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Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study

Optimal therapy of biochemically relapsed prostate cancer (BRPC) after local treatment is elusive. An established modified citrus pectin (PectaSol(®), P-MCP), a dietary polysaccharide, is an established antagonist of galectin-3, a carbohydrate-binding protein involved in cancer pathogenesis. Based o...

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Autores principales: Keizman, Daniel, Frenkel, Moshe, Peer, Avivit, Kushnir, Igal, Rosenbaum, Eli, Sarid, David, Leibovitch, Ilan, Mano, Roy, Yossepowitch, Ofer, Margel, David, Wolf, Ido, Geva, Ravit, Dresler, Hadas, Rouvinov, Keren, Rapoport, Noa, Eliaz, Isaac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706421/
https://www.ncbi.nlm.nih.gov/pubmed/34959847
http://dx.doi.org/10.3390/nu13124295
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author Keizman, Daniel
Frenkel, Moshe
Peer, Avivit
Kushnir, Igal
Rosenbaum, Eli
Sarid, David
Leibovitch, Ilan
Mano, Roy
Yossepowitch, Ofer
Margel, David
Wolf, Ido
Geva, Ravit
Dresler, Hadas
Rouvinov, Keren
Rapoport, Noa
Eliaz, Isaac
author_facet Keizman, Daniel
Frenkel, Moshe
Peer, Avivit
Kushnir, Igal
Rosenbaum, Eli
Sarid, David
Leibovitch, Ilan
Mano, Roy
Yossepowitch, Ofer
Margel, David
Wolf, Ido
Geva, Ravit
Dresler, Hadas
Rouvinov, Keren
Rapoport, Noa
Eliaz, Isaac
author_sort Keizman, Daniel
collection PubMed
description Optimal therapy of biochemically relapsed prostate cancer (BRPC) after local treatment is elusive. An established modified citrus pectin (PectaSol(®), P-MCP), a dietary polysaccharide, is an established antagonist of galectin-3, a carbohydrate-binding protein involved in cancer pathogenesis. Based on PSA dynamics, we report on the safety and the primary outcome analysis of a prospective phase II study of P-MCP in non-metastatic BRPC based. Sixty patients were enrolled, and one patient withdrew after a month. Patients (n = 59) were given P-MCP, 4.8 grams X 3/day, for six months. The primary endpoint was the rate without PSA progression and improved PSA doubling time (PSADT). Secondary endpoints were the rate without radiologic progression and toxicity. Patients that did not progress by PSA and radiologically at six months continued for an additional twelve months. After six months, 78% (n = 46) responded to therapy, with a decreased/stable PSA in 58% (n = 34), or improvement of PSADT in 75% (n = 44), and with negative scans, and entered the second twelve months treatment phase. Median PSADT improved significantly (p = 0.003). Disease progression during the first 6 months was noted in only 22% (n = 13), with PSA progression in 17% (n = 10), and PSA and radiologic progression in 5% (n = 3). No patients developed grade 3 or 4 toxicity.
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spelling pubmed-87064212021-12-25 Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study Keizman, Daniel Frenkel, Moshe Peer, Avivit Kushnir, Igal Rosenbaum, Eli Sarid, David Leibovitch, Ilan Mano, Roy Yossepowitch, Ofer Margel, David Wolf, Ido Geva, Ravit Dresler, Hadas Rouvinov, Keren Rapoport, Noa Eliaz, Isaac Nutrients Article Optimal therapy of biochemically relapsed prostate cancer (BRPC) after local treatment is elusive. An established modified citrus pectin (PectaSol(®), P-MCP), a dietary polysaccharide, is an established antagonist of galectin-3, a carbohydrate-binding protein involved in cancer pathogenesis. Based on PSA dynamics, we report on the safety and the primary outcome analysis of a prospective phase II study of P-MCP in non-metastatic BRPC based. Sixty patients were enrolled, and one patient withdrew after a month. Patients (n = 59) were given P-MCP, 4.8 grams X 3/day, for six months. The primary endpoint was the rate without PSA progression and improved PSA doubling time (PSADT). Secondary endpoints were the rate without radiologic progression and toxicity. Patients that did not progress by PSA and radiologically at six months continued for an additional twelve months. After six months, 78% (n = 46) responded to therapy, with a decreased/stable PSA in 58% (n = 34), or improvement of PSADT in 75% (n = 44), and with negative scans, and entered the second twelve months treatment phase. Median PSADT improved significantly (p = 0.003). Disease progression during the first 6 months was noted in only 22% (n = 13), with PSA progression in 17% (n = 10), and PSA and radiologic progression in 5% (n = 3). No patients developed grade 3 or 4 toxicity. MDPI 2021-11-28 /pmc/articles/PMC8706421/ /pubmed/34959847 http://dx.doi.org/10.3390/nu13124295 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Keizman, Daniel
Frenkel, Moshe
Peer, Avivit
Kushnir, Igal
Rosenbaum, Eli
Sarid, David
Leibovitch, Ilan
Mano, Roy
Yossepowitch, Ofer
Margel, David
Wolf, Ido
Geva, Ravit
Dresler, Hadas
Rouvinov, Keren
Rapoport, Noa
Eliaz, Isaac
Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title_full Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title_fullStr Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title_full_unstemmed Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title_short Modified Citrus Pectin Treatment in Non-Metastatic Biochemically Relapsed Prostate Cancer: Results of a Prospective Phase II Study
title_sort modified citrus pectin treatment in non-metastatic biochemically relapsed prostate cancer: results of a prospective phase ii study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706421/
https://www.ncbi.nlm.nih.gov/pubmed/34959847
http://dx.doi.org/10.3390/nu13124295
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