Table 1

Clinical characteristics of exome-sequenced T-LGL leukemia patients and patients with STAT5b mutation

No.LGL leukemia typeMutationsSexAge at diagnosis, yWBC count at diagnosis, 109/LLymph count at diagnosis, 109/LLymphocyte count, 109/L*CD8+Concomitant disordersTherapy
CD3+CD8+CD56+ T cell STAT5b Y665F 71 11.8 7.0 8.5 Vb22, 91% Collagenosis No 
CD3+CD8+CD56+ T cell STAT5b Y665F 49 16.1 12.9 13.7 Vb17, 94% None No 
CD3+CD8+CD56+ T cell STAT5b N642H 74 90.0 85.5 85.5 Vb21, 87%§ Pancytopenia, neutropenia, splenomegaly Yes 
CD3negCD56+ NK cell STAT5b N642H 75 164.7 131.8 131.8 Vb7, 27%§Vb3, 16%§ Hemolytic anemia, neutropenia, splenomegaly, MGUS Yes 
No.LGL leukemia typeMutationsSexAge at diagnosis, yWBC count at diagnosis, 109/LLymph count at diagnosis, 109/LLymphocyte count, 109/L*CD8+Concomitant disordersTherapy
CD3+CD8+CD56+ T cell STAT5b Y665F 71 11.8 7.0 8.5 Vb22, 91% Collagenosis No 
CD3+CD8+CD56+ T cell STAT5b Y665F 49 16.1 12.9 13.7 Vb17, 94% None No 
CD3+CD8+CD56+ T cell STAT5b N642H 74 90.0 85.5 85.5 Vb21, 87%§ Pancytopenia, neutropenia, splenomegaly Yes 
CD3negCD56+ NK cell STAT5b N642H 75 164.7 131.8 131.8 Vb7, 27%§Vb3, 16%§ Hemolytic anemia, neutropenia, splenomegaly, MGUS Yes 

F, female; M, male; MGUS, monoclonal gammapathy of unknown significance; WBC, white blood cell.

*

Lymphocyte count at the time point when the sample was taken.

Proportion of Vβ clone of CD8+ cells.

Pharmacological treatment at any time point.

§

Proportion from total T-cell fraction.

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