Table 1.
Baseline Demographic and Clinical Characteristics of the Patients.
Characteristic | Total (N = 85) |
---|---|
Age | |
Median — yr | 66 |
Range — yr | 37–82 |
≥70 yr — no. (%) | 30 (35) |
Sex — no. (%) | |
Male | 65 (76) |
Female | 20 (24) |
Diagnosis — no. (%) | |
Chronic lymphocytic leukemia | 82 (96) |
Small lymphocytic lymphoma | 3 (4) |
Time since most recent systemic anticancer therapy — mo | |
Median | 3 |
Range | 1–98 |
Rai stage at treatment initiation — no. (%)* | |
0, I, or II | 29 (34) |
III or IV | 55 (65) |
Data missing | 1 (1) |
No. of previous therapies | |
Median | 4 |
Range | 1–12 |
Previous therapy — no. (%) | |
Nucleoside analogue | 81 (95) |
Rituximab | 83 (98) |
Alkylator | 76 (89) |
Alemtuzumab | 18 (21) |
Bendamustine | 33 (39) |
Ofatumumab | 22 (26) |
Bulky nodes — no. (%) | |
≥5 cm in diameter | 44 (52) |
≥10 cm in diameter | 13 (15) |
Data missing | 3 (4) |
Unmutated immunoglobulin variable-region heavy-chain gene — no. (%) | |
Patients with data that could be evaluated | 69 (81) |
Data missing | 4 (5) |
Interphase cytogenetic abnormality — no. (%)† | |
17p13.1 deletion | 28 (33) |
11q22.3 deletion | 31 (36) |
β2-microglobulin level — no. (%) | |
>3 mg/liter | 39 (46) |
Data missing | 5 (6) |
Disease resistant to purine analogue — no. (%)‡ | 41 (48) |
Rai stage 0 indicates low-risk, stage I or II intermediate-risk, and stage III or IV high-risk disease.
Cutoff points were defined according to the assay specifications as performed in the central laboratory.
Resistance to a purine analogue was defined as treatment failure (stable disease or progressive disease) or disease progression within 12 months after receipt of a regimen containing a purine analogue.