G
Giovanni Barosi
Researcher at University of Pavia
Publications - 352
Citations - 21433
Giovanni Barosi is an academic researcher from University of Pavia. The author has contributed to research in topics: Myelofibrosis & Essential thrombocythemia. The author has an hindex of 69, co-authored 334 publications receiving 19225 citations.
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Journal ArticleDOI
Extended anticoagulation for prevention of recurrent venous thromboembolism in carriers of factor V Leiden--cost-effectiveness analysis.
TL;DR: Screening was a cost-effective strategy, since it provided 2 additional quality-adjusted days of life per patient at the cost of $12,833 per quality- adjusted year of life saved, as compared to standard management, however, screening was not cost- effective in patients who were predicted to incur fatal bleeding at a rate higher than 0.34% per year.
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Next-generation sequencing for BCR-ABL1 kinase domain mutation testing in patients with chronic myeloid leukemia: a position paper.
Simona Soverini,Elisabetta Abruzzese,Monica Bocchia,Massimiliano Bonifacio,Sara Galimberti,Antonella Gozzini,Alessandra Iurlo,Luigiana Luciano,Patrizia Pregno,Gianantonio Rosti,Giuseppe Saglio,Fabio Stagno,Mario Tiribelli,Paolo Vigneri,Giovanni Barosi,Massimo Breccia +15 more
TL;DR: A group discussion among an ad hoc expert panel producing recommendations on the appropriateness of clinical decisions about the indication for NGS, the performance characteristics of NGS platforms, and the therapeutic changes that could be applied based on the use of N GS in CML are reported.
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JAK2V617F mutational status and allele burden have little influence on clinical phenotype and prognosis in patients with post-polycythemia vera and post-essential thrombocythemia myelofibrosis
Paola Guglielmelli,Giovanni Barosi,Lisa Pieri,Elisabetta Antonioli,Alberto Bosi,Alessandro M. Vannucchi +5 more
TL;DR: The JAK2V617F mutational status and mutated allele burden were evaluated in 65 patients with post-poly-cythemia vera or post-essential thrombocythemia myelofibrosis (PPV/PET-MF) and it is concluded that presence and burden of JAK1v617F mutation provide little clinically relevant information in patients with PPV/ PET-MF.
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Comparison of placebo and best available therapy for the treatment of myelofibrosis in the phase 3 COMFORT studies
Ruben A. Mesa,Jean-Jacques Kiladjian,Srdan Verstovsek,Haifa Kathrin Al-Ali,Jason Gotlib,Heinz Gisslinger,Richard S. Levy,Andres Siulnik,Vikas Gupta,Mahmudul Khan,John F. DiPersio,Mari McQuitty,John Catalano,Deborah S. Hunter,Laurent Knoops,Michael W. Deininger,Francisco Cervantes,Carole B. Miller,Alessandro M. Vannucchi,Richard T. Silver,Tiziano Barbui,Moshe Talpaz,Giovanni Barosi,Elliott F. Winton,Estella Mendeson,Jimmie H. Harvey,Murat O. Arcasoy,Elizabeth O. Hexner,Roger M. Lyons,Ronald Paquette,Azra Raza,William Sun,Victor Sandor,Hagop M. Kantarjian,Claire N. Harrison +34 more
TL;DR: Analysis of efficacy outcomes of patients with myelofibrosis in the control arms from the two phase 3 COntrolled MyeloFibrosis study with ORal JAK inhibitor Treatment (COMFORT) studies suggests that non–Janus kinase inhibitor therapies provide little improvement in splenomegaly, symptoms or quality of life as compared with placebo.
Journal ArticleDOI
Estimation of Ferrokinetic Parameters by a Mathematical Model in Patients with Primary Acquired Sideroblastic Anaemia
TL;DR: Close agreement between experimental and theoretical data proved that the model can describe iron kinetics in sideroblastic anaemia and found ineffective erythropoiesis was found to be the major factor in the production of the anaemia.