Skip to main content

Table 4 Comparison of clinical characteristics between the MPR group and the non-MPR group

From: Safety and effectiveness of neoadjuvant PD-1 inhibitor (toripalimab) plus chemotherapy in stage II–III NSCLC (LungMate 002): an open-label, single-arm, phase 2 trial

 

Non-MPR

MPR

P

Patients

16 (44.4%)

20 (55.6%)

 

Age

66.5 (62.0–68.0)

60.5 (54.5–67.8)

0.147

Sex

 Male

12 (75.0%)

16 (80.0%)

 

 Female

4 (25.0%)

4 (20.0%)

1.000

Smoking history

 No

6 (37.5%)

6 (30.0%)

 

 Yes

10 (62.5%)

14 (70.0%)

0.729

Treatment cycles

 2

8 (50.0%)

10 (50.0%)

 

 3

6 (37.5%)

4 (20.0%)

 

 4

2 (12.5%)

6 (30.0%)

0.321

Adverse effect

 No

0

2 (10.0%)

 

 Grades 1–2

13 (81.2%)

12 (60.0%)

 

 Grades 3–5

3 (18.8%)

6 (30.0%)

0.184

Pre-treatment PD-L1 expression

 Negative

6 (37.5%)

2 (10.0%)

 

 Positive

2 (12.5%)

8 (40.0%)

 

 Unknown

8 (50.0%)

6 (30.0%)

0.054

Pathology

 Squamous cell carcinoma

8 (50.0%)

11 (55.0%)

 

 Adenocarcinoma

5 (31.3%)

4 (20.0%)

 

 Non-small-cell lung cancer

3 (18.8%)

5 (25.0%)

0.724

Clinical stage

 IIB

1 (6.3%)

3 (15.0%)

 

 IIIA

13 (81.2%)

7 (35.0%)

 

 IIIB

2 (12.5%)

7 (35.0%)

 

 IIIC

0

3 (15.0%)

0.023

Radiological response

 CR

0

8 (40.0%)

 

 PR

12 (75.0%)

12 (60.0%)

 

 SD

4 (25.0%)

0

<0.001

  1. MPR major pathologic response, CR complete response, PR partial response, SD stable disease, PD-L1 programmed cell death ligand 1