Ignite Creation Date:
2025-12-24 @ 4:54 PM
Ignite Modification Date:
2025-12-29 @ 2:48 PM
Study NCT ID:
NCT05209750
Status:
UNKNOWN
Last Update Posted:
2023-09-21
First Post:
2022-01-13
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
FAPI PET/CT for Lymph Node Staging in Colorectal Carcinoma
Sponsor:
The Netherlands Cancer Institute
Organization:
Study Overview
Official Title:
Pilot Study of FAPI PET/CT for Locoregional (re)Staging of Lymph Nodes in Colorectal Carcinoma
Status:
UNKNOWN
Status Verified Date:
2023-09
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
FAPI-CRC1
Brief Summary:
To describe the accuracy of FAPI PET/CT in the detection of regional lymph node metastases in patients with colorectal cancer in comparison with standard diagnostic imaging and (in operated patients) histopathology, aiming to provide early evidence of the diagnostic value of FAPI PET/CT.
Detailed Description:
Rationale: In patients with colorectal cancer the detection of small nodal metastases with standard diagnostic imaging (CT and/or MRI) is challenging. This may result in suboptimal staging and ultimately in suboptimal treatment. Colorectal cancer is typically associated with a tumour stroma containing large numbers of activated tumour-associated fibroblasts. Radiolabelled fibroblast activation protein inhibitor (FAPI) compounds bind selectively to these fibroblasts, and thereby allow sensitive and specific imaging of tumour stroma with FAPI PET/CT. Recently published research has indicated that FAPI PET/CT can accurately detect macroscopic colorectal cancer lesions. We have recently demonstrated that tumour stroma also develops in lymph node metastases with a tumour diameter of just a millimetre. Improved detection in the primary tumour area and in regional lymph nodes provided by FAPI PET/CT may contribute to more accurate staging with potential impact on patient management e.g., selection for neoadjuvant treatment. However, until now FAPI PET/CT has mainly been used to visualise tumour in metastatic patients with various tumour types in the scope of palliative treatment, and its specific diagnostic value for detection and locoregional staging of colorectal cancer is currently unknown. We will now use FAPI PET/CT in a pilot study to explore the potential diagnostic value in the detection of regional lymph node metastases, and to identify opportunities for further prospective research in the areas of diagnostics, radiotherapy, and FAPI-based theragnostic therapy.
Objective: To describe the accuracy of FAPI PET/CT in the detection of regional lymph node metastases in patients with colorectal cancer in comparison with standard diagnostic imaging and (in operated patients) histopathology, aiming to provide early evidence of the diagnostic value of FAPI PET/CT.
Study design: Multicentre prospective cross-sectional diagnostic pilot study. Study population: The study involves 30 patients with newly detected clinically node positive colorectal cancer stratified by 20 patients with colon cancer and 10 patients with rectal cancer. All patients undergo local treatment of the primary colorectal tumour.
Intervention: Participants receive standard diagnostic imaging with contrast enhanced CT thorax-abdomen (all patients) and pelvic MRI for initial staging and restaging after neoadjuvant treatment (rectal cancer patients only). In patients with colon cancer, one FAPI PET/CT scan is added as a diagnostic intervention in the scope of this study early after standard diagnostic imaging and prior to planned surgery. In patients with rectal cancer, two FAPI PET/CT scans are added as diagnostic interventions i.e., for initial staging and restaging (pre and post neoadjuvant therapy). The FAPI PET/CT results will not guide treatment decisions.
Main study parameters: The main objective is to describe the diagnostic accuracy of FAPI PET/CT in detecting regional lymph node metastases relative to standard of care diagnostic imaging. FAPI PET/CT will be visually correlated with contrast-enhanced CT in colon cancer patients, and pelvic MRI pre- and post-neoadjuvant treatment in rectal cancer patients. Histopathology of the resected specimen will serve as reference test for operated patients. Secondary outcomes include description of additional findings on FAPI PET/CT, correlation between tumour stroma in resected lymph node metastases and tracer uptake of regional lymph nodes on FAPI PET/CT, and evaluation of response to neoadjuvant treatment on FAPI PET/CT in rectal cancer. All outcomes are descriptive and serve as pilot for a potential subsequent larger prospective diagnostic study.
Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: Participation in this study has no significant risks and will not induce a delay in diagnosis or treatment because the outcomes of the FAPI PET/CT will not guide treatment decisions. The FAPI PET/CT scan involves a total procedure duration of maximally 2 hours and an estimated radiation dose of 6 mSv per procedure (3 mSv for an administered dose of 200 MBq Fluor-18-FAPI, and 3 mSv for the associated low dose CT scan). This radiation dose (6 mSv in colon cancer patients of \> 18 years and 12 mSv in rectal cancer patients of \> 50 years) is well within the range of normal diagnostic procedures and does not induce a significant risk in the selected population with colorectal cancer. In addition, the Fluor-18-FAPI radiopharmaceutical is thus far not associated with side effects after injection.
Objective: To describe the accuracy of FAPI PET/CT in the detection of regional lymph node metastases in patients with colorectal cancer in comparison with standard diagnostic imaging and (in operated patients) histopathology, aiming to provide early evidence of the diagnostic value of FAPI PET/CT.
Study design: Multicentre prospective cross-sectional diagnostic pilot study. Study population: The study involves 30 patients with newly detected clinically node positive colorectal cancer stratified by 20 patients with colon cancer and 10 patients with rectal cancer. All patients undergo local treatment of the primary colorectal tumour.
Intervention: Participants receive standard diagnostic imaging with contrast enhanced CT thorax-abdomen (all patients) and pelvic MRI for initial staging and restaging after neoadjuvant treatment (rectal cancer patients only). In patients with colon cancer, one FAPI PET/CT scan is added as a diagnostic intervention in the scope of this study early after standard diagnostic imaging and prior to planned surgery. In patients with rectal cancer, two FAPI PET/CT scans are added as diagnostic interventions i.e., for initial staging and restaging (pre and post neoadjuvant therapy). The FAPI PET/CT results will not guide treatment decisions.
Main study parameters: The main objective is to describe the diagnostic accuracy of FAPI PET/CT in detecting regional lymph node metastases relative to standard of care diagnostic imaging. FAPI PET/CT will be visually correlated with contrast-enhanced CT in colon cancer patients, and pelvic MRI pre- and post-neoadjuvant treatment in rectal cancer patients. Histopathology of the resected specimen will serve as reference test for operated patients. Secondary outcomes include description of additional findings on FAPI PET/CT, correlation between tumour stroma in resected lymph node metastases and tracer uptake of regional lymph nodes on FAPI PET/CT, and evaluation of response to neoadjuvant treatment on FAPI PET/CT in rectal cancer. All outcomes are descriptive and serve as pilot for a potential subsequent larger prospective diagnostic study.
Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: Participation in this study has no significant risks and will not induce a delay in diagnosis or treatment because the outcomes of the FAPI PET/CT will not guide treatment decisions. The FAPI PET/CT scan involves a total procedure duration of maximally 2 hours and an estimated radiation dose of 6 mSv per procedure (3 mSv for an administered dose of 200 MBq Fluor-18-FAPI, and 3 mSv for the associated low dose CT scan). This radiation dose (6 mSv in colon cancer patients of \> 18 years and 12 mSv in rectal cancer patients of \> 50 years) is well within the range of normal diagnostic procedures and does not induce a significant risk in the selected population with colorectal cancer. In addition, the Fluor-18-FAPI radiopharmaceutical is thus far not associated with side effects after injection.
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: