Peripheral blood 8 colour flow cytometry monitoring of hairy cell leukaemia allows detection of high-risk patients

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TitrePeripheral blood 8 colour flow cytometry monitoring of hairy cell leukaemia allows detection of high-risk patients
Type de publicationJournal Article
Year of Publication2014
AuteursOttou FGarnache, Chandesris M-O, Lhermitte L, Callens C, Beldjord K, Garrido M, Bedin A-S, Brouzes C, Villemant S, Rubio M-T, Belanger C, Suarez F, Deau B, Lefrere F, Hermine O, Asnafi V, Varet B, Macintyre E
JournalBRITISH JOURNAL OF HAEMATOLOGY
Volume166
Pagination50-59
Date PublishedJUL
Type of ArticleArticle
ISSN0007-1048
Mots-clésblood minimal residual disease, hairy cell leukaemia, multicolour flow cytometry
Résumé

Although purine analogues have significantly improved the outcome of hairy cell leukaemia (HCL) patients, 30-40% relapse, illustrating the need for minimal residual disease (MRD) markers that can aid personalized therapeutic management. Diagnostic samples from 34 HCL patients were used to design an 8-colour flow cytometry (8-FC) tube for blood MRD (B/RD) analysis (188 samples) which was compared to quantitative IGH polymerase chain reaction (Q-PCR) on 83 samples and to qualitative consensus IGH PCR clonality analysis on 165 samples. Despite heterogeneous HCL phenotypes at diagnosis, discrimination from normal B lymphocytes was possible in all cases using a single 8-FC tube, with a robust sensitivity of detection of 10(-4), comparable to Q-PCR at this level, but preferable in terms of informativeness, simplicity and cost. B/RD assessment of 15 patients achieving haematological complete remission after purine analogues was predictive of a clinically significant relapse risk: with a median follow-up of 95 months; only one of the nine patients with reproducible 8-FC B/RD levels below 10(-4) (B/RDneg) relapsed, compared to 5/6 in the B/RDpos group (P = 0-003). These data demonstrate the clinical interest of a robust 8-FC HCL B/RD strategy that could become a surrogate biomarker for therapeutic stratification and new drug assessment, which should be evaluated prospectively.

DOI10.1111/bjh.12839