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. 2013 Dec 4;35(5):992–1002. doi: 10.1093/carcin/bgt396

Table I.

Characteristics of the patients

Resequencing analysis (n = 98; 105 samples) miR-16-1 analysis; Sanger sequencing (n = 193) miR-29b-2/29c analysis; Sanger sequencing (n = 213)
Rai stage (at the time of sample collection)
    0–2 (low/intermediate stage) 72/98 (74%) 135/193 (70%) 153/213 (72%)
    3–4 (advanced stage) 17/98 (17%) 46/193 (24%) 48/213 (22%)
    NA 9/98 (9%) 12/193 (6%) 12/213 (6%)
Sex ratio (M:F) 60:38 118:75 131:82
Age at diagnosis - years (median) 62.3 60 60
IGHV mutation status
    Unmut 81/98 (83%) 122/193 (63%) 135/213 (63%)
    Mut 16/98 (16%) 67/193 (35%) 74/213 (35%)
    NA 1/98 (1%) 4/193 (2%) 4/213 (2%)
Cytogenetic aberrations (I-FISH) according to hierarchical cytogenetics (8) (at the time of sample collection)
    Del17p 23/105 (22%) 38/193 (20%) 40/213 (19%)
    Del11q 47/105 (45%) 21/193 (11%) 31/213 (15%)
    Trisomy 12 3/105 (3%) 29/193 (15%) 30/213 (14%)
    Del13q 20/105 (19%) 65/193 (34%) 71/213 (33%)
    Normal karyotype 12/105 (11%) 40/193 (21%) 41/213 (19%)
TP53 mutation status (60) (at the time of sample collection)
    del17p + mutTP53 19/105 (18%) 32/193 (17%) 34/213 (16%)
    Sole mutTP53 29/105 (28%) 8/193 (4%) 9/213 (4%)
    wtTP53 57/105 (54%) 153/193 (79%) 170/213 (80%)

NA, not available.