ZMB Member Thomas Günther
ZMB Member
Thomas Günther
Next ZMB-Member
Prof. Dr. Thomas Günther
Clinic for Nuclear Medicine
University Hospital Essen
Hufelandstr. 55
45122 Essen
- +49 201 723 4165
- Website
- Press Releases
- Selected Publications
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Web of Science ResearcherID:QUT-1471-2026
- ORCiD ID
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- ZMB Research Program
Oncology
Research Overview
Our group focuses on the development and optimization of novel radiolabeled compounds to improve in vitro (target affinity, lipophilicity, internalization, albumin binding) and in vivo (stability, pharmacokinetics, clearance kinetics, tumor uptake and retention) aspects, aiming at clinical translation and improving patient care. In general, diseases like cancer overexpress certain targets (receptors, enzymes, transporters, etc.) while healthy organs do not. Hence, radiolabeled molecules designed to specifically bind to these targets will help to identify and treat areas in the body that show increased activity uptake compared with those that do not show elevated uptake. By combining diagnostic radionuclides such as fluorine-18 or gallium-68, among others, with molecules that specifically bind to the overexpressed target, we are able to diagnose and monitor diseases that correlate with target expression using positron emission tomography (PET). By combining the same or a similar ligand with therapeutic radionuclides such as lutetium-177, high-energy beta or alpha radiation can be delivered to and deposited at the target site. This ultimately results in the damage of malignant and adjacent cells, which enables site-specific treatment and usually leads to less side effects. Despite significant progress in the field of nuclear medicine in the last decades, there are still a lot of challenges, particularly in treating late-stage cancers. Together with the Preclinical Theranostics group and the Department of Nuclear Medicine we intend to identify and address unmet clinical needs. Our group will focus to address potential drawbacks of existing radioligands by chemical design, for example, stabilizing the biovector by introducing unnatural instead of natural amino acids or reducing the number of charged moieties within the molecule to prevent unspecific accumulation in healthy organs like the kidneys. Developed radioligands will be extensively studied in in vitro and in vivo studies, while constantly optimizing identified drawbacks. We will use established and novel labeling techniques and radionuclides which might improve imaging and therapy outcomes. The ultimate goal of our group represents the design of best-in-class radiopharmaceuticals for different targets and diseases, which will be translated in our clinic and improve patient care.
Selected Publications
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Evaluation of treatment efficacy of the 161Tb- and 177Lu-Labeled GRPR antagonists AMTG and RM2 in a mouse model of prostate cancerIn: European Journal of Nuclear Medicine and Molecular Imaging, 2026, in pressDOI (Open Access)
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Synthesis and in vitro evaluation of pharmacokinetically optimized ⁹⁹mTc-labeled cholecystokinin-2 receptor-targeted peptides for improved SPECT imagingIn: EJNMMI Radiopharmacy and Chemistry, Vol. 11, 2026, Nr. 1, 48DOI (Open Access)
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A Vision for Gastrin-Releasing Peptide Receptor Targeting for Imaging and Therapy : Perspective from Academia and IndustryIn: Journal of Nuclear Medicine (JNM), Vol. 66, 2025, Nr. 8, pp. 1160 – 1167DOI (Open Access)
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CCK₂ Receptor Ligand [⁶⁸Ga]Ga-DOTA-CCK-66 PET/CT Outperforms [⁶⁸Ga]Ga-DOTATOC PET/CT in a Patient with Small Cell Lung CancerIn: Journal of Nuclear Medicine (JNM), Vol. 66, 2025, Nr. 4, pp. 662DOI (Open Access)
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First-in-Human Serum Stability Studies of [¹⁷⁷Lu]Lu-AMTG : A Step Toward Improved GRPR-Targeted Radiopharmaceutical TherapyIn: Journal of Nuclear Medicine (JNM), Vol. 66, 2025, Nr. 6, pp. 896 – 899DOI (Open Access)
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Preclinical evaluation of ²²⁵Ac-labeled minigastrin analog DOTA-CCK-66 for Targeted Alpha TherapyIn: European Journal of Nuclear Medicine and Molecular Imaging, Vol. 52, 2025, Nr. 2, pp. 458 – 468DOI (Open Access)
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Studies on the impact of modifications at the Gln-Trp site in RM2-based GRPR ligandsIn: EJNMMI Research, Vol. 15, 2025, Nr. 1, 114DOI (Open Access)
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Biodistribution and Radiation Dosimetry for ⁶⁸Ga-DOTA-CCK-66, a Novel CCK₂ R-Targeting Compound for Imaging of Medullary Thyroid CancerIn: Clinical Nuclear Medicine, Vol. 49, 2024, Nr. 12, pp. 1091 – 1097
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Biodistribution and radiation dosimetry of [99mTc]Tc-N4-BTG in patients with biochemical recurrence of prostate cancerIn: EJNMMI Research, Vol. 14, 2024, Nr. 1, 42DOI (Open Access)
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CCK₂ Receptor–Targeted PET/CT in Medullary Thyroid Cancer Using [⁶⁸Ga]Ga-DOTA-CCK-66In: Journal of Nuclear Medicine (JNM), Vol. 65, 2024, Nr. 3, pp. 493 – 494DOI (Open Access)
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Preclinical Evaluation of Gastrin-Releasing Peptide Receptor Antagonists Labeled with ¹⁶¹Tb and ¹⁷⁷Lu : A Comparative StudyIn: Journal of Nuclear Medicine (JNM), Vol. 65, 2024, Nr. 3, pp. 481 – 484DOI (Open Access)
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Preclinical Evaluation of Minigastrin Analogs and Proof-of-Concept [⁶⁸Ga]Ga-DOTA-CCK-66 PET/CT in 2 Patients with Medullary Thyroid CancerIn: Journal of Nuclear Medicine (JNM), Vol. 65, 2024, Nr. 1, pp. 33 – 39DOI (Open Access)
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Significant reduction of activity retention in the kidneys via optimized linker sequences in radiohybrid-based minigastrin analogsIn: EJNMMI Research, Vol. 14, 2024, Nr. 1, 23DOI (Open Access)
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Development of the First ¹⁸F-Labeled Radiohybrid-Based Minigastrin Derivative with High Target Affinity and Tumor Accumulation by Substitution of the Chelating MoietyIn: Pharmaceutics, Vol. 15, 2023, Nr. 3, 826DOI (Open Access)
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Investigation of the structure-activity relationship at the N-terminal part of minigastrin analogsIn: EJNMMI Research, Vol. 13, 2023, Nr. 1, 65DOI (Open Access)
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Preclinical Comparison of the ⁶⁴Cu- and ⁶⁸Ga-Labeled GRPR-Targeted Compounds RM2 and AMTG, as Well as First-in-Humans [⁶⁸Ga]Ga-AMTG PET/CTIn: Journal of Nuclear Medicine (JNM), Vol. 64, 2023, Nr. 10, pp. 1654 – 1659DOI (Open Access)
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Synthesis and preclinical evaluation of novel 99mTc-labeled PSMA ligands for radioguided surgery of prostate cancerIn: EJNMMI Research, Vol. 13, 2023, Nr. 1, 2DOI (Open Access)
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Synthesis of ¹⁷⁷Lu-Labeled, Somatostatin-2 Receptor-Targeted Metalla-Assemblies : Challenges in the Design of Supramolecular RadiotherapeuticsIn: Inorganic Chemistry, Vol. 62, 2023, Nr. 50, pp. 20710 – 20720
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Introduction of a SiFA Moiety into the D-Glutamate Chain of DOTA-PP-F11N Results in Radiohybrid-Based CCK-2R-Targeted Compounds with Improved Pharmacokinetics In VivoIn: Pharmaceuticals, Vol. 15, 2022, Nr. 12, 1467DOI (Open Access)
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Optimization of the Pharmacokinetic Profile of [99mTc]Tc-N4-Bombesin Derivatives by Modification of the Pharmacophoric Gln-Trp SequenceIn: Pharmaceuticals, Vol. 15, 2022, Nr. 9, 1133DOI (Open Access)
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Substitution of L-Tryptophan by α-Methyl-L-Tryptophan in ¹⁷⁷Lu-RM2 Results in ¹⁷⁷Lu-AMTG, a High-Affinity Gastrin-Releasing Peptide Receptor Ligand with Improved in Vivo StabilityIn: Journal of Nuclear Medicine (JNM), Vol. 63, 2022, Nr. 9, pp. 1364 – 1370DOI (Open Access)
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Preclinical comparison of four [18F, natGa]rhPSMA-7 isomers : influence of the stereoconfiguration on pharmacokineticsIn: EJNMMI Research, Vol. 10, 2020, Nr. 1, 149DOI (Open Access)
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Synthesis and in vitro and in vivo evaluation of urea-based PSMA inhibitors with increased lipophilicityIn: EJNMMI Research, Vol. 8, 2018, Nr. 1, 84DOI (Open Access)
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Synthesis and preclinical evaluation of novel 18F-labeled Glu-urea-Glu-based PSMA inhibitors for prostate cancer imaging : a comparison with 18F-DCFPyl and 18F-PSMA-1007In: EJNMMI Research, Vol. 8, 2018, Nr. 1, 30DOI (Open Access)

