Your browser doesn't support javascript.
loading
Management of chronic myeloid leukaemia patients treated with ponatinib in a real-life setting: A retrospective analysis from the monitoring registries of the Italian Medicines Agency (AIFA).
Breccia, Massimo; Olimpieri, Pier Paolo; Celant, Simone; Olimpieri, Odoardo; Pane, Fabrizio; Iurlo, Alessandra; Summa, Valentina; Corradini, Paolo; Russo, Pierluigi.
Afiliación
  • Breccia M; Department of Translational and Precision Medicine, Az. Policlinico Umberto I-Sapienza University, Rome, Italy.
  • Olimpieri PP; Italian Medicines Agency, Rome, Italy.
  • Celant S; Italian Medicines Agency, Rome, Italy.
  • Olimpieri O; Italian Medicines Agency, Rome, Italy.
  • Pane F; Università degli Studi di Napoli Federico II, Naples, Italy.
  • Iurlo A; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Summa V; Italian Medicines Agency, Rome, Italy.
  • Corradini P; Università degli Studi di Milano & Divisione Ematologia, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
  • Russo P; Italian Medicines Agency, Rome, Italy.
Br J Haematol ; 198(6): 965-973, 2022 09.
Article en En | MEDLINE | ID: mdl-35904979
ABSTRACT
Real-world data on daily practice management, treatment modifications and outcome of a large cohort of chronic myeloid leukaemia (CML) patients treated with ponatinib was performed through monitoring Registries of the Italian Medicines Agency (AIFA). Overall, 666 CML subjects were included in the ponatinib registry from February 2015 to December 2020 and were eligible for

analysis:

515 in chronic phase (CP), 50 in accelerated phase (AP) and 101 in blast crisis (BC). Median age at baseline was 58.7 years with a predominance of male subjects (57.1%). The median time from diagnosis to start of ponatinib was 2.35 years 259 (38.9%) subjects had received two previous lines of treatment, 260 (39.0%) three lines and 147 (22.1%) four or more lines. A molecular response [from major molecular response (MMR) to a score of ≤0.01% on the international reporting scale (IS)] was reported for 59% of patients out of 593 patients analysed. With a median follow-up of 14.4 months, 136 subjects (20.4%) required at least one dose reduction due to adverse events (AEs), whereas 309 patients (46.4%) required dose reduction in the absence of any evidence of side effects. Treatment discontinuation occurred in 261 patients (39%). This real-life analysis shows that dose reductions were made primarily as a precaution rather than due to the occurrence of adverse reactions.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Antineoplásicos Tipo de estudio: Observational_studies Límite: Female / Humans / Male Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Antineoplásicos Tipo de estudio: Observational_studies Límite: Female / Humans / Male Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Italia