Imatinib, the first BCR/ABL kinase inhibitor approved for the treatment of chronic myeloid leukemia (CML), has changed the long-term outcome of patients affected by this disease. The aim of our analysis was to report, after a median follow-up of 10.2 years (range 5.8–14.8), the long-term outcome, efficacy, and safety of imatinib treatment (frontline and after interferon failure) in a single institution cohort of 459 patients with CML in chronic phase treated outside of clinical trials. The 10-year overall survival of the whole cohort was 77.1%, while the 10-year probability of dying due to CML and other causes was 7.8% and 16%, respectively. The prognostic value of the BCR-ABL1 ratio at 3 months (⩽ 10%) and of complete cytogenetic response and major molecular response at 1 year was confirmed also in the real-life practice. The EUTOS long-term survival score better stratified the baseline risk of dying of CML compared with other risk scores. Two hundred thirty-six (51.4%) patients achieved a deep molecular response during imatinib treatment after a median time of 4.57 years, and 95 (20.6%) had a stable deep molecular response maintained for at least 2 consecutive years. Imatinib was associated with a low rate of serious cardiovascular events and second neoplasia. This 10-year real-life follow-up study shows that imatinib maintains efficacy over time and that long-term administration of imatinib is not associated with notable cumulative or late toxic effects.

Ten-year outcome of chronic-phase chronic myeloid leukemia patients treated with imatinib in real life / Molica, M.; Colafigli, G.; Scalzulli, E.; Alunni Fegatelli, D.; CHIATAMONE RANIERI, Sofia; Rizzo, L.; Diverio, D.; Efficace, F.; Latagliata, R.; Foa, R.; Breccia, M.. - In: ANNALS OF HEMATOLOGY. - ISSN 0939-5555. - (2019). [10.1007/s00277-019-03706-x]

Ten-year outcome of chronic-phase chronic myeloid leukemia patients treated with imatinib in real life

Molica M.;Colafigli G.;Scalzulli E.;Alunni Fegatelli D.;CHIATAMONE RANIERI, SOFIA;Rizzo L.;Efficace F.;Latagliata R.;Foa R.;Breccia M.
2019

Abstract

Imatinib, the first BCR/ABL kinase inhibitor approved for the treatment of chronic myeloid leukemia (CML), has changed the long-term outcome of patients affected by this disease. The aim of our analysis was to report, after a median follow-up of 10.2 years (range 5.8–14.8), the long-term outcome, efficacy, and safety of imatinib treatment (frontline and after interferon failure) in a single institution cohort of 459 patients with CML in chronic phase treated outside of clinical trials. The 10-year overall survival of the whole cohort was 77.1%, while the 10-year probability of dying due to CML and other causes was 7.8% and 16%, respectively. The prognostic value of the BCR-ABL1 ratio at 3 months (⩽ 10%) and of complete cytogenetic response and major molecular response at 1 year was confirmed also in the real-life practice. The EUTOS long-term survival score better stratified the baseline risk of dying of CML compared with other risk scores. Two hundred thirty-six (51.4%) patients achieved a deep molecular response during imatinib treatment after a median time of 4.57 years, and 95 (20.6%) had a stable deep molecular response maintained for at least 2 consecutive years. Imatinib was associated with a low rate of serious cardiovascular events and second neoplasia. This 10-year real-life follow-up study shows that imatinib maintains efficacy over time and that long-term administration of imatinib is not associated with notable cumulative or late toxic effects.
2019
Chronic myeloid leukemia; Imatinib; Long-term follow-up; Real-life experience
01 Pubblicazione su rivista::01a Articolo in rivista
Ten-year outcome of chronic-phase chronic myeloid leukemia patients treated with imatinib in real life / Molica, M.; Colafigli, G.; Scalzulli, E.; Alunni Fegatelli, D.; CHIATAMONE RANIERI, Sofia; Rizzo, L.; Diverio, D.; Efficace, F.; Latagliata, R.; Foa, R.; Breccia, M.. - In: ANNALS OF HEMATOLOGY. - ISSN 0939-5555. - (2019). [10.1007/s00277-019-03706-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1285954
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