| Literature DB >> 29360622 |
Yasuhiko Harada1, Yasunobu Nagata2, Rika Kihara1, Yuichi Ishikawa1, Norio Asou3, Shigeki Ohtake4, Shuichi Miyawaki5, Toru Sakura6, Yukiyasu Ozawa7, Noriko Usui8, Heiwa Kanamori9, Yoshikazu Ito10, Kiyotoshi Imai11, Youko Suehiro12, Shinichi Kobayashi13, Kunio Kitamura14, Emiko Sakaida15, Makoto Onizuka16, Akihiro Takeshita17, Fumihiro Ishida18, Hitoshi Suzushima19, Kenichi Ishizawa20, Tomoki Naoe21, Itaru Matsumura22, Yasushi Miyazaki23, Seishi Ogawa24, Hitoshi Kiyoi25.
Abstract
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.Entities:
Keywords: Acute myeloid leukemia; European LeukemiaNet; Genetics; Prognosis; Risk stratification
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Year: 2018 PMID: 29360622 DOI: 10.1016/j.leukres.2018.01.008
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156