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Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer

Radionuclide molecular imaging of human epidermal growth factor receptor type 2 (HER2) expression may enable a noninvasive discrimination between HER2-positive and HER2-negative breast cancers for stratification of patients for HER2-targeted treatments. DARPin (designed ankyrin repeat proteins) G3 i...

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Autores principales: Bragina, Olga, Chernov, Vladimir, Schulga, Alexey, Konovalova, Elena, Garbukov, Eugeniy, Vorobyeva, Anzhelika, Orlova, Anna, Tashireva, Liubov, Sörensen, Jens, Zelchan, Roman, Medvedeva, Anna, Deyev, Sergey, Tolmachev, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Nuclear Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973295/
https://www.ncbi.nlm.nih.gov/pubmed/34385343
http://dx.doi.org/10.2967/jnumed.121.262542
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author Bragina, Olga
Chernov, Vladimir
Schulga, Alexey
Konovalova, Elena
Garbukov, Eugeniy
Vorobyeva, Anzhelika
Orlova, Anna
Tashireva, Liubov
Sörensen, Jens
Zelchan, Roman
Medvedeva, Anna
Deyev, Sergey
Tolmachev, Vladimir
author_facet Bragina, Olga
Chernov, Vladimir
Schulga, Alexey
Konovalova, Elena
Garbukov, Eugeniy
Vorobyeva, Anzhelika
Orlova, Anna
Tashireva, Liubov
Sörensen, Jens
Zelchan, Roman
Medvedeva, Anna
Deyev, Sergey
Tolmachev, Vladimir
author_sort Bragina, Olga
collection PubMed
description Radionuclide molecular imaging of human epidermal growth factor receptor type 2 (HER2) expression may enable a noninvasive discrimination between HER2-positive and HER2-negative breast cancers for stratification of patients for HER2-targeted treatments. DARPin (designed ankyrin repeat proteins) G3 is a small (molecular weight, 14 kDa) scaffold protein with picomolar affinity to HER2. The aim of this first-in-humans study was to evaluate the safety, biodistribution, and dosimetry of (99m)Tc-(HE)(3)-G3. Methods: Three cohorts of patients with primary breast cancer (each including at least 4 patients with HER2-negative and 5 patients with HER2-positive tumors) were injected with 1,000, 2,000, or 3,000 μg of (99m)Tc-(HE)(3)-G3 (287 ± 170 MBq). Whole-body planar imaging followed by SPECT was performed at 2, 4, 6, and 24 h after injection. Vital signs and possible side effects were monitored during imaging and up to 7 d after injection. Results: All injections were well tolerated. No side effects were observed. The results of blood and urine analyses did not differ before and after studies. (99m)Tc-(HE)(3)-G3 cleared rapidly from the blood. The highest uptake was detected in the kidneys and liver followed by the lungs, breasts, and small intestinal content. The hepatic uptake after injection of 2,000 or 3,000 μg was significantly (P < 0.05) lower than the uptake after injection of 1,000 μg. Effective doses did not differ significantly between cohorts (average, 0.011 ± 0.004 mSv/MBq). Tumor–to–contralateral site ratios for HER-positive tumors were significantly (P < 0.05) higher than for HER2-negative at 2 and 4 h after injection. Conclusion: Imaging of HER2 expression using (99m)Tc-(HE)(3)-G3 is safe and well tolerated and provides a low absorbed dose burden on patients. This imaging enables discernment of HER2-positive and HER2-negative breast cancer. Phase I study data justify further clinical development of (99m)Tc-(HE)(3)-G3.
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spelling pubmed-89732952022-04-15 Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer Bragina, Olga Chernov, Vladimir Schulga, Alexey Konovalova, Elena Garbukov, Eugeniy Vorobyeva, Anzhelika Orlova, Anna Tashireva, Liubov Sörensen, Jens Zelchan, Roman Medvedeva, Anna Deyev, Sergey Tolmachev, Vladimir J Nucl Med Clinical (Molecular Imaging: Peptides) Radionuclide molecular imaging of human epidermal growth factor receptor type 2 (HER2) expression may enable a noninvasive discrimination between HER2-positive and HER2-negative breast cancers for stratification of patients for HER2-targeted treatments. DARPin (designed ankyrin repeat proteins) G3 is a small (molecular weight, 14 kDa) scaffold protein with picomolar affinity to HER2. The aim of this first-in-humans study was to evaluate the safety, biodistribution, and dosimetry of (99m)Tc-(HE)(3)-G3. Methods: Three cohorts of patients with primary breast cancer (each including at least 4 patients with HER2-negative and 5 patients with HER2-positive tumors) were injected with 1,000, 2,000, or 3,000 μg of (99m)Tc-(HE)(3)-G3 (287 ± 170 MBq). Whole-body planar imaging followed by SPECT was performed at 2, 4, 6, and 24 h after injection. Vital signs and possible side effects were monitored during imaging and up to 7 d after injection. Results: All injections were well tolerated. No side effects were observed. The results of blood and urine analyses did not differ before and after studies. (99m)Tc-(HE)(3)-G3 cleared rapidly from the blood. The highest uptake was detected in the kidneys and liver followed by the lungs, breasts, and small intestinal content. The hepatic uptake after injection of 2,000 or 3,000 μg was significantly (P < 0.05) lower than the uptake after injection of 1,000 μg. Effective doses did not differ significantly between cohorts (average, 0.011 ± 0.004 mSv/MBq). Tumor–to–contralateral site ratios for HER-positive tumors were significantly (P < 0.05) higher than for HER2-negative at 2 and 4 h after injection. Conclusion: Imaging of HER2 expression using (99m)Tc-(HE)(3)-G3 is safe and well tolerated and provides a low absorbed dose burden on patients. This imaging enables discernment of HER2-positive and HER2-negative breast cancer. Phase I study data justify further clinical development of (99m)Tc-(HE)(3)-G3. Society of Nuclear Medicine 2022-04 /pmc/articles/PMC8973295/ /pubmed/34385343 http://dx.doi.org/10.2967/jnumed.121.262542 Text en © 2022 by the Society of Nuclear Medicine and Molecular Imaging. https://creativecommons.org/licenses/by/4.0/Immediate Open Access: Creative Commons Attribution 4.0 International License (CC BY) allows users to share and adapt with attribution, excluding materials credited to previous publications. License: https://creativecommons.org/licenses/by/4.0/. Details: http://jnm.snmjournals.org/site/misc/permission.xhtml.
spellingShingle Clinical (Molecular Imaging: Peptides)
Bragina, Olga
Chernov, Vladimir
Schulga, Alexey
Konovalova, Elena
Garbukov, Eugeniy
Vorobyeva, Anzhelika
Orlova, Anna
Tashireva, Liubov
Sörensen, Jens
Zelchan, Roman
Medvedeva, Anna
Deyev, Sergey
Tolmachev, Vladimir
Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title_full Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title_fullStr Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title_full_unstemmed Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title_short Phase I Trial of (99m)Tc-(HE)(3)-G3, a DARPin-Based Probe for Imaging of HER2 Expression in Breast Cancer
title_sort phase i trial of (99m)tc-(he)(3)-g3, a darpin-based probe for imaging of her2 expression in breast cancer
topic Clinical (Molecular Imaging: Peptides)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973295/
https://www.ncbi.nlm.nih.gov/pubmed/34385343
http://dx.doi.org/10.2967/jnumed.121.262542
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