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Results in pediatric T-ALL patients treated in trial AIEOP-BFM ALL 2009: Prognostic factors in the context of modern risk-adapted therapy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F25%3A10501446" target="_blank" >RIV/00064203:_____/25:10501446 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11130/25:10501446

  • Result on the web

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

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/hem3.70206" target="_blank" >10.1002/hem3.70206</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Results in pediatric T-ALL patients treated in trial AIEOP-BFM ALL 2009: Prognostic factors in the context of modern risk-adapted therapy

  • Original language description

    To improve the outcome of pediatric T-cell acute lymphoblastic leukemia (T-ALL) patients, the AIEOP-BFM ALL 2009 trial modified T-ALL stratification and treatment based on AIEOP-BFM ALL 2000 and other pediatric ALL groups&apos; results. This report aims to describe the outcome of T-ALL patients in trial AIEOP-BFM ALL 2009 and evaluate prognostic features defined within the end of induction (EOI) therapy, for future protocols stratification and interventions. From 06/2010 to 02/2017, 872 T-ALL patients, aged 1-17, were enrolled. High risk (HR) criteria were prednisone poor response (PPR), Day 15 flow cytometry minimal residual disease (MRD) &gt;= 10%, no complete remission at EOI, or polymerase chain reaction (PCR)-MRD &gt;= 5 x 10(-4) at end of consolidation (EOC). Three Cox regression models on event-free survival (EFS) evaluated prognostic factors. Overall, 5-year EFS and survival were 79.9% +- 1.4% and 84.9% +- 1.2% with cumulative incidence of relapse (CIR) and death of 13.0% +- 1.2% and 5.9% +- 0.8%. Five-year EFS and CIR were 86.8% +- 1.6% and 8.7% +- 1.3% in non-HR patients (n = 470); 71.9% +- 2.3% and 18.0% +- 1.9% in HR patients (n = 402). High PCR-MRD levels at EOI and EOC were prognostic in all models, with EOC-MRD &gt;= 5 x 10(-3) related to a hazard ratio of 6.22 (P &lt; 0.001). When a model considered factors identified at EOI only, central nervous system (CNS)3 (hazard ratio = 2.3, P &lt; 0.001), PPR (hazard ratio = 1.74, P = 0.02), and high EOI-MRD (hazard ratio 4.71 for &gt;=5 x 10(-2) vs. negative, P &lt; 0.001) significantly impacted EFS. Results of T-ALL patients in AIEOP-BFM ALL 2009 were favorable. While EOC-MRD remained the strongest prognostic predictor, PPR, CNS3 disease, and EOI-MRD showed relevant prognostic value, with CNS3 and EOI-MRD &gt;= 5 x 10(-2) being candidate criteria for early stratification and intervention modifications.

  • 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

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    HemaSphere

  • ISSN

    2572-9241

  • e-ISSN

    2572-9241

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    e70206

  • UT code for WoS article

    001565324400001

  • EID of the result in the Scopus database

    2-s2.0-105014736424