TY - JOUR
T1 - International Consensus Classification of acute lymphoblastic leukemia/lymphoma
AU - Duffield, Amy S.
AU - Mullighan, Charles G.
AU - Borowitz, Michael J.
N1 - Funding Information:
M.J.B.: Financial support was received from U10 CA180886 (National Cancer Institute, National Institutes of Health).
Funding Information:
The authors thank the members of the working group including Elias Jabbour, Ching-Hon Pui, Kathryn Foucar, Nicola Goekbuget, Hartmut Doehner, and Mignon Loh, as well as Daniel Arber for thoughtful discussion. Additionally, the authors thank Dr. Qingsong Gao (St. Jude Children’s Research Hospital, Memphis, TN), who created Fig. 1.
Funding Information:
Authors A.S.D. and M.J.B. declare no competing interests. Author C.G.M. has received speaker (Illumina and Amgen) and consultant (Faze, Beam) honoraria, and receives research funding from AbbVie and Pfizer.
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2023/1
Y1 - 2023/1
N2 - The updated International Consensus Classification (ICC) of B-acute lymphoblastic leukemia (B-ALL) and T-acute lymphoblastic leukemia (T-ALL) includes both revisions to subtypes previously outlined in the 2016 WHO classification and several newly described entities. The ICC classification incorporates recent clinical, cytogenetic, and molecular data, with a particular emphasis on whole transcriptome analysis and gene expression (GEX) clustering studies. B-ALL classification is modified to further subclassify BCR::ABL1-positive B-ALL and hypodiploid B-ALL. Additionally, nine new categories of B-ALL are defined, including seven that contain distinguishing gene rearrangements, as well as two new categories that are characterized by a specific single gene mutation. Four provisional entities are also included in the updated B-ALL classification, although definitive identification of these subtypes requires GEX studies. T-ALL classification is also updated to incorporate BCL11B-activating rearrangements into early T-precursor (ETP) ALL taxonomy. Additionally, eight new provisional entities are added to the T-ALL subclassification. The clinical implications of the new entities are discussed, as are practical approaches to the use of different technologies in diagnosis. The enhanced specificity of the new classification will allow for improved risk stratification and optimized treatment plans for patients with ALL.
AB - The updated International Consensus Classification (ICC) of B-acute lymphoblastic leukemia (B-ALL) and T-acute lymphoblastic leukemia (T-ALL) includes both revisions to subtypes previously outlined in the 2016 WHO classification and several newly described entities. The ICC classification incorporates recent clinical, cytogenetic, and molecular data, with a particular emphasis on whole transcriptome analysis and gene expression (GEX) clustering studies. B-ALL classification is modified to further subclassify BCR::ABL1-positive B-ALL and hypodiploid B-ALL. Additionally, nine new categories of B-ALL are defined, including seven that contain distinguishing gene rearrangements, as well as two new categories that are characterized by a specific single gene mutation. Four provisional entities are also included in the updated B-ALL classification, although definitive identification of these subtypes requires GEX studies. T-ALL classification is also updated to incorporate BCL11B-activating rearrangements into early T-precursor (ETP) ALL taxonomy. Additionally, eight new provisional entities are added to the T-ALL subclassification. The clinical implications of the new entities are discussed, as are practical approaches to the use of different technologies in diagnosis. The enhanced specificity of the new classification will allow for improved risk stratification and optimized treatment plans for patients with ALL.
KW - B-lymphoblastic leukemia
KW - B-lymphoblastic lymphoma
KW - Gene expression clustering
KW - T-lymphoblastic leukemia
KW - T-lymphoblastic lymphoma
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U2 - 10.1007/s00428-022-03448-8
DO - 10.1007/s00428-022-03448-8
M3 - Review article
C2 - 36422706
AN - SCOPUS:85142539578
SN - 0945-6317
VL - 482
SP - 11
EP - 26
JO - Virchows Archiv - Abteilung A Pathologische Anatomie
JF - Virchows Archiv - Abteilung A Pathologische Anatomie
IS - 1
ER -