Gynecologic Oncology Group protocols 71 and 123 enrolled 464 patients randomly allocated to pelvic radiation (75 Gy, n = 291) plus hysterectomy (RTH) or to pelvic radiation (75 Gy) and cisplatin (40 mg/m2, n = 176) plus hysterectomy (RTCH). Risk of progression and death were evaluated by posttherapy hysterectomy response (good: <10 % viable; poor: ≥10 % viable).
Median survivor follow-up was 112 months. Relative risks of disease progression and death were 0.656 (95 % confidence interval, 0.472–0.912) and 0.638 (95 % confidence interval, 0.449–0.908), favoring RTCH. Good response patients (345; 74 % ) had similar 10 year overall survival (OS) and progression-free survival (PFS) after RTH or RTCH (P > .47). Poor response patients after RTCH had superior OS (P = .046) and PFS (P = .084). Extrapelvic recurrences occurred more often in poor response patients.
Posttherapy viable residual disease less than 10 % was associated with reduced risk of progression and cancer-related death.