<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(2)</volume><submitter>Aghemo A</submitter><funding>AbbVie</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Glecaprevir/pibrentasvir (G/P) has demonstrated high rates (>95%) of sustained virologic response at posttreatment Week 12 (SVR12) in treatment-naïve (TN) patients with hepatitis C virus (HCV) infection and compensated cirrhosis (CC). Here, in a key real-world subset of TN Italian patients with CC, we evaluated the effectiveness and safety of 8-week G/P treatment, including subgroups of interest such as those with genotype 3 (GT3) infection, elderly patients, and those with more advanced liver disease.&lt;h4>Methods&lt;/h4>Subanalysis of Italian patients enrolled in the CREST study. The full analysis set (FAS) included all patients enrolled in the study; the modified analysis set (MAS) excluded patients who discontinued G/P for nonvirologic failure or who had missing SVR12 r</pubmed_abstract><journal>PloS one</journal><pagination>e0280165</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9894491</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety and effectiveness of 8 weeks of Glecaprevir/Pibrentasvir in challenging HCV patients: Italian data from the CREST study.</pubmed_title><pmcid>PMC9894491</pmcid><pubmed_authors>D'Ambrosio R</pubmed_authors><pubmed_authors>Bhagat A</pubmed_authors><pubmed_authors>Gasbarrini A</pubmed_authors><pubmed_authors>Gualberti G</pubmed_authors><pubmed_authors>Villa E</pubmed_authors><pubmed_authors>Gallinaro V</pubmed_authors><pubmed_authors>Merolla RCD</pubmed_authors><pubmed_authors>Aghemo A</pubmed_authors><pubmed_authors>Persico M</pubmed_authors><pubmed_authors>Andreoni M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and effectiveness of 8 weeks of Glecaprevir/Pibrentasvir in challenging HCV patients: Italian data from the CREST study.</name><description>&lt;h4>Introduction&lt;/h4>Glecaprevir/pibrentasvir (G/P) has demonstrated high rates (>95%) of sustained virologic response at posttreatment Week 12 (SVR12) in treatment-naïve (TN) patients with hepatitis C virus (HCV) infection and compensated cirrhosis (CC). Here, in a key real-world subset of TN Italian patients with CC, we evaluated the effectiveness and safety of 8-week G/P treatment, including subgroups of interest such as those with genotype 3 (GT3) infection, elderly patients, and those with more advanced liver disease.&lt;h4>Methods&lt;/h4>Subanalysis of Italian patients enrolled in the CREST study. The full analysis set (FAS) included all patients enrolled in the study; the modified analysis set (MAS) excluded patients who discontinued G/P for nonvirologic failure or who had missing SVR12 r</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-03-31T10:39:57.067Z</modification><creation>2025-04-06T14:06:10.708Z</creation></dates><accession>S-EPMC9894491</accession><cross_references><pubmed>36730135</pubmed><doi>10.1371/journal.pone.0280165</doi></cross_references></HashMap>