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. Author manuscript; available in PMC: 2018 Oct 30.
Published in final edited form as: Lancet Oncol. 2017 Jul 19;18(9):1182–1191. doi: 10.1016/S1470-2045(17)30422-9

Table 2:

Objective response rate, best overall response, and disease control rate per investigator and BICR assessments in patients with metastatic or recurrent colorectal cancer locally assessed as dMMR/MSI-H

Patients, n (%) dMMR/MSI-H
per local assessment
(N=74)
dMMR/MSI-H
per central assessment
(N=53)
Investigator BICR Investigator BICR
      19 (35·8) 19 (35·8)
Objective response rate 23 (31·1) 24 (32·4)    
 [95% CI] [20·8–42·9] [22·0–44·3]
      [23·1–50·2] [23·1–50·2]
Best overall response        
 Complete response 0 2 (2.7) 0 1 (1·9)
 Partial response 23 (31·1) 22 (29·7) 19 (35·8) 18 (34·0)
 Stable disease 28 (37·8) 25 (33·8) 20 (37·0) 19 (35·8)
 Progressive disease 19 (25·7) 21 (28·4) 11 (20·8) 12 (22·6)
 Not determined 4 (5·4) 4 (5·4) 3 (5·7) 3 (5·7)
Disease control for ≥12
  51 (68·9) 47 (63·5) 39 (73·6) 37 (69·8)
weeks        
  [57·1–79·2] [51·5–74·4]    
 [95% CI]        
      [59·7–84·7] [55·7–81·7]

BICR=blinded independent central review; dMMR/MSI-H=DNA mismatch repair deficient/microsatellite instability–high.