Maria Teresa Voso, MD, University Tor Vergata, Rome, Italy, presents the findings from the final analysis of the APOLLO trial (NCT0268840), a Phase III randomized study that compared arsenic trioxide (ATO) plus all-trans retinoic acid (ATRA) to the classical AIDA regimen (ATRA + idarubicin) in patients with high-risk acute promyelocytic leukemia (APL). Dr Voso highlights that the trial met its primary endpoint, demonstrating superior event-free survival and fewer hematological side effects in the experimental arm, with updated follow-up confirming superiority and a significantly lower probability of relapse. This interview took place at the 31st Congress of the European Hematology Association (EHA) in Stockholm, Sweden.
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