Session: 613. Acute Myeloid Leukemias: Clinical and Epidemiological: Poster III
Hematology Disease Topics & Pathways:
Acute Myeloid Malignancies, AML, adult, Clinical Practice (Health Services and Quality), elderly, Diseases, Myeloid Malignancies, Study Population, Human
Aim: We investigated whether an integrated clinical fitness (according to SIE/SIES/GITMO criteria) and biological (according to ELN2017 risk stratification) assessment could help re-defining risk-category assignment of our pts, and better discriminating their outcome both in terms of complete remission (CR) probability and Overall Survival (OS).
Methods: This retrospective analysis includes 285 consecutive pts affected with non-promyelocytic AML, diagnosed at our institution between January 2013 and December 2021. SIE, SIES, GITMO operational criteria were retrospectively applied through medical files backtracking. Molecular risk was attributed according to ELN2017 risk stratification.
Results: Median age was 68 years (range 21-93). According to SIE/SIES/GITMO criteria, 142 (49.8%) pts qualified as fit (Fi-P), 57 (20%) as unfit (UF-P) and 86 (30.2%) as frail (Fr-P). According to ELN2017 risk stratification, 46 (16.1%) pts were classified as favorable [ELN2017-FR], 107(37.5%) as intermediate [ELN2017-IR] and 69 (24.2%) as adverse risk [ELN2017-AR]. Overall, 63 (22.2%) pts were not classifiable due to the lack of cytogenetic and/or molecular data. One hundred-32 (46.6%) pts received IC, 65 (22.8%) N-IC, 88 (30.9%) best supportive therapy (BST), with an overall 93% concordance rate between clinical fitness status and treatment received (90.1% of Fi-P received IC, 91.2% of UF-P received N-IC and 97.7% of Fr-P received BST, respectively). Such a concordance improved over the time (from 87.8% in 2013 up to 95.2% in 2021). We then focused on pts receiving active therapy (UF-P submitted to N-IC and Fi-P to IC, respectively). In the UF-P group, 12-months CR incidence was similar between ELN2017-IR (37.5%) and ELN2017-AR (28.6%) pts, with no difference in terms of median OS between the 2 groups (9.1 months vs. 6.6 months for ELN2017-IR and ELN2017-AR pts, respectively) [Figure 1A]. Five ELN2017-FR unfit patients submitted to N-IC were excluded from these analyses because of low numbers. Among Fi-P, 12-months CR incidence was proportional to ELN2017 risk (87.5% vs. 69.7% vs 51.4% for ELN2017-FR, ELN2017-IR, and ELN2017-AR, respectively; p=0.0012), with an OS advantage for ELN2017-FR pts over ELN2017-IR and ELN2017-AR ones (median: not reached for ELN2017-FR vs 12.2 months for ELN2017-IR and ELN2017-AR, respectively; p=0.0051) [Figure 1B].
Conclusions: We confirmed that a real-life therapeutic allocation relying on a comprehensive clinical (SIE/SIES/GITMO criteria) and biological (ELN2017) risk assessment is feasible. Based on their superimposable outcomes, pts unfit for N-IC may be candidate to an active, non-intensive approach, even if belonging to the ELN2017-AR category. For Fi-P belonging to the ELN2017-IR and ELN2017-AR categories, there is room for further improvement of clinical outcome by taking advantage of new strategies (targeted agents, biomarker driven approaches).
Disclosures: Del Principe: Jansenn: Honoraria; Gilead Sciences: Honoraria; Incyte: Honoraria. Voso: Celgene/BMS: Consultancy, Honoraria, Research Funding, Speakers Bureau; Astellas: Speakers Bureau; jazz: Consultancy, Speakers Bureau; Novartis: Research Funding, Speakers Bureau. Venditti: Pfizer: Honoraria, Speakers Bureau; Janssen & Cylag: Honoraria; Astellas: Membership on an entity's Board of Directors or advisory committees; Amgen: Membership on an entity's Board of Directors or advisory committees; astrazeneca: Honoraria; abbvie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Jazz Pharmaceuticals: Honoraria, Research Funding; Medac: Consultancy; Novartis: Membership on an entity's Board of Directors or advisory committees; Servier: Membership on an entity's Board of Directors or advisory committees.
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