| Literature DB >> 28187514 |
Michael N Dworzak1, Barbara Buldini2, Giuseppe Gaipa3, Richard Ratei4, Ondrej Hrusak5, Drorit Luria6, Eti Rosenthal7, Jean-Pierre Bourquin8, Mary Sartor9, Angela Schumich1, Leonid Karawajew10, Ester Mejstrikova5, Oscar Maglia3, Georg Mann1, Wolf-Dieter Ludwig4, Andrea Biondi3, Martin Schrappe11, Giuseppe Basso2.
Abstract
Immunophenotyping by flow cytometry (FCM) is a worldwide mainstay in leukemia diagnostics. For concordant multicentric application, however, a gap exists between available classification systems, technologic standardization, and clinical needs. The AIEOP-BFM consortium induced an extensive standardization and validation effort between its nine national reference laboratories collaborating in immunophenotyping of pediatric acute lymphoblastic leukemia (ALL). We elaborated common guidelines which take advantage of the possibilities of multi-color FCM: marker panel requirements, immunological blast gating, in-sample controls, tri-partite antigen expression rating (negative vs. weak or strong positive) with capturing of blast cell heterogeneities and subclone formation, refined ALL subclassification, and a dominant lineage assignment algorithm able to distinguish "simple" from bilineal/"complex" mixed phenotype acute leukemia (MPAL) cases, which is essential for choice of treatment. These guidelines are a first step toward necessary inter-laboratory standardization of pediatric leukemia immunophenotyping for a concordant multicentric application.Entities:
Keywords: flow cytometry; immunophenotyping:; leukemia; pediatric; standardization
Mesh:
Year: 2017 PMID: 28187514 DOI: 10.1002/cyto.b.21518
Source DB: PubMed Journal: Cytometry B Clin Cytom ISSN: 1552-4949 Impact factor: 3.058