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WT1 Expression in Peripheral Blood at Diagnosis and During the Course of Early Consolidation Treatment Correlates With Survival in Patients With Intermediate and Poor-Risk Acute Myeloid Leukemia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F20%3A10418633" target="_blank" >RIV/00216208:11110/20:10418633 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023736:_____/20:00013103

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=2r7cKlZjBh" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=2r7cKlZjBh</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.clml.2020.07.014" target="_blank" >10.1016/j.clml.2020.07.014</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    WT1 Expression in Peripheral Blood at Diagnosis and During the Course of Early Consolidation Treatment Correlates With Survival in Patients With Intermediate and Poor-Risk Acute Myeloid Leukemia

  • Original language description

    Dynamics of WT1 expression during the course of chemotherapy was tested in 106 cases of intermediate and high-risk acute myeloid leukemia in peripheral blood. High WT1 expression after 2 cycles of chemotherapy was a significant prognostic factor for overall and event-free survival in the whole cohort, as well as in patients treated without allogeneic stem cell transplantation. Background: Up to 55% of non-APL acute myeloid leukemias (AML) lack a molecular target suitable for standardized disease monitoring. We aimed to evaluate the prognostic significance of WT1 gene expression at early stages of intensive treatment. Patients and Methods: A total of 10(6) consecutive patients with intermediate and high-risk AML who had WT1 expression at diagnosis &gt;500 copies/10(4) ABL and who achieved remission after 1 to 2 cycles of induction treatment were analyzed. WT1 expression was measured in peripheral blood using a standardized European LeukemiaNet method. Overexpression was defined as &gt;50 copies/10(4) ABL. The median follow-up was 30 months. Results: Patients with normal versus high WT1 expression after 2 cycles of chemotherapy had overall survival (OS) at 3 years of 66% versus 41% (P=.01); event-free survival (EFS) 45% versus 22% (P=.01). Prognostic significance of WT1 expression after 2 cycles of treatment was maintained in the group of patients treated with chemotherapy alone without hematopoietic stem cell transplantation in first line treatment (OS 70% vs. 36%, P=.02; EFS 35% vs. 0%, P=.03). Significant prognostic factors for EFS on multivariate analysis were the achievement of molecular remission (&lt;50 copies of WT1) at any time during treatment (hazard ratio [HR] 0.47, P=.04) and increased WT1 expression after 2 cycles of chemotherapy (HR 2.0, P=.03). Conclusion: Increased WT1 expression after 2 cycles of chemotherapy is a negative prognostic factor for survival. WT1 remains a valuable molecular marker in AML without any leukemiaspecific mutation, especially if next generation sequencing and/or digital polymerase chain reaction are not routinely available.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Clinical Lymphoma, Myeloma &amp; Leukemia

  • ISSN

    2152-2650

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    "e998"-"e1009"

  • UT code for WoS article

    000593321200009

  • EID of the result in the Scopus database

    2-s2.0-85090066450