A1 Refereed original research article in a scientific journal
High white blood cell count at diagnosis of childhood acute lymphoblastic leukaemia: biological background and prognostic impact. Results from the NOPHO ALL-92 and ALL-2000 studies
Authors: Vaitkeviciene G, Forestier E, Hellebostad M, Heyman M, Jonsson OG, Lahteenmaki PM, Rosthoej S, Soderhall S, Schmiegelow K
Publisher: WILEY-BLACKWELL PUBLISHING, INC
Publication year: 2011
Journal: European Journal of Haematology
Journal name in source: EUROPEAN JOURNAL OF HAEMATOLOGY
Journal acronym: EUR J HAEMATOL
Number in series: 1
Volume: 86
Issue: 1
First page : 38
Last page: 46
Number of pages: 9
ISSN: 0902-4441
DOI: https://doi.org/10.1111/j.1600-0609.2010.01522.x
Abstract
Prognostic impact of peripheral blood white blood cell count (WBC) at the diagnosis of childhood acute lymphoblastic leukaemia (ALL) was evaluated in a population-based consecutive series of 2666 children aged 1-15 treated for ALL between 1992 and 2008 in the five Nordic countries (Denmark, Finland, Iceland, Norway and Sweden). Ten-year event-free (pEFS(10y)) survival and overall (pOS(10y)) survival were 0.75 +/- 0.01 and 0.85 +/- 0.01, respectively. Although treatment intensity was determined by WBC, non-remission and relapsed patients still had significantly higher WBC than those in remission for B-cell precursor (BCP) (median WBC: 24.8 vs. 14.0 vs. 8.3 x 109/L, P < 0.001), but not for T-lineage (T-ALL) (median WBC: 127.8 vs. 113.0 vs. 86.8 x 109/L, P = 0.22). pEFS was inversely related to WBC for BCP (P < 0.001), but not for T-ALL. WBC was not associated with risk of event for BCP or T-ALL for patients with minimal residual disease at the end of induction (MRD(d29)) < 10-3. In contrast, for MRD(d29) >= 10-3 and < 5% leukaemic blasts in bone marrow at day 29, the pEFS(5y) for WBC < 100.0 (N = 152) vs. >= 100.0 (N = 19) was 0.76 vs. 0.50 (P = 0.001). That was the case both for BCP (pEFS(5y) 0.76 vs. 0.58) and for T-ALL (pEFS(5y) 0.71 vs. 0.38). Whether the inferior EFS for the subset of patients with high WBC and slow initial response to treatment reflects rare or overlooked cytogenetic aberrations as well as the factors that determine WBC levels at diagnosis awaits exploration.
Prognostic impact of peripheral blood white blood cell count (WBC) at the diagnosis of childhood acute lymphoblastic leukaemia (ALL) was evaluated in a population-based consecutive series of 2666 children aged 1-15 treated for ALL between 1992 and 2008 in the five Nordic countries (Denmark, Finland, Iceland, Norway and Sweden). Ten-year event-free (pEFS(10y)) survival and overall (pOS(10y)) survival were 0.75 +/- 0.01 and 0.85 +/- 0.01, respectively. Although treatment intensity was determined by WBC, non-remission and relapsed patients still had significantly higher WBC than those in remission for B-cell precursor (BCP) (median WBC: 24.8 vs. 14.0 vs. 8.3 x 109/L, P < 0.001), but not for T-lineage (T-ALL) (median WBC: 127.8 vs. 113.0 vs. 86.8 x 109/L, P = 0.22). pEFS was inversely related to WBC for BCP (P < 0.001), but not for T-ALL. WBC was not associated with risk of event for BCP or T-ALL for patients with minimal residual disease at the end of induction (MRD(d29)) < 10-3. In contrast, for MRD(d29) >= 10-3 and < 5% leukaemic blasts in bone marrow at day 29, the pEFS(5y) for WBC < 100.0 (N = 152) vs. >= 100.0 (N = 19) was 0.76 vs. 0.50 (P = 0.001). That was the case both for BCP (pEFS(5y) 0.76 vs. 0.58) and for T-ALL (pEFS(5y) 0.71 vs. 0.38). Whether the inferior EFS for the subset of patients with high WBC and slow initial response to treatment reflects rare or overlooked cytogenetic aberrations as well as the factors that determine WBC levels at diagnosis awaits exploration.
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