Skip to content

Efficacy and Safety of Sequential Maintenance Therapy with Camrelizumab Combined with Apatinib after Radical Radiotherapy for FIGO Stage III - IVA Cervical Cancer: A Single - arm, Single - center, Exploratory Clinical Study

Efficacy and Safety of Sequential Maintenance Therapy with Camrelizumab Combined with Apatinib after Radical Radiotherapy for FIGO Stage III - IVA Cervical Cancer: A Single - arm, Single - center, Exploratory Clinical Study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104656
Enrollment
Unknown
Registered
2025-06-20
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

cervical cancer

Interventions

Interventions group:Sequential camrelizumab combined with apatinib after radical radiotherapy

Sponsors

CAS Hefei Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Pathologically diagnosed as cervical squamous cell carcinoma. 2. Age > 18 years old. 3. Locally advanced cervical squamous cell carcinoma at FIGO 2018 stage ? - ?A. 4. No history of radical radiotherapy in the past. 5. Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0 - 1. 6. PD-L1 >= 1%; Or PD-L1 expression negative 7. Before treatment, there are no significant abnormalities in white blood cells, red blood cells, platelets, hemoglobin, liver and kidney functions, coagulation function, cardiopulmonary function, etc., and the patient is expected to tolerate radiotherapy and chemotherapy. 8. Signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Synchronous double primary malignant tumors; other pathological types such as adenocarcinoma, small - cell carcinoma, sarcoma, etc. 2. History of previous radiotherapy and chemotherapy. 3. Poor patient compliance, failure to return for regular follow - up or receive treatment on schedule. 4. Suffering from autoimmune diseases such as rheumatoid arthritis, ulcerative colitis; infectious diseases such as active hepatitis, pulmonary tuberculosis, etc. 5. Abnormal coagulation function with a bleeding tendency; history of thromboembolic events within 1 year. 6. Cardiopulmonary function is not expected to tolerate radiotherapy and chemotherapy.

Design outcomes

Primary

MeasureTime frame
Progress free survival;

Secondary

MeasureTime frame
Overall Survival;Objective Response Rate;Disease Control Rate;Duration of continuous;Safety;

Countries

China

Contacts

Public ContactXiaotao Qian

CAS Hefei Cancer Hospital

moranqxt@163.com+86 138 5583 3820

Outcome results

None listed

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