A Prospective Study on the Prediction Model of Para-aortic Lymph Node Metastasis
NCT06068387
Summary
The goal of this prospective single-arm trial is to investigate the accuracy and feasibility of the para-aortic lymph node metastasis prediction model in locally advanced cervical cancer, as well as its impact on patients' prognosis. The main questions it aims to answer are: * Is the para-aortic lymph node metastasis prediction model accurate and feasible? * Whether the para-aortic lymph node metastasis prediction model can affect the prognosis of patients.
Eligibility
Inclusion Criteria: * In 2018, the International Federation of Obstetrics and Gynecology (FIGO) stage was Ib3 IIA2-IVA; * It was treated initially without surgical and chemotherapy. * Squamous cell carcinoma, adenocarcinoma and adeno-squamous cell carcinoma were confirmed by histopathology. * Pelvic MRI ± abdominal CT or MRI or PET/CT were performed before treatment. * ECOG score:0 \~ 1. * The expected survival time\>6 months; * There is no absolute contraindication of surgery and and chemoradiotherapy and the patients with good compliance. Exclusion Criteria: * History of immune disease who need to take immunosuppressive drugs. * History of serious mental illness and brain functional disorder. * Other malignancies were diagnosed within five years or needed treatments. * Those who are unable or unwilling to accept surgical treatment/sign informed consent/comply with research requirements. * Without surgical conditions: 1) Chronic renal insufficiency or renal failure; 2) Liver insufficiency; 3)Chronic lung disease with restrictive respiratory dysfunction; 4) Cardiac dysfunction (patients with relative and absolute contraindications to surgery after consultation by cardiac physicians. * Patients who cannot understand the research regimen and refuse to sign the informed consent form. * Other concomitant diseases or special conditions seriously endanger the patient's health or interfere with the trial.
Conditions2
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NCT06068387