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. Author manuscript; available in PMC: 2014 Jan 4.
Published in final edited form as: N Engl J Med. 2013 Jun 19;369(1):32–42. doi: 10.1056/NEJMoa1215637

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.

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