Dose optimisation of ponatinib in chronic phase chronic myeloid leukemia.
Expert Rev Hematol
; 16(9): 633-639, 2023.
Article
en En
| MEDLINE
| ID: mdl-37427999
ABSTRACT
INTRODUCTION:
Ponatinib exhibits a high inhibition potency on wild-type and most mutated forms of the BCRABL1 kinase, but also a significant cardiovascular toxicity. Improving the efficacy/safety ratio should allow patients to safely draw benefit from the drug. AREAS COVERED Based on pharmacological findings and international guidelines on chronic myeloid leukemia and cardiovascular risk management, as well as on the most recent data collected in real-life studies and in a randomized phase II trial, we propose a decision-tree of dose selection of the drug. EXPERT OPINION We distinguish (1) highly resistant patients according to poor previous response to second generation tyrosine kinase inhibitors (complete hematologic response or less) or to mutational status (T315I, E255V, alone or within compound mutations), requiring a starting daily dose of 45 mg, reduced to 15 or 30 mg according to the patient's profile, preferentially upon major molecular achievement (3-log reduction or MR3, BCRABL1 ≤ 0.1%IS); (2) less-resistant patients justifying an initial dose of 30 mg, reduced to 15 mg upon MR2 (BCRABL1 ≤ 1%IS) or preferentially MR3 in patients with a favorable safety profile; (3) intolerant patients to be treated by 15 mg.Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Piridazinas
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Leucemia Mielógena Crónica BCR-ABL Positiva
/
Leucemia Mieloide de Fase Crónica
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Antineoplásicos
Tipo de estudio:
Clinical_trials
/
Prognostic_studies
Límite:
Humans
Idioma:
En
Año:
2023
Tipo del documento:
Article