<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Heo ST</submitter><funding>National Institutes of Health and Astellas Pharma</funding><funding>Pfizer, Inc</funding><funding>John S. Dunn Foundation</funding><funding>Institutional Core</funding><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>MD Anderson Cancer Center</funding><pagination>216-225</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5850538</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>65(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Azole-resistant aspergillosis in high-risk patients with hematological malignancy or hematopoietic stem cell transplantation (HSCT) is a cause of concern.&lt;h4>Methods&lt;/h4>We examined changes over time in triazole minimum inhibitory concentrations (MICs) of 290 sequential Aspergillus isolates recovered from respiratory sources during 1999-2002 (before introduction of the Aspergillus-potent triazoles voriconazole and posaconazole) and 2003-2015 at MD Anderson Cancer Center. We also tested for polymorphisms in ergosterol biosynthetic genes (cyp51A, erg3C, erg1) in the 37 Aspergillus fumigatus isolates isolated from both periods that had non-wild-type (WT) MICs. For the 107 patients with hematologic cancer and/or HSCT with invasive pulmonary aspergillosis, we correlated in vi</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pubmed_title>Changes in In Vitro Susceptibility Patterns of Aspergillus to Triazoles and Correlation With Aspergillosis Outcome in a Tertiary Care Cancer Center, 1999-2015.</pubmed_title><pmcid>PMC5850538</pmcid><funding_grant_id>CA16672</funding_grant_id><funding_grant_id>R01 CA180279</funding_grant_id><funding_grant_id>R01 AI109025</funding_grant_id><funding_grant_id>AI109025</funding_grant_id><pubmed_authors>Mikos AG</pubmed_authors><pubmed_authors>Verweij PE</pubmed_authors><pubmed_authors>Tarrand J</pubmed_authors><pubmed_authors>Tverdek F</pubmed_authors><pubmed_authors>Meis JF</pubmed_authors><pubmed_authors>Heo ST</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Lewis RE</pubmed_authors><pubmed_authors>Albert ND</pubmed_authors><pubmed_authors>Tatara AM</pubmed_authors><pubmed_authors>Kontoyiannis DP</pubmed_authors><pubmed_authors>Perlin DS</pubmed_authors><pubmed_authors>Jimenez-Ortigosa C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Changes in In Vitro Susceptibility Patterns of Aspergillus to Triazoles and Correlation With Aspergillosis Outcome in a Tertiary Care Cancer Center, 1999-2015.</name><description>&lt;h4>Background&lt;/h4>Azole-resistant aspergillosis in high-risk patients with hematological malignancy or hematopoietic stem cell transplantation (HSCT) is a cause of concern.&lt;h4>Methods&lt;/h4>We examined changes over time in triazole minimum inhibitory concentrations (MICs) of 290 sequential Aspergillus isolates recovered from respiratory sources during 1999-2002 (before introduction of the Aspergillus-potent triazoles voriconazole and posaconazole) and 2003-2015 at MD Anderson Cancer Center. We also tested for polymorphisms in ergosterol biosynthetic genes (cyp51A, erg3C, erg1) in the 37 Aspergillus fumigatus isolates isolated from both periods that had non-wild-type (WT) MICs. For the 107 patients with hematologic cancer and/or HSCT with invasive pulmonary aspergillosis, we correlated in vi</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2026-05-02T06:58:24.575Z</modification><creation>2019-03-26T23:46:21Z</creation></dates><accession>S-EPMC5850538</accession><cross_references><pubmed>28379304</pubmed><doi>10.1093/cid/cix297</doi></cross_references></HashMap>