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Clinical Research on Moderately Hypofractionated Adaptive Postoperative Radiotherapy for High-Risk Endometrial Cancer

Clinical Research on Moderately Hypofractionated Adaptive Postoperative Radiotherapy for High-Risk Endometrial Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105258
Enrollment
Unknown
Registered
2025-07-01
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High-Risk Endometrial Cancer

Interventions

Moderately Hypofractionated Radiotherapy Group:Moderately Hypofractionated Adaptive Postoperative Radiotherapy

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.18–70 years old; 2.ECOG score 0–2, ??expected to comply with oART procedures; 3.Primary surgery including ??total hysterectomy and bilateral salpingo-oophorectomy??, with or without pelvic/para-aortic lymph node dissection/sampling or sentinel lymph node biopsy; 4.FIGO 2009 Stage I?? (Grade 3 endometrioid adenocarcinoma with superficial myometrial invasion and extensive LVSI; Grade 2 endometrioid carcinoma with deep myometrial invasion and extensive LVSI; Grade 3 endometrioid carcinoma with deep myometrial invasion), ??Stage II–IIIC1 endometrioid carcinoma??, and ??Stage I–IIIC1 serous carcinoma or clear cell carcinoma??; 5.Patients and families fully understood the protocol and provided ??written informed consent?? prior to enrollment.

Exclusion criteria

Exclusion criteria: 1.History of abdominal or pelvic radiotherapy; 2.If no adjuvant chemotherapy, over 12 weeks between surgery and radiotherapy initiation; if combined with adjuvant chemotherapy, over 6 months between surgery and radiotherapy; 3.History of other malignant tumors; 4.Pregnant or breastfeeding women; 5.Uncontrolled active infection or fever; 6.Diagnosis of IBD (regardless of activity status); 7.Severe diseases affecting trial compliance, including: Unstable cardiac disease requiring treatment, renal impairment, chronic hepatitis, poorly controlled diabetes and psychiatric disorders;

Design outcomes

Primary

MeasureTime frame
Acute Toxicity;

Secondary

MeasureTime frame
Quality of Life;Chronic Toxicity;3-year treatment failure-free survival rate;

Countries

China

Contacts

Public ContactXiaorong Hou

Peking Union Medical College Hospital

hxr_pumch@163.com+86 10 69155485

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026