Early T precursor acute lymphoblastic leukaemia/lymphoma shows differential immunophenotypic characteristics including frequent CD33 expression and in vitro response to targeted CD33 therapy

Summary The differential immunophenotypic characteristics of early T precursor (ETP) acute lymphoblastic leukaemia/lymphoma (ALL) remain incompletely characterized. The study group (n = 142) included 106 (74·7%) men and 36 (25·3%) women with a median age of 34·9 years (range, 2–79) at diagnosis. Pat...

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Veröffentlicht in:British journal of haematology 2019-08, Vol.186 (4), p.538-548
Hauptverfasser: Khogeer, Haitham, Rahman, Haitham, Jain, Nitin, Angelova, Evgeniya A., Yang, Hong, Quesada, Andres, Ok, Chi Y., Sui, Dawen, Wei, Peng, Al Fattani, Areej, Pierce, Sherry, Loghavi, Sanam, Lamb, Audrey, Hu, Peter, Thakral, Beenu, Kanagal‐Shamanna, Rashmi, Jorgensen, Jeffrey L., Jabbour, Elias J., Kantarjian, Hagop M., Medeiros, L. Jeffrey, Khoury, Joseph D.
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Sprache:eng
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Zusammenfassung:Summary The differential immunophenotypic characteristics of early T precursor (ETP) acute lymphoblastic leukaemia/lymphoma (ALL) remain incompletely characterized. The study group (n = 142) included 106 (74·7%) men and 36 (25·3%) women with a median age of 34·9 years (range, 2–79) at diagnosis. Patients were subtyped by flow cytometry immunophenotyping as follows: 33 (23·2%) ETP; 32 (22·5%) early non‐ETP; 60 (42·2%) thymic; and 17 (12·1%) mature. Excepting definitional markers, there was a significant differential expression of the markers CD2, CD10, CD33 and TdT between ETP‐ALL and non‐ETP‐ALL. Positive CD33 expression (≥20% of leukaemic blasts) was detected in 21/33 (63%) ETP‐ALL compared with 17/95 (17·9%) non‐ETP‐ALL (P 
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.15960