Literature DB >> 25041880

First-line treatment of 102 chronic myeloid leukemia patients with imatinib: a long-term single institution analysis.

Ilaria Viganò1, Nunzio Di Giacomo, Sofia Bozzani, Laura Antolini, Rocco Piazza, Carlo Gambacorti Passerini.   

Abstract

Imatinib mesylate radically changed the natural history of chronic myeloid leukemia (CML). The recent availability of alternative tyrosine kinase inhibitors (TKIs) renders the clinical management of CML more complex. In this article, we summarize our long-term single institution experience. From 2003 to 2012, 102 patients with newly diagnosed chronic phase CML were referred to our institution and treated with imatinib mesylate as first-line therapy. All patients were followed inside a dedicated CML clinic. At 1 year, 82/95 patients (86.3%) achieved complete cytogenetic response (CCyR) using a treatment performed analysis (TPA); when using an intention to treat analysis, 85/102 patients (83.3%) obtained CCyR. At 3 months, 58 patients (64.4% TPA) obtained a BCR-ABL transcripts level <10%. A major molecular response (MMR) was obtained by 38% and 53% of patients at 1 and 2 years. Twenty patients (19.6%) discontinued treatment with imatinib; six of them did so in the initial 2 years of treatment (4 for resistance and 2 for adverse events). We observed seven deaths (6.86%). Overall survival (OS) at 6 years is 95.1% (95% C.I. 90-100%) and is not different from that of the general population. No patient experienced progression of disease (95% C.I.: 0-3%). Our results suggest that patient management is a crucial point to obtain a successful therapeutic outcome: at 1 year CCyR and MMR rates are similar to the results obtained with second generation TKIs and OS is not different from that of the general population.
© 2014 Wiley Periodicals, Inc.

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Year:  2014        PMID: 25041880     DOI: 10.1002/ajh.23804

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  4 in total

1.  Long-term evaluation of cardiac and vascular toxicity in patients with Philadelphia chromosome-positive leukemias treated with bosutinib.

Authors:  Jorge E Cortes; H Jean Khoury; Hagop Kantarjian; Tim H Brümmendorf; Michael J Mauro; Ewa Matczak; Dmitri Pavlov; Jean M Aguiar; Kolette D Fly; Svetoslav Dimitrov; Eric Leip; Mark Shapiro; Jeff H Lipton; Jean-Bernard Durand; Carlo Gambacorti-Passerini
Journal:  Am J Hematol       Date:  2016-04-13       Impact factor: 10.047

2.  Chronic myeloid leukaemia patients at diagnosis and resistant to tyrosine kinase inhibitor therapy display exhausted T-cell phenotype.

Authors:  Patrick Harrington; Richard Dillon; Deepti Radia; Donal McLornan; Claire Woodley; Susan Asirvatham; Kavita Raj; Natalia Curto-Garcia; Jamie Saunders; Shahram Kordasti; Claire Harrison; Hugues de Lavallade
Journal:  Br J Haematol       Date:  2022-07-08       Impact factor: 8.615

3.  Caution in using second generation tyrosine kinase inhibitor, especially for first line therapy of chronic myeloid leukemia.

Authors:  Carlo Gambacorti-Passerini; Franck Emmanuel Nicolini; Richard A Larson; Andrea Aroldi; Diletta Fontana; Rocco Piazza; Philipp le Coutre; Laura Antolini; Sarit Assouline
Journal:  Am J Hematol       Date:  2022-06-09       Impact factor: 13.265

4.  Safety and efficacy of second-line bosutinib for chronic phase chronic myeloid leukemia over a five-year period: final results of a phase I/II study.

Authors:  Carlo Gambacorti-Passerini; Jorge E Cortes; Jeff H Lipton; Hagop M Kantarjian; Dong-Wook Kim; Philippe Schafhausen; Rocco Crescenzo; Nathalie Bardy-Bouxin; Mark Shapiro; Kay Noonan; Eric Leip; Liza DeAnnuntis; Tim H Brümmendorf; H Jean Khoury
Journal:  Haematologica       Date:  2018-05-17       Impact factor: 9.941

  4 in total

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