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Ponatinib in the Treatment of Chronic Myeloid Leukemia and Philadelphia Chromosome-Positive Acute Leukemia: Recommendations of a German Expert Consensus Panel with Focus on Cardiovascular Management.
Saussele, Susanne; Haverkamp, Wilhelm; Lang, Fabian; Koschmieder, Steffen; Kiani, Alexander; Jentsch-Ullrich, Kathleen; Stegelmann, Frank; Pfeifer, Heike; La Rosée, Paul; Goekbuget, Nicola; Rieger, Christina; Waller, Cornelius F; Franke, Georg-Nikolaus; le Coutre, Philipp; Kirchmair, Rudolf; Junghanss, Christian.
Afiliação
  • Saussele S; Department of Haematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany, susanne.saussele@medma.uni-heidelberg.de.
  • Haverkamp W; Department of Cardiology, Charité Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany.
  • Lang F; Department of Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.
  • Koschmieder S; Department of Medicine, Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Faculty of Medicine, RWTH Aachen University, Aachen, Germany.
  • Kiani A; Department of Medicine IV, Klinikum Bayreuth GmbH, Bayreuth, Germany.
  • Jentsch-Ullrich K; Practice for Hematology and Oncology, Magdeburg, Germany.
  • Stegelmann F; Department of Internal Medicine III, University Hospital Ulm, Ulm, Germany.
  • Pfeifer H; Department of Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.
  • La Rosée P; Department of Medicine II, Schwarzwald-Baar Klinikum, Villingen-Schwenningen, Germany.
  • Goekbuget N; Department of Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.
  • Rieger C; Hemato-Oncology Germering, Germering, Germany and Ludwig Maximilians University Munich, Munich, Germany.
  • Waller CF; Department of Haematology, Oncology and Stem Cell Transplantation, University Medical Centre Freiburg, and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Franke GN; Medical Clinic I, University Hospital of Leipzig, Leipzig, Germany.
  • le Coutre P; Department of Medicine, Hematology and Oncology, Charité Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Kirchmair R; Department of Internal Medicine III: Cardiology and Angiology, Medical University Innsbruck, Innsbruck, Austria.
  • Junghanss C; Department of Medicine, Clinic III: Hematology, Oncology, Palliative Medicine, Rostock University Medical Center, Rostock, Germany.
Acta Haematol ; 143(3): 217-231, 2020.
Article em En | MEDLINE | ID: mdl-31590170
Treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute leukemia (Ph+ ALL) has been revolutionized with the advent of tyrosine kinase inhibitors (TKIs). Most patients with CML achieve long-term survival similar to individuals without CML due to treatment with TKIs not only in frontline but also in further lines of therapy. The third-generation TKI ponatinib has demonstrated efficacy in patients with refractory CML and Ph+ ALL. Ponatinib is currently the most potent TKI in this setting demonstrating activity against T315I mutant clones. However, ponatinib's safety data revealed a dose-dependent, increased risk of serious cardiovascular (CV) events. Guidance is needed to evaluate the benefit-risk profile of TKIs, such as ponatinib, and safety measures to prevent treatment-associated CV events. An expert panel of German hematologists and cardiologists summarize current evidence regarding ponatinib's efficacy and CV safety profile. We propose CV management strategies for patients who are candidates for ponatinib.
Assuntos
Antineoplásicos/uso terapêutico; Doenças Cardiovasculares/induzido quimicamente; Proteínas de Fusão bcr-abl/antagonistas & inibidores; Imidazóis/uso terapêutico; Leucemia Mielogênica Crônica BCR-ABL Positiva/tratamento farmacológico; Leucemia-Linfoma Linfoblástico de Células Precursoras/tratamento farmacológico; Inibidores de Proteínas Quinases/uso terapêutico; Piridazinas/uso terapêutico; Adulto; Idoso; Antineoplásicos/administração & dosagem; Antineoplásicos/efeitos adversos; Doenças Cardiovasculares/fisiopatologia; Doenças Cardiovasculares/prevenção & controle; Ensaios Clínicos como Assunto; Relação Dose-Resposta a Droga; Resistencia a Medicamentos Antineoplásicos; Feminino; Humanos; Hiperglicemia/complicações; Hiperglicemia/tratamento farmacológico; Hiperlipidemias/complicações; Hiperlipidemias/tratamento farmacológico; Hipertensão/complicações; Hipertensão/tratamento farmacológico; Imidazóis/administração & dosagem; Imidazóis/efeitos adversos; Leucemia Mielogênica Crônica BCR-ABL Positiva/enzimologia; Leucemia Mielogênica Crônica BCR-ABL Positiva/genética; Masculino; Pessoa de Meia-Idade; Cromossomo Filadélfia; Leucemia-Linfoma Linfoblástico de Células Precursoras/enzimologia; Leucemia-Linfoma Linfoblástico de Células Precursoras/genética; Intervalo Livre de Progressão; Inibidores de Proteínas Quinases/administração & dosagem; Inibidores de Proteínas Quinases/efeitos adversos; Piridazinas/administração & dosagem; Piridazinas/efeitos adversos; Medição de Risco
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Piridazinas / Doenças Cardiovasculares / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Inibidores de Proteínas Quinases / Leucemia-Linfoma Linfoblástico de Células Precursoras / Imidazóis / Antineoplásicos Tipo de estudo: Etiology_studies / Guideline Idioma: En Revista: Acta Haematol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Piridazinas / Doenças Cardiovasculares / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Inibidores de Proteínas Quinases / Leucemia-Linfoma Linfoblástico de Células Precursoras / Imidazóis / Antineoplásicos Tipo de estudo: Etiology_studies / Guideline Idioma: En Revista: Acta Haematol Ano de publicação: 2020 Tipo de documento: Article