The Latest News and Updates in Acute Myeloid Leukemia

August 31, 2020
Ryan McDonald
Ryan McDonald

Ryan McDonald, Associate Editorial Director for CURE®, has been with the team since February 2020 and has previously covered medical news across several specialties prior to joining MJH Life Sciences. He is a graduate of Temple University, where he studied journalism and minored in political science and history. He considers himself a craft beer snob and would like to open a brewery in the future. During his spare time, he can be found rooting for all major Philadelphia sports teams. Follow Ryan on Twitter @RMcDonald11 or email him at rmcdonald@curetoday.com.

A roundup of the latest news and updates for patients with acute myeloid leukemia from CURE®.

There have been several updates in the field of acute myeloid leukemia (AML) over the last several weeks. Here, CURE® looks back at some of the latest news and updates affecting patients with that cancer type.

  • “If this data is positive, then (eprenetapopt) will be approved and this will be the standard of care for patients with (TP53-mutant myelodysplastic syndrome),” said Dr. Guillermo Garcia-Manero in an interview with CURE® where he discussed the phase 3 trial currently investigating eprenetapopt plus Vidaza (azacytidine) in this patient population.
  • A health-related quality of life assessment tool, known as Functional Assessment of Cancer Therapy—Leukemia (FACT-Leu), provided a viable and valid outcome measure for patients with AML who are not eligible for intensive therapy.
  • The Food and Drug Administration (FDA) has granted a fast track designation to BST-236 (aspacytarabine) to treat adults aged 75 years or older with AML, or who have comorbidities that prevent the use of intensive induction chemotherapy.
  • Researchers have found the combination of Tibsovo (ivosenidib) plus Venclexta (venetoclax) — with or without Vidaza (azacytidine) – to be safe and effective in the treatment of patients with IDH1-mutated acute myeloid leukemia (AML), according to the results of a recent trial presented at the 2020 ASCO Virtual Scientific Program.
  • The FDA extended the indication of Mylotarg (gemtuzumab ozogamicin) to include the treatment of children aged one month or older with newly diagnosed CD33-positive AML.