B-cell lymphoma/leukaemia 11B (BCL11B) expression status helps distinguish early T-cell precursor acute lymphoblastic leukaemia/lymphoma (ETP-ALL/LBL) from other subtypes of T-cell ALL/LBL

Hong Fang, Wei Wang, Siba El Hussein, Kiyomi Morita, Hannah C. Beird, Akash Mitra, Sanam Loghavi, Pei Lin, Elias J. Jabbour, Joseph D. Khoury

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

B-cell lymphoma/leukaemia 11B (BCL11B) is an essential transcription factor for T-cell lineage commitment and maturation. We investigated BCL11B expression by immunohistochemistry in T-lymphoblastic leukaemia/lymphoma (T-ALL/LBL) (n = 115). The majority (83%) of early T-cell precursor T-ALL/LBL (ETP-ALL) cases showed negative BCL11B expression, while most (84%) of non-ETP-ALL/LBL were positive for BCL11B. A simplified three-marker [BCL11B, cluster of differentiation 5 (CD5), CD13] immunophenotypic score discriminated reliably between ETP-ALL and non-ETP-ALL/LBL. In ETP-ALL, patients with positive BCL11B expression had a better overall survival than those with negative BCL11B (P = 0·009). In summary, BCL11B is a valuable marker for T-ALL/LBL subtyping and serves as a potential prognostic marker in patients with ETP-ALL.

Original languageEnglish (US)
Pages (from-to)1034-1038
Number of pages5
JournalBritish Journal of Haematology
Volume194
Issue number6
DOIs
StatePublished - Sep 2021

Keywords

  • BCL11B
  • T-cell differentiation
  • T-lymphoblastic leukaemia/lymphoma
  • early T-cell precursor lymphoblastic leukaemia
  • immunohistochemistry

ASJC Scopus subject areas

  • Hematology

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