G. Butera
University of Palermo
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Publication
Featured researches published by G. Butera.
Alimentary Pharmacology & Therapeutics | 2011
Salvatore Petta; V. Di Marco; Calogero Cammà; G. Butera; Daniela Cabibi; A. Craxì
Background Liver stiffness measurement (LSM) using transient elastography (TE) is used to stage fibrosis in patients with liver disease, diagnostic reliability and the factors affecting its performance in patients with non‐alcoholic fatty liver disease (NAFLD) are incompletely understood.
Expert Review of Anticancer Therapy | 2013
Chiara Genco; Giuseppe Cabibbo; Marcello Maida; Giuseppe Brancatelli; Massimo Galia; Nicola Alessi; G. Butera; Claudio Genova; Romano P; Maurizio Raineri; Antonello Giarratano; Massimo Midiri; Calogero Cammà
Hepatocellular carcinoma is a major health problem. It is the sixth most common cancer worldwide and the third most common cause of cancer-related death. Despite the availability of several treatment opportunities, diagnosis is still made in an advanced phase, limiting application of most therapeutic choices that currently are based on the Barcelona Clinic Cancer Liver Classification and include surgical resection, orthotopic liver transplantation and ablative methods for very early and early disease, arterial chemoembolization for intermediate stages and systemic therapy with sorafenib for advanced hepatocellular carcinoma. Thanks to novel advancements in knowledge of molecular pathogenesis of this tumor, many new systemic agents and locoregional treatments are in different stages of clinical development and they represent an important promise of further improvements in patients’ survival.
Alimentary Pharmacology & Therapeutics | 2009
Salvatore Petta; Calogero Cammà; V. Di Marco; V. Calvaruso; Marco Enea; F. Bronte; G. Butera; Daniela Cabibi; A. Craxì
Background In patients with chronic hepatitis C (CHC), liver stiffness measurement (LSM) by transient elastography (TE), is closely related to the stage of fibrosis, but may be affected by necroinflammation. Other factors, such as insulin resistance (IR), might influence the performance of LSM.
PLOS ONE | 2013
Giuseppe Cabibbo; Marcello Maida; Chiara Genco; Nicola Alessi; Marco Peralta; G. Butera; Massimo Galia; Giuseppe Brancatelli; Claudio Genova; Maurizio Raineri; Emanuele Orlando; Simona Attardo; Antonino Giarratano; Massimo Midiri; Vito Di Marco; A. Craxì; Calogero Cammà
Background Radio-frequency ablation (RFA) has been employed in the treatment of Barcelona Clinic Liver Cancer (BCLC) early stage hepatocellular carcinoma (HCC) as curative treatments. Aim To assess the effectiveness and the safety of RFA in patients with early HCC and compensated cirrhosis. Methods A cohort of 151 consecutive patients with early stage HCC (122 Child-Pugh class A and 29 class B patients) treated with RFA were enrolled. Clinical, laboratory and radiological follow-up data were collected from the time of first RFA. A single lesion was observed in 113/151 (74.8%), two lesions in 32/151 (21.2%), and three lesions in 6/151 (4%) of patients. Results The overall survival rates were 94%, 80%, 64%, 49%, and 41% at 12, 24, 36, 48 and 60 months, respectively. Complete response (CR) at 1 month (p<0.0001) and serum albumin levels (p = 0.0004) were the only variables indipendently linked to survival by multivariate Cox model. By multivariate analysis, tumor size (p = 0.01) is the only variable associated with an increased likehood of CR. The proportion of major complications after treatment was 4%. Conclusions RFA is safe and effective for managing HCC with cirrhosis, especially for patients with HCC ≤3 cm and higher baseline albumin levels. Complete response after RFA significantly increases survival.
Journal of Clinical Gastroenterology | 2012
Anna Licata; Claudia Randazzo; M. Cappello; V. Calvaruso; G. Butera; Ada Maria Florena; Sergio Peralta; Calogero Cammà; A. Craxì
Background: Surrogate markers of colorectal inflammation are increasingly being recognized as important in differentiating organic from functional intestinal disorders. Fecal calprotectin (FC) can be easily measured in the stool, being released by leukocytes in inflammatory conditions. Aim: We evaluated FC as an index of inflammation in consecutive outpatients referred for colonoscopy for chronic, nonbloody diarrhea. Methods: Stool specimens of 346 outpatients with chronic, nonbloody diarrhea, referred for colonoscopy, were measured for FC levels. The proportion of patients correctly diagnosed with the test and the relationship with endoscopic and histologic findings were measured. Results: Abnormal endoscopic findings were detected in 104 patients (30.1%). Histologic findings included 142 patients (41.0%) with inflammation and 204 (59.0%) without inflammation. Fecal excretion of calprotectin significantly correlated with the finding of inflammation at endoscopy and histology (P<0.0001). When 150 mcg/g of stool was used as the upper reference limit, FC showed 75.4% sensitivity and 88.3% specificity, with 81.7% positive and 83.7% negative predictive values for histologic inflammation. Conclusions: In outpatients referred for colonoscopy a measurement of FC is accurate to identify those with histologic inflammation. Assay of FC may be a reliable and noninvasive screening tool to identify inflammatory causes of chronic, nonbloody diarrhea.
Digestive and Liver Disease | 2014
Anna Licata; Marcello Maida; Daniela Cabibi; G. Butera; Fabio Salvatore Macaluso; Nicola Alessi; Calogero Caruso; A. Craxì; Piero Luigi Almasio
BACKGROUND Drugs and herbal products can induce autoimmune hepatitis. We assessed frequency and clinical outcomes of patients suffering from drug-induced autoimmune hepatitis. METHODS All patients with drug-induced liver injury admitted between 2000 and 2011 were retrospectively studied. Diagnoses of drug-induced autoimmune hepatitis and idiopathic autoimmune hepatitis were made according to simplified criteria. After discharge, all patients had regular follow-up and were contacted to update outcomes. RESULTS Among 10,270 in-hospital patients, 136 (1.3%) were diagnosed with drug-induced liver injury. Among them, 12 (8.8%) were diagnosed as drug-induced autoimmune hepatitis (41.7% males, age range 17-73); 8 (66.7%) were with jaundice at admission. Liver biopsies showed a pattern compatible with drug-induced autoimmune hepatitis, featured by severe portal inflammation and lymphoplasmacytic infiltrate. Drug-induced autoimmune hepatitis group had a shorter duration of drug intake, and higher values of transaminases and gamma globulins. All patients received immunosuppressive therapy with subsequent clinical remission, and five achieved a steroid-free long-term remission. CONCLUSIONS A diagnosis of drug-induced autoimmune hepatitis was quite rare in our cohort, and clinical pattern was similar to idiopathic autoimmune hepatitis. Severe portal inflammation, prominent portal-plasma cells, rosette formation and severe focal necrosis were significantly more frequent in drug-induced autoimmune hepatitis as compared to drug-induced liver injury.
Internal and Emergency Medicine | 2012
Anna Licata; M. Cappello; Andrea Arini; Ada Maria Florena; Claudia Randazzo; G. Butera; Piero Luigi Almasio; A. Craxì
European Journal of Clinical Pharmacology | 2012
Anna Licata; Claudia Randazzo; Ilaria Morreale; G. Butera; Natale D’Alessandro; A. Craxì
Journal of Hepatology | 2010
V. Calvaruso; V. Di Marco; F. Bronte; Giuseppe Licata; F. Simone; G. Butera; G. Pecoraro; D. Cabibbi; Nicola Alessi; C. Cammà; A. Craxì
Digestive and Liver Disease | 2015
Mauro Bernardi; Oliviero Riggio; Paolo Angeli; Carlo Alessandria; Sergio Neri; F.G. Foschi; F. Levantesi; S. Boccia; A. Airoldi; S. Fagiuoli; G. Svegliati-Baroni; Giacomo Laffi; R. Cozzolongo; G. Butera; V. Sangiovanni; Pierluigi Toniutto; M.A. Zocco; R. De Marco; F. Morisco; F. De Leonardis; Irene Cacciola; G. Elia; A. Federico; Sara Massironi; R. Guarisco; A. Marin; Salvatore Piano; C. Elia; Silvia Nardelli; D. Maiorca