Онкогематология (Dec 2015)

Flow cytometric minimal residual disease monitoring in children with acute lymphoblastic leukemia treated by regimens with reduced intensity

  • A. M. Popov,
  • Y. Yu. Verzhbitskaya,
  • G. A. Tsaur,
  • A. G. Solodovnikov,
  • O. R. Arakaev,
  • O. V. Streneva,
  • O. P Khlebnikova,
  • E. V. Shorikov,
  • L. I. Saveliev,
  • S. N. Lagoyko,
  • Yu. V. Rumyantseva,
  • A. I. Karachunskiy,
  • L. G. Fechina

DOI
https://doi.org/10.17650/1818-8346-2015-10-4-44-55
Journal volume & issue
Vol. 10, no. 4
pp. 44 – 55

Abstract

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191 consecutive unselected children with acute lymphoblastic leukemia aged from 1 to 16 years were enrolled in the study. Bone marrow samples were obtained at the time of initial diagnostics as well as at days 15 (n = 188), 36 (n = 191), and 85 (n = 187) of remission induction. Minimal residual disease (MRD) was assessed by 6–10-color flow cytometry. Flow cytometry data at day 15 allowed distinguishing three patients groups with significantly different outcome (p ˂ 0.0001): 35.64 % patients with MRD < 0.1 % represented 5-year event-free survival (EFS) of 100 %; 48.40 % cases with 0.1 % ≤ MRD< 10 % had EFS 84.6 ± 4.2 %; 15.96 % patients with very high MRD (≥ 10 %) belonged to group with poor outcome (EFS 56.7 ± 9.0 %). At the end of remission induction (day 36) 36 children (18.85 %) with MRD higher than 0.1 % had significantly worse outcome compared to remaining ones (EFS 49.4 ± 9.0 and 93.5 ± 2.1 % respectively; p ˂ 0.0001). From a clinical standpoint it is relevant to evaluate both low-risk and high-risk criteria. Multivariate analysis showed that day 15 MRD data is better for low-risk patients definition while end-induction MRD is the strongest unfavorable prognostic factor.

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