医学
伊马替尼
肿瘤科
甲磺酸伊马替尼
酪氨酸激酶
断点群集区域
临床实习
重症监护医学
内科学
免疫学
髓系白血病
危险分层
家庭医学
受体
作者
Daniel Egan,Jerald P. Radich
标识
DOI:10.1016/j.beha.2016.10.015
摘要
The implementation of cytogenetic and molecular techniques into standard clinical practice has improved our ability to more accurately diagnose and monitor CML. Routine peripheral blood BCR-ABL transcript testing can help monitor response, predict outcome, and detect early resistance or poor adherence to TKI therapy. The widely-used Sokal, Hasford and EUTOS clinical risk stratification scores were developed in patients receiving chemotherapy, interferon and imatinib, respectively; their predictive ability in patients receiving next-generation tyrosine kinase inhibitors (TKIs) remains to be established. Newer more sensitive molecular techniques are being developed that may aid in the expanding emphasis on discontinuing therapy in patients with a deep and consistent molecular response.
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