A. Porro
University of Bologna
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Featured researches published by A. Porro.
Journal of Viral Hepatitis | 2017
F. Conti; Stefano Brillanti; Federica Buonfiglioli; Ranka Vukotic; Maria Cristina Morelli; Claudine Lalanne; Marco Massari; Francesco Giuseppe Foschi; Veronica Bernabucci; Ilaria Serio; Gian Maria Prati; Elisa Negri; Lorenzo Badia; Paolo Caraceni; Paolo Muratori; Giovanni Vitale; A. Porro; Marta Morotti; G. Mazzella; Pietro Andreone
The availability of direct‐acting antiviral agents (DAA) regimens has expanded the pool of patients eligible for treatment. However, data on the virologic response and tolerability of DAAs in elderly patients are lacking. We evaluated the efficacy and safety of DAAs in patients with advanced fibrosis/cirrhosis in real‐life practice with the focus on those aged ≥65 years. Between January and December 2015, all consecutive patients with HCV‐related advanced fibrosis/cirrhosis treated with DAA at eleven tertiary referral centres in Emilia Romagna (Italy) were enrolled. Regimen choice was based on viral genotype and stage of disease, according to guidelines. The primary end point was sustained virologic response 12 weeks after the end of treatment (SVR12). Overall, 282 of 556 (50.7%) patients evaluated were elderly, most of them with cirrhosis. Antiviral therapy was stopped prematurely in four (1.4%) patients. Two patients, both with cirrhosis, died during treatment due to worsening of liver/renal function. SVR12 was achieved by 94.7% and was comparable to that obtained in patients aged <65 (P=.074). Similar data were also reported in subgroup of patients aged ≥75 years. All patients with advanced fibrosis achieved virologic response. SVR12 was 80.8% in Child‐Pugh‐Turcotte (CTP)‐B cirrhosis and 95.4% in CTP‐A (P=.013). According to genotype, the SVR12 was achieved in 172 of 181 (95%) with genotype 1b cirrhosis and in 44 of 48 (91.7%) with genotype 2 cirrhosis. In conclusions, in a real‐world setting, DAAs are safe and effective in elderly patients with HCV‐related advanced fibrosis/cirrhosis, but SVR12 is lower with worsening CTP class.
Journal of Gastroenterology | 2014
Andrea Lisotti; Francesco Azzaroli; Marco Montagnani; A. Porro; G. Mazzella
We recently read with great interest the manuscript entitled ‘‘Prophylactic impact of endoscopic treatment for esophageal varices in liver resection: a prospective study’’ [1] in which Dr. Yamazaki et al. demonstrated the usefulness of endoscopic prophylactic treatment of esophageal varices (EV) and evaluated different risk factors for post-operative progression and bleeding. The authors observed that in patients with hepatocellular carcinoma (HCC), various laboratory variables were significantly different according to the presence or absence of EV; for example, indocyanine green (ICG) retention rate at 15 min (ICG-r15) was 10.9 % (2.1–37.7) in patients without EV and 15.4 % (3.7–46.0) in patients with EV (P \ 0.001). Finally, they observed that ICG-r15 [ 30 % is independently correlated with the risk of worsening varices. We recently reported our experience [2] aimed to evaluate ICG 15-min retention test as a non-invasive marker of PH and EV in patients with compensated liver cirrhosis in which we demonstrated that among patients with well-preserved liver function, ICG retention tests indirectly correlate with the presence and degree of portal hypertension and its complications (EV). According to the observations of Dr. Yamazaki et al., ICG-r15 correlated with the presence of esophageal varices; we found two different ICG-r15 cut-off points able to accurately rule out and rule in the presence of EV (\10 % and C22.9 %, respectively). Liver-mediated uptake of organic anions (drugs or xenobiotics) is mainly mediated by organic anion transporting polypeptides (OATPs) and organic anion transporters (OATs); ICG presents a potent inhibitor effect on OATP isoforms and Na-taurocholate transporting polypeptide (NTCP). OATP1B3 and NTCP are the transporters involved in the hepatic uptake of ICG [3]. The organic anion transporter peptides (OATP) 1B1 and 1B3 are variably and progressively lost during liver carcinogenesis; a previous study performed on patients who underwent OLT because of HCC demonstrated a correlation between the loss of OATP 1B1/ 1B3 and tumor morphological features [4]. These molecular findings could, in our opinion, justify the higher ICG-r15 values observed by Dr. Yamazaki et al. in their population. Indeed, the ICG retention test, among patients with liver cirrhosis, represents both liver parenchymal reserve and hepatic blood flow; in patients with HCC, this interplay is altered by the introduction of a third variable (cancer biology) and could not be argued. This comment refers to the article available at doi:10.1007/s00535013-0841-y.
Journal of Hepatology | 2013
Andrea Lisotti; Federica Buonfiglioli; Paolo Cecinato; Marco Montagnani; R. Arena; C. Calvanese; Patrizia Simoni; S. Belvisi; A. Porro; Alessandro Cucchetti; Antonio Colecchia; Davide Festi; Rita Golfieri; G. Mazzella
211 INDOCYANINE GREEN CLEARANCE (ICG) AS A PREDICTOR OF 2-YEARS CLINICAL DECOMPENSATION AND MORTALITY IN PATIENTS WITH COMPENSATED LIVER CIRRHOSIS A. Lisotti, F. Azzaroli, F. Buonfiglioli, P. Cecinato, M. Montagnani, R. Arena, C. Calvanese, P. Simoni, S. Belvisi, A. Porro, A. Cucchetti, A. Colecchia, D. Festi, R. Golfieri, G. Mazzella. Hospital S. Orsola-Malpighi, Bologna, Italy E-mail: [email protected]
Digestive and Liver Disease | 2018
A. Simili; G. Mazzella; F. Ravaioli; F. Davide; Maria Letizia Bacchi-Reggiani; A. Porro; Franco Bazzoli
Digestive and Liver Disease | 2018
A. Simili; G. Mazzella; F. Ravaioli; Davide Festi; M. L. Bacchi Reggiani; A. Porro; Franco Bazzoli
Journal of Hepatology | 2017
Patrizia Simoni; R. Arena; R.M. Zagari; A. Porro; C. Camborata; A. Belardinelli; S. Spinozzi; Marco Montagnani; F. Bazzoli; Aldo Roda; G. Mazzella
Journal of Hepatology | 2017
F. Ravaioli; Giovanni Marasco; Maria Letizia Bacchi Reggiani; G. Mazzella; Federica Buonfiglioli; A. Porro; Stefano Brillanti; Antonio Colecchia; Davide Festi
Digestive and Liver Disease | 2017
F. Ravaioli; Giovanni Marasco; M. L. Bacchi Reggiani; G. Mazzella; Federica Buonfiglioli; A. Porro; Stefano Brillanti; Antonio Colecchia; Davide Festi
Digestive and Liver Disease | 2016
F. Conti; A. Scuteri; Giovanni Vitale; G. Lazzarini; A. Porro; Paolo Muratori; Ilaria Serio; Federica Buonfiglioli; Lorenzo Badia; A. Lanzi; Marianna Mastroroberto; L. Appolloni; M. Morotti; Maria Cristina Morelli; Francesco Giuseppe Foschi; Gabriella Verucchi; Stefano Brillanti; C. Crespi; Marco Lenzi; G. Mazzella; P. Andreone
Future Virology | 2014
Francesco Azzaroli; Marco Montagnani; A. Porro; Domenico Fiorillo; G. Mazzella