Velocity of early BCR-ABL transcript elimination as an optimized predictor of outcome in chronic myeloid leukemia (CML) patients in chronic phase on treatment with imatinib.

Unlabelled: Early assessment of response at 3 months of tyrosine kinase inhibitor treatment has become an important tool to predict favorable outcome. We sought to investigate the impact of relative changes of BCR-ABL transcript levels within the initial 3 months of therapy. In order to achieve accu...

Descripción completa

Detalles Bibliográficos
Publicado en:Leukemia (08876924) Vol. 28; no. 10; pp. 1988 - 1993
Autores principales: Hanfstein, B, Shlyakhto, V, Lauseker, M, Hehlmann, R, Saussele, S, Dietz, C, Erben, P, Fabarius, A, Proetel, U, Schnittger, S, Krause, S W, Schubert, J, Einsele, H, Hänel, M, Dengler, J, Falge, C, Kanz, L, Neubauer, A, Kneba, M, Stegelmann, F
Formato: research randomized controlled trial Journal Article
Publicado: Springer Nature Oct2014
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=103849605&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 103849605
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        08876924
        DZG
      jtl: Leukemia (08876924)
      issn: 08876924
      maglogo: Y
    pubinfo:
      dt: Oct2014
      vid: 28
      iid: 10
      pid: 2579
      pub: Springer Nature
      place: Dordrecht, <Blank>
    artinfo:
      ui:
        103849605
        NLM24798484
        2012761099
        10.1038/leu.2014.153
        NLM24798484
        103849605
      ppf: 1988
      ppct: 5
      formats:
      tig:
        atl: Velocity of early BCR-ABL transcript elimination as an optimized predictor of outcome in chronic myeloid leukemia (CML) patients in chronic phase on treatment with imatinib.
      aug:
        au:
          Hanfstein, B
          Shlyakhto, V
          Lauseker, M
          Hehlmann, R
          Saussele, S
          Dietz, C
          Erben, P
          Fabarius, A
          Proetel, U
          Schnittger, S
          Krause, S W
          Schubert, J
          Einsele, H
          Hänel, M
          Dengler, J
          Falge, C
          Kanz, L
          Neubauer, A
          Kneba, M
          Stegelmann, F
      sug:
        subj:
          Antineoplastic Agents Therapeutic Use
          Benzamides Therapeutic Use
          Proteins Metabolism
          Leukemia, Myeloid, Chronic Drug Therapy
          Leukemia, Myeloid, Chronic
          Heterocyclic Compounds Therapeutic Use
          Adolescence
          Adult
          Aged
          Aged, 80 and Over
          Prognosis
          Female
          Glycoside Hydrolases Metabolism
          Human
          Leukemia, Myeloid, Chronic Metabolism
          Male
          Middle Age
          Cox Proportional Hazards Model
          Relative Risk
          Sensitivity and Specificity
          Treatment Outcomes
          Young Adult
          Adolescent: 13-18 years
          Adult: 19-44 years
          Aged: 65+ years
          Aged, 80 & over
          Middle Aged: 45-64 years
          Female
          Male
      ab: Unlabelled: Early assessment of response at 3 months of tyrosine kinase inhibitor treatment has become an important tool to predict favorable outcome. We sought to investigate the impact of relative changes of BCR-ABL transcript levels within the initial 3 months of therapy. In order to achieve accurate data for high BCR-ABL levels at diagnosis, beta glucuronidase (GUS) was used as a reference gene. Within the German CML-Study IV, samples of 408 imatinib-treated patients were available in a single laboratory for both times, diagnosis and 3 months on treatment. In total, 301 of these were treatment-naïve at sample collection.Results: (i) with regard to absolute transcript levels at diagnosis, no predictive cutoff could be identified; (ii) at 3 months, an individual reduction of BCR-ABL transcripts to the 0.35-fold of baseline level (0.46-log reduction, that is, roughly half-log) separated best (high risk: 16% of patients, 5-year overall survival (OS) 83% vs 98%, hazard ratio (HR) 6.3, P=0.001); (iii) at 3 months, a 6% BCR-ABL(IS) cutoff derived from BCR-ABL/GUS yielded a good and sensitive discrimination (high risk: 22% of patients, 5-year OS 85% vs 98%, HR 6.1, P=0.002). Patients at risk of disease progression can be identified precisely by the lack of a half-log reduction of BCR-ABL transcripts at 3 months.
      pubtype: Academic Journal
      doctype:
        research
        randomized controlled trial
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N