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Prognostic analysis according to the 2017 ELN risk stratification by genetics in adult acute myeloid leukemia patients treated in the Japan Adult Leukemia Study Group (JALSG) AML201 study

医学 髓系白血病 肿瘤科 净现值1 危险分层 内科学 CEBPA公司 白血病 队列 儿科 突变 遗传学 基因 生物 染色体 核型
作者
Yoshio Harada,Yasunobu Nagata,Rika Kihara,Yuichi Ishikawa,Norio Asou,Shigeki Ohtake,Shuichi Miyawaki,Toru Sakura,Yukiyasu Ozawa,Noriko Usui,Heiwa Kanamori,Yoshikazu Ito,Kiyotoshi Imai,Yutaka Suehiro,Shinichi Kobayashi,Kazuo Kïtamura,Emiko Sakaida,Makoto Onizuka,Akira Takeshita,Fumihiro Ishida,Hitoshi Suzushima,Kenichi Ishizawa,Tomoki Naoe,Itaru Matsumura,Yasushi Miyazaki,Seishi Ogawa,Hitoshi Kiyoi
出处
期刊:Leukemia Research [Elsevier BV]
卷期号:66: 20-27 被引量:43
标识
DOI:10.1016/j.leukres.2018.01.008
摘要

Many genetic alterations that are associated with the prognosis of acute myeloid leukemia (AML) have been identified, and several risk stratification systems based on the genetic status have been recommended. The European LeukemiaNet (ELN) first proposed the risk stratification system for AML in 2010 (ELN-2010), and recently published the revised system (ELN-2017). We validated the long-term prognosis and clinical characteristics of each ELN-2017 risk category in Japanese adult AML patients who were treated in the Japan Adult Leukemia Study Group (JALSG) AML-201 study. We demonstrated that the 3-risk category system of the ELN-2017 successfully discriminated the overall survival and complete remission rates in our cohort in comparison with the 4-risk category of the ELN-2010. However, there were still genetic categories in which stratification of patients into favorable or intermediate risk categories was controversial; the low allelic ratio of FLT3-ITD was not necessarily associated with a better prognosis in patients with FLT3-ITD, and cytogenetic abnormalities may affect the prognosis in patients with favorable genetic lesions such as NPM1 and CEBPA mutations. As many molecular targeting agents, such as FLT3 inhibitors, have been developed, we must continue to modify the genetic risk stratification system to match the progression of therapeutic strategies.

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