# [68Ga]Ga-PSMA-11 PET/CT in medullary thyroid carcinoma: comparison with [18F]FDG PET/CT and immunohistochemical analysis

**Authors:** Klaudia Zajkowska, Elwira Bakuła-Zalewska, Paulina Cegla, Marta Wojewódzka-Mirocha, Paweł Ochman, Agata Sackiewicz, Joanna Januszkiewicz-Caulier, Joanna Długosińska, Małgorzata Czetwertyńska, Marek Dedecjus

PMC · DOI: 10.3389/fendo.2025.1627500 · Frontiers in Endocrinology · 2025-10-01

## TL;DR

This study compares [68Ga]Ga-PSMA-11 PET/CT with [18F]FDG PET/CT for detecting medullary thyroid carcinoma and finds the former to be more effective.

## Contribution

The study provides the first comparative evidence of [68Ga]Ga-PSMA-11 PET/CT's superior detection rates in medullary thyroid carcinoma.

## Key findings

- [68Ga]Ga-PSMA-11 PET/CT detected 100% of lesions and 36.4% of patients, compared to 12.5% and 9.1% with [18F]FDG PET/CT.
- PSMA neovascular expression was confirmed in 55% of patients via immunohistochemistry.
- Higher target-to-background ratios were observed with [68Ga]Ga-PSMA-11 PET/CT than with [18F]FDG PET/CT.

## Abstract

Medullary thyroid carcinoma (MTC) is a rare neuroendocrine malignancy. Despite the use of various imaging modalities, including positron emission tomography combined with computed tomography (PET/CT), a significant proportion of patients with biochemical evidence of disease have no detectable lesions. Prostate-specific membrane antigen (PSMA) is expressed by the neovasculature of several solid tumours, including thyroid cancer. While case reports suggest that PSMA-targeted PET/CT may detect MTC lesions, its diagnostic value remains unverified. This study aimed to compare the clinical utility of [68Ga]Ga-PSMA-11 PET/CT with that of 2-[18F]fluoro-2-deoxy-D-glucose ([18F]FDG) PET/CT in MTC patients, assess PSMA expression by immunohistochemistry, and correlate PSMA expression with [68Ga]Ga-PSMA-11 PET/CT findings.

Twelve patients with MTC who had undergone total thyroidectomy and presented with elevated serum calcitonin and/or carcinoembryonic antigen levels underwent prospective evaluation with [68Ga]Ga-PSMA-11 and [18F]FDG PET/CT. Immunohistochemical staining for PSMA and CD31 was performed.

The detection rate by [68Ga]Ga-PSMA-11 PET/CT was 100% (8/8) for lesion-based analysis, and 36.4% (4/11) for patient-based analysis, whereas those for [18F]FDG PET/CT were 12.5% (1/8) and 9.1% (1/11), respectively. [68Ga]Ga-PSMA-11 PET/CT led to a change in the clinical management of one (8.3%) patient. TBRBlood, and TBRLiver were significantly higher on [68Ga]Ga-PSMA-11 PET/CT than on [18F]FDG PET/CT (p = 0.018 and p = 0.038, respectively). Immunohistochemistry confirmed neovascular expression of PSMA in 55% of patients. Expression was significantly higher in patients with positive [68Ga]Ga-PSMA-11 PET/CT results (p = 0.042).

[68Ga]Ga-PSMA-11 PET/CT demonstrated higher detection rates than [18F]FDG PET/CT in both lesion-based and patient-based analyses.

## Linked entities

- **Proteins:** FOLH1 (folate hydrolase 1), PECAM1 (platelet and endothelial cell adhesion molecule 1)
- **Chemicals:** [68Ga]Ga-PSMA-11 (PubChem CID 154572876), [18F]FDG (PubChem CID 68614)
- **Diseases:** medullary thyroid carcinoma (MONDO:0007958), thyroid cancer (MONDO:0002108)

## Full-text entities

- **Genes:** FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}
- **Diseases:** MTC (MESH:C536914), neuroendocrine malignancy (MESH:D018358), thyroid cancer (MESH:D013964), solid (MESH:D018250), tumours (MESH:D009369)
- **Chemicals:** 2-[18F]fluoro-2-deoxy-D-glucose (-), [18F]FDG (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12520941/full.md

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Source: https://tomesphere.com/paper/PMC12520941