[68Ga]Ga-FAPI-46 in Staging of Head and Neck Carcinomas

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohn O. Prior

About this trial

The trial focuses on assessing the role of \[68Ga\]Ga-FAPI-46 in head and neck squamous cell carcinomas (HNSCC) staging before surgery. In the context of metastasis, cancer-associated fibroblasts (CAFs) emerge as pivotal contributors to the creation of a microenvironment conducive to future metastases. CAFs exert their influence through intricate mechanisms, including the remodeling of the extracellular matrix by secreting proteins such as collagen and fibronectin. This process enhances the structural support for cancer cell invasion into adjacent tissues. Additionally, CAFs play a central role in promoting angiogenesis, ensuring an adequate blood supply to the tumor, which may also facilitate the entry of cancer cells into the bloodstream. Through modulation of immune responses within the tumor microenvironment, CAFs establish an immunosuppressive milieu, providing a permissive environment for cancer cell survival and dissemination. Collectively, the orchestrated activities of CAFs contribute to the preparation of a metastatic niche, influencing the microenvironment at both primary and secondary sites and enhancing the likelihood of successful metastasis.

Employing \[68Ga\]Ga-FAPI-46 PET/CT imaging to target activated CAFs may hold the potential to discern lymph nodes (LNs) predisposed to future metastases in HNSCC. The use of this imaging modality offers a unique opportunity to visualize and assess the presence and activity of CAFs within the tumor microenvironment. By targeting the fibroblast activation protein (FAP), a receptor enriched on CAFs, this imaging approach provides a specific and sensitive mean to identify regions where the microenvironment may favor metastatic progression.

In this research endeavor, the primary objective is to highlight the additional value of \[68Ga\]Ga-FAPI-46 PET/CT into the standard pre-surgical imaging protocol. Additionally, the study will evaluate the efficacy of FAP positon emission tomography (PET) in primary tumor delineation. Imaging based on \[68Ga\]Ga-FAPI-46 allows the identification of CAFs, specifically by exploiting their increased FAP expression. The study aims also to systematically compare the \[68Ga\]Ga-FAPI-46 PET/CT signals with the characteristics of resected lymph nodes, seeking to ascertain the capability of FAPI PET imaging in identifying premetastatic conditions. By comparing the \[68Ga\]Ga-FAPI-46 PET signal and the histopathological features of resected lymph nodes, the goal is to validate the potential of \[68Ga\]Ga-FAPI-46 PET imaging as a tool for early detection of premalignant or metastatic conditions in the lymphatic system before surgical intervention. The ability to pinpoint lymph nodes at risk for future metastases could revolutionize clinical decision-making, by facilitating a more nuanced understanding of disease spread, thereby informing personalized treatment strategies and potentially improving patient outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years old

Karnofsky index ≥80%

Patients with operable head and neck cancer presenting histologically proven HNSCC (including Oral Cavity Cancer, Pharyngeal Cancer, Laryngeal Cancer)

Patients with at least one nodal metastasis

Disqualifiers

Known pregnancy or ongoing breast feeding

Claustrophobia

Severe renal insufficiency (GFR<30 mL/min/1,73 m2)

Liver enzymes (ALAT, ASAT)>5 times the standard upper limit

Trial design

Design model

Single group

Treatments tested in this trial

  • [68Ga]Ga-FAPI-46 PET/CT

    Drug

    \[68Ga\]Ga-FAPI-46 PET/CT

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: HNSCC patientsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

[68Ga]Ga-FAPI-46 PET/CT imaging results: tumor size

The tumor size (mm\*mm) measured by 68Ga-FAPI-46 PET/CT will be reported. Results will be compared to the clinically indicated standard imaging (FDG PET/CT, ceCT and MRI).

Time frame
6 weeks
2

[68Ga]Ga-FAPI-46 PET/CT imaging results: tumor volume

The tumor volume (mm\^3) measured by 68Ga-FAPI-46 PET/CT will be reported. Results will be compared to the clinically indicated standard imaging (FDG PET/CT).

Time frame
6 weeks
3

[68Ga]Ga-FAPI-46 PET/CT imaging results: tumor SUVmax

The SUVmax of the tumor measured by 68Ga-FAPI-46 PET/CT will be reported. Results will be compared to the clinically indicated standard imaging (FDG PET/CT).

Time frame
6 weeks
4

[68Ga]Ga-FAPI-46 PET/CT imaging results: number of lesions

The number of lesions (for nearby lymph nodes and distant metastases) visible by 68Ga-FAPI-46 PET/CT will be reported. Results will be compared to the clinically indicated standard imaging (FDG PET/CT, ceCT and MRI).

Time frame
6 weeks

Secondary outcomes

1

Ability of [68Ga]Ga-FAPI-46 PET/CT to visualize tumor infiltration in lymph nodes

Histopathology of clinically indicated resected lymph node specimen will be performed. \[68Ga\]Ga-FAPI-46 PET/CT results and tumor infiltration findings by histology will be compared (lesions defined positive/negative as a result of the two techniques).

Time frame
2 months

Other outcomes

1

Evaluation of FAP+ CAFs distribution

Presence (positive/negative) of FAP+ cells in tumor center, tumor invasive margin and adjacent normal tissue.

Time frame
1 year
2

Comparison of [68Ga]Ga-FAPI-46 PET/CT with FAP immunoistochemistry

The ability of \[68Ga\]Ga-FAPI-46 PET/CT to identify FAP+ cells in lymph node lesions will be evaluated. The measurement will compare if lesions are defined as positive/negative by FAPI PET (positive/negative) and by histology showing FAP+ CAFs in the lesion.

Time frame
1 year
3

Evaluation of desmoplastic changes

Resected LNs will be analyzed by histopathology to determine the presence of desmoplastic changes. Desmoplastic changes will be expressed as the expression of specific molecular markers.

Time frame
1 year
4

Evaluation of modifications to the current therapeutic approach (questionnaire)

Modifications to the current therapeutic approach will be evaluated by the head and neck surgeon, who will fill out a questionnaire about the foreseen therapeutic approach with and without taking into account the results of the \[68Ga\]Ga-FAPI-46 PET/CT. The questionnaire will contain yes/no questions or multiple choice questions.

Time frame
Questionnaire 2 ± 1 week after surgery

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

John O. Prior

Lead sponsor

University of Lausanne Hospitals

Sponsor institution