Concurrent Radiochemotherapy Plus Anlotinib for Locally Advanced Cervical Cancer

NARecruitingINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

March 12, 2021

Primary Completion Date

October 31, 2025

Study Completion Date

January 31, 2026

Conditions
Uterine Cervical NeoplasmsChemoradiotherapyAngiogenesis
Interventions
DRUG

Hydrochloride anlotinib

Hydrochloride anlotinib is a small molecular anti-angiogenesis drug with multiple targets. It will be taken at a starting dose of 12 mg for 14 days. Then participants will rest for 7 days and start a new cycles. At most of 3 cycles will be administrated. If intolerable toxicity happen, dosage of 10mg or 8mg will be taken.

DRUG

cis Platinum/carboplatin

Concurrent chemotherapy will be administrated weekly during radiation for a total of 5-6 doses. Cisplatin of 40mg/m2 will be the most preferred regime. For patients with intolerable toxicity of cisplatin, carboplatin of AUC 2 will be the alternative drug.

RADIATION

External beam radiotherapy and brachytherapy

Radiation will be given by external beam of 45Gy total dose and 3D-brachytherapy of 30Gy/5F or 28Gy/4F. Duration of radiotherapy will be no more than 8 weeks.

Trial Locations (1)

430071

RECRUITING

Zhongnan Hospital of Wuhan University, Wuhan

All Listed Sponsors
lead

Zhongnan Hospital

OTHER