Table 1 Demographics and baseline characteristics

From: Addition of SHR-1701 to first-line capecitabine and oxaliplatin (XELOX) plus bevacizumab for unresectable metastatic colorectal cancer

Characteristic

All patients (n = 62)

Age, years, median (range)

56 (23–73)

Sex, n (%)

 Male

36 (58.1)

 Female

26 (41.9)

BMI, kg/m2, mean ± SD

22.8 ± 3.2

Primary tumor location, n (%)

 Colon

40 (64.5)

 Rectum

22 (35.5)

Tumor site, n (%)

 Left or rectum

40 (64.5)

 Right

22 (35.5)

MSS/pMMR, n (%)

62 (100.0)

Surgery on primary tumor, n (%)

 Radical surgery

26 (41.9)

 Palliative surgery

13 (21.0)

 Diagnostic procedure

2 (3.2)

Previous (neo) adjuvant therapy, n (%)

12 (19.4)

ECOG performance status, n (%)

 0

17 (27.4)

 1

45 (72.6)

Metastasis sites, n (%)

 Liver

43 (69.4)

 Peritoneum

12 (19.4)

RAS gene status, n (%)a

 Wild-type

24 (38.7)

 Mutant-type

36 (58.1)

BRAF gene status, n (%)a

 Wild-type

47 (75.8)

 Mutant-type

4 (6.5)

RAS/BRAF, n (%)a

RAS and BRAF wild-type

11 (17.7)

RAS or BRAF mutant-type

40 (64.5)

PD-L1 expression, n (%)a,b

 Positive (TPS ≥ 1% or CPS ≥ 1)

33 (53.2)

 Negative

26 (41.9)

TGF-β1, n (%)a

 Positive

10 (16.1)

 Negative

9 (14.5)

pSMAD 2/3 expression, n (%)a

 ≥80%

10 (16.1)

 <80%

9 (14.5)

  1. aThe status was not detected in remaining patients
  2. b PD-L1 positive was defined as TPS ≥ 1% or CPS ≥ 1; PD-L1 negative was defined as any values other than TPS ≥ 1% or CPS ≥ 1 in cases with CPS or TPS detection
  3. BMI body mass index, SD standard deviation, ECOG Eastern Cooperative Oncology Group, MSS microsatellite stable, pMMR mismatch repair-proficient, PD-L1 programmed death-ligand 1, TPS tumor proportion score, CPS combined positive score