A Multicenter Randomized Controlled Study of Modalities of Adjuvant Radiotherapy and Chemotherapy for Stage Ⅲ Endometrial Cancer

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Endometrial cancer is the most common gynecological malignancy affecting women's health. About 15% of the patients will have local late disease (stage III) with high risk of recurrence and tumor related mortality. There is a consensus that adjuvant radiochemotherapy is needed for stage Ⅲ endometrial cancer, but the best modality of radiochemotherapy is still uncertain. The retrospective data of our center showed that the sequential radiochemotherapy of chemotherapy-radiotherapy-chemotherapy in the sanwich mode could improve the survival outcome in patients with advanced endometrial cancer. A multicenter, prospective, randomized controlled study to compare the sanwich mode of radiochemotherapy and the concurrent chemoradiotherapy followed by chemotherapy mode will be carried out to determine the better modality of radiochemotherapy in stage III endometrial adenocarcinoma.

Eligibility
Participation Requirements
Sex: Female
Healthy Volunteers: f
View:

• patients of primary treatment

• All patients must have undertaken comprehensive staging operation(Surgery must have included a hysterectomy and bilateral salpingooophorectomy and surgical staging).

• Patients with endometrial adenocarcinoma confirmed by postoperative patholog.

• All patients with Surgical Stage III endometrial carcinoma according to FIGO 2009 staging criteria.

• Entry into the study is limited to no more than 8 weeks from the date of surgery.

• Patients with adequate organ function, reflected by the following parameters:

‣ WBC ≥ Normal value of the institution;

⁃ Absolute neutrophil count (ANC) ≥ Normal value of the institution;

⁃ Platelet count ≥ 100,000/mcl;

⁃ SGOT, SGPT, and alkaline phosphatase ≤ 1.25 X upper limit of normal (ULN) ;

⁃ Bilirubin ≤ 1.5 X ULN;

⁃ Creatinine ≤ institutional ULN.

• Patients with a Karnofsky score≥60.

• The patients should voluntarily join the study, sign an approved informed consent with good compliance and cooperation with the follow-up.

Locations
Other Locations
China
Jianliu Wang
RECRUITING
Beijing
Contact Information
Primary
Guo Zhang, Ph.D
zhangguo-2005@163.com
+861088324381
Time Frame
Start Date: 2020-05-12
Estimated Completion Date: 2027-04
Participants
Target number of participants: 654
Treatments
Experimental: sequential radiochemotherapy in a sanwich mode
Two courses of TC regimen chemotherapy (paclitaxel 135-175mg / m2; carboplatin AUC = 5; once every 21 days) will be given first, followed by external pelvic radiation (± vaginal brachytherapy), and then four courses of the same regime consolidation chemotherapy.
Active_comparator: concurrent chemoradiotherapy followed by chemotherapy
External pelvic radiation (± vaginal brachytherapy) will be given after operation. On the first day and the 29th day of radiotherapy, concurrent intravenous cisplatin (50mg/m2) will be given. After the concurrent radiochemotherapy, four courses of TC regimen (paclitaxel 135-175mg / m2; carboplatin AUC = 5; once every 21 days) chemotherapy will be given.
Related Therapeutic Areas
Sponsors
Leads: Peking University People's Hospital

This content was sourced from clinicaltrials.gov