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The use of molecularly targeted therapy in acute promyelocytic leukaemia BJCM, Volume 3, Issue 2.
Acute promyelocytic leukaemia (APL) is one of the most common subtypes of acute myeloid leukaemia (AML), accounting for 10–15% of cases. It has been of particular interest as it is the first form of leukaemia for which molecularly targeted therapies, such as all-transretinoic acid (ATRA) and arsenic trioxide (ATO), have been successfully used in clinical practice.1
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