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AML risk stratification models utilizing ELN-2017 guidelines and additional prognostic factors: a SWOG report.
Pogosova-Agadjanyan, Era L; Moseley, Anna; Othus, Megan; Appelbaum, Frederick R; Chauncey, Thomas R; Chen, I-Ming L; Erba, Harry P; Godwin, John E; Jenkins, Isaac C; Fang, Min; Huynh, Mike; Kopecky, Kenneth J; List, Alan F; Naru, Jasmine; Radich, Jerald P; Stevens, Emily; Willborg, Brooke E; Willman, Cheryl L; Wood, Brent L; Zhang, Qing; Meshinchi, Soheil; Stirewalt, Derek L.
Afiliação
  • Pogosova-Agadjanyan EL; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Moseley A; SWOG Statistical Center, Fred Hutch, Seattle, WA USA.
  • Othus M; SWOG Statistical Center, Fred Hutch, Seattle, WA USA.
  • Appelbaum FR; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Chauncey TR; Departments of Oncology and Hematology, University of Washington, Seattle, WA USA.
  • Chen IL; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Erba HP; Departments of Oncology and Hematology, University of Washington, Seattle, WA USA.
  • Godwin JE; VA Puget Sound Health Care System, Seattle, WA USA.
  • Jenkins IC; Department of Pathology, University of New Mexico, UNM Comprehensive Cancer Center, Albuquerque, NM USA.
  • Fang M; Duke Cancer Institute, Durham, NC USA.
  • Huynh M; Providence Cancer Center, Earle A. Chiles Research Institute, Portland, OR USA.
  • Kopecky KJ; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • List AF; Clinical Biostatistics, Fred Hutch, Seattle, WA USA.
  • Naru J; Departments of Laboratory Medicine and Pathology, University of Washington, Seattle, WA USA.
  • Radich JP; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Stevens E; SWOG Statistical Center, Fred Hutch, Seattle, WA USA.
  • Willborg BE; Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL USA.
  • Willman CL; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Wood BL; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Zhang Q; Departments of Oncology and Hematology, University of Washington, Seattle, WA USA.
  • Meshinchi S; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
  • Stirewalt DL; Clinical Research Division, Fred Hutch, 1100 Fairview Ave N, D5-112, Seattle, WA 98109 USA.
Biomark Res ; 8: 29, 2020.
Article em En | MEDLINE | ID: mdl-32817791
ABSTRACT

BACKGROUND:

The recently updated European LeukemiaNet risk stratification guidelines combine cytogenetic abnormalities and genetic mutations to provide the means to triage patients with acute myeloid leukemia for optimal therapies. Despite the identification of many prognostic factors, relatively few have made their way into clinical practice.

METHODS:

In order to assess and improve the performance of the European LeukemiaNet guidelines, we developed novel prognostic models using the biomarkers from the guidelines, age, performance status and select transcript biomarkers. The models were developed separately for mononuclear cells and viable leukemic blasts from previously untreated acute myeloid leukemia patients (discovery cohort, N = 185) who received intensive chemotherapy. Models were validated in an independent set of similarly treated patients (validation cohort, N = 166).

RESULTS:

Models using European LeukemiaNet guidelines were significantly associated with clinical outcomes and, therefore, utilized as a baseline for comparisons. Models incorporating age and expression of select transcripts with biomarkers from European LeukemiaNet guidelines demonstrated higher area under the curve and C-statistics but did not show a substantial improvement in performance in the validation cohort. Subset analyses demonstrated that models using only the European LeukemiaNet guidelines were a better fit for younger patients (age < 55) than for older patients. Models integrating age and European LeukemiaNet guidelines visually showed more separation between risk groups in older patients. Models excluding results for ASXL1, CEBPA, RUNX1 and TP53, demonstrated that these mutations provide a limited overall contribution to risk stratification across the entire population, given the low frequency of mutations and confounding risk factors.

CONCLUSIONS:

While European LeukemiaNet guidelines remain a critical tool for triaging patients with acute myeloid leukemia, the findings illustrate the need for additional prognostic factors, including age, to improve risk stratification.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article