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PET/MR Evaluation of Regression Grading After Neoadjuvant Therapy for Rectal Cancer

Research Focused on Developing and Assessing a Non-intrusive Diagnostic Approach for Grading Tumor Regression Post-neoadjuvant Treatment in Rectal Cancer, Utilizing 18F-FAPI in Conjunction With FDG PET/MR Imaging.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06318234
Enrollment
32
Registered
2024-03-19
Start date
2024-01-01
Completion date
2025-12-31
Last updated
2024-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Cancer

Keywords

Rectal cancer, Immunotherapy, New assistance, Efficacy evaluation, 18F-FAPI, 18F-FDG, PET/MRI

Brief summary

This project aims to evaluate the role of 18F-FAPI combined with 18F-FDG PET/MRI imaging in quantitatively and accurately evaluating the grading of rectal cancer after SCRT neoadjuvant therapy in patients with advanced rectal cancer as the research object, with postoperative histopathological analysis as the reference index, and to assess the ability of patients to achieve pCR. A diagnostic model and evaluation system will also be constructed.

Detailed description

1. Correlation analysis between the expression levels of FAP and GLUT1 and the degree of tumor regression in rectal cancer The study focuses on patients with advanced rectal cancer treated with SCRT neoadjuvant therapy, and conducts immunohistochemical staining of FAP and GLUT1 (glucose transporter 1) on postoperative specimens to evaluate histopathological changes related to the degree of rectal cancer tumor regression. The expression levels of FAP and GLUT1 and the grading of tumor regression are quantitatively analyzed, and their correlation is analyzed to explore the correlation between the expression levels of FAP and GLUT1 in the lesions of neoadjuvant therapy patients and the degree of tumor regression. 2. Construction and validation of a diagnostic model for the degree of tumor regression in rectal cancer after neoadjuvant therapy using 18F-FAPI combined with 18F-FDG PET/MRI imaging The patient underwent preoperative 18F-FAPI and 18F-FDG PET/MRI imaging, followed by immunohistochemical staining of FAP and GLUT1 on postoperative specimens and evaluation of histopathological changes related to the degree of rectal cancer tumor regression. The patient's uptake of 18F-FAPI and 18F-FDG (SUVmax, SUVmean, SUVpeak, FAPI metabolic volume, MTV, TBR, TLG), expression levels of FAP and GLUT1, and degree of tumor regression were quantitatively analyzed, and the correlation between the patient's uptake of 18F-FAPI and 18F-FDG and the degree of tumor regression was explored. A graded diagnostic model and evaluation system were constructed to verify their effectiveness. 3. Comparison of the efficacy of PET/MR-TRG and MR-TRG in assessing pTRG after neoadjuvant therapy for rectal cancer Compare the constructed PET/MR tumor regression grading diagnostic model with the commonly used clinical imaging diagnostic method MRI in evaluating the efficacy, pTRG, and pCR of neoadjuvant therapy for rectal cancer.

Interventions

DIAGNOSTIC_TEST18F-FAPI,18F-FDG

FAPI and FDG combined with PET/MR imaging in patients with rectal cancer after neoadjuvant therapy

Sponsors

Xiao Chen
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pathologically confirmed as rectal adenocarcinoma, with baseline clinical staging of T3\ 4 and/or N+; * No distant metastasis; * Not receiving chemotherapy or any other anti-tumor treatment before enrollment; * Has not received immunotherapy before enrollment and is able to adhere to the protocol during the study period (neoadjuvant therapy of short-term radiotherapy sequential chemotherapy combined with immunotherapy); * After neoadjuvant therapy, 18F-FAPI and 18F-FDG PET/MRI imaging were performed within 7 days before surgery, and the two scans were collected over two days; * Patient age ≥ 18 years old

Exclusion criteria

* Pregnant or lactating patients; * Patients with severe heart disease in clinical practice; * Organ transplantation requires immunosuppressive therapy and long-term use of hormone therapy; * Patients with autoimmune diseases; * Serious uncontrolled recurrent infections or other serious uncontrolled comorbidities; * The imaging quality is poor and cannot be used for diagnosis and evaluation; * Fasting blood glucose levels are higher than 11.1 mmol/L; * Patients with contraindications for MRI examination.

Design outcomes

Primary

MeasureTime frameDescription
Evaluation efficacy of tumor regression levelCompleted within half year after end of the studyThe sensitivity, specificity, positive predictive value (PPV), negative predictive value

Secondary

MeasureTime frameDescription
expression of FAPcompleted within one week after surgeryImmunohistochemical evaluation of the expression of FAP in postoperative tumor tissue
expression of GLUT1completed within one week after surgeryImmunohistochemical evaluation of the expression of GLUT1 in postoperative tumor tissue
SUVCompleted within one week after PET examinationStandardized uptake value (SUV) of 18F-FDG and 18F-FAPI for each target lesion of subject or suspected primary tumor or/and metastasis.

Countries

China

Contacts

Primary ContactXiao Chen, Ph.D
xiaochen229@foxmail.com+8615922970174

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026