Advances in Clinical and Experimental Medicine
2019, vol. 28, nr 2, February, p. 271–276
doi: 10.17219/acem/81610
Publication type: review
Language: English
Download citation:
The new perspectives of targeted therapy in acute myeloid leukemia
1 Department and Clinic of Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Poland
Abstract
Acute myeloid leukemia (AML) is a heterogeneous disease and the results of previous treatment with cytotoxic drugs have not been satisfactory. This situation has prompted investigations into novel approaches. The breakthrough in therapy brought by all-trans retinoic acid (ATRA) in acute promyelocytic leukemia (APL) and tyrosine kinase inhibitors in neoplasms with the Philadelphia chromosome has encouraged the search for other effective targeted therapies. Among the tested substances are higher molecular mass drugs such as antibodies and various small molecules: kinase inhibitors, cell pathway inhibitors and epigenetic modulators. So far, the U.S. Food and Drug Administration (FDA) has approved the antibody-drug conjugate gemtuzumab ozogamycin (GO), the tyrosine kinase inhibitor midostaurin and the IDH2 inhibitor enasidenib. These studies have led to a better understanding of the mechanisms of leukemogenesis and may soon allow for differentiating treatments depending on baseline mutational complements. Some innovative drugs described in this article have strong therapeutic potential, but there is still a long way to go before actual success in targeted treatment.
Key words
immunotherapy, target therapy, acute myeloid leukemia
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