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- W4285159197 endingPage "816" @default.
- W4285159197 startingPage "798" @default.
- W4285159197 abstract "FLT3 mutations are one of the most common genetic aberrations found in nearly 30% of acute myeloid leukemias (AML). The mutations are associated with poor prognosis despite advances in the understanding of the biological mechanisms of AML. Numerous small molecule FLT3 inhibitors have been developed in an effort to combat AML. Even with the development of these inhibitors, the five-year overall survival for newly diagnosed AML is less than 30%. In 2017, midostaurin received FDA approval to treat AML, which was the first approved FLT3 inhibitor in the U.S. and Europe. Following, gilteritinib received FDA approval in 2018 and in 2019 quizartinib received approval in Japan. This review parallels these clinical success stories along with other pre-clinical and clinical investigations of FLT3 inhibitors." @default.
- W4285159197 created "2022-07-14" @default.
- W4285159197 creator A5039675686 @default.
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- W4285159197 creator A5077242280 @default.
- W4285159197 creator A5080382070 @default.
- W4285159197 creator A5086385428 @default.
- W4285159197 date "2022-01-01" @default.
- W4285159197 modified "2023-10-16" @default.
- W4285159197 title "FLT3 inhibitors for acute myeloid leukemia: successes, defeats, and emerging paradigms" @default.
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