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Ponatinib in chronic myeloid leukemia (CML): Consensus on patient treatment and management from a European expert panel.
Müller, Martin C; Cervantes, Francisco; Hjorth-Hansen, Henrik; Janssen, Jeroen J W M; Milojkovic, Dragana; Rea, Delphine; Rosti, Gianantonio.
Afiliação
  • Müller MC; Institute for Hematology and Oncology (IHO GmbH), Mannheim, Germany. Electronic address: Martin.c.mueller@gmail.com.
  • Cervantes F; Hematology Department, Hospital Clinic, IDIBAPS, Barcelona, Spain.
  • Hjorth-Hansen H; Department of Hematology, St Olavs Hospital, Trondheim, Norway; Department of Cancer Research and Molecular Medicine (IKM), NTNU, Trondheim, Norway.
  • Janssen JJWM; Department of Hematology, VU University Medical Center, Amsterdam, Netherlands.
  • Milojkovic D; Department of Medicine, Imperial College London, London, United Kingdom.
  • Rea D; Department of Hematology, Hôpital Saint-Louis, Paris, France.
  • Rosti G; Department of Hematology and Oncology "L. and A. Seràgnoli," St Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Crit Rev Oncol Hematol ; 120: 52-59, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29198338
ABSTRACT
Five tyrosine kinase inhibitors (TKIs) are currently approved in the European Union for treatment of chronic myeloid leukemia (CML) and all have considerable overlap in their indications. While disease-specific factors such as CML phase, mutational status, and line of treatment are key to TKI selection, other important features must be considered, such as patient-specific comorbidities and TKI safety profiles. Ponatinib, the TKI most recently approved, has demonstrated efficacy in patients with refractory CML, but is associated with an increased risk of arterial hypertension, sometimes severe, and serious arterial occlusive and venous thromboembolic events. A panel of European experts convened to discuss their clinical experience in managing patients with CML. Based on the panel discussions, scenarios in which a CML patient may be an appropriate candidate for ponatinib therapy are described, including presence of the T315I mutation, resistance to other TKIs without the T315I mutation, and intolerance to other TKIs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piridazinas / Leucemia Mielogênica Crônica BCR-ABL Positiva / Imidazóis Tipo de estudo: Guideline Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Crit Rev Oncol Hematol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piridazinas / Leucemia Mielogênica Crônica BCR-ABL Positiva / Imidazóis Tipo de estudo: Guideline Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Crit Rev Oncol Hematol Ano de publicação: 2017 Tipo de documento: Article