J 2018

Reproducible diagnosis of chronic lymphocytic leukemia by flow cytometry: An European Research Initiative on CLL (ERIC) & European Society for Clinical Cell Analysis (ESCCA) Harmonisation project

RAWSTRON, A.C.; K.A. KREUZER; A. SOOSAPILLA; M. SPACEK; Olga STEHLÍKOVÁ et al.

Základní údaje

Originální název

Reproducible diagnosis of chronic lymphocytic leukemia by flow cytometry: An European Research Initiative on CLL (ERIC) & European Society for Clinical Cell Analysis (ESCCA) Harmonisation project

Autoři

RAWSTRON, A.C.; K.A. KREUZER; A. SOOSAPILLA; M. SPACEK; Olga STEHLÍKOVÁ; P. GAMBELL; N. MCIVER-BROWN; N. VILLAMOR; K. PSARRA; M. ARROZ; R. MILANI; J. DE LA SERNA; M.T. CEDENA; O. JAKSIC; J. NOMDEDEU; C. MORENO; G.M. RIGOLIN; A. CUNEO; P. JOHANSEN; H.E. JOHNSEN; R. ROSENQUIST; C.U. NIEMANN; W. KERN; D. WESTERMAN; M. TRNENY; S. MULLIGAN; Michael DOUBEK; Šárka POSPÍŠILOVÁ; P. HILLMEN; D. OSCIER; M. HALLEK; P. GHIA a E. MONTSERRAT

Vydání

Cytometry Part B ( Clinical cytometry), HOBOKEN, WILEY-BLACKWELL, 2018, 1552-4949

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30109 Pathology

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 2.938

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14740/18:00102937

Organizační jednotka

Středoevropský technologický institut

EID Scopus

Klíčová slova anglicky

chronic lymphocytic leukemia; flow cytometry; diagnosis

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 13. 3. 2019 16:49, Mgr. Pavla Foltynová, Ph.D.

Anotace

V originále

The diagnostic criteria for CLL rely on morphology and immunophenotype. Current approaches have limitations affecting reproducibility and there is no consensus on the role of new markers. The aim of this project was to identify reproducible criteria and consensus on markers recommended for the diagnosis of CLL. ERIC/ESCCA members classified 14 of 35 potential markers as required or recommended for CLL diagnosis, consensus being defined as >75% and >50% agreement, respectively. An approach to validate required markers using normal peripheral blood was developed. Responses were received from 150 participants with a diagnostic workload >20 CLL cases per week in 23/150 (15%), 5-20 in 82/150 (55%), and <5 cases per week in 45/150 (30%). The consensus for required diagnostic markers included: CD19, CD5, CD20, CD23, Kappa, and Lambda. Recommended markers potentially useful for differential diagnosis were: CD43, CD79b, CD81, CD200, CD10, and ROR1. Reproducible criteria for component reagents were assessed retrospectively in 14,643 cases from 13 different centers and showed >97% concordance with current approaches. A pilot study to validate staining quality was completed in 11 centers. Markers considered as required for the diagnosis of CLL by the participants in this study (CD19, CD5, CD20, CD23, Kappa, and Lambda) are consistent with current diagnostic criteria and practice. Importantly, a reproducible approach to validate and apply these markers in individual laboratories has been identified. Finally, a consensus recommended panel of markers to refine diagnosis in borderline cases (CD43, CD79b, CD81, CD200, CD10, and ROR1) has been defined and will be prospectively evaluated. (c) 2017 International Clinical Cytometry Society

Návaznosti

LQ1601, projekt VaV
Název: CEITEC 2020 (Akronym: CEITEC2020)
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, CEITEC 2020
NV15-30015A, projekt VaV
Název: Analýza klonální heterogenity chronické lymfocytární leukemie pomoci sekvenování nové generace genu pro B-buněčný receptor. Národní studie.