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多酪氨酸激酶抑制剂帕纳替尼治疗慢性髓性白血病:真实世界数据。

The multi-tyrosine kinase inhibitor ponatinib for chronic myeloid leukemia: Real-world data.

机构信息

Hematology - Department of Clinical Medicine and Surgery, Federico II University, Napoli, Italy.

Hematology Division, AORN Cardarelli, Naples, Italy.

出版信息

Eur J Haematol. 2020 Jul;105(1):3-15. doi: 10.1111/ejh.13408. Epub 2020 Mar 15.

Abstract

Development of the highly selective targeted tyrosine kinase inhibitors (TKIs) has expanded the therapeutic options for chronic myeloid leukemia (CML). Patients undergoing TKI therapy should be closely monitored to ensure that the best therapeutic response and quality of life are achieved, and to control suboptimal responses and adverse events. Despite the high rate of response using current first-line TKIs, treatment failure may still occur, and resistance is considered a challenge in the treatment of patients with CML. The third-generation TKI, ponatinib, is a potent orally bioavailable pan BCR-ABL inhibitor that inhibits both wild-type and mutant BCR-ABL1 kinase, including the "gatekeeper" T315I mutation, which is resistant to all other currently available TKIs. This paper reviews the effectiveness, feasibility, and safety of ponatinib in the real-life clinical management of CML. Potential prognostic factors in identifying patients most likely to benefit from ponatinib treatment will be discussed, and case presentations illustrating situations encountered in real-life clinical practice are described. Ponatinib is effective in patients who have received prior TKIs in clinical studies as well as under real-life conditions. Nevertheless, the risk/benefit balance must be evaluated for each patient, particularly considering disease state, mutational status, treatment line, intolerance/resistance to prior TKIs, age, frailty, and specific comorbidities.

摘要

高度选择性的靶向酪氨酸激酶抑制剂(TKI)的开发扩大了慢性髓性白血病(CML)的治疗选择。接受 TKI 治疗的患者应密切监测,以确保达到最佳的治疗反应和生活质量,并控制不理想的反应和不良事件。尽管目前一线 TKI 的反应率很高,但仍可能发生治疗失败,耐药性被认为是 CML 患者治疗的挑战。第三代 TKI 帕纳替尼是一种强效的口服生物可利用的 pan BCR-ABL 抑制剂,可抑制野生型和突变型 BCR-ABL1 激酶,包括对所有其他现有 TKI 耐药的“守门员”T315I 突变。本文综述了帕纳替尼在 CML 真实临床管理中的有效性、可行性和安全性。将讨论确定最有可能从帕纳替尼治疗中获益的患者的潜在预后因素,并描述说明在真实临床实践中遇到的情况的病例介绍。在临床试验和真实环境中,帕纳替尼对接受过先前 TKI 治疗的患者均有效。然而,必须为每位患者评估风险/获益平衡,特别是要考虑疾病状态、突变状态、治疗线、对先前 TKI 的不耐受/耐药性、年龄、虚弱和特定合并症。

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