The conversation focuses on AML treatments, including arsenic and another frontline approach. Preventing relapses through non-toxic drugs like masitinib is explored. Financial obstacles and customized treatments are discussed. The importance of precise timing for treatments is highlighted. Myelosuppression and new dosing ideas are brought up.
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Clinical trial design’s role in optimizing treatment is mentioned, with examples of challenges in drug approval. The need for data confidence, stepwise treatment, and MRD monitoring are emphasized.
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