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Validation and refinement of the 2022 European LeukemiaNet genetic risk stratification of acute myeloid leukemia.
Rausch, Christian; Rothenberg-Thurley, Maja; Dufour, Annika; Schneider, Stephanie; Gittinger, Hanna; Sauerland, Cristina; Görlich, Dennis; Krug, Utz; Berdel, Wolfgang E; Woermann, Bernhard J; Hiddemann, Wolfgang; Braess, Jan; von Bergwelt-Baildon, Michael; Spiekermann, Karsten; Herold, Tobias; Metzeler, Klaus H.
Afiliação
  • Rausch C; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • Rothenberg-Thurley M; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • Dufour A; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • Schneider S; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • Gittinger H; Institute of Human Genetics, University Hospital, LMU Munich, Munich, Germany.
  • Sauerland C; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • Görlich D; Institute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
  • Krug U; Institute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
  • Berdel WE; Department of Medicine 3, Klinikum Leverkusen, Leverkusen, Germany.
  • Woermann BJ; Department of Medicine A, University Hospital Münster, Münster, Germany.
  • Hiddemann W; German Society of Hematology and Oncology, Berlin, Germany.
  • Braess J; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
  • von Bergwelt-Baildon M; German Cancer Consortium (DKTK), Partner Site Munich, Munich, Germany.
  • Spiekermann K; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Herold T; Department of Oncology and Hematology, Hospital Barmherzige Brüder, Regensburg, Germany.
  • Metzeler KH; Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
Leukemia ; 37(6): 1234-1244, 2023 06.
Article em En | MEDLINE | ID: mdl-37041198
ABSTRACT
The revised 2022 European LeukemiaNet (ELN) AML risk stratification system requires validation in large, homogeneously treated cohorts. We studied 1118 newly diagnosed AML patients (median age, 58 years; range, 18-86 years) who received cytarabine-based induction chemotherapy between 1999 and 2012 and compared ELN-2022 to the previous ELN-2017 risk classification. Key findings were validated in a cohort of 1160 mostly younger patients. ELN-2022 reclassified 15% of patients, 3% into more favorable, and 12% into more adverse risk groups. This was mainly driven by patients reclassified from intermediate- to adverse-risk based on additional myelodysplasia-related mutations being included as adverse-risk markers. These patients (n = 79) had significantly better outcomes than patients with other adverse-risk genotypes (5-year OS, 26% vs. 12%) and resembled the remaining intermediate-risk group. Overall, time-dependent ROC curves and Harrel's C-index controlling for age, sex, and AML type (de novo vs. sAML/tAML) show slightly worse prognostic discrimination of ELN-2022 compared to ELN-2017 for OS. Further refinement of ELN-2022 without including additional genetic markers is possible, in particular by recognizing TP53-mutated patients with complex karyotypes as "very adverse". In summary, the ELN-2022 risk classification identifies a larger group of adverse-risk patients at the cost of slightly reduced prognostic accuracy compared to ELN-2017.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Idioma: En Ano de publicação: 2023 Tipo de documento: Article