Long-term treatment-free remission in patients with chronic myeloid leukemia after second-line nilotinib: ENESTop 5-year update

被引:0
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作者
Timothy P. Hughes
Nelma Cristina D. Clementino
Mikhail Fominykh
Jeffrey H. Lipton
Anna G. Turkina
Elena Beatriz Moiraghi
Franck E. Nicolini
Naoto Takahashi
Tomasz Sacha
Dong-Wook Kim
Rafik Fellague-Chebra
Ranjan Tiwari
Catherine Bouard
Francois-Xavier Mahon
机构
[1] University of Adelaide,South Australian Health and Medical Research Institute
[2] Hospital Das Clinicas Da UFMG,Hematology Department
[3] Russian Research Institute of Hematology and Transfusiology,Department of Hematology, Nephrology and Rheumatology
[4] Saint Petersburg State University,Department of Hematology
[5] Princess Margaret Cancer Centre,Seoul St. Mary’s Hospital
[6] National Research Center for Hematology,Cancer Center of Bordeaux, Institut Bergonié, INSERM U1218
[7] Hospital General De Agudos J. M. Ramos Mejia,undefined
[8] Centre Léon Berard,undefined
[9] Akita University Graduate School of Medicine,undefined
[10] Jagiellonian University Hospital,undefined
[11] The Catholic University of Korea,undefined
[12] Novartis Pharma SAS,undefined
[13] Rueil-Malmaison,undefined
[14] Novartis Healthcare Pvt. Ltd,undefined
[15] University of Bordeaux,undefined
来源
Leukemia | 2021年 / 35卷
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摘要
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.
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页码:1631 / 1642
页数:11
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