| Literature DB >> 33399480 |
Jan M Middeke1, Raphael Teipel1, Christoph Röllig1, Sebastian Stasik1, Armin Zebisch2,3, Heinz Sill2, Michael Kramer1, Sebastian Scholl4, Andreas Hochhaus4, Edgar Jost5, Tim H Brümmendorf5, Ralph Naumann6, Björn Steffen7, Hubert Serve7, Heidi Altmann1, Volker Kunzmann8, Hermann Einsele8, Stefani Parmentier9, Markus Schaich9, Andreas Burchert10, Andreas Neubauer10, Christoph Schliemann11, Wolfgang E Berdel11, Katja Sockel1, Friedrich Stölzel1, Uwe Platzbecker12, Gerhard Ehninger1, Martin Bornhäuser1, Johannes Schetelig1,13, Christian Thiede1.
Abstract
We performed a registry-based analysis of 311 AML patients treated with decitabine in a standard of care setting to assess response and survival data with a distinct focus on the impact of the TP53 mutation status. Median age was 73 years. 172 patients received decitabine first-line and 139 in r/r disease. The ORR (whole cohort) was 30% with a median overall survival of 4.7 months. First-line patients achieved better responses than r/r-patients (ORR: 38% vs. 21%) resulting in a median OS of 5.8 months vs. 3.9 months. NGS based mutation analysis was performed in 180 patients. 20 patients (11%) harbored a TP53 mutation. Response rates and survival did not differ significantly between TP53 mutated patients and wild-type patients. This analysis of a large cohort of AML patients provides response rates and OS data after decitabine treatment. Interestingly, outcome was not negatively influenced by a TP53 mutation.Entities:
Keywords: AML; TP53mutation; decitabine
Mesh:
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Year: 2021 PMID: 33399480 DOI: 10.1080/10428194.2020.1864354
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022