Prediction of Neoadjuvant Chemotherapy Efficacy in Locally Advanced Gastric Cancer

Sponsor
Ruijin Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05140746
Collaborator
(none)
40
1
1
84
0.5

Study Details

Study Description

Brief Summary

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).

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT
N/A

Detailed Description

Before the start of NAC, baseline 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT scans will be scheduled in all enrolled patients. Next, the patients with resectable LAGC will receive NAC treatment, surgery will follow 3~6 weeks after finishing NAC. Abdomen 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT will be scheduled after one cycle of NAC treatment or before surgery. Imaging response measurements will be compared with the histopathological tumor regression grade (TRG) of the resection specimen as gold standard.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Prospective Study on Predicting the Efficacy of Neoadjuvant Chemotherapy in Locally Advanced Gastric Cancer.
Actual Study Start Date :
Sep 10, 2020
Anticipated Primary Completion Date :
Sep 10, 2022
Anticipated Study Completion Date :
Sep 10, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: PET/CT for prediction of NAC efficacy

68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT will be scanned before, during or after NAC.

Diagnostic Test: 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT
Baseline 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT scans before NAC followed by abdomen 68Ga-FAPI-04 PET/CT and 18F-FDG PET/CT scans after one cycle of NAC treatment or before surgery.

Outcome Measures

Primary Outcome Measures

  1. Prediction for NAC efficacy [Two weeks after surgery]

    Predictive value of 68Ga-FAPI PET/CT and 18F-FDG PET/CT for LAGC in NAC response assessment.

  2. Standardized uptake value(SUV) [Two weeks after surgery]

    SUV of 68Ga-FAPI and 18F-FDG uptake on PET/CT images for primary gastric cancer.

  3. Target-to-background ratio(TBR) [Two weeks after surgery]

    68Ga-FAPI and 18F-FDG uptake ratio of primary gastric cancer to mediastinum blood pool on PET/CT images.

Secondary Outcome Measures

  1. Diagnostic efficacy for metastatic lymph nodes [Two weeks after surgery]

    The sensitivity, specificity, NPV, PPV and accuracy of 68Ga-FAPI PET/CT for metastatic lymph nodes in comparison with those of 18F-FDG PET/CT.

  2. Disease free survival [5 years]

    Disease free survival

  3. Overall survival [5 years]

    Overall survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion criteria

  1. Age between 18-75 years.

  2. Histologically confirmed gastric adenocarcinoma through gastroscopy.

  3. Resectable gastric cancer.

  4. ECOG performance status 0-1.

  5. White blood count >4x109/L, Absolute neutrophil count (ANC) >2x109/L, Hemoglobin (Hb)>90g/L, Platelets >100x109/L.

  6. Ejection Fraction>50%.

  7. Serum bilirubin <1.5x ULN; ALT and AST <1.5x ULN.

  8. Serum creatinine ≤1.5x ULN, or GFR> 60ml/min.

  9. Agreement to participate in this study with informed consent form.

  10. Willingness and ability to comply with the protocol for the duration of the study.

  11. No children bearing petential in the next six months before enrollment.

Exclusion criteria

  1. With second primary malignant diseases in past five years, exceptions include basal cell and squamous cell carcinoma of the skin that have been cured.

  2. Known hypersensitivity reaction to chemotherapy drugs or with contraindications.

  3. With severe disease or other unsuitable conditions determined by investigators. Inadequate organ function.

  4. With uncontrollable diabetic or fasting blood glucose level ≥11 mmol/L on the test-day.

  5. With severe mental symptoms, unconscious or unable to complete the examination.

  6. Pregnancy or possibly pregnant woman, breastfeeding woman.

  7. Lack of compliance.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Ruijin Hospital Shanghai Shanghai China 200025

Sponsors and Collaborators

  • Ruijin Hospital

Investigators

  • Principal Investigator: Zhenggang Zhu, Ruijin Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ruijin Hospital
ClinicalTrials.gov Identifier:
NCT05140746
Other Study ID Numbers:
  • PET-NAC-GC
First Posted:
Dec 1, 2021
Last Update Posted:
Dec 1, 2021
Last Verified:
Nov 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2021