Fallopian Tube Cancer Clinical Trial
Official title:
Stratified Evaluation and Prediction of Survival Benefit for PDS or NACT-IDS in Advanced Ovarian Cancer, A Randomized, Phase 3 Trial After the SUNNY Study
The purpose of this study is to answer the fundamental question 'The Optimal Timing of Surgery' in advanced ovarian cancer patients with different tumor burden, and to perform translational study.
OBJECTIVES: Compare the efficacy and safety in patients with advanced ovarian cancer treated
with NACT-IDS versus PDS, among different tumor burden groups. Compare survival benefit of
PARPi therapy in patients treated with PDS or NACT-IDS.
OUTLINE: This is a randomized phase III multicenter study. Patients will receive upfront
maximal cytoreductive surgery followed by at least 6 cycles of adjuvant chemotherapy or 3
cycles of neoadjuvant chemotherapy followed by interval debulking surgery, and then at least
3 cycles of adjuvant chemotherapy, and maintenance therapy of PARP inhibitor for patients
with gBRCA/sBRCA mutation who had a complete or partial clinical response after
platinum-based chemotherapy. Patients are followed every 3 months within the first 5 years,
and then every 6 months.
PROJECTED ACCRUAL: A total of 410 patients will be accrued for this study within 3 years.
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|---|---|---|---|
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