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Validation of the 2017 revision of the WHO chronic myelomonocytic leukemia categories.
Loghavi, Sanam; Sui, Dawen; Wei, Peng; Garcia-Manero, Guillermo; Pierce, Sherry; Routbort, Mark J; Jabbour, Elias J; Pemmaraju, Naveen; Kanagal-Shamanna, Rashmi; Gur, H Deniz; Hu, Shimin; Zuo, Zhuang; Medeiros, L Jeffrey; Kantarjian, Hagop M; Khoury, Joseph D.
Afiliación
  • Loghavi S; Department of Hematopathology.
  • Sui D; Department of Biostatistics, and.
  • Wei P; Department of Biostatistics, and.
  • Garcia-Manero G; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Pierce S; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Routbort MJ; Department of Hematopathology.
  • Jabbour EJ; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Pemmaraju N; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Kanagal-Shamanna R; Department of Hematopathology.
  • Gur HD; Department of Hematopathology.
  • Hu S; Department of Hematopathology.
  • Zuo Z; Department of Hematopathology.
  • Medeiros LJ; Department of Hematopathology.
  • Kantarjian HM; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Khoury JD; Department of Hematopathology.
Blood Adv ; 2(15): 1807-1816, 2018 08 14.
Article en En | MEDLINE | ID: mdl-30054307
The 2017 revision of the World Health Organization (WHO) classification includes substantial changes to the subclassification of chronic myelomonocytic leukemia (CMML): (1) a 3-tiered blast-based scheme including a novel "CMML-0" category replacing a 2-tiered system in place since 2001 and (2) 2 CMML subtypes, myelodysplastic (MDS-CMML) and myeloproliferative (MP-CMML), based on a white blood cell count cutoff of 13 × 109/L. The clinical utility of this subclassification scheme, particularly the expansion of blast-based subgroups, has not been validated. In this study, a large single-institution CMML patient cohort (n = 629) was used to assess the prognostic impact of the newly proposed categories. Patients were risk stratified according to the CMML-specific Prognostic Scoring System (CPSS) and the MD Anderson Prognostic Scoring System. MP-CMML patients had significantly shorter overall survival (OS; P < .0001; hazard ratio: 0.53, 95% confidence interval: 0.42-0.65) and median duration to acute myeloid leukemia (AML) transformation (P < .0001; 15.2 vs 22.0 months) compared with MDS-CMML patients. The CMML-0 group included 36.4% patients with higher risk CPSS categories and 11.2% of patients with high-risk cytogenetics. Among treatment-naïve patients (n = 499), there was a marginal difference in OS between the CMML-0 and CMML-12017 subgroups (P = .0552). The WHO 2017 blast-based categories were not associated with AML-free survival. Incorporation of the WHO 2017 blast-based subgroups in a modified CPSS scheme had a neutral effect and did not improve its prognostic strength. Our data support the inclusion of MP-CMML and MDS-CMML subtypes in the WHO 2017 revision. Although of some utility in MP-CMML, the 3-tiered blast-based system is not well supported in this study.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 11_ODS3_cobertura_universal / 2_ODS3 Problema de salud: 11_delivery_arrangements / 2_cobertura_universal Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 11_ODS3_cobertura_universal / 2_ODS3 Problema de salud: 11_delivery_arrangements / 2_cobertura_universal Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2018 Tipo del documento: Article
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