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NCT Number: NCT07552207

Comparison of [68Ga]Ga-CTR-FAPI and 18F-FDG PET/MRI for Lymph Node Staging in Rectal Cancer

This is a prospective, single-center, diagnostic study designed to compare the accuracy of [68Ga]Ga-CTR-FAPI PET/MRI and [18]F-FDG PET/MRI for the detection of lymph node metastasis in patients with initially untreated, resectable middle to high rectal cancer. The study aims to evaluate whether [68Ga]Ga-CTR-FAPI PET/MRI provides higher sensitivity and specificity than traditional 18F-FDG PET/MRI at both the patient level and the lymph node level.

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Key information

About this study

Accurate preoperative staging of colorectal cancer is crucial for formulating treatment plans and improving patient prognosis. While conventional MRI and 18F-FDG PET/MRI are utilized, they face limitations such as false positives due to inflammatory lymph nodes or fibrotic scars. Fibroblast activating protein inhibitor (FAPI) specifically targets tumor-associated fibroblasts, potentially reducing false-positive rates by avoiding non-specific uptake in inflammatory areas.

This study aims to cross-validate the diagnostic efficacy of these two probes through a precise imaging-pathology matching technique. All enrolled patients will sequentially undergo both [68Ga]Ga-CTR-FAPI PET/MRI and 18F-FDG PET/MRI within 30 days prior to radical surgery. Following surgery, fresh mesorectal specimens will be precisely sectioned and matched to preoperative anatomical imaging maps. By leveraging a well-established node-by-node matching and identification methodology with high accuracy, this study ensures the execution of spatial correlation between preoperative radiologic imaging and postoperative microscopic pathology. Through mapping individual lymph nodes, the study will analyze the root causes of false positives and negatives, and extract radiomics features to evaluate their correlation with the tumor microenvironment (e.g., fibroblast density, Ki-67 index).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed rectal adenocarcinoma by pathological biopsy.
  • Lower margin of the tumor is ≥ 5 cm and ≤15 cm from the anal verge.
  • Planned to undergo radical surgery.
  • ECOG performance status score ≤ 2.
  • Patient is willing to undergo PET/MRI examination.

Exclusion criteria

  • History of pelvic radiotherapy or chemotherapy.
  • Concurrent with other malignant tumors or active infections.
  • Pregnant or unable to sign the informed consent form.
  • Claustrophobia or inability to tolerate MRI examinations due to other reasons.

Treatment and study plan

PET/MRI with 18F-FDG and [68Ga]Ga-CTR-FAPI

Diagnostic Test

Diagnostic Test: 18F-FDG PET/MRI

Description: Patients receive an intravenous injection of 18F-FDG (3.7-5.5 MBq/kg).

Diagnostic Test: [68Ga]Ga-CTR-FAPI PET/MRI

Description: Patients receive an intravenous injection of [68Ga]Ga-CTR-FAPI (1.8-3.7 MBq/kg).

Primary outcomes

  1. Sensitivity and Specificity of Lymph Node Metastasis Detection

    Time frame: Up to 30 days post-surgery

    Comparison of the sensitivity and specificity of [68Ga]Ga-CTR-FAPI and 18F-FDG PET/MRI in determining lymph node metastasis at both the individual lymph node level and the patient level. Sensitivity is defined as the proportion of imaging-positive and pathology-positive nodes out of all pathology-positive nodes. Specificity is defined as the proportion of imaging-negative and pathology-negative nodes out of all pathology-negative nodes.

Secondary outcomes

  1. False Positive and False Negative Rates

    Time frame: Up to 30 days post-surgery

    Analysis of the false positive and false negative rates of FAPI and FDG imaging, exploring underlying pathological bases such as inflammation or micrometastasis.

  2. Correlation Between Radiomics Features and Tumor Microenvironment

    Time frame: Up to 30 days post-surgery

    Extraction of lymph node radiomics features to evaluate their association with tumor microenvironmental markers, determined via automatic immunohistochemistry scoring.

Study contacts

Contact information is provided by the study sponsor or research team.

Minghe Zhao

CONTACT

[email protected]

0086-15600896700

Sponsors and collaborators

Lead sponsor

Peking University Cancer Hospital & Institute

Other

Registry information

Official study title

Comparison of the Diagnostic Efficacy of [68Ga]Ga-CTR-FAPI PET/MRI and 18F-FDG PET/MRI for Lymph Node Metastasis in Middle to High Rectal Cancer

Acronym: PKUCH-R12

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Apr 27, 2026
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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