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Clinical Trial Summary

The purpose of this study is to compare the efficacy and toxicity of early stage endometrial cancer based on molecular classification and conventional risk stratification adjuvant therapy decision-making, and to provide high-quality evidence-based medical evidence for individualized adjuvant therapy selection under the guidance of fine stratification system of endometrial cancer.


Clinical Trial Description

This is an investigator-initiated prospective, national multicentre, phase III, randomised, open, non-inferiority clinical study. The study hypothesis is that adjuvant radiotherapy decision for early-stage endometrial cancer which is based on molecular classification can achieve de-escalation of adjuvant treatment without reducing local tumour control and survival, thereby potentially further reducing radiotherapy-related toxicity and improving quality of life, compared to using conventional risk stratification. The primary endpoint of this study is the 3-year local recurrence rate. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05524389
Study type Interventional
Source Peking Union Medical College Hospital
Contact Xiaorong Hou, PhD
Phone +86-13811963013
Email hxr_pumch@163.com
Status Not yet recruiting
Phase Phase 3
Start date December 1, 2022
Completion date June 30, 2027

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