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Comparison of Sequential Chemotherapy and Concurrent Chemotherapy and Adjuvant Chemotherapy in Postoperative Adjuvant Treatment of High-risk Endometrial Cancer: a Randomized, Controlled, Single Center Phase III Clinical Study

Comparison of Sequential Chemotherapy and Concurrent Chemotherapy and Adjuvant Chemotherapy in Postoperative Adjuvant Treatment of High-risk Endometrial Cancer: a Randomized, Controlled, Single Center Phase III Clinical Study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045675
Enrollment
Unknown
Registered
2021-04-21
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-06

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

Conditions

Endometrial cancer

Interventions

Group one:Simultaneous radiotherapy and chemotherapy + adjuvant chemotherapy for 6 cycles
Group two:3 cycles of chemotherapy + concurrent radiotherapy and chemotherapy + 3 cycles of chemotherapy

Sponsors

Anhui Cancer Hospita
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Women between 18 and 70 years old; (1) Stage I endometrial cancer has the following high-risk factors: (any stage of serous adenocarcinoma, any stage of clear cell adenocarcinoma, grade 3 deep invasive endometrial carcinoma); (2) The pathological stage is stage II-III, any histological type; 2. Karnofsky score >= 70; ECOG score 0-2 points; 3. There is a possibility of follow-up; 4. The patient signs an informed consent form; 5. The patient shall not receive any definite pelvic history radiotherapy before; 6. The investigator assessed that it is suitable for accepting and tolerating radiotherapy and chemotherapy.

Exclusion criteria

Exclusion criteria: 1. Accompanied by severe active infection or severe heart, liver, kidney and hematopoietic system diseases; 2. Poor compliance; 3. The withdrawal time of other clinical trial drugs is less than 4 weeks; 4. History of other primary malignant tumors, except for the following conditions: malignant tumors that have been cured, and there is no known active disease >= 5 years before the first administration of IP, and the potential risk of recurrence is low.

Design outcomes

Primary

MeasureTime frame
Overall survival;Disease-free survival;

Secondary

MeasureTime frame
safety;Quality of Life;

Countries

China

Contacts

Public ContactLiu Yunqin

Anhui Cancer Hospital

liuyunq@163.com+86 13696528788

Outcome results

None listed

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