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Peer-reviewedCC BY 4.0Frontiers in Nuclear Medicine

FAP-targeted [68Ga]BED003-PET compared with [18F]DOPA-PET in patients with recurrent medullary thyroid carcinoma

4 affiliations
  1. 1Department of Nuclear Medicine, University Hospital Münster, Münster, Germany
  2. 2West German Cancer Center, University Hospital Münster, Münster, Germany
  3. 3European Institute for Molecular Imaging (EIMI), University of Münster, Münster, Germany
  4. 4Clinic for Radiology, University Hospital Münster, Münster, Germany

Abstract

Aim: Molecular imaging of recurrent or advanced medullary thyroid carcinoma (MTC) remains clinically challenging. [18F]DOPA-PET is an established reference standard, but its sensitivity is limited and dependent on tumour burden and biomarker levels. Fibroblast activation protein (FAP)-targeted PET has emerged as a promising imaging approach across several malignancies. This study aimed to compare the detection rate and quantitative imaging characteristics of [68Ga]BED003-PET, recently known as [68Ga]OncoFAP-DOTAGA, with [18F]DOPA-PET in patients with recurrent or advanced MTC.

Methods: Eight patients with histologically proven MTC and suspected recurrence or progression based on elevated calcitonin levels underwent both [18F]DOPA-PET and an additional [68Ga]BED003-PET. All patients presented with inconclusive findings in [18F]DOPA-PET. Comparative analyses were performed on a patient- and lesion-based level. Quantitative parameters included maximum and mean standardized uptake values (SUVmax/SUVmean), metabolic tumour volume (MTV), and maximum tumour-to-background ratios (TBRmax). Potential theranostic suitability was explored based on lesional FAP uptake.

Results: The median interval between PET acquisitions was 33 days (range, 7–56 days). In total, 35 tracer-avid lesions were detected. [68Ga]BED003-PET detected significantly more lesions than [18F]DOPA-PET (34/35 [97%] vs. 16/35 [46%], P < 0.001). 15 lesions (43%) were positive on both modalities, 19 (54%) were only [68Ga]BED003-positive, and 1 (2.9%) was only [18F]DOPA-positive. Quantitative analysis demonstrated significantly higher uptake and contrast for [68Ga]BED003, including higher blood-pool TBRmax than [18F]DOPA (6.02 vs. 2.23, Bonferroni adjusted P < 0.001).

Conclusion: In this small MTC cohort, [68Ga]BED003-PET demonstrated higher lesion detection and TBRs in patients with inconsistent findings in [18F]DOPA-PET. Prospective multicenter validation is warranted.

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BibTeX
@article{ventura2026faptargeted,
  title = {{FAP-targeted [68Ga]BED003-PET compared with [18F]DOPA-PET in patients with recurrent medullary thyroid carcinoma}},
  author = {David Ventura and Benjamin Noto and Philipp Backhaus and Philipp Schindler and Kambiz Rahbar and Michael Schäfers and Burkhard Riemann and Wolfgang Roll},
  journal = {Frontiers in Nuclear Medicine},
  year = {2026},
  month = oct,
  doi = {10.3389/fnume.2026.1949036},
  url = {https://doi.org/10.3389/fnume.2026.1949036},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - FAP-targeted [68Ga]BED003-PET compared with [18F]DOPA-PET in patients with recurrent medullary thyroid carcinoma
AU  - David Ventura
AU  - Benjamin Noto
AU  - Philipp Backhaus
AU  - Philipp Schindler
AU  - Kambiz Rahbar
AU  - Michael Schäfers
AU  - Burkhard Riemann
AU  - Wolfgang Roll
PY  - 2026
DA  - 2026/10/21
JO  - Frontiers in Nuclear Medicine
DO  - 10.3389/fnume.2026.1949036
UR  - https://doi.org/10.3389/fnume.2026.1949036
AB  - Aim: Molecular imaging of recurrent or advanced medullary thyroid carcinoma (MTC) remains clinically challenging. [18F]DOPA-PET is an established reference standard, but its sensitivity is limited and dependent on tumour burden and biomarker levels. Fibroblast activation protein (FAP)-targeted PET has emerged as a promising imaging approach across several malignancies. This study aimed to compare the detection rate and quantitative imaging characteristics of [68Ga]BED003-PET, recently known as [68Ga]OncoFAP-DOTAGA, with [18F]DOPA-PET in patients with recurrent or advanced MTC.  Methods: Eight patients with histologically proven MTC and suspected recurrence or progression based on elevated calcitonin levels underwent both [18F]DOPA-PET and an additional [68Ga]BED003-PET. All patients presented with inconclusive findings in [18F]DOPA-PET. Comparative analyses were performed on a patient- and lesion-based level. Quantitative parameters included maximum and mean standardized uptake values (SUVmax/SUVmean), metabolic tumour volume (MTV), and maximum tumour-to-background ratios (TBRmax). Potential theranostic suitability was explored based on lesional FAP uptake.  Results: The median interval between PET acquisitions was 33 days (range, 7–56 days). In total, 35 tracer-avid lesions were detected. [68Ga]BED003-PET detected significantly more lesions than [18F]DOPA-PET (34/35 [97%] vs. 16/35 [46%], P < 0.001). 15 lesions (43%) were positive on both modalities, 19 (54%) were only [68Ga]BED003-positive, and 1 (2.9%) was only [18F]DOPA-positive. Quantitative analysis demonstrated significantly higher uptake and contrast for [68Ga]BED003, including higher blood-pool TBRmax than [18F]DOPA (6.02 vs. 2.23, Bonferroni adjusted P < 0.001).  Conclusion: In this small MTC cohort, [68Ga]BED003-PET demonstrated higher lesion detection and TBRs in patients with inconsistent findings in [18F]DOPA-PET. Prospective multicenter validation is warranted.
SN  - 2673-8880
ER  -