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

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, Kjeld Schmiegelow, Nordic Society of Pediatric Hematology and Oncology (NOPHO)

20 Citationer (Scopus)

Abstract

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 × 109/l vs. 10 × 109/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.

OriginalsprogEngelsk
TidsskriftPediatric Blood & Cancer
Vol/bind63
Udgave nummer11
Sider (fra-til)1935-42
Antal sider8
ISSN1545-5009
DOI
StatusUdgivet - 1 nov. 2016

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