Leukemic blasts are present at low levels in spinal fluid in one-third of childhood acute lymphoblastic leukemia cases

Research output: Contribution to journalJournal articleResearchpeer-review

  • Mette Levinsen
  • Hanne V Marquart
  • Line Groth-Pedersen
  • Jonas Abrahamsson
  • Birgitte Klug Albertsen
  • Mette K Andersen
  • Thomas L Frandsen
  • Arja Harila-Saari
  • Cornelis J H Pronk
  • Aina Ulvmoen
  • Goda Vaitkevičienė
  • Päivi M Lähteenmäki
  • Riitta Niinimäki
  • Mervi Taskinen
  • Maria Jeppesen
  • Schmiegelow, K.
  • Nordic Society of Pediatric Hematology and Oncology (NOPHO)

BACKGROUND: Central nervous system (CNS) involvement is associated with relapse in childhood acute lymphoblastic leukemia (ALL) and is a diagnostic challenge.

PROCEDURE: In a Nordic/Baltic prospective study, we assessed centralized flow cytometry (FCM) of locally fixed cerebrospinal fluid (CSF) samples versus local conventional cytospin-based cytology (CC) for detecting leukemic cells and evaluating kinetics of elimination of leukemic cells in CSF.

RESULTS: Among 300 patients with newly diagnosed ALL, 87 (29%) had CSF involvement by FCM, while CC was positive in 30 (10%) of 299 patients with available CC data (P < 0.001). Patients with FCM+/CC+ had higher CSF leukemic blast counts compared to patients positive by FCM only (medians: 0.10 vs. 0.017 leukemic blasts/μl, P = 0.006). Patients positive by FCM had higher white blood cell counts in peripheral blood than patients negative by FCM (medians: 45 × 10(9) /l vs. 10 × 10(9) /l, P < 0.001), were younger (medians: 3 years vs. 4 years, P = 0.03), and more frequently had T-cell ALL (18/87 vs. 16/213, P = 0.001). At treatment day 15, five of 52 patients (10%) who had CSF positive by FCM at diagnosis remained so despite at least two doses of weekly intrathecal chemotherapy.

CONCLUSIONS: Longer follow-up is needed to clarify whether FCM positivity has prognostic significance and is an indicator for intensified CNS-directed therapy.

Original languageEnglish
JournalPediatric Blood & Cancer
Volume63
Issue number11
Pages (from-to)1935-42
Number of pages8
ISSN1545-5009
DOIs
Publication statusPublished - Nov 2016

    Research areas

  • Journal Article

ID: 177483987