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. 2018 Apr 27;32(8):1778–1786. doi: 10.1038/s41375-018-0146-5

Table 4.

Disease characteristics and response (MRD or clinical) at the final response assessment in patients receiving G-B in cohort 1 of the GREEN study

Factor, n/N (%) patients MRD negativea (blood) MRD negativea (bone marrow) CR/Crib
All patients 94/104 (90.4) 44/65 (67.7) 55/158 (34.8)
Binet stage A 32/32 (100) 13/18 (72.2) 19/48 (39.6)
Binet stage B+C 62/72 (86.1) 31/47 (66.0) 36/110 (32.7)
Disease bulk ≥5 cm 57/64 (89.1) 27/39 (69.2) 29/95 (30.5)
ALC ≥50 × 109/l 52/59 (88.1) 25/38 (65.8) 33/88 (37.5)
17p deletion 3/6 (50.0) 2/3 (66.7) 2/11 (18.2)
11q deletion 18/23 (78.3) 5/15 (33.3) 7/26 (26.9)
12q trisomy 18/20 (90.0) 12/14 (85.7) 8/26 (30.8)
13q deletion 32/32 (100) 13/19 (68.4) 22/52 (42.3)
CD38 positive 49/55 (89.1) 17/28 (60.7) 22/70 (31.4)
CD38 negative 37/41 (90.2) 22/30 (73.3) 22/59 (37.3)
ZAP70 positive 54/60 (90.0) 22/34 (64.7) 30/82 (36.6)
ZAP70 negative 32/36 (88.9) 17/24 (70.8) 14/47 (29.8)
IGHV mutated 31/31 (100) 12/17 (70.6) 17/44 (38.6)
IGHV unmutated 58/68 (85.3) 28/44 (63.6) 30/92 (32.6)

ALC absolute lymphocyte count, CR complete response, CRi complete response with incomplete marrow recovery, G-B obinutuzumab plus bendamustine, IGHV immunoglobulin heavy variable chain, MRD minimal residual disease

a Patients with evaluable (laboratory sample with a valid result at the final response assessment) MRD

b Patients who achieved CR/CRi at the final response assessment in the intent-to-treat population