Carbon ion radiotherapy with brachytherapy for locally advanced cervical cancer

Trial details

Who runs it

Zhejiang Cancer Hospital

Trial code

NCT07702838

Record updated

14 July 2026

Original description

This study explores the therapeutic effect of carbon ion radiotherapy plus immunotherapy and chemotherapy for locally advanced cervical cancer.Read full original descriptionShow less

A Prospective Clinical Study of Immunotherapy Combined With Carbon Ion Radiotherapy for Locally Advanced Cervical Cancer

This study explores the therapeutic effect of carbon ion radiotherapy plus immunotherapy and chemotherapy for locally advanced cervical cancer.

Inclusion: Female patients aged ≥ 18 years at the time of signing the informed consent form; Histopathologically confirmed diagnosis of cervical cancer (squamous cell carcinoma, adenocarcinoma, and adenosquamous carcinoma); Stage IIB-IVA disease per the 2018 FIGO staging system; Presence of measurable lesions as defined by RECIST version 1.1; Patients reviewed by the carbon ion radiotherapy multidisciplinary team (MDT) with an indication for carbon ion radiotherapy; Patients voluntarily receiving carbon ion radiotherapy at Zhejiang Cancer Hospital and bearing all relevant treatment expenses; Complete clinical and imaging data available; Patients willing to participate in the trial and complete questionnaire surveys; Patients willing to participate in the trial and provide biospecimens, including cervical tissue, various body fluid specimens and tissue samples; Patients willing to attend regular standardised outpatient follow-up visits at our hospital; Eastern Cooperative 11. Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-2; No prior history of surgery, radiotherapy or chemotherapy for cervical cancer; Adequate function of major vital organs (bone marrow, liver, kidney, etc.), with laboratory values meeting the following criteria within 1 week prior to treatment: Absolute neutrophil count (ANC) ≥ 1500/μL; Platelet count ≥ 100,000/μL; Haemoglobin ≥ 9.0 g/dL (or ≥ 5.6 mmol/L); Creatinine clearance ≥ 50 mL/min; Total bilirubin ≤ 1.5 × upper limit of normal (ULN); if total bilirubin > 1.5 × ULN, direct bilirubin shall be ≤ ULN; Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN; International Normalised Ratio (INR), prothrombin time (PT), and activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (excluding patients receiving anticoagulant therapy within the therapeutic range); Estimated overall survival ≥ 6 months.

Exclusion: Presence of severe concomitant complications (e.g., uncontrolled cardiovascular disease, hypertension, diabetes mellitus, refractory infection, active peptic ulcer, uncontrolled psychiatric disorders, etc.); Concurrent active second primary malignancy; Prior receipt of immunotherapy agents (including anti-PD-1, anti-PD-L1, anti-CTLA-4, etc.); Prior radical surgery, radiotherapy, or systemic therapy (including investigational agents) for cervical cancer. Note: Conisation of the cervix is permitted; Administration of any investigational drug within 4 weeks before the initiation of immunotherapy; Confirmed immunodeficiency or receipt of chronic systemic corticosteroid therapy (prednisone equivalent dose >10 mg/day) or other immunosuppressive therapy within 7 days prior to immunotherapy; Prior history of non-infectious pneumonitis/interstitial lung disease requiring steroid treatment, or current active pneumonitis/interstitial lung disease; Previous allogeneic tissue or solid organ transplantation; Metallic implants within the radiation field path that may compromise the accuracy of radiotherapy dose calculation; History of grade ≥3 severe hypersensitivity reactions to immunotherapeutic agents; Active autoimmune disease requiring systemic therapy within the past 2 years (replacement therapies such as thyroxine, insulin and physiological glucocorticoids are excluded); Active infection requiring systemic treatment; History of active hepatitis B (HBsAg positive) or active hepatitis C (detectable HCV RNA); Known psychiatric illness or substance abuse that may impair subject compliance; pregnant or breastfeeding females, or those planning conception/pregnancy during the study period (from screening to 120 days after the last study treatment); History of HIV infection; Any disease, treatment, laboratory abnormality or other condition that, in the investigator's judgement, may confound study results, hinder full study participation or pose additional risks to the subject; Tumour invasion of the rectum (Stage IVA) or peritoneal metastasis (M1); Subject requests withdrawal from the study.

ClinicalTrials.gov NCT07702838