Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid

Most therapeutic approaches for keloids remain clinically unsatisfactory. In the last years, intralesional botulinum toxin-A (IL BTX-A) was proposed for treatment of keloids. Our aim of the study was to compare the clinical efficacy of IL BTX-A and IL 5-Fluorouracil (IL 5-FU) in treatment of keloids...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Archives of Dermatological Research 2021-09, Vol.313 (7), p.549-556
Hauptverfasser: Ismail, Sahar A., Mohammed, Noorhan H. K., Sotohy, Muhammad, Abou-Taleb, Doaa A. E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 556
container_issue 7
container_start_page 549
container_title Archives of Dermatological Research
container_volume 313
creator Ismail, Sahar A.
Mohammed, Noorhan H. K.
Sotohy, Muhammad
Abou-Taleb, Doaa A. E.
description Most therapeutic approaches for keloids remain clinically unsatisfactory. In the last years, intralesional botulinum toxin-A (IL BTX-A) was proposed for treatment of keloids. Our aim of the study was to compare the clinical efficacy of IL BTX-A and IL 5-Fluorouracil (IL 5-FU) in treatment of keloids. A total of 50 patients with keloids were included in the study, 22 patients (with 26 keloids) were treated with IL BTX-A monthly for up to 6 months and other 22 patients (with 27 keloids) were treated with IL 5-FU weekly for up to 6 weeks, while the remaining 6 patients, each having multiple keloids, were treated with both IL BTX-A for some lesions (8 keloids) and IL 5-FU for their remaining lesions (8 keloids). The clinical improvement was assessed according to flattening of the lesions. Side effects were recorded. A significantly better therapeutic response of keloids was detected after IL BTX-A than IL 5-FU ( P  = 0.041). IL BTX-A achieved excellent and good flattening of the lesions (58.8% and 20.6%) compared to (31.4% and 17.1%) after IL 5-FU, respectively. In BTX-A treated group, there was no statistically significant difference between the clinical response in small lesions compared to medium and large ones ( P  = 0.476). While in 5-FU treated group, small and medium lesions showed significantly better response than larger ones ( P  = 0.009). IL BTX-A caused fewer side effects than IL 5-FU, less pain, itching, no hyperpigmentation and less recurrence. Both IL BTX-A and IL 5-FU showed positive results in treatment of keloids. However, IL BTX-A showed higher clinical efficacy even in large size keloids with less side effects.
doi_str_mv 10.1007/s00403-020-02132-8
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2440666221</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2440666221</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-8079c9f3b4356868e38253bd68d76145c4bd12bbc8fa2dd8ad3e1990e061135d3</originalsourceid><addsrcrecordid>eNp9kE9LwzAYh4Mobsx9AQ9S8OKl-uZ_epzDqTDwouAttE0qnW0zk1bctzdzU8GDgZDA-7y_N3kQOsVwiQHkVQBgQFMgEDemJFUHaIxZvIDIng_RGCiDlIpMjNA0hBXEJYERkMdoRInKCGFijObXrh-auhvapHcfdZf0m7VNZsm79WEICU8XzeC8G3xe1k2yrXub963t-sRVyattXG1O0FGVN8FO9-cEPS1uHud36fLh9n4-W6YllbxPFciszCpaMMqFEspSRTgtjFBGCsx4yQqDSVGUqsqJMSo31OIsAwsCY8oNnaCLXe7au7fBhl63dSht0-SddUPQhDEQQpCoY4LO_6Cr-Icuvk4TzhmVAuSWIjuq9C4Ebyu99nWb-43GoLeW9c6yjpb1l2WtYtPZPnooWmt-Wr6dRoDugBBL3Yv1v7P_if0ESxaFUA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2554376071</pqid></control><display><type>article</type><title>Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid</title><source>MEDLINE</source><source>Springer Journals</source><creator>Ismail, Sahar A. ; Mohammed, Noorhan H. K. ; Sotohy, Muhammad ; Abou-Taleb, Doaa A. E.</creator><creatorcontrib>Ismail, Sahar A. ; Mohammed, Noorhan H. K. ; Sotohy, Muhammad ; Abou-Taleb, Doaa A. E.</creatorcontrib><description>Most therapeutic approaches for keloids remain clinically unsatisfactory. In the last years, intralesional botulinum toxin-A (IL BTX-A) was proposed for treatment of keloids. Our aim of the study was to compare the clinical efficacy of IL BTX-A and IL 5-Fluorouracil (IL 5-FU) in treatment of keloids. A total of 50 patients with keloids were included in the study, 22 patients (with 26 keloids) were treated with IL BTX-A monthly for up to 6 months and other 22 patients (with 27 keloids) were treated with IL 5-FU weekly for up to 6 weeks, while the remaining 6 patients, each having multiple keloids, were treated with both IL BTX-A for some lesions (8 keloids) and IL 5-FU for their remaining lesions (8 keloids). The clinical improvement was assessed according to flattening of the lesions. Side effects were recorded. A significantly better therapeutic response of keloids was detected after IL BTX-A than IL 5-FU ( P  = 0.041). IL BTX-A achieved excellent and good flattening of the lesions (58.8% and 20.6%) compared to (31.4% and 17.1%) after IL 5-FU, respectively. In BTX-A treated group, there was no statistically significant difference between the clinical response in small lesions compared to medium and large ones ( P  = 0.476). While in 5-FU treated group, small and medium lesions showed significantly better response than larger ones ( P  = 0.009). IL BTX-A caused fewer side effects than IL 5-FU, less pain, itching, no hyperpigmentation and less recurrence. Both IL BTX-A and IL 5-FU showed positive results in treatment of keloids. However, IL BTX-A showed higher clinical efficacy even in large size keloids with less side effects.</description><identifier>ISSN: 0340-3696</identifier><identifier>EISSN: 1432-069X</identifier><identifier>DOI: 10.1007/s00403-020-02132-8</identifier><identifier>PMID: 32892246</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>5-Fluorouracil ; Adolescent ; Adult ; Botulinum toxin ; Botulinum toxin type A ; Botulinum Toxins, Type A - administration &amp; dosage ; Botulinum Toxins, Type A - adverse effects ; Clinical outcomes ; Dermatology ; Female ; Fluorouracil - administration &amp; dosage ; Fluorouracil - adverse effects ; Follow-Up Studies ; Humans ; Hyperpigmentation ; Hyperpigmentation - chemically induced ; Hyperpigmentation - epidemiology ; Injection Site Reaction - epidemiology ; Injection Site Reaction - etiology ; Injections, Intralesional - adverse effects ; Keloid - drug therapy ; Lesions ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Original Paper ; Patients ; Pruritus ; Scars ; Side effects ; Skin ; Statistical analysis ; Treatment Outcome ; Young Adult</subject><ispartof>Archives of Dermatological Research, 2021-09, Vol.313 (7), p.549-556</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>2020. Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-8079c9f3b4356868e38253bd68d76145c4bd12bbc8fa2dd8ad3e1990e061135d3</citedby><cites>FETCH-LOGICAL-c375t-8079c9f3b4356868e38253bd68d76145c4bd12bbc8fa2dd8ad3e1990e061135d3</cites><orcidid>0000-0002-9642-8233</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00403-020-02132-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00403-020-02132-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32892246$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ismail, Sahar A.</creatorcontrib><creatorcontrib>Mohammed, Noorhan H. K.</creatorcontrib><creatorcontrib>Sotohy, Muhammad</creatorcontrib><creatorcontrib>Abou-Taleb, Doaa A. E.</creatorcontrib><title>Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid</title><title>Archives of Dermatological Research</title><addtitle>Arch Dermatol Res</addtitle><addtitle>Arch Dermatol Res</addtitle><description>Most therapeutic approaches for keloids remain clinically unsatisfactory. In the last years, intralesional botulinum toxin-A (IL BTX-A) was proposed for treatment of keloids. Our aim of the study was to compare the clinical efficacy of IL BTX-A and IL 5-Fluorouracil (IL 5-FU) in treatment of keloids. A total of 50 patients with keloids were included in the study, 22 patients (with 26 keloids) were treated with IL BTX-A monthly for up to 6 months and other 22 patients (with 27 keloids) were treated with IL 5-FU weekly for up to 6 weeks, while the remaining 6 patients, each having multiple keloids, were treated with both IL BTX-A for some lesions (8 keloids) and IL 5-FU for their remaining lesions (8 keloids). The clinical improvement was assessed according to flattening of the lesions. Side effects were recorded. A significantly better therapeutic response of keloids was detected after IL BTX-A than IL 5-FU ( P  = 0.041). IL BTX-A achieved excellent and good flattening of the lesions (58.8% and 20.6%) compared to (31.4% and 17.1%) after IL 5-FU, respectively. In BTX-A treated group, there was no statistically significant difference between the clinical response in small lesions compared to medium and large ones ( P  = 0.476). While in 5-FU treated group, small and medium lesions showed significantly better response than larger ones ( P  = 0.009). IL BTX-A caused fewer side effects than IL 5-FU, less pain, itching, no hyperpigmentation and less recurrence. Both IL BTX-A and IL 5-FU showed positive results in treatment of keloids. However, IL BTX-A showed higher clinical efficacy even in large size keloids with less side effects.</description><subject>5-Fluorouracil</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Botulinum toxin</subject><subject>Botulinum toxin type A</subject><subject>Botulinum Toxins, Type A - administration &amp; dosage</subject><subject>Botulinum Toxins, Type A - adverse effects</subject><subject>Clinical outcomes</subject><subject>Dermatology</subject><subject>Female</subject><subject>Fluorouracil - administration &amp; dosage</subject><subject>Fluorouracil - adverse effects</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Hyperpigmentation</subject><subject>Hyperpigmentation - chemically induced</subject><subject>Hyperpigmentation - epidemiology</subject><subject>Injection Site Reaction - epidemiology</subject><subject>Injection Site Reaction - etiology</subject><subject>Injections, Intralesional - adverse effects</subject><subject>Keloid - drug therapy</subject><subject>Lesions</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Original Paper</subject><subject>Patients</subject><subject>Pruritus</subject><subject>Scars</subject><subject>Side effects</subject><subject>Skin</subject><subject>Statistical analysis</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0340-3696</issn><issn>1432-069X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9LwzAYh4Mobsx9AQ9S8OKl-uZ_epzDqTDwouAttE0qnW0zk1bctzdzU8GDgZDA-7y_N3kQOsVwiQHkVQBgQFMgEDemJFUHaIxZvIDIng_RGCiDlIpMjNA0hBXEJYERkMdoRInKCGFijObXrh-auhvapHcfdZf0m7VNZsm79WEICU8XzeC8G3xe1k2yrXub963t-sRVyattXG1O0FGVN8FO9-cEPS1uHud36fLh9n4-W6YllbxPFciszCpaMMqFEspSRTgtjFBGCsx4yQqDSVGUqsqJMSo31OIsAwsCY8oNnaCLXe7au7fBhl63dSht0-SddUPQhDEQQpCoY4LO_6Cr-Icuvk4TzhmVAuSWIjuq9C4Ebyu99nWb-43GoLeW9c6yjpb1l2WtYtPZPnooWmt-Wr6dRoDugBBL3Yv1v7P_if0ESxaFUA</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Ismail, Sahar A.</creator><creator>Mohammed, Noorhan H. K.</creator><creator>Sotohy, Muhammad</creator><creator>Abou-Taleb, Doaa A. E.</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9642-8233</orcidid></search><sort><creationdate>20210901</creationdate><title>Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid</title><author>Ismail, Sahar A. ; Mohammed, Noorhan H. K. ; Sotohy, Muhammad ; Abou-Taleb, Doaa A. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-8079c9f3b4356868e38253bd68d76145c4bd12bbc8fa2dd8ad3e1990e061135d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>5-Fluorouracil</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Botulinum toxin</topic><topic>Botulinum toxin type A</topic><topic>Botulinum Toxins, Type A - administration &amp; dosage</topic><topic>Botulinum Toxins, Type A - adverse effects</topic><topic>Clinical outcomes</topic><topic>Dermatology</topic><topic>Female</topic><topic>Fluorouracil - administration &amp; dosage</topic><topic>Fluorouracil - adverse effects</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Hyperpigmentation</topic><topic>Hyperpigmentation - chemically induced</topic><topic>Hyperpigmentation - epidemiology</topic><topic>Injection Site Reaction - epidemiology</topic><topic>Injection Site Reaction - etiology</topic><topic>Injections, Intralesional - adverse effects</topic><topic>Keloid - drug therapy</topic><topic>Lesions</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Original Paper</topic><topic>Patients</topic><topic>Pruritus</topic><topic>Scars</topic><topic>Side effects</topic><topic>Skin</topic><topic>Statistical analysis</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ismail, Sahar A.</creatorcontrib><creatorcontrib>Mohammed, Noorhan H. K.</creatorcontrib><creatorcontrib>Sotohy, Muhammad</creatorcontrib><creatorcontrib>Abou-Taleb, Doaa A. E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of Dermatological Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ismail, Sahar A.</au><au>Mohammed, Noorhan H. K.</au><au>Sotohy, Muhammad</au><au>Abou-Taleb, Doaa A. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid</atitle><jtitle>Archives of Dermatological Research</jtitle><stitle>Arch Dermatol Res</stitle><addtitle>Arch Dermatol Res</addtitle><date>2021-09-01</date><risdate>2021</risdate><volume>313</volume><issue>7</issue><spage>549</spage><epage>556</epage><pages>549-556</pages><issn>0340-3696</issn><eissn>1432-069X</eissn><abstract>Most therapeutic approaches for keloids remain clinically unsatisfactory. In the last years, intralesional botulinum toxin-A (IL BTX-A) was proposed for treatment of keloids. Our aim of the study was to compare the clinical efficacy of IL BTX-A and IL 5-Fluorouracil (IL 5-FU) in treatment of keloids. A total of 50 patients with keloids were included in the study, 22 patients (with 26 keloids) were treated with IL BTX-A monthly for up to 6 months and other 22 patients (with 27 keloids) were treated with IL 5-FU weekly for up to 6 weeks, while the remaining 6 patients, each having multiple keloids, were treated with both IL BTX-A for some lesions (8 keloids) and IL 5-FU for their remaining lesions (8 keloids). The clinical improvement was assessed according to flattening of the lesions. Side effects were recorded. A significantly better therapeutic response of keloids was detected after IL BTX-A than IL 5-FU ( P  = 0.041). IL BTX-A achieved excellent and good flattening of the lesions (58.8% and 20.6%) compared to (31.4% and 17.1%) after IL 5-FU, respectively. In BTX-A treated group, there was no statistically significant difference between the clinical response in small lesions compared to medium and large ones ( P  = 0.476). While in 5-FU treated group, small and medium lesions showed significantly better response than larger ones ( P  = 0.009). IL BTX-A caused fewer side effects than IL 5-FU, less pain, itching, no hyperpigmentation and less recurrence. Both IL BTX-A and IL 5-FU showed positive results in treatment of keloids. However, IL BTX-A showed higher clinical efficacy even in large size keloids with less side effects.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32892246</pmid><doi>10.1007/s00403-020-02132-8</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9642-8233</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0340-3696
ispartof Archives of Dermatological Research, 2021-09, Vol.313 (7), p.549-556
issn 0340-3696
1432-069X
language eng
recordid cdi_proquest_miscellaneous_2440666221
source MEDLINE; Springer Journals
subjects 5-Fluorouracil
Adolescent
Adult
Botulinum toxin
Botulinum toxin type A
Botulinum Toxins, Type A - administration & dosage
Botulinum Toxins, Type A - adverse effects
Clinical outcomes
Dermatology
Female
Fluorouracil - administration & dosage
Fluorouracil - adverse effects
Follow-Up Studies
Humans
Hyperpigmentation
Hyperpigmentation - chemically induced
Hyperpigmentation - epidemiology
Injection Site Reaction - epidemiology
Injection Site Reaction - etiology
Injections, Intralesional - adverse effects
Keloid - drug therapy
Lesions
Male
Medicine
Medicine & Public Health
Middle Aged
Original Paper
Patients
Pruritus
Scars
Side effects
Skin
Statistical analysis
Treatment Outcome
Young Adult
title Botulinum toxin type A versus 5-Fluorouracil in treatment of keloid
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T16%3A28%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Botulinum%20toxin%20type%20A%20versus%205-Fluorouracil%20in%20treatment%20of%20keloid&rft.jtitle=Archives%20of%20Dermatological%20Research&rft.au=Ismail,%20Sahar%20A.&rft.date=2021-09-01&rft.volume=313&rft.issue=7&rft.spage=549&rft.epage=556&rft.pages=549-556&rft.issn=0340-3696&rft.eissn=1432-069X&rft_id=info:doi/10.1007/s00403-020-02132-8&rft_dat=%3Cproquest_cross%3E2440666221%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2554376071&rft_id=info:pmid/32892246&rfr_iscdi=true