Efficacy and safety of nilotinib in chronic myeloid leukaemia patients who failed to achieve a treatment-free remission period after imatinib discontinuation: Results of the French Nilo post-STIM study.
Stephanie DulucqFrançoise Rigal-HuguetFranck Emmanuel NicoliniPascale Cony-MakhoulMartine Escoffre-BarbeMartine GardembasLaurence LegrosPhilippe RousselotJixing LiuDelphine ReaVéronique De MasSandrine HayetteSophie RaynaudCaroline Lacoste-RoussillonFanny RobbesynEmilie KleinStéphane MorissetFrançois-Xavier MahonGabriel EtiennePublished in: British journal of haematology (2023)
Molecular recurrence (MRec) occurs in about half of all patients with chronic myeloid leukaemia (CML) who discontinue tyrosine kinase inhibitors (TKI) in sustained deep molecular response. A second TKI discontinuation has been attempted in some patients who regain the discontinuation criteria after resuming treatment. Nilotinib treatment affords faster and deeper molecular responses than imatinib as first-line therapy. We prospectively evaluated the efficacy and safety of nilotinib (300 mg twice daily) in chronic-phase CML patients who experienced MRec, after imatinib discontinuation and analysed the probability of TFR after a new attempt in patients treated for 2 years with sustained MR 4.5 for at least 1 year. A total of 31 patients were included in the study between 2013 and 2018. Seven (23%) patients experienced serious adverse events after a median of 2 months of nilotinib treatment leading to discontinuation of treatment. One patient was excluded from the study for convenience. Among the 23 patients treated for 2 years with nilotinib, 22 maintained their molecular response for at least 1 year (median: 22 months) and stopped nilotinib. The TFR rates at 24 and 48 months after nilotinib discontinuation were 59.1% (95% confidence interval [CI]: 41.7%-83.7%) and 42.1% (95% CI: 25%-71%) respectively (NCT #01774630).
Keyphrases
- chronic myeloid leukemia
- ejection fraction
- acute myeloid leukemia
- stem cells
- physical activity
- bone marrow
- bariatric surgery
- combination therapy
- computed tomography
- dendritic cells
- tyrosine kinase
- epidermal growth factor receptor
- ulcerative colitis
- roux en y gastric bypass
- patient reported outcomes
- disease activity