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Ilaria Iacobucci
Researcher at University of Bologna
Publications - 228
Citations - 7050
Ilaria Iacobucci is an academic researcher from University of Bologna. The author has contributed to research in topics: Myeloid leukemia & Leukemia. The author has an hindex of 41, co-authored 201 publications receiving 6217 citations.
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Journal ArticleDOI
Contribution of ABL Kinase Domain Mutations to Imatinib Resistance in Different Subsets of Philadelphia-Positive Patients: By the GIMEMA Working Party on Chronic Myeloid Leukemia
Simona Soverini,Sabrina Colarossi,Alessandra Gnani,Gianantonio Rosti,Fausto Castagnetti,Angela Poerio,Ilaria Iacobucci,Marilina Amabile,Elisabetta Abruzzese,Ester Orlandi,F. Radaelli,Fabrizio Ciccone,Mario Tiribelli,Roberto Di Lorenzo,Clementina Caracciolo,Barbara Izzo,Fabrizio Pane,Giuseppe Saglio,Michele Baccarani,Giovanni Martinelli +19 more
TL;DR: P-loop and T315I mutations were particularly frequent in advanced-phase chronic myeloid leukemia and Ph+ ALL patients, and often accompanied progression from chronic phase to accelerated phase/blast crisis, and should warn the clinician to reconsider the therapeutic strategy.
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Dasatinib as first-line treatment for adult patients with Philadelphia chromosome–positive acute lymphoblastic leukemia
Robin Foà,Antonella Vitale,Marco Vignetti,Giovanna Meloni,Anna Guarini,Maria Stefania De Propris,Loredana Elia,Francesca Paoloni,Paola Fazi,Giuseppe Cimino,Francesco Nobile,Felicetto Ferrara,Carlo Castagnola,Simona Sica,Pietro Leoni,Eliana Zuffa,Claudio Fozza,Mario Luppi,Anna Candoni,Ilaria Iacobucci,Simona Soverini,Franco Mandelli,Giovanni Martinelli,Michele Baccarani +23 more
TL;DR: In adult Ph(+) ALL, induction treatment with dasatinib plus steroids is associated with a CHR in virtually all patients, irrespective of age, good compliance, no deaths, and a very rapid debulking of the neoplastic clone.
Journal ArticleDOI
PAX5 -driven subtypes of B-progenitor acute lymphoblastic leukemia
Zhaohui Gu,Michelle L. Churchman,Kathryn G. Roberts,Ian Moore,Xin Zhou,Joy Nakitandwe,Kohei Hagiwara,Stephane Pelletier,Sebastien Gingras,Hartmut Berns,Debbie Payne-Turner,Ashley Hill,Ilaria Iacobucci,Lei Shi,Stanley Pounds,Cheng Cheng,Deqing Pei,Chunxu Qu,Scott Newman,Meenakshi Devidas,Yunfeng Dai,Shalini C. Reshmi,Julie M. Gastier-Foster,Elizabeth A. Raetz,Michael J. Borowitz,Brent L. Wood,William L. Carroll,Patrick A. Zweidler-McKay,Karen R. Rabin,Leonard A. Mattano,Kelly W. Maloney,Alessandro Rambaldi,Orietta Spinelli,Jerald P. Radich,Mark D. Minden,Jacob M. Rowe,Selina M. Luger,Mark R. Litzow,Martin S. Tallman,Janis Racevskis,Yanming Zhang,Ravi Bhatia,Jessica Kohlschmidt,Krzysztof Mrózek,Clara D. Bloomfield,Wendy Stock,Steven M. Kornblau,Hagop M. Kantarjian,Marina Konopleva,Williams E. Evans,Sima Jeha,Ching-Hon Pui,Jun J. Yang,Elisabeth Paietta,James R. Downing,Mary V. Relling,Jinghui Zhang,Mignon L. Loh,Stephen P. Hunger,Charles G. Mullighan +59 more
TL;DR: Analysis of 1,988 cases of B-cell acute lymphoblastic leukemia characterizes 23 subtypes defined by genomic features and shows that two of the subtypes have frequent PAX5 alterations, demonstrating the utility of transcriptome sequencing to classify B-ALL.
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Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group
Libi Hertzberg,Libi Hertzberg,Libi Hertzberg,Elena Vendramini,Ithamar Ganmore,Ithamar Ganmore,Giovanni Cazzaniga,Maike Schmitz,Jane Chalker,Ruth Shiloh,Ilaria Iacobucci,Chen Shochat,Chen Shochat,Chen Shochat,Sharon Zeligson,Gunnar Cario,Martin Stanulla,Sabine Strehl,Lisa J. Russell,Christine J. Harrison,Beat Bornhauser,Akinori Yoda,Gideon Rechavi,Gideon Rechavi,Dani Bercovich,Arndt Borkhardt,Helena Kempski,Geertruy te Kronnie,Jean-Pierre Bourquin,Eytan Domany,Shai Izraeli,Shai Izraeli +31 more
TL;DR: The data suggest that the majority of DS children with ALL may benefit from therapy blocking the CRLF2/JAK2 pathways, and the gene expression signature of DS-ALL is enriched with DNA damage and BCL6 responsive genes, suggesting the possibility of B-cell lymphocytic genomic instability.
Journal ArticleDOI
IKZF1 (Ikaros) Deletions in BCR-ABL1–Positive Acute Lymphoblastic Leukemia Are Associated With Short Disease-Free Survival and High Rate of Cumulative Incidence of Relapse: A GIMEMA AL WP Report
Giovanni Martinelli,Ilaria Iacobucci,Clelia Tiziana Storlazzi,Marco Vignetti,Francesca Paoloni,Daniela Cilloni,Simona Soverini,Antonella Vitale,Sabina Chiaretti,Giuseppe Cimino,Cristina Papayannidis,Stefania Paolini,Loredana Elia,Paola Fazi,Giovanna Meloni,Amadori S,Giuseppe Saglio,Fabrizio Pane,Michele Baccarani,Robin Foà +19 more
TL;DR: IKZF1 deletions are likely to be a genomic alteration that significantly affects the prognosis of Ph-positive ALL in adults, andMultivariate analysis confirmed the negative prognostic impact of IKzF1 deletion on DFS.