Table 2.
Baseline characteristics for patients with T-LGLL.
Variable | Total (%) (n=14) |
---|---|
Age at T-LGLL, mean (SD) | 62.8 (10.1) |
Age at PCD diagnosis, mean (SD) | 63.6 (9.3) |
Sex | |
Male | 9 (64.3) |
Female | 5 (35.7) |
Race | |
Caucasian | 13 (92.9) |
African American | 1 (7.1) |
Plasma Cell Dyscrasia | |
MGUS | 8 (57.1) |
MM | 4 (28.6) |
Plasmacytosis | 2 (14.3) |
Presenting Cytopenia at T-LGLL Diagnosis | |
Neutropenia (ANC <1500) | 1 (7.1) |
Anemia (Hgb <12) | 7 (50.0) |
Both | 3 (21.4) |
Unknown | 3 (21.4) |
TCR V-Beta Positive at T-LGLL Diagnosis | |
Yes | 8 (57.1) |
No | 4 (28.6) |
Unknown | 2 (14.3) |
LGL Count (CD3CD8+) at Diagnosis | |
<1,500 | 6 (42.9) |
≥1,500 | 5 (35.7) |
Unknown | 3 (21.4) |
LDH at T-LGLL Diagnosis | |
≤190 | 10 (71.4) |
>190 | 3 (21.4) |
Unknown | 1 (7.1) |
Splenomegaly | |
Yes | 4 (28.6) |
No | 10 (71.4) |
Associated Autoimmune Disease | |
Rheumatoid arthritis | 5 (35.7) |
ITP | 1 (7.1) |
Anti-MAG neuropathy | 1 (7.1) |
ANCA-associated vasculitis | 1 (7.1) |
Cryoglobulinemia | 1 (7.1) |
Anemia (Hgb <12) at PCD Diagnosis | |
Yes | 9 (64.3) |
No | 4 (28.6) |
Unknown | 1 (7.1) |
Bone Disease at PCD Diagnosis | |
Yes | 2 (14.3) |
No | 6 (42.9) |
Unknown | 6 (42.9) |
Creatinine at PCD Diagnosis | |
<1.0 | 6 (42.9) |
1.0–1.5 | 4 (28.6) |
1.5–2.0 | 2 (14.3) |
2.0–2.5 | 0 (0.0) |
2.5–3.0 | 0 (0.0) |
>3.0 | 1 (7.1) |
Unknown | 1 (7.1) |
Monoclonal Protein-Light Chain | |
IgA-Unk | 1 (7.1) |
IgG-K | 2 (14.3) |
IgG-L | 3 (21.4) |
IgM-K | 2 (14.3) |
IgM-L | 1 (7.1) |
N/A-K | 1 (7.1) |
N/A-L | 2 (14.3) |
None detected | 2 (14.3) |
ISS Staging For PCD | |
1 | 2 (14.3) |
2 | 1 (7.1) |
3 | 1 (7.1) |
N/A | 10 (71.4) |
First-Line LGL Therapy | 10/14* (71.4) |
Methotrexate | 5 (35.7) |
Cyclophosphamide | 1 (7.1) |
Cyclosporine | 3 (21.4) |
CHOP | 1 (7.1) |
First-Line PCD Therapy* | 3/14* (21.4) |
Bortezomib/Lenalidomide/Dexamethasone | 2 (14.3) |
Cyclophosphamide/Dexamethasone/Bortezomib | 1 (7.1) |
*One patient has not received treatment for either disease.