Comparison of the 2022 and 2017 European LeukemiaNet risk classifications in a real-life cohort of the PETHEMA group
Sargas, C.; Ayala, R.; Larráyoz, M.J.; Chillón, M.C.; Rodriguez-Arboli, E.; Bilbao, C.; Prados de la Torre, E.; Martínez-Cuadrón, D.; Rodríguez-Veiga, R.; Boluda, B.; Gil, C.; Bernal, T.; Bergua, J.; Algarra, L.; Tormo, M.; Martínez-Sánchez, P.; Soria, E.; Serrano, J.; Alonso-Dominguez, J.M.; García, R.; Amigo, M.L.; Herrera-Puente, P.; Sayas, M.J.; Lavilla Rubira, Esperanza; Martínez-López, J.; Calasanz, M.J.; García-Sanz, R.; Pérez-Simón, J.A.; Gómez Casares, M.T.; Sánchez-García, J.; Barragán, E.; Montesinos, P.

Identificadores
Identificadores
Visualización ou descarga de ficheiros
Visualización ou descarga de ficheiros
Data de publicación
2023Título da revista
Blood Cancer Journal
Tipo de contido
Artigo
MeSH
Humans | Aged | Nucleophosmin | Leukemia, Myeloid, Acute | Prognosis | Risk Factors | MutationResumo
Next-Generation Sequencing is needed for the accurate genetic risk stratification of acute myeloid leukemia according to European LeukemiaNet (ELN) guidelines. We validated and compared the 2022 ELN risk classification in a real-life cohort of 546 intensively and 379 non-intensively treated patients. Among fit patients, those aged ?65 years old showed worse OS than younger regardless risk classification. Compared with the 2017 classification, 14.5% of fit patients changed the risk with the 2022 classification, increasing the high-risk group from 44.3% to 51.8%. 3.7% and 0.9% FLT3-ITD mutated patients were removed from the favorable and adverse 2017 categories respectively to 2022 intermediate risk group. We suggest that midostaurin therapy could be a predictor for 3 years OS (85.2% with vs. 54.8% without midostaurin, P = 0.04). Forty-seven (8.6%) patients from the 2017 intermediate group were assigned to the 2022 adverse-risk group as they harbored myelodysplasia (MDS)-related mutations. Patients with one MDS-related mutation did not reach median OS, while patients with ?2 mutations had 13.6 months median OS (P = 0.002). Patients with TP53 ± complex karyotype or inv(3) had a dismal prognosis (7.1 months median OS). We validate the prognostic utility of the 2022 ELN classification in a real-life setting providing supportive evidences to improve risk stratification guidelines.
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