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Actinium-225 targeted alpha particle therapy for prostate cancer
by
VanBrocklin, Henry F.
, Zerefa, Luann
, Yadav, Surekha
, Bidkar, Anil P.
, Flavell, Robert R.
in
Actinium - chemistry
/ Actinium - therapeutic use
/ Alpha Particles - therapeutic use
/ Animals
/ Humans
/ Male
/ Prostatic Neoplasms - radiotherapy
/ Prostatic Neoplasms - therapy
/ Radiopharmaceuticals - therapeutic use
/ Review
2024
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Actinium-225 targeted alpha particle therapy for prostate cancer
by
VanBrocklin, Henry F.
, Zerefa, Luann
, Yadav, Surekha
, Bidkar, Anil P.
, Flavell, Robert R.
in
Actinium - chemistry
/ Actinium - therapeutic use
/ Alpha Particles - therapeutic use
/ Animals
/ Humans
/ Male
/ Prostatic Neoplasms - radiotherapy
/ Prostatic Neoplasms - therapy
/ Radiopharmaceuticals - therapeutic use
/ Review
2024
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Do you wish to request the book?
Actinium-225 targeted alpha particle therapy for prostate cancer
by
VanBrocklin, Henry F.
, Zerefa, Luann
, Yadav, Surekha
, Bidkar, Anil P.
, Flavell, Robert R.
in
Actinium - chemistry
/ Actinium - therapeutic use
/ Alpha Particles - therapeutic use
/ Animals
/ Humans
/ Male
/ Prostatic Neoplasms - radiotherapy
/ Prostatic Neoplasms - therapy
/ Radiopharmaceuticals - therapeutic use
/ Review
2024
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Actinium-225 targeted alpha particle therapy for prostate cancer
Journal Article
Actinium-225 targeted alpha particle therapy for prostate cancer
2024
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Overview
Targeted alpha particle therapy (TAT) has emerged as a promising strategy for the treatment of prostate cancer (PCa). Actinium-225 (
Ac), a potent alpha-emitting radionuclide, may be incorporated into targeting vectors, causing robust and in some cases sustained antitumor responses. The development of radiolabeling techniques involving EDTA, DOTA, DOTPA, and Macropa chelators has laid the groundwork for advancements in this field. At the forefront of clinical trials with
Ac in PCa are PSMA-targeted TAT agents, notably [
Ac]Ac-PSMA-617, [
Ac]Ac-PSMA-I&T and [
Ac]Ac-J591. Ongoing investigations spotlight [
Ac]Ac-hu11B6, [
Ac]Ac-YS5, and [
Ac]Ac-SibuDAB, targeting hK2, CD46, and PSMA, respectively. Despite these efforts, hurdles in
Ac production, daughter redistribution, and a lack of suitable imaging techniques hinder the development of TAT. To address these challenges and additional advantages, researchers are exploring alpha-emitting isotopes including
Th,
Ra,
At,
Bi,
Pb or
Tb, providing viable alternatives for TAT.
Publisher
Ivyspring International Publisher
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