Prediction of Neoadjuvant Chemotherapy Efficacy in Locally Advanced Gastric Cancer
Recruiting now · Not applicable
Conditions studied: Gastric Cancer
In brief
This study intends to explore the value of 68Ga-FAPI-04 and 18F-FDG PET/CT in the evaluation of treatment response to neoadjuvant chemotherapy(NAC) for patients with locally advanced gastric cancer(LAGC).
Key facts
- Study ID
- NCT05140746
- Run by
- Ruijin Hospital
- People needed
- 40
- Starts
- 2020-09-10
- Expected to finish
- 2027-09-10
- Last updated by the study team
- 2024-01-09
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age between 18-75 years.
- Histologically confirmed gastric adenocarcinoma through gastroscopy.
- Resectable gastric cancer.
- ECOG performance status 0-1.
- White blood count >4x109/L, Absolute neutrophil count (ANC) >2x109/L, Hemoglobin (Hb)>90g/L, Platelets >100x109/L.
- Ejection Fraction>50%.
- Serum bilirubin <1.5x ULN; ALT and AST <1.5x ULN.
- Serum creatinine ≤1.5x ULN, or GFR> 60ml/min.
- Agreement to participate in this study with informed consent form.
- Willingness and ability to comply with the protocol for the duration of the study.
- No children bearing petential in the next six months before enrollment.
You may not qualify if…
- With second primary malignant diseases in past five years, exceptions include basal cell and squamous cell carcinoma of the skin that have been cured.
- Known hypersensitivity reaction to chemotherapy drugs or with contraindications.
- With severe disease or other unsuitable conditions determined by investigators. Inadequate organ function.
- With uncontrollable diabetic or fasting blood glucose level ≥11 mmol/L on the test-day.
- With severe mental symptoms, unconscious or unable to complete the examination.
- Pregnancy or possibly pregnant woman, breastfeeding woman.
- Lack of compliance.
Where it is running
- Shanghai Ruijin Hospital — Shanghai, Shanghai Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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