Esophageal Squamous Cell Carcinoma Clinical Trial
Official title:
Quantitative Analysis of 18F-FAPI Dynamic PET/CT for Accurate Differential Diagnosis of Metastatic Lymph Nodes of Esophageal Squamous Cell Carcinoma
Patients diagnosed with esophageal squamous cell carcinoma based on clinicopathology, laboratory examination and imaging criteria were selected as the research subjects, and compared with conventional 18F-FDG PET/CT. To evaluate the research value of quantitative analysis of 18F-FAPI PET/CT dynamic imaging in the classification of benign and malignant features of primary esophageal squamous cell carcinoma (ESCC) and lymphatic nodules, lesion localization, outcome and prognosis.
| Status | Not yet recruiting |
| Enrollment | 60 |
| Est. completion date | December 31, 2023 |
| Est. primary completion date | December 31, 2023 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 85 Years |
| Eligibility | Inclusion Criteria: 1. Esophageal squamous cell carcinoma was diagnosed according to gastroscopy and pathological diagnostic criteria; 2. Age above 18 years old, less than 85 years old, no gender restriction; 3. Untreated patients who have not received surgery, chemotherapy, biotherapy or radiotherapy; 4. Laboratory examination: (1) General physical condition score ECOG: 0-2; (2) No dysfunction of main organs; (3) Oxygen partial pressure = 10.64kPa; (4) WBC = 4×109 L-1; (5) Routine blood hemoglobin = 9.5 g· DL-1; (6) The absolute count of neutrophils = 1.5×109 L-1; (7) Platelet count = 100×109 L-1; (8) Total bilirubin = 1.5 times the upper limit of normal value; (9) Creatinine = 1.25 times the upper limit of normal value; (10) Creatinine clearance rate = 60 mL ·min-1; 5. Can obtain complete follow-up information, understand the situation of this study and sign the informed consent. Exclusion Criteria: 1. Has had any other malignant tumor within 5 years; 2. Nursing and/or pregnant women; 3. Patients with severe bleeding tendency; 4. Recent severe hemoptysis, severe cough, dyspnea or patients cannot cooperate; 5. Severe emphysema, pulmonary congestion and cor pulmonale; 6. In the opinion of the Investigator, the subject may not be able to complete the study or comply with the requirements of the study (for administrative or other reasons). |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Fifth Affiliated Hospital, Sun Yat-Sen University | Sun Yat-sen University, The First Affiliated Hospital of Guangzhou Medical University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Comparison of SUVmax between MLN and BLN. | Comparison of SUVmax between MLN and BLN. | 50 min to 60 min | |
| Primary | Comparison of K1 between MLN and BLN. | Comparison of K1 of 2TM between MLN and BLN. | 0 min to 60 min | |
| Primary | Comparison of k2 between MLN and BLN. | Comparison of k2 of 2TM between MLN and BLN. | 0 min to 60 min | |
| Primary | Comparison of k3 between MLN and BLN. | Comparison of k3 of 2TM between MLN and BLN. | 0 min to 60 min | |
| Primary | Comparison of k4 between MLN and BLN. | Comparison of k4 of 2TM between MLN and BLN. | 0 min to 60 min | |
| Primary | Comparison of BP between MLN and BLN. | Comparison of BP of LoganREF between MLN and BLN. | 30 min to 60 min |
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