Table 1

Patient characteristics at time of 17p− documentation

CharacteristicM. D. Anderson (n = 64)Mayo Clinic (n = 35)P
Median survivor follow-up after 17p− documentation, mos (range) 28 (7-60) 28 (1-70) NA 
Median age, y (range) 61 (40-84) 69 (45-87) .03 
Age ≥ 60 y, n (%) 34 (53) 25 (71) NS 
Male sex, n (%) 39 (61) 20 (57) NS 
Median months since diagnosis (range) 9 (0–142) 13 (0–313) NS 
Performance status ECOG 1 or higher, n (%) 31 (48) 6 (17) .002 
B-symptoms, n (%) 13 (20) 3 (9) NS 
Rai stage 0, n (%) 18 (28) 15 (43) NS 
Rai stage 1 or 2, n (%) 32 (50) 16 (46) NS 
Rai stage 3 or 4, n (%) 14 (22) 4 (11) NS 
Median white cell count, ×109/L (range) 44 (6-281) 19 (8-150) .002 
β2m ≥ 2 × upper limit of normal, n (%) 26 (41) 8 (40) NS 
Median FISH 17p deletion % (range) 46 (8-97) 64 (10-96) .05 
FISH 17p deletion < 25%, n (%) 21 (33) 7 (20) NS 
FISH 17p deletion 25%-49%, n (%) 11 (17) 5 (14) NS 
FISH 17p deletion 50%-74%, n (%) 10 (16) 8 (23) NS 
FISH 17p deletion ≥ 75%, n (%) 22 (34) 15 (43) NS 
FISH 17p deletion only, n (%) 25 (39) 6 (17) NS 
FISH 11q deletion in addition, n (%)* 9 (14) 8 (23) NS 
FISH trisomy 12 in addition, n (%)* 7 (11) 3 (9) NS 
FISH 13q deletion in addition, n (%)* 23 (36) 18 (51) NS 
Abnormal 17p on karyotype, n (%) 23 (40) 1 (25) NS 
CD38+, n (%) 17 (29) 13 (35) NS 
ZAP-70+, n (%) 19 (58) 11 (39) NS 
Unmutated IgVH, n (%) 39 (70) 15 (57) NS 
Commenced CLL therapy, n (%) 46 (72) 11 (31) <.001 
First CLL therapy type, n (%)    
    Rituximab without chemotherapy 5 (11) 1 (9) NA 
    PA + rituximab based 22 (48) 3 (27) NA 
    PA, alemtuzumab, + rituximab based 14 (30) 2 (18) NA 
    Other 5 (11) 5 (45) NA 
CharacteristicM. D. Anderson (n = 64)Mayo Clinic (n = 35)P
Median survivor follow-up after 17p− documentation, mos (range) 28 (7-60) 28 (1-70) NA 
Median age, y (range) 61 (40-84) 69 (45-87) .03 
Age ≥ 60 y, n (%) 34 (53) 25 (71) NS 
Male sex, n (%) 39 (61) 20 (57) NS 
Median months since diagnosis (range) 9 (0–142) 13 (0–313) NS 
Performance status ECOG 1 or higher, n (%) 31 (48) 6 (17) .002 
B-symptoms, n (%) 13 (20) 3 (9) NS 
Rai stage 0, n (%) 18 (28) 15 (43) NS 
Rai stage 1 or 2, n (%) 32 (50) 16 (46) NS 
Rai stage 3 or 4, n (%) 14 (22) 4 (11) NS 
Median white cell count, ×109/L (range) 44 (6-281) 19 (8-150) .002 
β2m ≥ 2 × upper limit of normal, n (%) 26 (41) 8 (40) NS 
Median FISH 17p deletion % (range) 46 (8-97) 64 (10-96) .05 
FISH 17p deletion < 25%, n (%) 21 (33) 7 (20) NS 
FISH 17p deletion 25%-49%, n (%) 11 (17) 5 (14) NS 
FISH 17p deletion 50%-74%, n (%) 10 (16) 8 (23) NS 
FISH 17p deletion ≥ 75%, n (%) 22 (34) 15 (43) NS 
FISH 17p deletion only, n (%) 25 (39) 6 (17) NS 
FISH 11q deletion in addition, n (%)* 9 (14) 8 (23) NS 
FISH trisomy 12 in addition, n (%)* 7 (11) 3 (9) NS 
FISH 13q deletion in addition, n (%)* 23 (36) 18 (51) NS 
Abnormal 17p on karyotype, n (%) 23 (40) 1 (25) NS 
CD38+, n (%) 17 (29) 13 (35) NS 
ZAP-70+, n (%) 19 (58) 11 (39) NS 
Unmutated IgVH, n (%) 39 (70) 15 (57) NS 
Commenced CLL therapy, n (%) 46 (72) 11 (31) <.001 
First CLL therapy type, n (%)    
    Rituximab without chemotherapy 5 (11) 1 (9) NA 
    PA + rituximab based 22 (48) 3 (27) NA 
    PA, alemtuzumab, + rituximab based 14 (30) 2 (18) NA 
    Other 5 (11) 5 (45) NA 

Percentages were calculated based on the total number of patients with evaluable information. Therapies listed under “Other” were: for M.D. Anderson, lenalidomide (n = 4), and R-CHOP (n = 1); for the Mayo Clinic, chlorambucil (n = 1), pentostatin plus cyclophosphamide (n = 1), R-CVP (n = 2) and R-CHOP (n = 1).

ECOG indicates Eastern Cooperative Oncology Group; FISH, fluorescent in situ hybridization; CLL, chronic lymphocytic leukemia; PA, purine analogue; NA, not applicable; and NS, not significant.

*

Patients were ranked in the hierarchical classification proposed by Dohner et al. For example, a patient with concomitant deletions of 11q and 13q would be classified as having 11q deletion.

Defined as ≥ 30% for CD38 and ≥ 20% for ZAP-70.

Excluding patients enrolled in early intervention trials for disease not meeting National Cancer Institute Working Group treatment criteria.

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