Effective Response Metric: a novel tool to predict relapse in childhood acute lymphoblastic leukaemia using time-series gene expression profiling
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu klinické zkoušky, časopisecké články, multicentrická studie, práce podpořená grantem
PubMed
29808917
DOI
10.1111/bjh.15252
Knihovny.cz E-zdroje
- Klíčová slova
- acute lymphoblastic leukaemia, effective response metric, gene expression, relapse, time-series,
- MeSH
- akutní lymfatická leukemie krev genetika mortalita MeSH
- dítě MeSH
- hodnocení rizik MeSH
- kojenec MeSH
- lidé MeSH
- míra přežití MeSH
- prediktivní hodnota testů MeSH
- předškolní dítě MeSH
- přežití bez známek nemoci MeSH
- recidiva MeSH
- regulace genové exprese u leukemie * MeSH
- stanovení celkové genové exprese * MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
Accurate risk assignment in childhood acute lymphoblastic leukaemia is essential to avoid under- or over-treatment. We hypothesized that time-series gene expression profiles (GEPs) of bone marrow samples during remission-induction therapy can measure the response and be used for relapse prediction. We computed the time-series changes from diagnosis to Day 8 of remission-induction, termed Effective Response Metric (ERM-D8) and tested its ability to predict relapse against contemporary risk assignment methods, including National Cancer Institutes (NCI) criteria, genetics and minimal residual disease (MRD). ERM-D8 was trained on a set of 131 patients and validated on an independent set of 79 patients. In the independent blinded test set, unfavourable ERM-D8 patients had >3-fold increased risk of relapse compared to favourable ERM-D8 (5-year cumulative incidence of relapse 38·1% vs. 10·6%; P = 2·5 × 10-3 ). ERM-D8 remained predictive of relapse [P = 0·05; Hazard ratio 4·09, 95% confidence interval (CI) 1·03-16·23] after adjusting for NCI criteria, genetics, Day 8 peripheral response and Day 33 MRD. ERM-D8 improved risk stratification in favourable genetics subgroups (P = 0·01) and Day 33 MRD positive patients (P = 1·7 × 10-3 ). We conclude that our novel metric - ERM-D8 - based on time-series GEP after 8 days of remission-induction therapy can independently predict relapse even after adjusting for NCI risk, genetics, Day 8 peripheral blood response and MRD.
2nd Faculty of Medicine Charles University Prague Czech Republic
Cancer Science Institute of Singapore National University of Singapore Singapore
Department of Paediatrics KK Women's and Children's Hospital Singapore
School of Computing National University of Singapore Singapore
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