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Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies

Radical treatment of malignant solid tumors should aim to be less traumatic, precise, and effective. OncoCiDia, as a noninvasive, sequential dual-targeting, small-molecule, broad spectrum anticancer theranostic approach, may fulfill these requirements of solid cancer (Onco) treatment with both tumor...

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Autores principales: Li, Yue, Wang, Shuncong, Chen, Lei, Feng, Yuanbo, Shen, Zhijun, Chen, Xin, Huang, Gang, Ni, Yicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647265/
https://www.ncbi.nlm.nih.gov/pubmed/36344243
http://dx.doi.org/10.1177/15330338221136716
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author Li, Yue
Wang, Shuncong
Chen, Lei
Feng, Yuanbo
Shen, Zhijun
Chen, Xin
Huang, Gang
Ni, Yicheng
author_facet Li, Yue
Wang, Shuncong
Chen, Lei
Feng, Yuanbo
Shen, Zhijun
Chen, Xin
Huang, Gang
Ni, Yicheng
author_sort Li, Yue
collection PubMed
description Radical treatment of malignant solid tumors should aim to be less traumatic, precise, and effective. OncoCiDia, as a noninvasive, sequential dual-targeting, small-molecule, broad spectrum anticancer theranostic approach, may fulfill these requirements of solid cancer (Onco) treatment with both tumoricidal (Ci) and diagnostic (Dia) effects. However, it is unlikely to cure patients with cancer, especially those with large and irregular tumors and with tumors residing in certain organs, such as the brain and pancreas, because of insufficient necrosis generation. To amplify ablative efficacy, this shortcoming could be overcome by combining high-intensity focused ultrasound (HIFU) with the use of a vascular-disrupting agent (VDA) and a radioactively labeled necrosis avid compound (NAC), such as (131)I-Hypericin ((131)I-Hyp), which are the first and second targeting drugs used in OncoCiDia. This study proposes the combined use of OncoCiDia and HIFU (Onco-HIFU-CiDia) as a synergistic treatment for malignant tumors to achieve a curative multimodality and multidrug regimen for patients with solid cancers, in accordance with the current trend of cancer patient care.
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spelling pubmed-96472652022-11-15 Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies Li, Yue Wang, Shuncong Chen, Lei Feng, Yuanbo Shen, Zhijun Chen, Xin Huang, Gang Ni, Yicheng Technol Cancer Res Treat Novel Biomarkers, Molecular Diagnostics and Targeted Therapies of Cancer Radical treatment of malignant solid tumors should aim to be less traumatic, precise, and effective. OncoCiDia, as a noninvasive, sequential dual-targeting, small-molecule, broad spectrum anticancer theranostic approach, may fulfill these requirements of solid cancer (Onco) treatment with both tumoricidal (Ci) and diagnostic (Dia) effects. However, it is unlikely to cure patients with cancer, especially those with large and irregular tumors and with tumors residing in certain organs, such as the brain and pancreas, because of insufficient necrosis generation. To amplify ablative efficacy, this shortcoming could be overcome by combining high-intensity focused ultrasound (HIFU) with the use of a vascular-disrupting agent (VDA) and a radioactively labeled necrosis avid compound (NAC), such as (131)I-Hypericin ((131)I-Hyp), which are the first and second targeting drugs used in OncoCiDia. This study proposes the combined use of OncoCiDia and HIFU (Onco-HIFU-CiDia) as a synergistic treatment for malignant tumors to achieve a curative multimodality and multidrug regimen for patients with solid cancers, in accordance with the current trend of cancer patient care. SAGE Publications 2022-11-07 /pmc/articles/PMC9647265/ /pubmed/36344243 http://dx.doi.org/10.1177/15330338221136716 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Novel Biomarkers, Molecular Diagnostics and Targeted Therapies of Cancer
Li, Yue
Wang, Shuncong
Chen, Lei
Feng, Yuanbo
Shen, Zhijun
Chen, Xin
Huang, Gang
Ni, Yicheng
Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title_full Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title_fullStr Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title_full_unstemmed Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title_short Sequential Administrations of a Vascular-Disrupting Agent, High-Intensity Focused Ultrasound, and a Radioactively labeled Necrosis Avid Compound for Eradicating Solid Malignancies
title_sort sequential administrations of a vascular-disrupting agent, high-intensity focused ultrasound, and a radioactively labeled necrosis avid compound for eradicating solid malignancies
topic Novel Biomarkers, Molecular Diagnostics and Targeted Therapies of Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647265/
https://www.ncbi.nlm.nih.gov/pubmed/36344243
http://dx.doi.org/10.1177/15330338221136716
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