Phase I Clinical Evaluation of Designed Ankyrin Repeat Protein [99mTc]Tc(CO)3-(HE)3-Ec1 for Visualization of EpCAM-Expressing Lung Cancer

Xehetasun bibliografikoak
Parent link:Cancers.— .— Basel: MDPI AG
Vol. 16, iss. 16.— 2024.— Article number 2815, 12 p.
Erakunde egilea: National Research Tomsk Polytechnic University (570)
Beste egile batzuk: Zelchan (Zeltchan) R. V. Roman Vladimirovich, Chernov V. I. Vladimir Ivanovich, Medvedeva А. А. Anna Aleksandrovna, Rybina A. N. Anastasiya Nikolaevna, Bragina O. D. Olga Dmitrievna, Mishina E. Elizaveta, Larkina M. S. Mariya Sergeevna, Varvashenya R. N. Ruslan Nikolaevich, Fominykh A. S. Anastasiya Sergeevna, Shulga (Schulga) A. A. Aleksey Anatolievich, Konovalova E. V. Elena Valerjevna, Vorobjeva (Vorobyeva) A. G. Anzhelika Grigorjevna, Orlova A. M. Anna Markovna, Tashireva L. A. Lyubov Aleksandrovna, Deev S. M. Sergey Mikhaylovich
Gaia:A high level of EpCAM overexpression in lung cancer makes this protein a promising target for targeted therapy. Radionuclide visualization of EpCAM expression would facilitate the selection of patients potentially benefiting from such treatment. Single-photon computed tomography (SPECT) using 99mTc-labeled engineered scaffold protein DARPin Ec1 has shown its effectiveness in imaging tumors with overexpression of EpCAM in preclinical studies, providing high contrast just a few hours after injection. This first-in-human study aimed to evaluate the safety and distribution of [99mTc]Tc(CO)3-(HE)3-Ec1 in patients with primary lung cancer. Twelve lung cancer patients were injected with 300.7 ± 103.2 MBq of [99mTc]Tc(CO)3-(HE)3-Ec1. Whole-body planar imaging (at 2, 4, 6 and 24 h after injection) and SPECT/CT of the lung (at 2, 4, and 6 h) were performed. The patients’ vital signs and possible side effects were monitored up to 7 days after injection. The patients tolerated the injection of [99mTc]Tc(CO)3-(HE)3-Ec1 well, and their somatic condition remained normal during the entire follow-up period. There were no abnormalities in blood and urine tests after injection of [99mTc]Tc(CO)3-(HE)3-Ec1. The highest absorbed doses were in the kidneys, liver, pancreas, thyroid, gallbladder wall, and adrenals. There was also a relatively high accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 in the small and large intestines, pancreas and thyroid. According to the SPECT/CT, accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 in the lung tumor was found in all patients included in the study. Intensive accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 was also noted in regional metastases. [99mTc]Tc(CO)3-(HE)3-Ec1 can potentially be considered a diagnostic tracer for imaging EpCAM expression in lung cancer patients and other tumors with overexpression of EpCAM
Текстовый файл
Hizkuntza:ingelesa
Argitaratua: 2024
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Sarrera elektronikoa:https://doi.org/10.3390/cancers16162815
Formatua: Baliabide elektronikoa Liburu kapitulua
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=677883

MARC

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200 1 |a Phase I Clinical Evaluation of Designed Ankyrin Repeat Protein [99mTc]Tc(CO)3-(HE)3-Ec1 for Visualization of EpCAM-Expressing Lung Cancer  |f Roman Zelchan, Vladimir Chernov, Anna Medvedeva [et al.] 
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330 |a A high level of EpCAM overexpression in lung cancer makes this protein a promising target for targeted therapy. Radionuclide visualization of EpCAM expression would facilitate the selection of patients potentially benefiting from such treatment. Single-photon computed tomography (SPECT) using 99mTc-labeled engineered scaffold protein DARPin Ec1 has shown its effectiveness in imaging tumors with overexpression of EpCAM in preclinical studies, providing high contrast just a few hours after injection. This first-in-human study aimed to evaluate the safety and distribution of [99mTc]Tc(CO)3-(HE)3-Ec1 in patients with primary lung cancer. Twelve lung cancer patients were injected with 300.7 ± 103.2 MBq of [99mTc]Tc(CO)3-(HE)3-Ec1. Whole-body planar imaging (at 2, 4, 6 and 24 h after injection) and SPECT/CT of the lung (at 2, 4, and 6 h) were performed. The patients’ vital signs and possible side effects were monitored up to 7 days after injection. The patients tolerated the injection of [99mTc]Tc(CO)3-(HE)3-Ec1 well, and their somatic condition remained normal during the entire follow-up period. There were no abnormalities in blood and urine tests after injection of [99mTc]Tc(CO)3-(HE)3-Ec1. The highest absorbed doses were in the kidneys, liver, pancreas, thyroid, gallbladder wall, and adrenals. There was also a relatively high accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 in the small and large intestines, pancreas and thyroid. According to the SPECT/CT, accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 in the lung tumor was found in all patients included in the study. Intensive accumulation of [99mTc]Tc(CO)3-(HE)3-Ec1 was also noted in regional metastases. [99mTc]Tc(CO)3-(HE)3-Ec1 can potentially be considered a diagnostic tracer for imaging EpCAM expression in lung cancer patients and other tumors with overexpression of EpCAM 
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461 1 |t Cancers  |c Basel  |n MDPI AG 
463 1 |t Vol. 16, iss. 16  |d 2024  |v Article number 2815, 12 p. 
610 1 |a [99mTc]Tc(CO)3-(HE)3-Ec1 
610 1 |a single-photon emission computed tomography 
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701 1 |a Zelchan (Zeltchan)  |b R. V.  |c specialist in the field of medical technology  |c Researcher of the Tomsk Polytechnic University, Candidate of Medical Sciences  |f 1984-  |g Roman Vladimirovich  |9 17728 
701 1 |a Chernov  |b V. I.  |c specialist in the field of medical technology  |c lead engineer of Tomsk Polytechnic University, doctor of medical sciences  |f 1962-  |g Vladimir Ivanovich  |9 17725 
701 1 |a Medvedeva  |b А. А.  |g Anna Aleksandrovna  |f 1975-  |c specialist in the field of medical technology  |c research fellow of Tomsk Polytechnic University, Doctor of Medical Sciences  |y Tomsk  |9 20294 
701 1 |a Rybina  |b A. N.  |g Anastasiya Nikolaevna  |f 1982-  |c specialist in the field of biophysics  |c Researcher of Tomsk Polytechnic University, Candidateof medical Sciences  |y Tomsk  |9 88810 
701 1 |a Bragina  |b O. D.  |c specialist in the field of medical technology  |c Senior Researcher of the Tomsk Polytechnic University, Doctor of Medical Sciences  |f 1986-  |g Olga Dmitrievna  |y Tomsk  |9 19084 
701 1 |a Mishina  |b E.  |g Elizaveta 
701 1 |a Larkina  |b M. S.  |g Mariya Sergeevna  |f 1984-  |c pharmacist  |c Professor; Senior Researcher of the Tomsk Polytechnic University, Doctor of Pharmaceutical Sciences  |y Tomsk  |9 22417 
701 1 |a Varvashenya  |b R. N.  |c pharmacist  |c engineer at Tomsk Polytechnic University  |f 1997-  |g Ruslan Nikolaevich  |9 88559 
701 1 |a Fominykh  |b A. S.  |g Anastasiya Sergeevna  |f 1998-  |c chemist  |c Engineer of Tomsk Polytechnic University  |y Tomsk  |9 88811 
701 1 |a Shulga (Schulga)  |b A. A.  |c biologist  |c Researcher, Tomsk Polytechnic University, Candidate of Biological Sciences  |f 1960-  |g Aleksey Anatolievich  |9 22432 
701 1 |a Konovalova  |b E. V.  |c specialist in the field of chemical technology and biotechnology  |c engineer at Tomsk Polytechnic University  |f 1985-  |g Elena Valerjevna  |9 88562 
701 1 |a Vorobjeva (Vorobyeva)  |b A. G.  |c specialist in the field of medical technology  |c Senior Researcher, Oncoteranostika Research Center, Tomsk Polytechnic University, Ph.D  |f 1990-  |g Anzhelika Grigorjevna  |9 22214 
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701 1 |a Tashireva  |b L. A.  |g Lyubov Aleksandrovna 
701 1 |a Deev  |b S. M.  |c biologist  |c Leading Researcher, Tomsk Polytechnic University, Doctor of Biological Sciences  |f 1951-  |g Sergey Mikhaylovich  |9 20959 
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