[18F]AlF-FAPI-74 PET/CT for preoperative assessment of the peritoneal cancer index and comparison with MRI-based, surgical and pathological assessment in colorectal cancer patients eligible for CRS-HIPEC: study protocol for a prospective observational proof-of-concept study.

Myrna van den Bos, Wouter V Vogel, Maurice van Duijvenvoorde, Niels F M Kok, Arend G J Aalbers, Petur Snaebjornsson, Miangela M Lacle, Jeroen R J Willemse, Walter Kool, Jeroen J M A Hendrikx, Ignace H J T de Hingh, Wilhelmina M U van Grevenstein, Djamila Boerma, Anya N Milne, Andor F van den Hoven, Sjoerd G Elias, Marnix G E H Lam, Max J Lahaye, Onno Kranenburg

Journal: BMJ open 2026;16(9):e125722

PMID: 42716685

Abstract

INTRODUCTION

Colorectal cancer patients with peritoneal metastases have a very poor prognosis. A minority of these patients is eligible for curative cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). The peritoneal cancer index (PCI) is an important criterion to select patients for CRS-HIPEC. Due to challenges in peritoneal metastasis detection by imaging, the PCI is currently routinely assessed by invasive diagnostic laparoscopy in addition to CT and/or MRI. Yet, open-close procedures and early disease recurrence following CRS-HIPEC are common, indicating the need for better patient selection tools. Fibroblast activation protein (FAP)-targeted imaging has recently emerged as a promising strategy for visualising peritoneal disease. The aim of this study is to assess the potential value of FAP inhibitor positron emission tomography/CT (FAPI-PET/CT) as an alternative non-invasive tool for quantitative PCI assessment.

METHODS AND ANALYSIS

TROMPET is a prospective observational proof-of-concept study. A total of 25 colorectal cancer patients with suspected or verified peritoneal metastases who are eligible for CRS-HIPEC based on MRI will be included in this study. Patients younger than 18, pregnant and/or breastfeeding, with any contraindication(s) for MRI, PET, CT and/or CRS-HIPEC, and/or with a known additional malignancy within the past five years are excluded. Participants will receive [18F]AlF-FAPI-74 PET/CT prior to surgery. The primary objective is to determine the correlation between PCI scores determined by FAPI-PET/CT and 'true' PCI scores determined by histopathological analysis of all resected lesions. The secondary objectives include the correlations between PCI scores determined by FAPI-PET/CT, by MRI and during surgery, the potential of FAPI-PET/CT to detect extraperitoneal metastases, and molecular and immunohistochemical analysis of resected tissue to provide insight into the nature of FAPI-PET-positive lesions. The primary endpoint is all PCI scores determined by FAPI-PET and histopathology and their correlation on patient level. If this study shows that the PCI score can be accurately determined preoperatively by FAPI-PET/CT, it will form the basis for further developing FAPI-PET/CT as a quantitative, standardised, non-invasive diagnostic tool for selecting patients for CRS-HIPEC. Moreover, the 'radiology-pathology' setup of the study will allow us to characterise FAPI-PET-positive and PET-negative lesions in detail, providing further insight into the strengths and potential pitfalls of FAPI-PET/CT in the detection of peritoneal metastases from colorectal cancer.

ETHICS AND DISSEMINATION

This study is approved by the assigned Medical-Research-Ethics-Committee (METC NedMec) on 19-08-2024. All participants will provide written informed consent. Study results will be disseminated through (inter)national meetings and peer-reviewed publications.

TRIAL REGISTRATION NUMBER

2024-512301-16-01.

© Author(s) (or their employer(s)) 2026. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.

Address: Department of Imaging and Oncology, Laboratory Translational Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Department of Radiology, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Nuclear Medicine, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Epidemiology and Health Economic Evaluation, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Department of Surgery, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Pathology, Netherlands Cancer Institute, Amsterdam, Netherlands.; Faculty of Medicine, University of Iceland, Reykjavík, Iceland.; Department of Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Department of Radiology, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Nuclear Medicine and Cyclotron Noordwest B.V, Noordwest Ziekenhuisgroep Alkmaar, Alkmaar, Noord-Holland, Netherlands.; Department of Nuclear Medicine, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Pharmacy & Pharmacology, Netherlands Cancer Institute, Amsterdam, Netherlands.; Department of Surgery, Catharina Hospital, Eindhoven, Netherlands.; GROW - School for Oncology and Reproduction, Maastricht University, Maastricht, Netherlands.; Department of Surgical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Department of Surgery, St Antonius Ziekenhuis, Nieuwegein, Netherlands.; Department of Pathology, St Antonius Ziekenhuis, Nieuwegein, Netherlands.; Department of Nuclear Medicine, St Antonius Ziekenhuis, Nieuwegein, Netherlands.; Department of Radiology and Nuclear Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Department of Radiology, Netherlands Cancer Institute, Amsterdam, Netherlands [email protected] [email protected].; Department of Imaging and Oncology, Laboratory Translational Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands [email protected] [email protected].
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