TY - JOUR
T1 - High white blood cell count at diagnosis of childhood acute lymphoblastic leukaemia
T2 - biological background and prognostic impact. Results from the NOPHO ALL-92 and ALL-2000 studies
AU - Vaitkeviciene, Goda
AU - Forestier, Erik
AU - Hellebostad, Marit
AU - Heyman, Mats
AU - Jonsson, Olafur G
AU - Lähteenmäki, Päivi M
AU - Rosthoej, Susanne
AU - Söderhäll, Stefan
AU - Schmiegelow, Kjeld
AU - Nordic Society of Paediatric Haematology and Oncology (NOPHO)
AU - Vaitkevičienė, Goda
N1 - © 2010 John Wiley & Sons A/S.
PY - 2011
Y1 - 2011
N2 - 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(10 y)) survival and overall (pOS(10 y)) 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 × 10(9) /L, P <0.001), but not for T-lineage (T-ALL) (median WBC: 127.8 vs. 113.0 vs. 86.8 × 10(9) /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) )
AB - 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(10 y)) survival and overall (pOS(10 y)) 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 × 10(9) /L, P <0.001), but not for T-lineage (T-ALL) (median WBC: 127.8 vs. 113.0 vs. 86.8 × 10(9) /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) )
U2 - 10.1111/j.1600-0609.2010.01522.x
DO - 10.1111/j.1600-0609.2010.01522.x
M3 - Journal article
SN - 0902-4441
VL - 86
SP - 38
EP - 46
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 1
ER -