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Lisaftoclax + daunorubicin + cytarabine (LDA) is an investigational combination therapy being studied for the treatment of newly diagnosed intermediate- and high-risk acute myeloid leukemia (AML) in young adults. The regimen combines lisaftoclax (APG-2575), a selective, orally administered small-molecule BCL-2 inhibitor, with the standard chemotherapy agents daunorubicin and cytarabine. Lisaftoclax works by blocking the anti-apoptotic BCL-2 protein, thereby sensitizing malignant cells to the cytotoxic effects of chemotherapy and promoting programmed cell death (apoptosis). This combination is designed to enhance the efficacy of the traditional '7+3' induction backbone in patients eligible for intensive chemotherapy.
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