Publication: A randomized, blinded, multicenter trial of lipid-associated amphotericin B alone versus in combination with an antibody-based inhibitor of heat shock protein 90 in patients with invasive candidiasis
| cris.virtualsource.author-orcid | 1faeeeef-6791-474f-9394-bedce1157a32 | |
| datacite.rights | open.access | |
| dc.contributor.author | Pachl, J | |
| dc.contributor.author | Svoboda, P | |
| dc.contributor.author | Jacobs, F | |
| dc.contributor.author | Vandewoude, K | |
| dc.contributor.author | van der Hoven, B | |
| dc.contributor.author | Spronk, P | |
| dc.contributor.author | Masterson, G | |
| dc.contributor.author | Malbrain, M | |
| dc.contributor.author | Aoun, M | |
| dc.contributor.author | Garbino, J | |
| dc.contributor.author | Takala, Jukka | |
| dc.contributor.author | Drgona, L | |
| dc.contributor.author | Burnie, J | |
| dc.contributor.author | Matthews, R | |
| dc.contributor.author | Mycograb, Invasive Candidiasis Study Group | |
| dc.date.accessioned | 2024-10-13T16:59:39Z | |
| dc.date.available | 2024-10-13T16:59:39Z | |
| dc.date.issued | 2006 | |
| dc.description.abstract | BACKGROUND: Mycograb (NeuTec Pharma) is a human recombinant monoclonal antibody against heat shock protein 90 that, in laboratory studies, was revealed to have synergy with amphotericin B against a broad spectrum of Candida species. METHODS: A double-blind, randomized study was conducted to determine whether lipid-associated amphotericin B plus Mycograb was superior to amphotericin B plus placebo in patients with culture-confirmed invasive candidiasis. Patients received a lipid-associated formulation of amphotericin B plus a 5-day course of Mycograb or placebo, having been stratified on the basis of Candida species (Candida albicans vs. non-albicans species of Candida). Inclusion criteria included clinical evidence of active infection at trial entry plus growth of Candida species on culture of a specimen from a clinically significant site within 3 days after initiation of study treatment. The primary efficacy variable was overall response to treatment (clinical and mycological resolution) by day 10. RESULTS: Of the 139 patients enrolled from Europe and the United States, 117 were included in the modified intention-to-treat population. A complete overall response by day 10 was obtained for 29 (48%) of 61 patients in the amphotericin B group, compared with 47 (84%) of 56 patients in the Mycograb combination therapy group (odds ratio [OR], 5.8; 95% confidence interval [CI], 2.41-13.79; P<.001). The following efficacy criteria were also met: clinical response (52% vs. 86%; OR, 5.4; 95% CI, 2.21-13.39; P<.001), mycological response (54% vs. 89%; OR, 7.1; 95% CI, 2.64-18.94; P<.001), Candida-attributable mortality (18% vs. 4%; OR, 0.2; 95% CI, 0.04-0.80; P = .025), and rate of culture-confirmed clearance of the infection (hazard ratio, 2.3; 95% CI, 1.4-3.8; P = .001). Mycograb was well tolerated. CONCLUSIONS: Mycograb plus lipid-associated amphotericin B produced significant clinical and culture-confirmed improvement in outcome for patients with invasive candidiasis. | |
| dc.description.numberOfPages | 10 | |
| dc.description.sponsorship | Universitätsklinik für Intensivmedizin | |
| dc.identifier.doi | 10.7892/boris.20406 | |
| dc.identifier.isi | 000237247400009 | |
| dc.identifier.pmid | 16619152 | |
| dc.identifier.publisherDOI | 10.1086/503428 | |
| dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/94136 | |
| dc.language.iso | en | |
| dc.publisher | The University of Chicago Press | |
| dc.publisher.place | Cary, N.C. | |
| dc.relation.isbn | 16619152 | |
| dc.relation.ispartof | Clinical infectious diseases | |
| dc.relation.issn | 1058-4838 | |
| dc.relation.organization | Clinic of Intensive Care Medicine | |
| dc.title | A randomized, blinded, multicenter trial of lipid-associated amphotericin B alone versus in combination with an antibody-based inhibitor of heat shock protein 90 in patients with invasive candidiasis | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| dspace.file.type | text | |
| oaire.citation.endPage | 13 | |
| oaire.citation.issue | 10 | |
| oaire.citation.startPage | 1404 | |
| oaire.citation.volume | 42 | |
| oairecerif.author.affiliation | Universitätsklinik für Intensivmedizin | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.contributor.role | creator | |
| unibe.date.licenseChanged | 2019-10-22 22:18:47 | |
| unibe.description.ispublished | pub | |
| unibe.eprints.legacyId | 20406 | |
| unibe.journal.abbrevTitle | CLIN INFECT DIS | |
| unibe.refereed | true | |
| unibe.subtype.article | journal |
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