Frédéric Millot1, Meinolf Suttorp2, Anne B Versluys3, Krzysztof Kalwak4, Brigitte Nelken5, Stephane Ducassou6, Yves Bertrand7, André Baruchel8. 1. Inserm CIC 1402, University Hospital, Poitiers, France. Electronic address: f.millot@chu-poitiers.fr. 2. Medical Faculty, Pediatric Hemato-oncology, Technical University, Dresden, Germany. 3. Department of Pediatric Oncology/Hematology, Princess Maxima Center, Utrecht, Netherlands. 4. Department of Pediatric Hematology Oncology and Transplantation, Wroclaw Medical University, Wroclaw, Poland. 5. Department of Pediatric Hematology-oncology, University Hospital, Lille, France. 6. Department of Pediatric Hematology-oncology, University Hospital, Bordeaux, France. 7. Department of Pediatric Hematology, Institut d'Hématologie et d'Oncologie Pédiatrique, Lyon, France. 8. Department of Pediatric Hematology, Robert Debré Hospital, Paris, France.
Abstract
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 + ALL in molecular (n = 1) or marrow (n = 2) relapses. The median dose administered was 21.4 mg/m2 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.
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 + ALL in molecular (n = 1) or marrow (n = 2) relapses. The median dose administered was 21.4 mg/m2 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.