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慢性粒细胞白血病患者二线及三线治疗的耐药原因及治疗选择

Causes of resistance and treatment choices of second- and third-line treatment in chronic myelogenous leukemia patients.

作者信息

Hochhaus Andreas, Ernst Thomas, Eigendorff Ekkehard, La Rosée Paul

机构信息

Abteilung Hämatologie/Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Erlanger Allee 101, 07740, Jena, Germany,

出版信息

Ann Hematol. 2015 Apr;94 Suppl 2:S133-40. doi: 10.1007/s00277-015-2323-1. Epub 2015 Mar 27.

Abstract

For patients with chronic myelogenous leukemia who fail first-line therapy, several factors should be considered for the decision of the next treatment option. Second-generation tyrosine kinase inhibitors (TKIs) dasatinib, nilotinib, and bosutinib offer improved potency and a high likelihood of success for these patients. Overall, efficacy data are comparable for these agents, and so physicians should consider the BCR-ABL1 mutation profile and the patient's history to make a decision on the best choice. Only a few BCR-ABL1 mutations seem to be less responsive to any of the three drugs, and it is recommended to choose the second-line TKI that has shown clinical activity against the specific mutation in these cases. For patients with all other mutations and for patients with no mutations, it is recommended to choose the second-generation TKI based on the patient's disease history. The third-generation TKI ponatinib is available after dasatinib or nilotinib failure or for patients with T315I mutations. However, optimal dose of ponatinib is still under investigation. Overall, it is recommended to select a drug that minimizes the likelihood of worsening the patient's past side effects or comorbid conditions. In any case, chance and risk of allogeneic stem cell transplantation should be compared with the long-term outcome of TKI therapy in patients eligible for this procedure.

摘要

对于一线治疗失败的慢性髓性白血病患者,在决定下一步治疗方案时应考虑多个因素。第二代酪氨酸激酶抑制剂(TKIs)达沙替尼、尼洛替尼和博舒替尼对这些患者具有更高的效力和成功可能性。总体而言,这些药物的疗效数据相当,因此医生应考虑BCR-ABL1突变情况和患者病史,以做出最佳选择。似乎只有少数BCR-ABL1突变对这三种药物中的任何一种反应较差,在这些情况下,建议选择对特定突变显示出临床活性的二线TKI。对于所有其他突变的患者以及无突变的患者,建议根据患者的病史选择第二代TKI。在达沙替尼或尼洛替尼治疗失败后或对于T315I突变的患者,可使用第三代TKI波纳替尼。然而,波纳替尼的最佳剂量仍在研究中。总体而言,建议选择一种能将患者既往副作用或合并症恶化可能性降至最低的药物。在任何情况下,对于适合该程序的患者,应将异基因干细胞移植的机会和风险与TKI治疗的长期结果进行比较。

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