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. 2022 Jan 12;54(4):1175–1190. doi: 10.4143/crt.2021.1133

Table 1.

Comparison of histopathologic characteristics among patients with dMMR/MSI-H according to treatment response

Histopathologic characteristic Responder (n=15) Non-responder (n=12) p-value
Histologic subtype
 Well-differentiated or moderately-differentiated 10 (66.7) 4 (33.3) 0.003
 Poorly-differentiated 4 (26.7) 0
 Mucinous or signet-ring cell carcinoma 1 (6.6) 8 (66.7)
Neutrophil infiltration grade
 0 or 1 8 (53.3) 11 (91.7) 0.043
 2 or 3 7 (46.7) 1 (8.3)
Lymphocyte infiltration grade
 0 or 1 6 (40.0) 12 (100) 0.001
 2 or 3 9 (60.0) 0
Crohn-like lymphoid aggregate
 Absent 6 (40.0) 9 (75.0) 0.120
 Present 9 (60.0) 3 (25.0)
Tumor border
 Expansile 8 (53.3) 0 0.003
 Infiltrative 7 (46.7) 12 (100)
Lymphovascular invasion
 Absent 8 (53.3) 7 (58.3) > 0.99
 Present 7 (46.7) 5 (41.7)
PD-L1 status 12 7
 PD-L1 immunohistochemistry
  Negative 2 (16.7) 3 (42.9) 0.305
  Positive 10 (83.3) 4 (57.1)
 Combined proportion score 5 (0–30) 5 (0–15) 0.290
RAS and RAF mutation 13 11
KRAS 7 (53.9) 5 (45.5) 0.827
NRAS 0 1 (9.0)
BRAF V600E 1 (7.6) 0
 None 5 (38.5) 5 (45.5)
Tumor mutational burden 7 6
 TMB (mutations/Mb) 110.9 (57.8–176.6) 101.6 (50.0–135.9) 0.656

Values are presented as number (%) or median (range). dMMR, deficient DNA mismatch repair; MSI-H, microsatellite instability–high; PD-L1, programmed death-ligand 1; TMB, tumor mutational burden.