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Residual disease detected by flow cytometry is an independent predictor of survival in childhood acute myeloid leukaemia; results of the NOPHO-AML 2004 study
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2016 (Engelska)Ingår i: British Journal of Haematology, ISSN 0007-1048, E-ISSN 1365-2141, Vol. 174, nr 4, s. 600-609Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Early response after induction is a prognostic factor for disease outcome in childhood acute myeloid leukaemia (AML). Residual disease (RD) detection by multiparameter flow cytometry (MFC) was performed at day 15 and before consolidation therapy in 101 patients enrolled in the Nordic Society of Paediatric Haemato-Oncology AML 2004 study. A multicentre laboratory approach to RD analysis was used. Event-free survival (EFS) and overall survival (OS) was significantly different in patients with and without RD at both time points, using a 0.1% RD cut-off level. RD-negative and -positive patients after first induction showed a 5-year EFS of 65.7% and 22.7%, respectively (P < 0.001) and an OS of 77.6% (P = 0.025) and 51.8%. RD-negative and -positive patients at start of consolidation therapy had a 5-year EFS of 57.7% and 11.7%, respectively (P < 0001) and an OS of 786% and 2811%) (P < 0001). In multivariate analysis only RD was significantly correlated with survival. RD before consolidation therapy was the strongest independent prognostic factor for EFS [hazard ratio (HR): 5.0; 95% confidence interval (CI): 1.9-133] and OS (HR: 7.0; 95% CI: 20-245). In conclusion, RD before consolidation therapy identifies patients at high risk of relapse in need of intensified treatment. In addition, RD detection can be performed in a multicentre setting and can be implemented in future trials.

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2016. Vol. 174, nr 4, s. 600-609
Nyckelord [en]
acute myeloid leukaemia, flow cytometry, minimal residual disease, prognosis, survival
Nationell ämneskategori
Hematologi
Identifikatorer
URN: urn:nbn:se:umu:diva-126752DOI: 10.1111/bjh.14093ISI: 000383774500014PubMedID: 27072379Scopus ID: 2-s2.0-84982993879OAI: oai:DiVA.org:umu-126752DiVA, id: diva2:1038571
Tillgänglig från: 2016-10-19 Skapad: 2016-10-13 Senast uppdaterad: 2023-03-23Bibliografiskt granskad

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Forestier, Erik

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