A Phase II Randomized Trial of Amphotericin B Alone or Combined with Fluconazole in the Treatment of HIV-Associated Cryptococcal Meningitis
Background. Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-...
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creator | Pappas, Peter G. Chetchotisakd, Ploenchan Larsen, Robert A. Manosuthi, Weerawat Morris, Michele I. Anekthananon, Thomansak Sungkanuparph, Somnuek Supparatpinyo, Khauncahi Nolen, Tracy L. Zimmer, Louise O. Kendrick, Amy S. Johnson, Phillip Sobel, Jack D. Filler, Scott G. |
description | Background. Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-label, phase II trial in Thailand and the United States that compared the safety and efficacy of intravenous amphotericin B deoxycholate (AmB) 0.7 mg/kg (the standard therapy) with that of AmB 0.7 mg/kg plus fluconazole 400 mg (the low-dosage combination) or AmB 0.7 mg/kg plus fluconazole 800 mg (the high-dosage combination) administered daily for 14 days, followed by fluconazole alone at the randomized dosage (400 or 800 mg per day) for 56 days. The primary safety end point was the number of severe or life-threatening treatment-related toxicities; the primary efficacy end point was a composite of survival, neurologic stability, and negative cerebrospinal fluid culture results after 14 days of therapy. Results. A total of 143 patients were enrolled. There were no differences in treatment-related toxicities among the 3 arms. Toxicity was predictable and was most often related to AmB, and it included electrolyte abnormalities, anemia, nephrotoxicity, and infusion-related events. At day 14, 41%, 27%, and 54% of patients in the standard therapy, low-dosage combination, and high-dosage combination therapy arms, respectively, demonstrated successful outcomes. A trend towards better outcomes in the combination therapy arms was seen at days 42 and 70. Conclusions. AmB plus fluconazole administered at a dosage of 800 mg for 14 days, followed by fluconazole administered at a dosage of 800 mg daily for 56 days, is well-tolerated and efficacious among HIV-positive patients with central nervous system cryptococcosis. These results have significant treatment implications and should be validated in a randomized phase III trial. Clinical trials registration. This clinical trial is registered in the National Library of Medicine's registry (http://www.clinicaltrials.gov) under the registration number NCT00145249. |
doi_str_mv | 10.1086/599112 |
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Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-label, phase II trial in Thailand and the United States that compared the safety and efficacy of intravenous amphotericin B deoxycholate (AmB) 0.7 mg/kg (the standard therapy) with that of AmB 0.7 mg/kg plus fluconazole 400 mg (the low-dosage combination) or AmB 0.7 mg/kg plus fluconazole 800 mg (the high-dosage combination) administered daily for 14 days, followed by fluconazole alone at the randomized dosage (400 or 800 mg per day) for 56 days. The primary safety end point was the number of severe or life-threatening treatment-related toxicities; the primary efficacy end point was a composite of survival, neurologic stability, and negative cerebrospinal fluid culture results after 14 days of therapy. Results. A total of 143 patients were enrolled. There were no differences in treatment-related toxicities among the 3 arms. Toxicity was predictable and was most often related to AmB, and it included electrolyte abnormalities, anemia, nephrotoxicity, and infusion-related events. At day 14, 41%, 27%, and 54% of patients in the standard therapy, low-dosage combination, and high-dosage combination therapy arms, respectively, demonstrated successful outcomes. A trend towards better outcomes in the combination therapy arms was seen at days 42 and 70. Conclusions. AmB plus fluconazole administered at a dosage of 800 mg for 14 days, followed by fluconazole administered at a dosage of 800 mg daily for 56 days, is well-tolerated and efficacious among HIV-positive patients with central nervous system cryptococcosis. These results have significant treatment implications and should be validated in a randomized phase III trial. Clinical trials registration. This clinical trial is registered in the National Library of Medicine's registry (http://www.clinicaltrials.gov) under the registration number NCT00145249.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/599112</identifier><identifier>PMID: 19441980</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: The University of Chicago Press</publisher><subject>Adult ; Amphotericin B - administration & dosage ; Amphotericin B - adverse effects ; Amphotericin B - therapeutic use ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal agents ; Antifungal Agents - administration & dosage ; Antifungal Agents - adverse effects ; Antifungal Agents - therapeutic use ; Antiretroviral drugs ; Biological and medical sciences ; Cerebrospinal Fluid - microbiology ; Clinical trials ; Comparative analysis ; Female ; Fluconazole - administration & dosage ; Fluconazole - adverse effects ; Fluconazole - therapeutic use ; HIV ; HIV Infections - complications ; Human immunodeficiency virus ; Human mycoses ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Medical treatment ; Meningitis ; Meningitis, Cryptococcal - drug therapy ; Middle Aged ; Miscellaneous mycoses ; Mycoses ; Nervous system ; Pharmacology. Drug treatments ; Survival Analysis ; Thailand ; Treatment Outcome ; United States ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>Clinical infectious diseases, 2009-06, Vol.48 (12), p.1775-1783</ispartof><rights>2009 Infectious Diseases Society of America 2009</rights><rights>2009 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Jun 15, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-9100bdaebc6dcda7356863dd3a385fa47515c2325f7d9f21fde75c9ba2a245cd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21551212$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19441980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pappas, Peter G.</creatorcontrib><creatorcontrib>Chetchotisakd, Ploenchan</creatorcontrib><creatorcontrib>Larsen, Robert A.</creatorcontrib><creatorcontrib>Manosuthi, Weerawat</creatorcontrib><creatorcontrib>Morris, Michele I.</creatorcontrib><creatorcontrib>Anekthananon, Thomansak</creatorcontrib><creatorcontrib>Sungkanuparph, Somnuek</creatorcontrib><creatorcontrib>Supparatpinyo, Khauncahi</creatorcontrib><creatorcontrib>Nolen, Tracy L.</creatorcontrib><creatorcontrib>Zimmer, Louise O.</creatorcontrib><creatorcontrib>Kendrick, Amy S.</creatorcontrib><creatorcontrib>Johnson, Phillip</creatorcontrib><creatorcontrib>Sobel, Jack D.</creatorcontrib><creatorcontrib>Filler, Scott G.</creatorcontrib><title>A Phase II Randomized Trial of Amphotericin B Alone or Combined with Fluconazole in the Treatment of HIV-Associated Cryptococcal Meningitis</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><addtitle>Clinical Infectious Diseases</addtitle><description>Background. Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-label, phase II trial in Thailand and the United States that compared the safety and efficacy of intravenous amphotericin B deoxycholate (AmB) 0.7 mg/kg (the standard therapy) with that of AmB 0.7 mg/kg plus fluconazole 400 mg (the low-dosage combination) or AmB 0.7 mg/kg plus fluconazole 800 mg (the high-dosage combination) administered daily for 14 days, followed by fluconazole alone at the randomized dosage (400 or 800 mg per day) for 56 days. The primary safety end point was the number of severe or life-threatening treatment-related toxicities; the primary efficacy end point was a composite of survival, neurologic stability, and negative cerebrospinal fluid culture results after 14 days of therapy. Results. A total of 143 patients were enrolled. There were no differences in treatment-related toxicities among the 3 arms. Toxicity was predictable and was most often related to AmB, and it included electrolyte abnormalities, anemia, nephrotoxicity, and infusion-related events. At day 14, 41%, 27%, and 54% of patients in the standard therapy, low-dosage combination, and high-dosage combination therapy arms, respectively, demonstrated successful outcomes. A trend towards better outcomes in the combination therapy arms was seen at days 42 and 70. Conclusions. AmB plus fluconazole administered at a dosage of 800 mg for 14 days, followed by fluconazole administered at a dosage of 800 mg daily for 56 days, is well-tolerated and efficacious among HIV-positive patients with central nervous system cryptococcosis. These results have significant treatment implications and should be validated in a randomized phase III trial. Clinical trials registration. This clinical trial is registered in the National Library of Medicine's registry (http://www.clinicaltrials.gov) under the registration number NCT00145249.</description><subject>Adult</subject><subject>Amphotericin B - administration & dosage</subject><subject>Amphotericin B - adverse effects</subject><subject>Amphotericin B - therapeutic use</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - administration & dosage</subject><subject>Antifungal Agents - adverse effects</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Antiretroviral drugs</subject><subject>Biological and medical sciences</subject><subject>Cerebrospinal Fluid - microbiology</subject><subject>Clinical trials</subject><subject>Comparative analysis</subject><subject>Female</subject><subject>Fluconazole - administration & dosage</subject><subject>Fluconazole - adverse effects</subject><subject>Fluconazole - therapeutic use</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>Human immunodeficiency virus</subject><subject>Human mycoses</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Meningitis</subject><subject>Meningitis, Cryptococcal - drug therapy</subject><subject>Middle Aged</subject><subject>Miscellaneous mycoses</subject><subject>Mycoses</subject><subject>Nervous system</subject><subject>Pharmacology. Drug treatments</subject><subject>Survival Analysis</subject><subject>Thailand</subject><subject>Treatment Outcome</subject><subject>United States</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10F1v1SAABuDGaNyH-hMMmri7Tj5KC5fd0XlOskWzzMV4QyhQD7OFCjRz-wv70zJ7Mq-8gouH9w1vUbxC8BhBVr-nnCOEnxT7iJKmrClHT_MdUlZWjLC94iDGawgRYpA-L_YQryrEGdwv7lvwZSujAZsNuJBO-9HeGQ0ug5UD8D1ox2nrkwlWWQdOQDt4Z4APYOXHzrosb2zagtNhVt7JOz8YkF3ampxgZBqNSw8p681V2cbolZUpv1mF2yl55ZXKJefGWffDJhtfFM96OUTzcnceFl9PP16u1uXZ50-bVXtWKsJZKjmCsNPSdKrWSsuG0JrVRGsiCaO9rBqKqMIE077RvMeo16ahincSS1xRpclh8XbJnYL_NZuYxLWfg8uVAiPOG8RondHRglTwMQbTiynYUYZbgaB4mFwsk2f4epc2d6PR_9hu4wze7YCM-cN9kE7Z-OgwohThv0FvFufn6f9l5WJsTOb3o5Lhp6gb0lCx_vZdfLigFVvjK4HIH5ddoYM</recordid><startdate>20090615</startdate><enddate>20090615</enddate><creator>Pappas, Peter G.</creator><creator>Chetchotisakd, Ploenchan</creator><creator>Larsen, Robert A.</creator><creator>Manosuthi, Weerawat</creator><creator>Morris, Michele I.</creator><creator>Anekthananon, Thomansak</creator><creator>Sungkanuparph, Somnuek</creator><creator>Supparatpinyo, Khauncahi</creator><creator>Nolen, Tracy L.</creator><creator>Zimmer, Louise O.</creator><creator>Kendrick, Amy S.</creator><creator>Johnson, Phillip</creator><creator>Sobel, Jack D.</creator><creator>Filler, Scott G.</creator><general>The 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></search><sort><creationdate>20090615</creationdate><title>A Phase II Randomized Trial of Amphotericin B Alone or Combined with Fluconazole in the Treatment of HIV-Associated Cryptococcal Meningitis</title><author>Pappas, Peter G. ; Chetchotisakd, Ploenchan ; Larsen, Robert A. ; Manosuthi, Weerawat ; Morris, Michele I. ; Anekthananon, Thomansak ; Sungkanuparph, Somnuek ; Supparatpinyo, Khauncahi ; Nolen, Tracy L. ; Zimmer, Louise O. ; Kendrick, Amy S. ; Johnson, Phillip ; Sobel, Jack D. ; Filler, Scott G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-9100bdaebc6dcda7356863dd3a385fa47515c2325f7d9f21fde75c9ba2a245cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Amphotericin B - administration & dosage</topic><topic>Amphotericin B - adverse effects</topic><topic>Amphotericin B - therapeutic use</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - administration & dosage</topic><topic>Antifungal Agents - adverse effects</topic><topic>Antifungal Agents - therapeutic use</topic><topic>Antiretroviral drugs</topic><topic>Biological and medical sciences</topic><topic>Cerebrospinal Fluid - microbiology</topic><topic>Clinical trials</topic><topic>Comparative analysis</topic><topic>Female</topic><topic>Fluconazole - administration & dosage</topic><topic>Fluconazole - adverse effects</topic><topic>Fluconazole - therapeutic use</topic><topic>HIV</topic><topic>HIV Infections - complications</topic><topic>Human immunodeficiency virus</topic><topic>Human mycoses</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Meningitis</topic><topic>Meningitis, Cryptococcal - drug therapy</topic><topic>Middle Aged</topic><topic>Miscellaneous mycoses</topic><topic>Mycoses</topic><topic>Nervous system</topic><topic>Pharmacology. Drug treatments</topic><topic>Survival Analysis</topic><topic>Thailand</topic><topic>Treatment Outcome</topic><topic>United States</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pappas, Peter G.</creatorcontrib><creatorcontrib>Chetchotisakd, Ploenchan</creatorcontrib><creatorcontrib>Larsen, Robert A.</creatorcontrib><creatorcontrib>Manosuthi, Weerawat</creatorcontrib><creatorcontrib>Morris, Michele I.</creatorcontrib><creatorcontrib>Anekthananon, Thomansak</creatorcontrib><creatorcontrib>Sungkanuparph, Somnuek</creatorcontrib><creatorcontrib>Supparatpinyo, Khauncahi</creatorcontrib><creatorcontrib>Nolen, Tracy L.</creatorcontrib><creatorcontrib>Zimmer, Louise O.</creatorcontrib><creatorcontrib>Kendrick, Amy S.</creatorcontrib><creatorcontrib>Johnson, Phillip</creatorcontrib><creatorcontrib>Sobel, Jack D.</creatorcontrib><creatorcontrib>Filler, Scott G.</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><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pappas, Peter G.</au><au>Chetchotisakd, Ploenchan</au><au>Larsen, Robert A.</au><au>Manosuthi, Weerawat</au><au>Morris, Michele I.</au><au>Anekthananon, Thomansak</au><au>Sungkanuparph, Somnuek</au><au>Supparatpinyo, Khauncahi</au><au>Nolen, Tracy L.</au><au>Zimmer, Louise O.</au><au>Kendrick, Amy S.</au><au>Johnson, Phillip</au><au>Sobel, Jack D.</au><au>Filler, Scott G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Phase II Randomized Trial of Amphotericin B Alone or Combined with Fluconazole in the Treatment of HIV-Associated Cryptococcal Meningitis</atitle><jtitle>Clinical infectious diseases</jtitle><stitle>Clinical Infectious Diseases</stitle><addtitle>Clinical Infectious Diseases</addtitle><date>2009-06-15</date><risdate>2009</risdate><volume>48</volume><issue>12</issue><spage>1775</spage><epage>1783</epage><pages>1775-1783</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. Cryptococcosis is a life-threatening infection among patients with human immunodeficientcy virus (HIV) infection. Therapeutic options for the treatment of central nervous system cryptococcosis are limited, especially in resource-limited settings. Methods. We conducted a randomized, open-label, phase II trial in Thailand and the United States that compared the safety and efficacy of intravenous amphotericin B deoxycholate (AmB) 0.7 mg/kg (the standard therapy) with that of AmB 0.7 mg/kg plus fluconazole 400 mg (the low-dosage combination) or AmB 0.7 mg/kg plus fluconazole 800 mg (the high-dosage combination) administered daily for 14 days, followed by fluconazole alone at the randomized dosage (400 or 800 mg per day) for 56 days. The primary safety end point was the number of severe or life-threatening treatment-related toxicities; the primary efficacy end point was a composite of survival, neurologic stability, and negative cerebrospinal fluid culture results after 14 days of therapy. Results. A total of 143 patients were enrolled. There were no differences in treatment-related toxicities among the 3 arms. Toxicity was predictable and was most often related to AmB, and it included electrolyte abnormalities, anemia, nephrotoxicity, and infusion-related events. At day 14, 41%, 27%, and 54% of patients in the standard therapy, low-dosage combination, and high-dosage combination therapy arms, respectively, demonstrated successful outcomes. A trend towards better outcomes in the combination therapy arms was seen at days 42 and 70. Conclusions. AmB plus fluconazole administered at a dosage of 800 mg for 14 days, followed by fluconazole administered at a dosage of 800 mg daily for 56 days, is well-tolerated and efficacious among HIV-positive patients with central nervous system cryptococcosis. These results have significant treatment implications and should be validated in a randomized phase III trial. Clinical trials registration. This clinical trial is registered in the National Library of Medicine's registry (http://www.clinicaltrials.gov) under the registration number NCT00145249.</abstract><cop>Oxford</cop><pub>The University of Chicago Press</pub><pmid>19441980</pmid><doi>10.1086/599112</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Amphotericin B - administration & dosage Amphotericin B - adverse effects Amphotericin B - therapeutic use Antibiotics. Antiinfectious agents. Antiparasitic agents Antifungal agents Antifungal Agents - administration & dosage Antifungal Agents - adverse effects Antifungal Agents - therapeutic use Antiretroviral drugs Biological and medical sciences Cerebrospinal Fluid - microbiology Clinical trials Comparative analysis Female Fluconazole - administration & dosage Fluconazole - adverse effects Fluconazole - therapeutic use HIV HIV Infections - complications Human immunodeficiency virus Human mycoses Human viral diseases Humans Infectious diseases Male Medical sciences Medical treatment Meningitis Meningitis, Cryptococcal - drug therapy Middle Aged Miscellaneous mycoses Mycoses Nervous system Pharmacology. Drug treatments Survival Analysis Thailand Treatment Outcome United States Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | A Phase II Randomized Trial of Amphotericin B Alone or Combined with Fluconazole in the Treatment of HIV-Associated Cryptococcal Meningitis |
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