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. Author manuscript; available in PMC: 2017 Jun 28.
Published in final edited form as: Genet Med. 2016 Feb 11;18(9):863–868. doi: 10.1038/gim.2015.184

Table 1.

Patient characteristics, stage and tumor location

Lynch syndrome (n=37) MLH1-hm (n=106) p-value
Age (median; Q1,Q3) 47 (35, 58) 70.5 (63,80) p< 0.0001
Sex
 Male 22 (59.5%) 45 (42.5%) p=0.074
 Female 15 (40.5%) 61 (57.5%)
Race
 Caucasian 33 (89.2%) 88 (89.8%) p=0.775
 AA 3 (8.1%) 9 (9.2%)
 Hispanic 1 (2.7%) 1 (1.0%)
Stage
 I 4 (10.8%) 15 (14.2%) p=0.022
 II 10 (27.0%) 48 (45.3%)
 III 17 (46.0%) 28 (26.4%)
 IV 3 (8.1%) 14 (13.2%)
 Stage I–III (unknown) 3 (8.1%) 1 (0.9%)
Location
 Right 27 (73.0%) 87 (82.9%) p=0.457
 Left 7 (18.9%) 11 (10.5%)
 Rectum 3 (8.1%) 7 (6.7%)
Synchronous 4 (10.8%) 6 (5.7%) p=0.459
Metachronous 7 (18.9%) 4 (3.8%) p=0.009
Received adjuvant chemotherapy
 Stage II 3 (30%) 4 (8.3%) p=0.058
 Stage III 10 (59%) 11 (39%) P=0.091
Recurrence (%) 9 (24.3%) 12 (11.3%) p=0.040
Other cancer diagnosis (%) 13 (34.2%) 27 (25.5%) p=0.301
Follow-up time (months)
(median; Q1,Q3) 30.0 (16, 117) 25 (5, 54) p=0.02
CEA (n, median; Q1, Q3) 1.2 (0.7, 2.6) 1.9 (1.0, 5.6) P=0.070

AA = African-American; Q = quartiles; Statistical significance was evaluated by Chi-square for categorical variables and t-test for continuous variables. Significance was set at p<0.05.