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PET Imaging of Solid Tumors by a Novel Tracer, 68Ga-FAPI

K

Karolinska University Hospital

Status and phase

Enrolling
Phase 1

Conditions

Epithelial Ovarian Cancer
Bile Duct Neoplasms
Stomach Neoplasms
Pancreatic Neoplasms

Treatments

Device: PET/CT
Drug: 68Ga-FAPI-46

Study type

Interventional

Funder types

Other

Identifiers

NCT05172310
2020-002568-30 (EudraCT Number)
H035-FAPI

Details and patient eligibility

About

Cancers of the pancreas, bile ducts, stomach and ovaries are dismal diseases with most patients being diagnosed in advanced stages leading to a bad prognosis. These cancers can be difficult to diagnose and sometimes impossible to differentiate from underlying benign conditions. Establishing the correct diagnosis of primary cancer lesions and possible spread to other organs in time is pivotal for choosing the right therapy. Routinely applied staging procedures are however not always reliable. The main aim in this study is to evaluate the diagnostic accuracy of PET/CT with a novel radiotracer, FAPI, in the primary diagnosis of cancers in the pancreas, stomach and bile ducts as well as in patients with primary and recurrent epithelial ovarian cancer (EOC).

Full description

Malignant tumors exceeding 1-2 mm in size require formation of a supporting stroma, which includes vascular cells, inflammatory cells and fibroblasts . Several organs in the upper gastro-intestinal tract are known to develop tumors with strong desmoplastic reaction characterized by pervasive growth of tumor stroma. The pancreas, stomach, bile ducts and ovaries are all organs with this property. Within tumor stroma, a subpopulation of fibroblasts called cancer-associated fibroblasts (CAFs) are known to be involved in growth, migration and progression of the tumor.

The Fibroblast Activation Protein (FAP) is one of the more prominent stroma markers and was the focus in the development of an agent for imaging and, eventually, even targeted radionuclide therapy. FAP is a type II membrane bound glycoprotein absent or only expressed at insignificant levels, in normal tissues in adults. The FAP inhibitor, FAPI, gets selectively enriched in tissues where its target protein is expressed and there is no or very limited FAPI uptake in all normal organs. This opens new possibilities for the detection of malignant lesions with higher stromal content based on the high contrast positron emission tomography (PET) images obtained with a 68-Gallium (68Ga) radiolabeled - FAPI compound. As cancers in pancreas, stomach, bile ducts and ovaries are all characterized by abundant desmoplasia that constitutes up to 90% of the total tumor volume and contains extracellular matrix, immune cells, vasculature and CAFs, it would be suitable for targeted imaging with FAPI.

Preliminary studies show elevated FAPI uptake in many tumors rich in fibroblasts along with low background uptake. The main objective of this prospective study is to improve non-invasive diagnostics of malignancy in tumors of pancreas, stomach, bile ducts and ovaries, all known for a strong desmoplastic reaction by evaluating the diagnostic accuracy of PET/CT with a novel radiotracer, FAPI in the primary diagnosis and staging of such cancers.

Enrollment

410 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Consecutive patients scheduled for surgical removal of either a pancreatic, biliary or gastric lesion.

    • Consecutive patients scheduled for primary surgical removal of early stage epithelial ovarian cancer (EOC), interval debulking surgery of EOC or surgical removal or tissue biopsy of recurrent EOC
  • Signed informed consent.

Common Exclusion Criteria for all study populations:

  • Age ≤18 year
  • Pregnancy and lactation
  • Significantly reduced renal function
  • Allergy to iodinated contrast media
  • Subjects that for some reason are unable to exercise their own rights, such as cognitive function impairment.

Additional Exclusion Criteria for study populations with either pancreatic-, gastric or bile duct cancer:

• Known metastatic disease

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

410 participants in 2 patient groups

Cancer patients
Experimental group
Description:
* Adults with suspected cancer of either pancreas, bile ducts or stomach * Adults with primary and recurrent epithelial ovarian cancer (EOC)
Treatment:
Drug: 68Ga-FAPI-46
Device: PET/CT
Non cancer patients
Active Comparator group
Description:
Non cancer patients operated for non-malignant diseases in pancreas during the same period of time will be investigated with the same procedure.
Treatment:
Drug: 68Ga-FAPI-46
Device: PET/CT

Trial contacts and locations

1

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Central trial contact

Siri af Burén, MD; Rimma Axelsson, Professor

Data sourced from clinicaltrials.gov

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