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Multi tyrosine kinase inhibitor dasatinib as novel cause of severe pre-capillary pulmonary hypertension?

机译:多酪氨酸激酶抑制剂达沙替尼可作为严重毛细血管前肺动脉高压的新病因?

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Background Pulmonary hypertension (PH) is a life-threatening disease with poor prognosis. Encouraging efforts have been made to target the main vasoproliferative aspects of the disease. Promising emerging therapeutics are tyrosine kinase inhibitors such as imatinib. Case presentation Here, we discuss the relevance of previously published cases and add another well-characterised patient who developed pre-capillary PH under long-term therapy with the multi-tyrosine kinase inhibitor dasatinib approved for therapy of chronic myeloic leukaemia (CML) and Philadelphia chromosome positive acute lymphocytic leukaemia (mean time of all patients on dasatinib: 26 months). Hence, we discuss the possibility of dasatinib itself causing PH after long-term therapy and turn specialist's attention to this possible severe side effect. At present, the true incidence of dasatinib-associated PH remains illusive and systematic data regarding haemodynamics are missing. Conclusion We therefore recommend systematic screening of dasatinib-treated patients for pulmonary hypertension and subsequent collection of haemodynamic data.
机译:背景技术肺动脉高压(PH)是威胁生命的疾病,预后不良。已经做出了令人鼓舞的努力来针对该疾病的主要血管增生方面。酪氨酸激酶抑制剂,例如伊马替尼,有望成为新兴疗法。病例介绍在这里,我们讨论了以前发表的病例的相关性,并增加了另一位特征明确的患者,该患者在长期治疗下与多酪氨酸激酶抑制剂dasatinib一起被批准用于慢性粒细胞白血病(CML)和费城治疗染色体阳性的急性淋巴细胞白血病(达沙替尼所有患者的平均时间:26个月)。因此,我们讨论了长期治疗后达沙替尼自身引起PH的可能性,并将专家的注意力转向这种可能的严重副作用。目前,达沙替尼相关PH的真实发生率仍是虚假的,有关血流动力学的系统性数据也缺失。结论因此,我们建议系统筛选达沙替尼治疗的患者的肺动脉高压,并随后收集血液动力学数据。

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