Your browser doesn't support javascript.
loading
Beat-AML 2024 ELN-refined risk stratification for older adults with newly diagnosed AML given lower-intensity therapy.
Hoff, Fieke W; Blum, William G; Huang, Ying; Welkie, Rina Li; Swords, Ronan T; Traer, Elie; Stein, Eytan M; Lin, Tara L; Archer, Kellie J; Patel, Prapti A; Collins, Robert H; Baer, Maria R; Duong, Vu H; Arellano, Martha L; Stock, Wendy; Odenike, Olatoyosi; Redner, Robert L; Kovacsovics, Tibor; Deininger, Michael W; Zeidner, Joshua F; Olin, Rebecca L; Smith, Catherine C; Foran, James M; Schiller, Gary J; Curran, Emily K; Koenig, Kristin L; Heerema, Nyla A; Chen, Timothy; Martycz, Molly; Stefanos, Mona; Marcus, Sonja G; Rosenberg, Leonard; Druker, Brian J; Levine, Ross L; Burd, Amy; Yocum, Ashley O; Borate, Uma M; Mims, Alice S; Byrd, John C; Madanat, Yazan F.
Afiliação
  • Hoff FW; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Blum WG; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA.
  • Huang Y; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Welkie RL; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Swords RT; Division of Hematology/Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
  • Traer E; Division of Hematology/Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
  • Stein EM; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Lin TL; Department of Internal Medicine, The University of Kansas Medical Center, Kansas City, KS.
  • Archer KJ; Division of Biostatistics, The Ohio State University, Columbus, OH.
  • Patel PA; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Collins RH; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
  • Baer MR; Department of Medicine, University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD.
  • Duong VH; Department of Medicine, University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD.
  • Arellano ML; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA.
  • Stock W; Department of Medicine, The University of Chicago, Chicago, IL.
  • Odenike O; Department of Medicine, The University of Chicago, Chicago, IL.
  • Redner RL; Department of Medicine, University of Pittsburgh Medical Center, Hillman Cancer Center, Pittsburgh, PA.
  • Kovacsovics T; Division of Hematology and Hematologic Malignancies, The University of Utah, Salt Lake City, UT.
  • Deininger MW; Department of Internal Medicine, Versiti Blood Research Institute and Medical College of Wisconsin, Milwaukee, WI.
  • Zeidner JF; Division of Hematology, Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Olin RL; Department of Medicine, University of California, San Francisco, San Francisco, CA.
  • Smith CC; Department of Medicine, University of California, San Francisco, San Francisco, CA.
  • Foran JM; Department of Internal Medicine, Mayo Clinic, Jacksonville, FL.
  • Schiller GJ; Department of Medicine, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA.
  • Curran EK; Deparrtment of Internal Medicine, University of Cincinnati, Cincinnati, OH.
  • Koenig KL; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Heerema NA; Department of Pathology, The Ohio State University, Columbus, OH.
  • Chen T; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Martycz M; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Stefanos M; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Marcus SG; Leukemia & Lymphoma Society, Rye Brook, NY.
  • Rosenberg L; Leukemia & Lymphoma Society, Rye Brook, NY.
  • Druker BJ; Division of Hematology/Medical Oncology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
  • Levine RL; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Burd A; Leukemia & Lymphoma Society, Rye Brook, NY.
  • Yocum AO; Leukemia & Lymphoma Society, Rye Brook, NY.
  • Borate UM; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Mims AS; Division of Hematology, Department of Medicine, The Ohio State University, Columbus, OH.
  • Byrd JC; Deparrtment of Internal Medicine, University of Cincinnati, Cincinnati, OH.
  • Madanat YF; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Blood Adv ; 8(20): 5297-5305, 2024 Oct 22.
Article em En | MEDLINE | ID: mdl-39110987
ABSTRACT
ABSTRACT Although the 2022 European LeukemiaNet (ELN) acute myeloid leukemia (AML) risk classification reliably predicts outcomes in younger patients treated with intensive chemotherapy, it is unclear whether it applies to adults ≥60 years treated with lower-intensity treatment (LIT). We aimed to test the prognostic impact of ELN risk in patients with newly diagnosed (ND) AML aged ≥60 years given LIT and to further refine risk stratification for these patients. A total of 595 patients were included 11% had favorable-, 11% intermediate-, and 78% had adverse-risk AML. ELN risk was prognostic for overall survival (OS) (P < .001) but did not stratify favorable- from intermediate-risk (P = .71). Within adverse-risk AML, the impact of additional molecular abnormalities was further evaluated. Multivariable analysis was performed on a training set (n = 316) and identified IDH2 mutation as an independent favorable prognostic factor, and KRAS, MLL2, and TP53 mutations as unfavorable (P < .05). A "mutation score" was calculated for each combination of these mutations, assigning adverse-risk patients to 2 risk groups -1 to 0 points ("Beat-AML intermediate") vs 1+ points ("Beat-AML adverse"). In the final refined risk classification, ELN favorable- and intermediate-risk were combined into a newly defined "Beat-AML favorable-risk" group, in addition to mutation scoring within the ELN adverse-risk group. This approach redefines risk for older patients with ND AML and proposes refined Beat-AML risk groups with improved discrimination for OS (2-year OS, 48% vs 33% vs 11%, respectively; P < .001), providing patients and providers additional information for treatment decision-making.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda Idioma: En Ano de publicação: 2024 Tipo de documento: Article