Literature DB >> 30267380

Leveraging Hypomethylating Agents for Better MDS Therapy.

Terrence J Bradley1, Justin M Watts2, Ronan T Swords2.   

Abstract

PURPOSE OF REVIEW: Myelodysplastic syndrome (MDS) is a clinically and molecularly heterogeneous disease, which primarily occurs in older adults. Although hypomethylating agents have survival benefit and are the current standard of care, many MDS patients will not garner a response from therapy. For those who do respond, most responses are not durable, and the only hope for a cure is allogeneic stem cell transplant. New therapies to improve outcomes are urgently needed. RECENT
FINDINGS: Clinical trials combining standard hypomethylating agents with novel experimental agents are underway in an effort to improve clinical outcomes in MDS patients. Several of these small molecules have demonstrated the ability to augment the response rates of hypomethylating agents alone, including complete remission rates, in both the front line and refractory settings. Combination approaches utilizing hypomethylating agents and novel-targeted therapies have demonstrated the ability to improve response rates in MDS patients in both the front line and salvage settings, and thus may change the standard of care.

Entities:  

Keywords:  Acute myeloid leukemia; Hypomethylating agents; Immunotherapy; Isocitrate dehydrogenase; Myelodysplastic syndrome; Pevonedistat

Mesh:

Substances:

Year:  2018        PMID: 30267380     DOI: 10.1007/s11899-018-0477-3

Source DB:  PubMed          Journal:  Curr Hematol Malig Rep        ISSN: 1558-8211            Impact factor:   3.952


  32 in total

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9.  Enasidenib in mutant IDH2 relapsed or refractory acute myeloid leukemia.

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10.  Clinical experience with the BCL2-inhibitor venetoclax in combination therapy for relapsed and refractory acute myeloid leukemia and related myeloid malignancies.

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