| Literature DB >> 33980976 |
Timothy P Hughes1, Nelma Cristina D Clementino2, Mikhail Fominykh3,4, Jeffrey H Lipton5, Anna G Turkina6, Elena Beatriz Moiraghi7, Franck E Nicolini8, Naoto Takahashi9, Tomasz Sacha10, Dong-Wook Kim11, Rafik Fellague-Chebra12, Ranjan Tiwari13, Catherine Bouard12, Francois-Xavier Mahon14.
Abstract
The ENESTop study evaluated treatment-free remission (TFR) in patients with chronic myeloid leukemia (CML) in chronic phase who had received ≥3 years of tyrosine kinase inhibitor therapy and achieved sustained deep molecular response only after switching from imatinib to nilotinib. After 1-year nilotinib consolidation, 126 patients attempted TFR. At 48 weeks (primary analysis), 57.9% (73/126) were in TFR. In the present analysis at 5 years, 42.9% (54/126) were in TFR. Since the 48-week analysis, among patients who left the TFR phase, 58% (11/19) did not have a loss of molecular response and discontinued for other reasons. Of the 59 patients who reinitiated nilotinib upon loss of major molecular response (MMR) or confirmed loss of MR4, 98.3% regained MMR, 94.9% regained MR4, and 93.2% regained MR4.5. Overall adverse event rates decreased over the 5 years of TFR. In patients reinitiating nilotinib, there was a cumulative increase in cardiovascular events with longer nilotinib exposure. No disease progression or CML-related deaths were reported. Overall, these results confirm the durability and safety of TFR for patients receiving second-line nilotinib. Cardiovascular risk should be carefully managed, particularly when reinitiating treatment after TFR.Entities:
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Year: 2021 PMID: 33980976 DOI: 10.1038/s41375-021-01260-y
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528