Interruption or Discontinuation of Tyrosine Kinase Inhibitor Treatment in Chronic Myeloid Leukaemia: A Retrospective Cohort Study (SPARKLE) in Belgium

被引:5
|
作者
Devos, Timothy [1 ]
Verhoef, Gregor [1 ]
Steel, Eva [2 ]
Mazure, Dominiek [2 ]
Lewalle, Philippe [3 ]
Bron, Dominique [3 ]
Berneman, Zwi [4 ]
Benghiat, Fleur Samantha [5 ]
Mineur, Philippe [6 ]
Theunissen, Koen [7 ]
Zachee, Pierre [8 ]
Doyen, Chantal [9 ]
Put, Natalie [10 ]
Lejeune, Marie [11 ]
Van Eygen, Koen [12 ]
Havelange, Violaine [13 ]
Reusens, Michael [14 ]
Pluymers, Wim [14 ]
Peeters, Karen [14 ]
机构
[1] Univ Hosp Leuven, Dept Hematol, Leuven, Belgium
[2] Univ Ziekenhuis Ghent, Ghent, Belgium
[3] Inst Jules Bordet, Brussels, Belgium
[4] Univ Ziekenhuis Antwerpen, Edegem, Belgium
[5] Hop Erasme, Brussels, Belgium
[6] Grand Hop Charleroi GHdC, Charleroi, Belgium
[7] Jessa Ziekenhuis, Campus Virga Jesse, Hasselt, Belgium
[8] Ziekenhuis Netwerk Antwerpen Stuivenberg, Antwerp, Belgium
[9] Ctr Hosp Univ UCL Namur, Yvoir, Belgium
[10] Ziekenhuis Oost Limburg, Campus Sint Jan, Genk, Belgium
[11] Ctr Hosp Univ Liege, Liege, Belgium
[12] AZ Groeninge, Campus Kennedylaan, Kortrijk, Belgium
[13] UCL St Luc, Woluwe St Lambert, Belgium
[14] Novartis Pharma NV SA, Vilvoorde, Belgium
关键词
Chronic myeloid leukaemia; Tyrosine kinase inhibitor; Treatment interruption; discontinuation; Molecular response; Imatinib; Nilotinib; Dasatinib; Ponatinib; TREATMENT-FREE REMISSION; MOLECULAR RESPONSE; ADVERSE EVENTS; IMATINIB; RECOMMENDATIONS; MANAGEMENT; THERAPY; NILOTINIB; TRIAL;
D O I
10.1159/000499329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To assess interruptions/discontinuations of tyrosine kinase inhibitor (TKI) treatment in Belgian patients with chronic myeloid leukaemia (CML). Methods: This retrospective study included patients with TKI interruptions/discontinuations of >= 4 continuous weeks (no clinical trial context) between May 2013 and May 2016. Data collection took place between October 2016 and February 2017. Results: All 60 participants (69 interruptions/discontinuations) had chronic-phase CML and 75% had at least a major molecular response (>= MMR) at interruption/discontinuation. Most interruptions/discontinuations occurred while on imatinib (36/69; 49%) and dasatinib (20/69; 29%). Most interruptions/discontinuations occurred due to side effects/intolerance (46/69; 67%); other reasons included a wish to conceive (6/69; 9%) and attempts to achieve treatment-free remission (TFR) (6/69; 9%). Interruptions due to side effects occurred later for imatinib- or dasatinib-treated patients than for those on nilotinib or ponatinib. Treatment was re-initiated in 62% (43/69) of cases. Most interruptions caused by side effects/intolerance were followed by treatment changes. All 4 patients with >= MR 4.5 at interruption/discontinuation and >= 11-month follow-up who had not restarted treatment maintained the response. Conclusion: Although TKIs are used for long-term CML treatment, physicians sometimes recommend interruptions/discontinuations. In this study, interruptions/discontinuations were mainly caused by side effects or intolerance, rather than TFR attempts.
引用
收藏
页码:197 / 207
页数:11
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