Study of Nimotuzumab Combined With IMRT in Elder Patients With Cervical Squamous Cell Carcinoma

Not yet recruitingOBSERVATIONAL
Enrollment

125

Participants

Timeline

Start Date

July 31, 2021

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2026

Conditions
Cervical Squamous Cell Carcinoma
Interventions
DRUG

Nimotuzumab

Patients receive Nimotuzumab: 200mg, intravenous infusion, weekly for 6 weeks.

RADIATION

EBRT combined with brachytherapy

"IMRT/VMAT are adopted. A total dose of 45-50.4 Gy, 1.8\~2.0Gy/f, 25\~ 28F in pelvic and/or extension filed. For patients with metastasis in pelvic lymph node and abdominal para-aortic lymph node, the dose of radiation in local lesion will be increased to 60\~66Gy. For patients at stage IIIB, concurrent radiation will be given in parametrial extension or in the late course the dose will be increased to 60Gy.~Brachytherapy: Three dimensional high dose rate brachytherapy is used with HR-CTV D90 cumulative dose of 80\~85Gy (EQD2); If the tumor diameter is ≥4cm, HR-CTV D90 cumulative dose is ≥87Gy (EQD2). Brachytherapy combined with external beam radiotherapy will be completed within 8 weeks."

Trial Locations (1)

100191

Peking University 3rd Hospital, Beijing

All Listed Sponsors
lead

Peking University Third Hospital

OTHER

NCT04976478 - Study of Nimotuzumab Combined With IMRT in Elder Patients With Cervical Squamous Cell Carcinoma | Biotech Hunter | Biotech Hunter