V
Vincenzo Liso
Researcher at University of Bari
Publications - 206
Citations - 8516
Vincenzo Liso is an academic researcher from University of Bari. The author has contributed to research in topics: Myeloid leukemia & Leukemia. The author has an hindex of 46, co-authored 206 publications receiving 8008 citations. Previous affiliations of Vincenzo Liso include University of Foggia & Sapienza University of Rome.
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Journal ArticleDOI
Definition of relapse risk and role of nonanthracycline drugs for consolidation in patients with acute promyelocytic leukemia: a joint study of the PETHEMA and GIMEMA cooperative groups.
Miguel A. Sanz,Francesco Lo Coco,Guillermo Martin,Giuseppe Avvisati,Consuelo Rayon,Tiziano Barbui,Joaquín Díaz-Mediavilla,Giuseppe Fioritoni,José D. González,Vincenzo Liso,Jordi Esteve,Felicetto Ferrara,Pascual Bolufer,Carlo Bernasconi,Marcos González,Francesco Rodeghiero,Dolors Colomer,Maria Concetta Petti,José M. Ribera,Franco Mandelli +19 more
TL;DR: The conclusions are that omission of nonanthracycline drugs from the AIDA regimen is not associated with reduced antileukemic efficacy and a simple predictive model may be used for risk-adapted therapy in this disease.
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Molecular Remission in PML/RARα-Positive Acute Promyelocytic Leukemia by Combined All-trans Retinoic Acid and Idarubicin (AIDA) Therapy
Franco Mandelli,Daniela Diverio,Giuseppe Avvisati,Anna Luciano,Tiziano Barbui,Carlo Bernasconi,Giorgio Broccia,Cerri R,Michele Falda,Giuseppe Fioritoni,Franco Leoni,Vincenzo Liso,Maria Concetta Petti,Francesco Rodeghiero,Giuseppe Saglio,M. L. Vegna,Giuseppe Visani,Ulrich Jehn,Roel Willemze,Petra Muus,Pier Giuseppe Pelicci,Andrea Biondi,Francesco Lo Coco +22 more
TL;DR: This study indicates that the AIDA protocol is a well-tolerated regimen that induces molecular remission in almost all patients with PML/RARα-positive APL and suggests that a remarkable cure rate can be obtained with this treatment.
Journal ArticleDOI
Clinical profile of homozygous JAK2 617V>F mutation in patients with polycythemia vera or essential thrombocythemia.
Alessandro M. Vannucchi,Elisabetta Antonioli,Paola Guglielmelli,Alessandro Rambaldi,Giovanni Barosi,Roberto Marchioli,Rosa Maria Marfisi,Guido Finazzi,Vittoria Guerini,Fabrizio Fabris,Maria Luigia Randi,Valerio De Stefano,Sabrina Caberlon,Agostino Tafuri,Marco Ruggeri,Giorgina Specchia,Vincenzo Liso,Edoardo Rossi,Enrico Pogliani,Luigi Gugliotta,Alberto Bosi,Tiziano Barbui +21 more
TL;DR: It is concluded that JAK2 617V>F homozygosity identifies PV or ET patients with a more symptomatic myeloproliferative disorder and is associated with a higher risk of major cardiovascular events in patients with ET.
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Allogeneic compared with autologous stem cell transplantation in the treatment of patients younger than 46 years with acute myeloid leukemia (AML) in first complete remission (CR1): an intention-to-treat analysis of the EORTC/GIMEMAAML-10 trial
Stefan Suciu,Franco Mandelli,Theo de Witte,Robert Zittoun,Eugenio Gallo,Boris Labar,Gennaro De Rosa,A Belhabri,Rosario Giustolisi,Richard Delarue,Vincenzo Liso,Salvatore Mirto,Giuseppe Leone,Jean-Henri Bourhis,Giuseppe Fioritoni,Ulrich Jehn,Sergio Amadori,Paola Fazi,Anne Hagemeijer,Roel Willemze +19 more
TL;DR: Intention-to-treat analysis revealed that the 4-year disease-free survival (DFS) rate of patients with a donor versus those without a donor was 52.2% versus 42.2%, and the strategy to perform early allo-SCT led to better overall results than auto-S CT, especially for younger patients or those with bad/very bad risk cytogenetics.
Journal ArticleDOI
Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party
David Grimwade,Andrea Biondi,M J Mozziconacci,Anne Hagemeijer,Roland Berger,M. Neat,Kathy Howe,Nicole Dastugue,Joop H. Jansen,Isabelle Radford-Weiss,F. Lo Coco,Michel Lessard,Jesús M. Hernández,Eric Delabesse,David R. Head,Vincenzo Liso,Danielle Sainty,G. Flandrin,Ellen Solomon,Françoise Birg,Marina Lafage-Pochitaloff +20 more
TL;DR: In this paper, the authors used morphologic, cytogenetic, and molecular analyses for optimal management of acute promyelocytic leukemia (APL) patients and better understanding of the pathogenesis of the disease.