Federica Latteri
University of Palermo
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Featured researches published by Federica Latteri.
Alimentary Pharmacology & Therapeutics | 2008
Calogero Cammà; V. Di Marco; Giuseppe Cabibbo; Federica Latteri; Luigi Sandonato; Pietro Parisi; Marco Enea; Massimo Attanasio; Massimo Galia; Nicola Alessi; Anna Licata; Latteri M; A. Craxì
Background A major problem in assessing the likelihood of survival of patients with hepatocellular carcinoma (HCC) arises from a lack of models capable of predicting outcome accurately.
Digestive and Liver Disease | 2008
Federica Latteri; Luigi Sandonato; V. Di Marco; Pietro Parisi; Giuseppe Cabibbo; G. Lombardo; Massimo Galia; Massimo Midiri; Latteri M; A. Craxì
BACKGROUND Neoplastic seeding of hepatocellular carcinoma may arise after radiofrequency ablation. AIMS In order to clarify the real risk of seeding, we observed a prospective cohort of patients undergoing radiofrequency ablation. METHODS Ninety-three (22.9%) out of 406 consecutive patients with hepatocellular carcinoma superimposed to cirrhosis diagnosed at our Liver Unit (2000-2005) were selected for radiofrequency ablation according to the Barcelona 2000 EASL guidelines. Seventy-one patients were treated by a percutaneous approach and 22 at laparotomy. After radiofrequency ablation ultrasound scan was repeated every 3 months and spiral-computed tomography every 6 months. RESULTS Overall 145 sessions were performed in 93 patients: 113 (77.9%) by a percutaneous approach and 32 (22.1%) at laparotomy. The median follow-up was 23 months (range 1-60). Only 1 of the 71 patients (1.4%; 95% C.I. 0.25-7.56) treated percutaneously and none of the 22 (0%; 95% C.I. 0-14.8) treated at laparotomy showed neoplastic seeding. CONCLUSION In our experience the risk of seeding of hepatocellular carcinoma after radiofrequency ablation was small (1.1% per patient, 95% C.I. 0.19-5.84; 0.7% per procedure, 95% C.I. 0.12-3.80). A stringent selection of patients for radiofrequency ablation and retraction of the needle with a hot tip may have been instrumental in obtaining this low frequency.
Expert Opinion on Pharmacotherapy | 2005
Calogero Cammà; Anna Licata; Giuseppe Cabibbo; Federica Latteri; A. Craxì
Chronic hepatitis C virus infection is currently the most common cause of end stage liver disease worldwide. Although the conclusions of the last National Institutes of Health Consensus Development Conferences on Hepatitis C have recently been published, several important issues remain unanswered. This paper reviews the available data using an evidence-based approach. Current evidence is sufficient to recommend IFN treatment for all patients with acute hepatitis. A later initiation of therapy yields the same likelihood of response as early treatment. A daily induction dose during month 1 is the best treatment option. The current gold standard of efficacy for treatment-naive patients with chronic hepatitis C is the combination of pegylated IFN and ribavirin. The overall sustained viral response rate to these regimens is 54 – 56% following a 48-week course of therapy. Patients with genotype 1 infection will have a 42 – 51% likelihood of response to 48weeks of therapy. Those with genotypes 2 or 3 infection will respond to 24weeks in 78 – 82% of cases. Debate continues regarding the optimal dose and duration of peginterferon (PEG-IFN), not only in patients infected with genotype 2 or 3 but also in those infected with genotype 1. The optimal dose of ribavirin has yet to be determined. Available data show the need to give the highest tolerable doses (1000–1200mg/day) to the difficult-to-treat patients (genotype 1, cirrhotics, obese), although there is a greater likelihood of intolerance. Genotypes 2 and 3 may receive 800mg/day, which is also the most appropriate lower dose for those patients who require dosage modification for anaemia or other side effects. Tolerability and compliance to therapy are still a problem, as ∼15– 20% of patients within trials and > 25% in clinical practice withdraw from therapy. New PEG-IFNs are more effective than conventional IFN in improving liver histology. Monotherapy with PEG-IFN induces a marked reduction in staging in virological sustained responders, and to a lesser degree in relapsers, but provides no benefit to nonresponders after 24–48weeks of treatment. The use of maintenance therapy in virological nonresponders aiming to improve histology should be considered experimental and of unproven benefit. Pooling data from the literature suggests a slight preventive effect of IFN on hepatocellular carcinoma development in patients with HCV-related cirrhosis. The magnitude of this effect is low and the observed benefit may be due to spurious associations. The preventive effect is more evident among sustained responders to IFN.
Cases Journal | 2009
Luigi Sandonato; Calogero Cipolla; Maurizio Soresi; Giuseppe Lo Re; Federica Latteri; Giuseppina Lombardo; Valentina Bova; Latteri M
IntroductionAt the present time, the best possible choice for the local management of a multifocal hepatocellular carcinoma (HCC) developing on liver cirrhosis is multimodal treatment of the disease. Combined approach based on simultaneous radiofrequency ablation (RFA) together with limited surgical resection represents a valid choice of treatment.Case presentationA 75-year-old white female patient affected of HCV-associated cirrhosis in Child-Pughs functional class A5, developed a bifocal HCC. The patient had undergone a limited surgical resection together with simultaneous RFA, without intraoperative and postoperative surgical complications. At 36 months after surgery, still shows no sign of disease relapse.ConclusionThis strategy directed at the management of multifocal HCC, may prove more useful for the reduction of surgical risk and post-operative progression of the liver cirrhosis than large-scale hepatectomy, since it presents no peri-operative mortality and a complication rate of less than 10%.
Journal of Hepatology | 2005
Calogero Cammà; Vito Di Marco; Ambrogio Orlando; Luigi Sandonato; Andrea Casaril; P. Parisi; Silvia Alizzi; Elio Sciarrino; Roberto Virdone; Salvatore Pardo; Danilo Di Bona; Anna Licata; Federica Latteri; Giuseppe Cabibbo; Giuseppe Montalto; Latteri M; Nicola Nicoli; A. Craxì
Nature Clinical Practice Gastroenterology & Hepatology | 2009
Giuseppe Cabibbo; Federica Latteri; Michela Antonucci; A. Craxì
Journal of Cancer Research and Clinical Oncology | 2002
Viviana Bazan; Manuela Migliavacca; Ines Zanna; Carla Tubiolo; Simona Corsale; Valentina Calò; Antonella Amato; Patrizia Cammareri; Federica Latteri; Nello Grassi; F. Fulfaro; Rossana Porcasi; Vincenza Morello; R. B. Nuara; Gabriella Dardanoni; S. Salerno; Maria Rosaria Valerio; Luisa Dusonchet; A. Gerbino; N. Gebbia; Rosa Maria Tomasino; A. Russo
Cancer | 2001
Antonio Russo; Viviana Bazan; Manuela Migliavacca; Carla Tubiolo; Marcella Macaluso; Ines Zanna; Simona Corsale; Federica Latteri; Maria Rosaria Valerio; Gianni Pantuso; Vincenza Morello; Gabriella Dardanoni; Latteri M; Giuseppe Colucci; Rosa Maria Tomasino; Nicola Gebbia
World Journal of Gastroenterology | 2008
Nello Grassi; Calogero Cipolla; Adriana Torcivia; Stefano Mandalà; Giuseppa Graceffa; Bottino A; Federica Latteri
American Surgeon | 2009
Luigi Sandonato; Cipolla C; Fulfaro F; Lo Re G; Federica Latteri; Terranova A; Mastrosimone A; Bova; Giuseppe Cabibbo; Latteri M