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Silymarin as a preventive or therapeutic measure for chemotherapy and radiotherapy-induced adverse reactions: a comprehensive review of preclinical and clinical data
Purpose Thus far, silymarin has been examined in several studies for prevention or treatment of various chemotherapy or radiotherapy-induced adverse reactions. In this review, we try to collect all available human, animal, and pre-clinical data in this field. Methods The search was done in Scopus, P...
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Published in: | European journal of clinical pharmacology 2023, Vol.79 (1), p.15-38 |
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container_title | European journal of clinical pharmacology |
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creator | Ghodousi, Mahsa Karbasforooshan, Hedyieh Arabi, Leila Elyasi, Sepideh |
description | Purpose
Thus far, silymarin has been examined in several studies for prevention or treatment of various chemotherapy or radiotherapy-induced adverse reactions. In this review, we try to collect all available human, animal, and pre-clinical data in this field.
Methods
The search was done in Scopus, PubMed, Medline, and systematic reviews in the Cochrane database, using the following keywords: “Cancer,” “Chemotherapy,” “Radiotherapy,” “Mucositis,” “Nephrotoxicity,” “Dermatitis,” “Ototoxicity,” “Cardiotoxicity,” “Nephrotoxicity,” “Hepatotoxicity,” “Reproductive system,” “Silybum marianum,” “Milk thistle,” and “Silymarin” and “Silybin.” We included all relevant in vitro, in vivo, and human studies up to the date of publication.
Results
Based on 64 included studies in this review, silymarin is considered a safe and well-tolerated compound, with no known clinical drug interaction. Notably, multiple adverse reactions of chemotherapeutic agents are effectively managed by its antioxidant, anti-apoptotic, anti-inflammatory, and anti-immunomodulatory properties.
Clinical trials suggest that oral silymarin may be a promising adjuvant with cancer treatments, particularly against hepatotoxicity (
n
= 10), nephrotoxicity (
n
= 3), diarrhea (
n
= 1), and mucositis (
n
= 3), whereas its topical formulation can be particularly effective against radiodermatitis (
n
= 2) and hand-foot syndrome (HFS) (
n
= 1).
Conclusion
Further studies are required to determine the optimal dose, duration, and the best formulation of silymarin to prevent and/or manage chemotherapy and radiotherapy-induced complications. |
doi_str_mv | 10.1007/s00228-022-03434-8 |
format | article |
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Thus far, silymarin has been examined in several studies for prevention or treatment of various chemotherapy or radiotherapy-induced adverse reactions. In this review, we try to collect all available human, animal, and pre-clinical data in this field.
Methods
The search was done in Scopus, PubMed, Medline, and systematic reviews in the Cochrane database, using the following keywords: “Cancer,” “Chemotherapy,” “Radiotherapy,” “Mucositis,” “Nephrotoxicity,” “Dermatitis,” “Ototoxicity,” “Cardiotoxicity,” “Nephrotoxicity,” “Hepatotoxicity,” “Reproductive system,” “Silybum marianum,” “Milk thistle,” and “Silymarin” and “Silybin.” We included all relevant in vitro, in vivo, and human studies up to the date of publication.
Results
Based on 64 included studies in this review, silymarin is considered a safe and well-tolerated compound, with no known clinical drug interaction. Notably, multiple adverse reactions of chemotherapeutic agents are effectively managed by its antioxidant, anti-apoptotic, anti-inflammatory, and anti-immunomodulatory properties.
Clinical trials suggest that oral silymarin may be a promising adjuvant with cancer treatments, particularly against hepatotoxicity (
n
= 10), nephrotoxicity (
n
= 3), diarrhea (
n
= 1), and mucositis (
n
= 3), whereas its topical formulation can be particularly effective against radiodermatitis (
n
= 2) and hand-foot syndrome (HFS) (
n
= 1).
Conclusion
Further studies are required to determine the optimal dose, duration, and the best formulation of silymarin to prevent and/or manage chemotherapy and radiotherapy-induced complications.</description><identifier>ISSN: 0031-6970</identifier><identifier>EISSN: 1432-1041</identifier><identifier>DOI: 10.1007/s00228-022-03434-8</identifier><identifier>PMID: 36450892</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Antioxidants - pharmacology ; Apoptosis ; Biomedical and Life Sciences ; Biomedicine ; Cardiotoxicity ; Chemical and Drug Induced Liver Injury - drug therapy ; Chemotherapy ; Clinical trials ; Dermatitis ; Diarrhea ; Drug interaction ; Hepatotoxicity ; Humans ; Immunomodulation ; Inflammation ; Mucositis ; Mucositis - drug therapy ; Neoplasms - drug therapy ; Neoplasms - radiotherapy ; Ototoxicity ; Pharmacology/Toxicology ; Radiation therapy ; Reproductive system ; Review ; Reviews ; Side effects ; Silymarin ; Silymarin - pharmacology ; Silymarin - therapeutic use</subject><ispartof>European journal of clinical pharmacology, 2023, Vol.79 (1), p.15-38</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-bfdab9a443d906145001aaedff0ccae0fcd498cd283f10f328a35e90b123e6573</citedby><cites>FETCH-LOGICAL-c375t-bfdab9a443d906145001aaedff0ccae0fcd498cd283f10f328a35e90b123e6573</cites><orcidid>0000-0001-9857-1175 ; 0000-0003-1623-3346</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36450892$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ghodousi, Mahsa</creatorcontrib><creatorcontrib>Karbasforooshan, Hedyieh</creatorcontrib><creatorcontrib>Arabi, Leila</creatorcontrib><creatorcontrib>Elyasi, Sepideh</creatorcontrib><title>Silymarin as a preventive or therapeutic measure for chemotherapy and radiotherapy-induced adverse reactions: a comprehensive review of preclinical and clinical data</title><title>European journal of clinical pharmacology</title><addtitle>Eur J Clin Pharmacol</addtitle><addtitle>Eur J Clin Pharmacol</addtitle><description>Purpose
Thus far, silymarin has been examined in several studies for prevention or treatment of various chemotherapy or radiotherapy-induced adverse reactions. In this review, we try to collect all available human, animal, and pre-clinical data in this field.
Methods
The search was done in Scopus, PubMed, Medline, and systematic reviews in the Cochrane database, using the following keywords: “Cancer,” “Chemotherapy,” “Radiotherapy,” “Mucositis,” “Nephrotoxicity,” “Dermatitis,” “Ototoxicity,” “Cardiotoxicity,” “Nephrotoxicity,” “Hepatotoxicity,” “Reproductive system,” “Silybum marianum,” “Milk thistle,” and “Silymarin” and “Silybin.” We included all relevant in vitro, in vivo, and human studies up to the date of publication.
Results
Based on 64 included studies in this review, silymarin is considered a safe and well-tolerated compound, with no known clinical drug interaction. Notably, multiple adverse reactions of chemotherapeutic agents are effectively managed by its antioxidant, anti-apoptotic, anti-inflammatory, and anti-immunomodulatory properties.
Clinical trials suggest that oral silymarin may be a promising adjuvant with cancer treatments, particularly against hepatotoxicity (
n
= 10), nephrotoxicity (
n
= 3), diarrhea (
n
= 1), and mucositis (
n
= 3), whereas its topical formulation can be particularly effective against radiodermatitis (
n
= 2) and hand-foot syndrome (HFS) (
n
= 1).
Conclusion
Further studies are required to determine the optimal dose, duration, and the best formulation of silymarin to prevent and/or manage chemotherapy and radiotherapy-induced complications.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Apoptosis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cardiotoxicity</subject><subject>Chemical and Drug Induced Liver Injury - drug therapy</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Dermatitis</subject><subject>Diarrhea</subject><subject>Drug interaction</subject><subject>Hepatotoxicity</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Mucositis</subject><subject>Mucositis - drug therapy</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - radiotherapy</subject><subject>Ototoxicity</subject><subject>Pharmacology/Toxicology</subject><subject>Radiation therapy</subject><subject>Reproductive system</subject><subject>Review</subject><subject>Reviews</subject><subject>Side effects</subject><subject>Silymarin</subject><subject>Silymarin - pharmacology</subject><subject>Silymarin - therapeutic use</subject><issn>0031-6970</issn><issn>1432-1041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kc2OVCEQhYnROO3oC7gwJK7RAu4f7szEv2QSF-qaVENhM-nLbeHeNv1Avqf03Jlx56YIVafOFziMvZTwRgL0bwuAUoOoRYBudCOGR2wjG62EhEY-ZhsALUVnerhgz0q5AZCtAf2UXeiuaWEwasP-fIv704g5Jo6FIz9kOlKa45H4lPm8o4wHWubo-EhYlkw81L7b0TitwxPH5HlGH-8bIia_OPIc_ZFyIZ4J3RynVN5VgJvGythRKmdGpUX6zadwBrt9TNHh_tbx4eJxxufsScB9oRd35yX78fHD96vP4vrrpy9X76-F0307i23wuDXYNNob6GR9I0hE8iGAc0gQnG_M4LwadJAQtBpQt2RgK5Wmru31JXu9-h7y9GuhMtubacmpIq3qOzCDNq2qKrWqXJ5KyRTsIcf6hycrwZ6TsWsythZ7m4wd6tKrO-tlO5J_WLmPogr0Kih1lH5S_sf-j-1fSued0Q</recordid><startdate>2023</startdate><enddate>2023</enddate><creator>Ghodousi, Mahsa</creator><creator>Karbasforooshan, Hedyieh</creator><creator>Arabi, Leila</creator><creator>Elyasi, Sepideh</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0001-9857-1175</orcidid><orcidid>https://orcid.org/0000-0003-1623-3346</orcidid></search><sort><creationdate>2023</creationdate><title>Silymarin as a preventive or therapeutic measure for chemotherapy and radiotherapy-induced adverse reactions: a comprehensive review of preclinical and clinical data</title><author>Ghodousi, Mahsa ; Karbasforooshan, Hedyieh ; Arabi, Leila ; Elyasi, Sepideh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-bfdab9a443d906145001aaedff0ccae0fcd498cd283f10f328a35e90b123e6573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Apoptosis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cardiotoxicity</topic><topic>Chemical and Drug Induced Liver Injury - drug therapy</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Dermatitis</topic><topic>Diarrhea</topic><topic>Drug interaction</topic><topic>Hepatotoxicity</topic><topic>Humans</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Mucositis</topic><topic>Mucositis - drug therapy</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - radiotherapy</topic><topic>Ototoxicity</topic><topic>Pharmacology/Toxicology</topic><topic>Radiation therapy</topic><topic>Reproductive system</topic><topic>Review</topic><topic>Reviews</topic><topic>Side effects</topic><topic>Silymarin</topic><topic>Silymarin - pharmacology</topic><topic>Silymarin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghodousi, Mahsa</creatorcontrib><creatorcontrib>Karbasforooshan, Hedyieh</creatorcontrib><creatorcontrib>Arabi, Leila</creatorcontrib><creatorcontrib>Elyasi, Sepideh</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghodousi, Mahsa</au><au>Karbasforooshan, Hedyieh</au><au>Arabi, Leila</au><au>Elyasi, Sepideh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silymarin as a preventive or therapeutic measure for chemotherapy and radiotherapy-induced adverse reactions: a comprehensive review of preclinical and clinical data</atitle><jtitle>European journal of clinical pharmacology</jtitle><stitle>Eur J Clin Pharmacol</stitle><addtitle>Eur J Clin Pharmacol</addtitle><date>2023</date><risdate>2023</risdate><volume>79</volume><issue>1</issue><spage>15</spage><epage>38</epage><pages>15-38</pages><issn>0031-6970</issn><eissn>1432-1041</eissn><abstract>Purpose
Thus far, silymarin has been examined in several studies for prevention or treatment of various chemotherapy or radiotherapy-induced adverse reactions. In this review, we try to collect all available human, animal, and pre-clinical data in this field.
Methods
The search was done in Scopus, PubMed, Medline, and systematic reviews in the Cochrane database, using the following keywords: “Cancer,” “Chemotherapy,” “Radiotherapy,” “Mucositis,” “Nephrotoxicity,” “Dermatitis,” “Ototoxicity,” “Cardiotoxicity,” “Nephrotoxicity,” “Hepatotoxicity,” “Reproductive system,” “Silybum marianum,” “Milk thistle,” and “Silymarin” and “Silybin.” We included all relevant in vitro, in vivo, and human studies up to the date of publication.
Results
Based on 64 included studies in this review, silymarin is considered a safe and well-tolerated compound, with no known clinical drug interaction. Notably, multiple adverse reactions of chemotherapeutic agents are effectively managed by its antioxidant, anti-apoptotic, anti-inflammatory, and anti-immunomodulatory properties.
Clinical trials suggest that oral silymarin may be a promising adjuvant with cancer treatments, particularly against hepatotoxicity (
n
= 10), nephrotoxicity (
n
= 3), diarrhea (
n
= 1), and mucositis (
n
= 3), whereas its topical formulation can be particularly effective against radiodermatitis (
n
= 2) and hand-foot syndrome (HFS) (
n
= 1).
Conclusion
Further studies are required to determine the optimal dose, duration, and the best formulation of silymarin to prevent and/or manage chemotherapy and radiotherapy-induced complications.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36450892</pmid><doi>10.1007/s00228-022-03434-8</doi><tpages>24</tpages><orcidid>https://orcid.org/0000-0001-9857-1175</orcidid><orcidid>https://orcid.org/0000-0003-1623-3346</orcidid></addata></record> |
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issn | 0031-6970 1432-1041 |
language | eng |
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source | Springer Nature |
subjects | Animals Antioxidants - pharmacology Apoptosis Biomedical and Life Sciences Biomedicine Cardiotoxicity Chemical and Drug Induced Liver Injury - drug therapy Chemotherapy Clinical trials Dermatitis Diarrhea Drug interaction Hepatotoxicity Humans Immunomodulation Inflammation Mucositis Mucositis - drug therapy Neoplasms - drug therapy Neoplasms - radiotherapy Ototoxicity Pharmacology/Toxicology Radiation therapy Reproductive system Review Reviews Side effects Silymarin Silymarin - pharmacology Silymarin - therapeutic use |
title | Silymarin as a preventive or therapeutic measure for chemotherapy and radiotherapy-induced adverse reactions: a comprehensive review of preclinical and clinical data |
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