Ponatinib in childhood Philadelphia chromosome-positive leukaemias: an international registry of childhood chronic myeloid leukaemia study

被引:16
作者
Millot, Frederic [1 ]
Suttorp, Meinolf [2 ]
Versluys, Anne B. [3 ]
Kalwak, Krzysztof [4 ]
Nelken, Brigitte [5 ]
Ducassou, Stephane [6 ]
Bertrand, Yves [7 ]
Baruchel, Andre [8 ]
机构
[1] Univ Hosp, Inserm CIC 1402, Poitiers, France
[2] Tech Univ, Med Fac, Pediat Hematooncol, Dresden, Germany
[3] Princess Maxima Ctr, Dept Pediat Oncol Hematol, Utrecht, Netherlands
[4] Wroclaw Med Univ, Dept Pediat Hematol Oncol & Transplantat, Wroclaw, Poland
[5] Univ Hosp, Dept Pediat Hematol Oncol, Lille, France
[6] Univ Hosp, Dept Pediat Hematol Oncol, Bordeaux, France
[7] Inst Hematol & Oncol Pediat, Dept Pediat Hematol, Lyon, France
[8] Robert Debre Hosp, Dept Pediat Hematol, Paris, France
关键词
Children; Ponatinib; Chronic myeloid leukaemia; Philadelphia chromosome-positive acute lymphoblastic leukaemia; TYROSINE KINASE INHIBITORS; RECOMMENDATIONS; MUTATION; IMATINIB; OUTCOMES;
D O I
10.1016/j.ejca.2020.05.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Ponatinib is effective in adults with Philadelphia chromosome-positive (Ph+) leukaemias, but scant data are available regarding the use of this tyrosine kinase inhibitor in children. Aims: The aim of this study isto describe the tolerance and efficacy of compassionate use of ponatinib in a paediatric cohort of patients with Ph+ leukaemias. Methods: Data from 11 children with chronic myeloid leukaemia (CML) registered to the international registry of childhood chronic myeloid leukaemia and from 3 children with Ph+ acute lymphoblastic leukaemia (Ph+ ALL) treated with ponatinib were collected retrospectively. Results: In 11 girls and 3 boys (median age 14 years), ponatinib was used as a second- to eighth-line treatment. Ponatinib was administered as single therapy (9 patients) or in combination with chemotherapy (8 patients). The status of the disease when ponatinib was started was as follows: CML in advanced phases (n = 8), CML in chronic phase without achievement of molecular response (n = 2) or presence of T315I mutation (n = 1) and Ph thorn ALL in molecular (n = 1) or marrow (n = 2) relapses. The median dose administered was 21.4 mg/m(2) and median duration of ponatinib was 2.5 months. Ponatinib alone or in combination with chemotherapy administered on 16 occasions led to achievement of major molecular response in 50% of cases. Ponatinib was used as a bridge to transplant in 4 cases. Among the 9 patients treated with ponatinib alone, toxicity grade III-IV (2 patients) was exclusively haematologic. No vascular events related to ponatinib were observed. Conclusion: Ponatinib may be a reasonable additional treatment option for children with Ph + leukaemias who have failed several lines of therapy. (C) 2020 Elsevier Ltd. All rights reserved.
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收藏
页码:107 / 112
页数:6
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