to RT+ADT in high-risk prostate cancer.
Week ending May 23, 2026
Five recent oncology studies with immediate practice implications for radiation oncologists
8-variable model predicts grade ≥2 radiation esophagitis after concurrent CRT for unresectable stage III NSCLC
In 1,288 patients from 8 trials, grade ≥2 esophagitis occurred in 15% and grade ≥3 in 2.0% during concurrent chemoradiotherapy. An LASSO-derived model using eight baseline factors achieved a c-statistic of 0.85 for predicting grade ≥2 esophagitis. Grade ≥2 esophagitis did not affect PFS or OS, whereas grade ≥3 esophagitis associated with worse PFS only. The model can guide anticipatory supportive care and toxicity counseling for unresectable stage III NSCLC patients.
Reduced-dose (36 Gy) preoperative RT yields durable local control in myxoid liposarcoma
Ninety patients received 36 Gy preoperative RT and surgery with median follow-up 66 months and 5-year local recurrence-free survival 97.4%. Five-year overall survival was 88.5% and progression-free survival 81.0% after the reduced-dose regimen. Wound complications occurred in 21%, with 16% requiring intervention; late grade ≥3 toxicity was uncommon. These phase 2, nonrandomized results support discussing 36 Gy as a reasonable preoperative option for localized myxoid liposarcoma.
Baseline testosterone modifies mortality benefit of docetaxel added to RT+ADT in high-risk prostate cancer
In discovery (n=255) and validation (n=563) cohorts, adding docetaxel to RT+ADT reduced all-cause mortality only in men with normal baseline testosterone. A significant treatment-by-testosterone interaction was present in both cohorts (p=.048 and p=.042). The predictive signal was strongest for patients with PSA >20, T3/4 disease, or Gleason 9–10. Baseline testosterone may inform selection for docetaxel but requires prospective validation before guideline adoption.
References
Numbered in order of appearance. Click any reference to view details.
Additional Reads
Optional additional studies from this edition.