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. 2018 Nov 17;68(2):283–296. doi: 10.1007/s00262-018-2275-0

Table 1.

Clinicopathologic characteristics and PD-L1 expression status of enrolled patients (n = 104)

Clinicopathological characteristics Total cases, n (%) Tumor PD-L1 (pre-neoCRT) Tumor PD-L1 (post-neoCRT)
High, n (%) Low, n (%) p value High, n (%) Low, n (%) p value NA, n (%)
104 (100%) 53 (51%) 51 (49%) 57 (64%) 32 (36%) 15 (100%)
Age 0.88 0.3
 < 65 66 (63%) 34 (64%) 32 (63%) 40 (70%) 19 (59%) 7 (47%)
 ≥ 65 38 (37%) 19 (36%) 19 (37%) 17 (30%) 13 (41%) 8 (53%)
Sex 0.24 0.97
 Female 33 (32%) 14 (26%) 19 (37%) 18 (32%) 10 (31%) 5 (33%)
 Male 71 (68%) 39 (74%) 32 (63%) 39 (68%) 22 (69%) 10 (67%)
cN stage 0.56 0.42
 Negative 52 (50%) 28 (53%) 24 (47%) 30 (53%) 14 (44%) 8 (53%)
 Positive 52 (50%) 25 (47%) 27 (53%) 27 (47%) 18 (56%) 7 (47%)
Clinical TNM stage (7th AJCC) 0.04* 0.04*
 I 4 (4%) 3 (6%) 1 (2%) 2 (4%) 2 (6%) 0 (0%)
 II 48 (46%) 25 (47%) 23 (45%) 28 (49%) 12 (38%) 8 (53%)
 III 52 (50%) 25 (47%) 27 (53%) 27 (47%) 18 (56%) 7 (47%)
pN stage 0.32 0.57
 Negative 74 (71%) 40 (75%) 34 (67%) 39 (68%) 20 (63%) 15 (100%)
 Positive 30 (29%) 13 (25%) 17 (33%) 18 (32%) 12 (38%) 0 (0%)
TRG 0.004* 0.4
 4 15 (14%) 6 (11%) 9 (18%) 0 (0%) 0 (0%) 15 (100%)
 3 57 (55%) 32 (60%) 25 (49%) 37 (65%) 20 (63%) 0 (0%)
 2 23 (22%) 12 (23%) 11 (22%) 16 (28%) 7 (22%) 0 (0%)
 1 9 (9%) 3 (6%) 6 (12%) 4 (7%) 5 (16%) 0 (0%)
Clinical response 0.002* 0.04*
 CR 15 (14%) 5 (9%) 10 (20%) 1 (2%) 0 (0%) 14 (93%)
 PR 39 (38%) 22 (42%) 17 (33%) 24 (42%) 14 (44%) 1 (7%)
 SD 45 (43%) 22 (42%) 23 (45%) 29 (51%) 16 (50%) 0 (0%)
 PD 5 (5%) 4 (8%) 1 (2%) 3 (5%) 2 (6%) 0 (0%)
Chemotherapy 0.002* 0.02*
 Capecitabine 50 (48%) 30 (57%) 20 (39%) 29 (51%) 15 (47%) 6 (40%)
 UFT 38 (37%) 15 (28%) 23 (45%) 20 (35%) 12 (38%) 6 (40%)
 5-FU 11 (11%) 6 (11%) 5 (10%) 6 (11%) 4 (13%) 1 (7%)
 Others 5 (5%) 2 (4%) 3 (6%) 2 (4%) 1 (3%) 2 (13%)
Local recurrence 0.1 0.13
 Negative 93 (89%) 50 (94%) 43 (84%) 53 (93%) 27 (84%) 13 (87%)
 Positive 11 (11%) 3 (6%) 8 (16%) 4 (7%) 5 (16%) 2 (13%)
Distant metastasis 0.04* 0.62
 Negative 84 (81%) 47 (89%) 37 (73%) 47 (82%) 25 (78%) 12 (80%)
 Positive 20 (19%) 6 (11%) 14 (27%) 10 (18%) 7 (22%) 3 (20%)
Tumor IFN-γ (pre-neoCRT) 0.0001*
 High 44 (42%) 32 (60%) 12 (24%)
 Low 60 (58%) 21 (40%) 39 (76%)
Tumor IFN-γ (post-neoCRT) 0.26
 High 50 (88%) 28 (88%) 0 (0%)
 Low 7 (12%) 4 (13%) 0 (0%)
 NA 15 (100%)
Tumor TGF-β (pre-neoCRT) 0.3
 High 62 (70%) 35 (74%) 27 (62%)
 Low 27 (30%) 12 (26%) 15 (36%)
Tumor TGF-β (post-neoCRT) 0.1
 High 52 (91%) 26 (81%) 0 (0%)
 Low 5 (9%) 6 (19%) 0 (0%)
 NA 15 (100%)
Microsatellite instability (MSI) status 1.0 1.0
 Proficient 102 (98%) 52 (98%) 50 (98%) 56 (98%) 31 (97%) 15 (100%)
 Deficient 2 (2%) 1 (2%) 1 (2%) 1 (2%) 1 (3%) 0 (0%)

Chi-squared test was used. Fisher’s exact test was used when > 25% of the cells had expected counts < 5

The contrast test did not include the “NA” group

*p < 0.05

cN stage positive (stage 1 + 2) vs. negative (stage 0), pN stage positive (stage 1a + 1b + 2) vs. negative (stage 0 + X), CR complete response, PR partial response, SD stable disease, PD progressive disease, tumor PD-L1 high (grade 2 + 3) vs. low (grade 0 + 1), tumor IFN-γ high (grade 2 + 3) vs. low (grade 0 + 1), tumor TGF-β high (grade 2 + 3) vs. low (grade 0 + 1), NA surgical specimen is TRG4 with no residue tumor tissue after neoCRT treatment