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

被引:26
作者
Hughes, Timothy P. [1 ]
Clementino, Nelma Cristina D. [2 ]
Fominykh, Mikhail [3 ,4 ]
Lipton, Jeffrey H. [5 ]
Turkina, Anna G. [6 ]
Moiraghi, Elena Beatriz [7 ]
Nicolini, Franck E. [8 ]
Takahashi, Naoto [9 ]
Sacha, Tomasz [10 ]
Kim, Dong-Wook [11 ]
Fellague-Chebra, Rafik [12 ]
Tiwari, Ranjan [13 ]
Bouard, Catherine [12 ]
Mahon, Francois-Xavier [14 ]
机构
[1] Univ Adelaide, South Australian Hlth & Med Res Inst, Adelaide, SA, Australia
[2] Hosp Clin UFMG, Belo Horizonte, MG, Brazil
[3] Russian Res Inst Hematol & Transfusiol, St Petersburg, Russia
[4] St Petersburg State Univ, St Petersburg, Russia
[5] Princess Margaret Canc Ctr, Toronto, ON, Canada
[6] Natl Res Ctr Hematol, Moscow, Russia
[7] Hosp Gen Agudos JM Ramos Mejia, Buenos Aires, DF, Argentina
[8] Ctr Leon Berard, Hematol Dept, Lyon, France
[9] Akita Univ, Dept Hematol Nephrol & Rheumatol, Grad Sch Med, Akita, Japan
[10] Jagiellonian Univ Hosp, Dept Hematol, Krakow, Poland
[11] Catholic Univ Korea, Seoul St Marys Hosp, Seoul, South Korea
[12] Novartis Pharma SAS, Paris, France
[13] Novartis Healthcare Pvt Ltd, Hyderabad, India
[14] Univ Bordeaux, Canc Ctr Bordeaux, Inst Bergonie, INSERM U1218, Bordeaux, France
关键词
TYROSINE KINASE INHIBITORS; MAJOR MOLECULAR RESPONSE; IMATINIB; DISCONTINUATION; THERAPY;
D O I
10.1038/s41375-021-01260-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:1631 / 1642
页数:12
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