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Search / Trial NCT06061874

Ga68-FAPI-46 PET/CT for Preoperative Assessment of Peritoneal Carcinomatosis

Launched by JULES BORDET INSTITUTE · Sep 25, 2023

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Colorectal Cancer Ovarian Cancer Peritoneal Carcinomatosis Fibroblast Activation Protein Inhibitor Positron Emission Tomography Fapi 46 Pet Fapi Pet/Ct Fibroblast Activation Protein

ClinConnect Summary

This clinical trial is studying a new imaging technique called Ga68-FAPI-46 PET/CT to help doctors better assess patients with peritoneal carcinomatosis, which is a type of cancer spread in the abdominal cavity. The goal is to see how accurately this imaging method can identify cancer in patients with colorectal and ovarian cancer who are preparing for surgery intended to remove the tumors.

To participate in this trial, individuals must have a confirmed diagnosis of colorectal or ovarian cancer and either known or suspected spread of the cancer to the peritoneum (the lining of the abdominal cavity). They should be scheduled for surgery aimed at removing these tumors and must be in good overall health. Participants will undergo the Ga68-FAPI-46 PET/CT scan as part of their preoperative assessment, which could help doctors plan the best treatment approach. The study is currently recruiting patients aged 65 to 74, and both men and women are welcome to join.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Histologically proven colorectal and ovarian cancer.
  • Known or suspected peritoneal metastases from the tumour of origin.
  • Scheduled for peritoneal complete cytoreductive surgery with curative intent with or without neoadjuvant chemotherapy.
  • ECOG (Eastern Cooperative Oncology Group) Performance status ≤2.
  • Signed written informed consent obtained before any study-specific screening procedures.
  • Exclusion Criteria:
  • Non-resectable extra-abdominal metastasis and/or \>3 hepatic metastases on standard work-up
  • Known chronic inflammatory conditions including the intestinal system (eg. inflammatory bowel disease, Crohn's disease)
  • Pregnant and lactating women
  • Previous or concurrent malignancy diagnosed within the last 3 years except adequately treated in situ carcinoma of the cervix uteri and basal or squamous cell skin cancer.
  • Subjects with another significant medical condition which, in the investigator's opinion, may interfere with the completion of the study.

About Jules Bordet Institute

The Jules Bordet Institute is a prestigious cancer research and treatment center located in Brussels, Belgium, dedicated to advancing oncology through innovative clinical trials and multidisciplinary care. As a leading sponsor of clinical research, the institute focuses on developing novel therapeutic approaches and improving patient outcomes in various cancer types. With a commitment to scientific excellence and collaboration, the Jules Bordet Institute leverages cutting-edge technologies and a robust network of healthcare professionals to foster breakthroughs in cancer treatment and enhance the quality of life for patients.

Locations

Brussels, , Belgium

Patients applied

0 patients applied

Trial Officials

Patrick Flamen

Principal Investigator

Jules Bordet Institute

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported