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Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome.
Patnaik, M M; Wassie, E A; Padron, E; Onida, F; Itzykson, R; Lasho, T L; Kosmider, O; Finke, C M; Hanson, C A; Ketterling, R P; Komrokji, R; Tefferi, A; Solary, E.
Afiliación
  • Patnaik MM; Department of Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Wassie EA; Department of Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Padron E; Malignant Hematology and Immunology Program, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
  • Onida F; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Itzykson R; Hematology département, Hospital Saint-Louis, Paris, France.
  • Lasho TL; Department of Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Kosmider O; 1] Université Paris Descartes, Paris, France [2] Institut Cochin, Paris, France.
  • Finke CM; Department of Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Hanson CA; Division of Hematopathology, Mayo Clinic, Rochester, MN, USA.
  • Ketterling RP; Division of Cytogenetics, Mayo Clinic, Rochester, MN, USA.
  • Komrokji R; Malignant Hematology and Immunology Program, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
  • Tefferi A; Department of Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Solary E; 1] Institut Gustave Roussy, Paris, France [2] INSERM U1009, Institut Gustave Roussy, Paris, France.
Blood Cancer J ; 5: e270, 2015 Jan 02.
Article en En | MEDLINE | ID: mdl-25555161
ABSTRACT
In patients with chronic myelomonocytic leukemia (CMML), age>65 years is an adverse prognostic factor. Our objective in the current study was to examine risk factors for survival and treatment outcome in 261 'young' adults with CMML, as defined by age ⩽65 years. In multivariable analysis, lower HB (P=0.01), higher circulating blast % (P=0.002), ASXL1 (P=0.0007) and SRSF2 mutations (P=0.008) and Mayo-French cytogenetic stratification (P=0.04) negatively impacted survival. Similarly, leukemia-free survival was independently affected by higher circulating blast % (P<0.0001), higher bone marrow blast % (P=0.0007) and the presence of circulating immature myeloid cells (P=0.0002). Seventy-five (29%) patients received hypomethylating agents (HMA), with the median number of cycles being 5, and the median duration of therapy being 5 months. The over-all response rate was 40% for azacitidine and 30% for decitabine. Fifty-three (24%) patients underwent an allogeneic hematopoietic stem cell transplant (AHSCT), with a response rate of 56% and a non-relapse mortality of 19%. Survival in young adults with CMML, although higher than in older patients, is poor and even worse in the presence of ASXL1 and SRSF2 mutations. Treatment outcome was more impressive with AHSCT than with HMA and neither was influenced by ASXL1/SRSF2 mutations or karyotype.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Pronóstico / Ribonucleoproteínas / Proteínas Nucleares / Leucemia Mielomonocítica Crónica Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Blood Cancer J Año: 2015 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Pronóstico / Ribonucleoproteínas / Proteínas Nucleares / Leucemia Mielomonocítica Crónica Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Blood Cancer J Año: 2015 Tipo del documento: Article