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Role of Imiquimod and Parenteral Meglumine Antimoniate in the Initial Treatment of Cutaneous Leishmaniasis
Background. Cutaneous leishmaniasis is a serious public health problem in the developing world. The main therapeutic agent—pentavalent antimony, developed >50 years ago—is expensive, often accompanied by severe adverse effects, and complicated by the emergence of drug resistance. Better therapies...
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Published in: | Clinical infectious diseases 2007-06, Vol.44 (12), p.1549-1554 |
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description | Background. Cutaneous leishmaniasis is a serious public health problem in the developing world. The main therapeutic agent—pentavalent antimony, developed >50 years ago—is expensive, often accompanied by severe adverse effects, and complicated by the emergence of drug resistance. Better therapies are urgently needed. In the present pilot study, we compared the use of imiquimod, an immunomodulatory molecule, to the use of meglumine antimoniate alone and in combination for the initial treatment of cutaneous leishmaniasis. Materials and methods. Patients with newly diagnosed cutaneous leishmaniasis were enrolled from a single referral center in Lima, Peru, from August 2005 through October 2005. Patients were randomly assigned to 1 of 3 treatment groups and received either imiquimod 7.5% cream administered topically every other day for 20 days, intravenous meglumine antimoniate administered at a dosage of 20 mg/kg per day every day for 20 days, or combination therapy with both intravenous meglumine antimoniate and imiquimod 7.5% cream. Patients were evaluated weekly and at 1 and 3 months after treatment. Patients who had healed lesions at 3 months were considered to be clinically cured. Results. Although several patients showed initial resolution of symptoms with imiquimod treatment alone, all of these patients experienced relapse after treatment discontinuation. Four (57%) of 7 patients treated with meglumine antimoniate alone and 7 (100%) of 7 patients treated with combination therapy were cured. Combination therapy was not only more effective than the other 2 treatments (P < .05) but also led to faster healing and better cosmetic results. Conclusion. Combination therapy with imiquimod and meglumine antimoniate is a promising regimen for the initial treatment of cutaneous leishmaniasis that warrants additional larger studies. |
doi_str_mv | 10.1086/518172 |
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Cutaneous leishmaniasis is a serious public health problem in the developing world. The main therapeutic agent—pentavalent antimony, developed >50 years ago—is expensive, often accompanied by severe adverse effects, and complicated by the emergence of drug resistance. Better therapies are urgently needed. In the present pilot study, we compared the use of imiquimod, an immunomodulatory molecule, to the use of meglumine antimoniate alone and in combination for the initial treatment of cutaneous leishmaniasis. Materials and methods. Patients with newly diagnosed cutaneous leishmaniasis were enrolled from a single referral center in Lima, Peru, from August 2005 through October 2005. Patients were randomly assigned to 1 of 3 treatment groups and received either imiquimod 7.5% cream administered topically every other day for 20 days, intravenous meglumine antimoniate administered at a dosage of 20 mg/kg per day every day for 20 days, or combination therapy with both intravenous meglumine antimoniate and imiquimod 7.5% cream. Patients were evaluated weekly and at 1 and 3 months after treatment. Patients who had healed lesions at 3 months were considered to be clinically cured. Results. Although several patients showed initial resolution of symptoms with imiquimod treatment alone, all of these patients experienced relapse after treatment discontinuation. Four (57%) of 7 patients treated with meglumine antimoniate alone and 7 (100%) of 7 patients treated with combination therapy were cured. Combination therapy was not only more effective than the other 2 treatments (P < .05) but also led to faster healing and better cosmetic results. Conclusion. Combination therapy with imiquimod and meglumine antimoniate is a promising regimen for the initial treatment of cutaneous leishmaniasis that warrants additional larger studies.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/518172</identifier><identifier>PMID: 17516397</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Administration, Topical ; Adult ; Adverse effects ; Aged ; Aged, 80 and over ; Aminoquinolines - therapeutic use ; Animals ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiprotozoal Agents - therapeutic use ; Antirheumatic Agents - therapeutic use ; Antiviral agents ; Articles and Commentaries ; Biological and medical sciences ; Clinical outcomes ; Clinical trials ; Comparative analysis ; Cream ; Cutaneous leishmaniasis ; Dosage ; Drug therapy ; Drug Therapy, Combination ; Female ; Healing ; Human protozoal diseases ; Humans ; Immunomodulators ; Infectious diseases ; Injections, Intravenous ; Leishmaniasis ; Leishmaniasis, Cutaneous - drug therapy ; Leshmaniasis ; Lesions ; Male ; Medical sciences ; Meglumine - therapeutic use ; Middle Aged ; Organometallic Compounds - therapeutic use ; Parasitic diseases ; Pharmacology. Drug treatments ; Pilot Projects ; Protozoal diseases ; Relapse ; Scars ; Skin diseases ; Treatment Outcome</subject><ispartof>Clinical infectious diseases, 2007-06, Vol.44 (12), p.1549-1554</ispartof><rights>Copyright 2007 The Infectious Diseases Society of America</rights><rights>2007 Infectious Diseases Society of America 2007</rights><rights>2008 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Jun 15, 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-73c6c6ebb7339bb8beab7b9849c6abb037fa45ca1504dd391e85bf3665e2a02d3</citedby><cites>FETCH-LOGICAL-c513t-73c6c6ebb7339bb8beab7b9849c6abb037fa45ca1504dd391e85bf3665e2a02d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4485448$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4485448$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20291162$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17516397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arevalo, Iracema</creatorcontrib><creatorcontrib>Tulliano, Gianfranco</creatorcontrib><creatorcontrib>Quispe, Ana</creatorcontrib><creatorcontrib>Spaeth, Gerald</creatorcontrib><creatorcontrib>Matlashewski, Greg</creatorcontrib><creatorcontrib>Llanos-Cuentas, Alejandro</creatorcontrib><creatorcontrib>Pollack, Henry</creatorcontrib><title>Role of Imiquimod and Parenteral Meglumine Antimoniate in the Initial Treatment of Cutaneous Leishmaniasis</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><addtitle>Clinical Infectious Diseases</addtitle><description>Background. Cutaneous leishmaniasis is a serious public health problem in the developing world. The main therapeutic agent—pentavalent antimony, developed >50 years ago—is expensive, often accompanied by severe adverse effects, and complicated by the emergence of drug resistance. Better therapies are urgently needed. In the present pilot study, we compared the use of imiquimod, an immunomodulatory molecule, to the use of meglumine antimoniate alone and in combination for the initial treatment of cutaneous leishmaniasis. Materials and methods. Patients with newly diagnosed cutaneous leishmaniasis were enrolled from a single referral center in Lima, Peru, from August 2005 through October 2005. Patients were randomly assigned to 1 of 3 treatment groups and received either imiquimod 7.5% cream administered topically every other day for 20 days, intravenous meglumine antimoniate administered at a dosage of 20 mg/kg per day every day for 20 days, or combination therapy with both intravenous meglumine antimoniate and imiquimod 7.5% cream. Patients were evaluated weekly and at 1 and 3 months after treatment. Patients who had healed lesions at 3 months were considered to be clinically cured. Results. Although several patients showed initial resolution of symptoms with imiquimod treatment alone, all of these patients experienced relapse after treatment discontinuation. Four (57%) of 7 patients treated with meglumine antimoniate alone and 7 (100%) of 7 patients treated with combination therapy were cured. Combination therapy was not only more effective than the other 2 treatments (P < .05) but also led to faster healing and better cosmetic results. Conclusion. Combination therapy with imiquimod and meglumine antimoniate is a promising regimen for the initial treatment of cutaneous leishmaniasis that warrants additional larger studies.</description><subject>Administration, Topical</subject><subject>Adult</subject><subject>Adverse effects</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aminoquinolines - therapeutic use</subject><subject>Animals</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antiprotozoal Agents - therapeutic use</subject><subject>Antirheumatic Agents - therapeutic use</subject><subject>Antiviral agents</subject><subject>Articles and Commentaries</subject><subject>Biological and medical sciences</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Comparative analysis</subject><subject>Cream</subject><subject>Cutaneous leishmaniasis</subject><subject>Dosage</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Healing</subject><subject>Human protozoal diseases</subject><subject>Humans</subject><subject>Immunomodulators</subject><subject>Infectious diseases</subject><subject>Injections, Intravenous</subject><subject>Leishmaniasis</subject><subject>Leishmaniasis, Cutaneous - drug therapy</subject><subject>Leshmaniasis</subject><subject>Lesions</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Meglumine - therapeutic use</subject><subject>Middle Aged</subject><subject>Organometallic Compounds - therapeutic use</subject><subject>Parasitic diseases</subject><subject>Pharmacology. Drug treatments</subject><subject>Pilot Projects</subject><subject>Protozoal diseases</subject><subject>Relapse</subject><subject>Scars</subject><subject>Skin diseases</subject><subject>Treatment Outcome</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqF0VtrFDEUB_BBFFurfgKRKOjbaM5kcnssi9rFFaVWKH0JycwZm3UubZIB_fZmmWULgvQhJHB--edyiuI50HdAlXjPQYGsHhTHwJksBdfwMK8pV2WtmDoqnsS4pRRAUf64OALJQTAtj4vt-dQjmTqyHvzt7IepJXZsyTcbcEwYbE--4M9-HvyI5HRMGYzeJiR-JOkayXr0yWd0EdCmIW_ZRa3mZEec5kg26OP1YPOW6OPT4lFn-4jP9vNJ8ePjh4vVWbn5-mm9Ot2UDQeWSska0Qh0TjKmnVMOrZNOq1o3wjpHmexszRsLnNZtyzSg4q5jQnCsLK1adlK8XXJvwnQ7Y0xm8LHBvl8uZSTlUFWC3gsrmv-Uwv0QtIQsRYav_4HbaQ5jfq2pQGuucgvu0powxRiwMzfBDzb8MUDNrplmaWaGL_dpsxuwvWP77mXwZg9sbGzfBTs2Ph5cRSsNIHZBrxY3zTf_P-zFYrYxTeGg6lrxPHK5XMo-Jvx9KNvwywjJJDdnl1dGnH-_FFefayPZX6TTyDg</recordid><startdate>20070615</startdate><enddate>20070615</enddate><creator>Arevalo, Iracema</creator><creator>Tulliano, Gianfranco</creator><creator>Quispe, Ana</creator><creator>Spaeth, Gerald</creator><creator>Matlashewski, Greg</creator><creator>Llanos-Cuentas, Alejandro</creator><creator>Pollack, Henry</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QL</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070615</creationdate><title>Role of Imiquimod and Parenteral Meglumine Antimoniate in the Initial Treatment of Cutaneous Leishmaniasis</title><author>Arevalo, Iracema ; Tulliano, Gianfranco ; Quispe, Ana ; Spaeth, Gerald ; Matlashewski, Greg ; Llanos-Cuentas, Alejandro ; Pollack, Henry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-73c6c6ebb7339bb8beab7b9849c6abb037fa45ca1504dd391e85bf3665e2a02d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Administration, Topical</topic><topic>Adult</topic><topic>Adverse effects</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aminoquinolines - therapeutic use</topic><topic>Animals</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antiprotozoal Agents - therapeutic use</topic><topic>Antirheumatic Agents - therapeutic use</topic><topic>Antiviral agents</topic><topic>Articles and Commentaries</topic><topic>Biological and medical sciences</topic><topic>Clinical outcomes</topic><topic>Clinical trials</topic><topic>Comparative analysis</topic><topic>Cream</topic><topic>Cutaneous leishmaniasis</topic><topic>Dosage</topic><topic>Drug therapy</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Healing</topic><topic>Human protozoal diseases</topic><topic>Humans</topic><topic>Immunomodulators</topic><topic>Infectious diseases</topic><topic>Injections, Intravenous</topic><topic>Leishmaniasis</topic><topic>Leishmaniasis, Cutaneous - drug therapy</topic><topic>Leshmaniasis</topic><topic>Lesions</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Meglumine - therapeutic use</topic><topic>Middle Aged</topic><topic>Organometallic Compounds - therapeutic use</topic><topic>Parasitic diseases</topic><topic>Pharmacology. Drug treatments</topic><topic>Pilot Projects</topic><topic>Protozoal diseases</topic><topic>Relapse</topic><topic>Scars</topic><topic>Skin diseases</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arevalo, Iracema</creatorcontrib><creatorcontrib>Tulliano, Gianfranco</creatorcontrib><creatorcontrib>Quispe, Ana</creatorcontrib><creatorcontrib>Spaeth, Gerald</creatorcontrib><creatorcontrib>Matlashewski, Greg</creatorcontrib><creatorcontrib>Llanos-Cuentas, Alejandro</creatorcontrib><creatorcontrib>Pollack, Henry</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arevalo, Iracema</au><au>Tulliano, Gianfranco</au><au>Quispe, Ana</au><au>Spaeth, Gerald</au><au>Matlashewski, Greg</au><au>Llanos-Cuentas, Alejandro</au><au>Pollack, Henry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Imiquimod and Parenteral Meglumine Antimoniate in the Initial Treatment of Cutaneous Leishmaniasis</atitle><jtitle>Clinical infectious diseases</jtitle><stitle>Clinical Infectious Diseases</stitle><addtitle>Clinical Infectious Diseases</addtitle><date>2007-06-15</date><risdate>2007</risdate><volume>44</volume><issue>12</issue><spage>1549</spage><epage>1554</epage><pages>1549-1554</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. Cutaneous leishmaniasis is a serious public health problem in the developing world. The main therapeutic agent—pentavalent antimony, developed >50 years ago—is expensive, often accompanied by severe adverse effects, and complicated by the emergence of drug resistance. Better therapies are urgently needed. In the present pilot study, we compared the use of imiquimod, an immunomodulatory molecule, to the use of meglumine antimoniate alone and in combination for the initial treatment of cutaneous leishmaniasis. Materials and methods. Patients with newly diagnosed cutaneous leishmaniasis were enrolled from a single referral center in Lima, Peru, from August 2005 through October 2005. Patients were randomly assigned to 1 of 3 treatment groups and received either imiquimod 7.5% cream administered topically every other day for 20 days, intravenous meglumine antimoniate administered at a dosage of 20 mg/kg per day every day for 20 days, or combination therapy with both intravenous meglumine antimoniate and imiquimod 7.5% cream. Patients were evaluated weekly and at 1 and 3 months after treatment. Patients who had healed lesions at 3 months were considered to be clinically cured. Results. Although several patients showed initial resolution of symptoms with imiquimod treatment alone, all of these patients experienced relapse after treatment discontinuation. Four (57%) of 7 patients treated with meglumine antimoniate alone and 7 (100%) of 7 patients treated with combination therapy were cured. Combination therapy was not only more effective than the other 2 treatments (P < .05) but also led to faster healing and better cosmetic results. Conclusion. Combination therapy with imiquimod and meglumine antimoniate is a promising regimen for the initial treatment of cutaneous leishmaniasis that warrants additional larger studies.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>17516397</pmid><doi>10.1086/518172</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Topical Adult Adverse effects Aged Aged, 80 and over Aminoquinolines - therapeutic use Animals Antibiotics. Antiinfectious agents. Antiparasitic agents Antiprotozoal Agents - therapeutic use Antirheumatic Agents - therapeutic use Antiviral agents Articles and Commentaries Biological and medical sciences Clinical outcomes Clinical trials Comparative analysis Cream Cutaneous leishmaniasis Dosage Drug therapy Drug Therapy, Combination Female Healing Human protozoal diseases Humans Immunomodulators Infectious diseases Injections, Intravenous Leishmaniasis Leishmaniasis, Cutaneous - drug therapy Leshmaniasis Lesions Male Medical sciences Meglumine - therapeutic use Middle Aged Organometallic Compounds - therapeutic use Parasitic diseases Pharmacology. Drug treatments Pilot Projects Protozoal diseases Relapse Scars Skin diseases Treatment Outcome |
title | Role of Imiquimod and Parenteral Meglumine Antimoniate in the Initial Treatment of Cutaneous Leishmaniasis |
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