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Table 1 Baseline characteristics of the studies included in the network Meta-analysis

From: Comparative efficacy and safety of first-line neoadjuvant therapy for early-stage non-small cell lung cancer based on immune checkpoint inhibitor therapy: a systematic review and network meta-analysis

Source

Registered ID(date)

Phase

Treatment

Participants

EFS

median,95%CI

Months

HR

(95%CI)

PCR No./total

(%)

MPR

No./total

(%)

Grade ≥ 3AEs

No./total

(%)

Rates of undergoing surgery No./total

(%)

R0 resection rate No./total

(%)

Forde 2022

NCT02998528

(2016)

III

Nivolumab Q3W plus ChemotherapyQ3W

179

31.6

(30.2-NE)

0.63

(0.43–0.91)

43/179

(24.0)

66/179

(36.9)

59/176

(33.5)

149/179(83.2)

124/149(83.2)

Chemotherapy Q3W

179

20.8

(14.0−26.7)

4/179

(2.2)

16/179

(8.9)

65/176

(36.9)

135/179(75.4)

105/135(77.8)

Provencio 2023

NCT03838159

(2019)

II

Nivolumab Q3W plus Chemotherapy Q3W

57

NR

NR

21/57

(36.8)

30/57

(53.0)

12/57

(21.1)

53/57(93.0)

50/53

(94.3)

Chemotherapy Q3W

29

NR

2/29

(6.9)

4/29

(14.0)

3/29

(10.3)

20/29(69.0)

17/20

(85.0)

John

2023

NCT03800134

(2019)

III

Durvalumab Q3W plus Chemotherapy Q3W

366

NR

(31.9-NE)

0.68

(0.53–0.88)

63/366

(17.2)

122/366

(33.3)

130/400

(32.4)

284/366(77.6)

269/284(94.7)

Placebo plus Chemotherapy Q3W

374

25.9

(18.9-NE)

16/374

(4.3)

46/374

(12.3)

131/398

(32.9)

287/374(76.7)

262/287(91.3)

Shun

2023

NCT04158440

(2019)

III

Toripalimab Q3W plus Chemotherapy Q3W

202

NR

(24.4-NE)

0.40

(0.28–0.57)

50/202

(24.8)

98/202

(48.5)

157/202

(77.7)

166/202(82.2)

159/166(95.8)

Placebo plus Chemotherapy Q3W

202

15.1

(10.6–21.9)

2(1.0)

17/202

(8.4)

113/202

(55.9)

148/202(73.3)

137/148(92.6)

Lei

2022

NCT04338620

(2020)

II

Camrelizumab Q3W plus

Chemotherapy Q3W

43

NR

(NE-NE)

0.52

(0.21–1.29)

14/43

(32.6)

28/43

(65.1)

11/43

(25.6)

40/43(93.0)

37/40(92.5)

Chemotherapy Q3W

45

NR

(NE-NE)

4/45

(8.9)

7/45

(15.6)

5/45

(11.1)

42/45(93.3)

36/42(85.7)

Wakelee

2023

NCT03425643

(2018)

III

Pembrolizumab Q3W plus

Chemotherapy Q3W

397

NR

(34.1-NE)

0.58

(0.46–0.72)

72/397

(18.1)

120/397

(30.2)

77/396

(19.4)

325/396(82.1)

299/325(92.0)

Chemotherapy Q3W

400

17

(14.3–22)

16/400

(4.0)

44/400

(11.0)

78/399

(19.5)

317/399(79.4)

266/317(84.0)

Cascone

2022

NCT03158129

(2017)

II

Ipilimumab plus nivolumab plus Chemotherapy

22

NR

NR

4/22

(18.2)

11/22

(50.0)

4/22

(18.0)

20/22(91.0)

19/20(95.0)

Nivolumab plus Chemotherapy

22

NR

4/22

(18.2)

7/22

(32.1)

10/22(45)

22/22(100)

20/22(91.0)

Yue

2023

NCT04379635

(2020)

III

Tislelizumab Q3W plus Chemotherapy Q3W

226

NR(NE-NE)

0.56(0.40–0.79)

92/226(40.7)

127/226

(56.2)

157/226(69.5)

190/226(84.1)

NR

Chemotherapy Q3W

227

NR(16.6-NE)

13/227

(5.7)

34/227

(15.0)

148/226

(65.5)

173/227(76.2)

NR

Cascone

2023

NCT04025879

(2019)

III

Nivolumab Q3W plus Chemotherapy Q3W

229

NR(28.9-NE)

0.58(0.42–0.81)

58/229(25.3)

81/229(35.4)

66/194

(34.0)

178/229(77.7)

159/178(89.0)

Chemotherapy Q3W

232

18.4

(13.5–28.1)

11/232(4.7)

28/232(12.1)

55/205

(27.0)

178/232(76.6)

161/178

(90.0)

  1. PCR: Pathological complete response; MPR: Major Pathological response; EFS: Event-free survival; Grade ≥ 3 AEs: adverseevents of grade 3 or higher(During neoadjuvant therapy); NE: Not Evaluated; NR: not reported; Q3W: every three weeks, HR: hazard ratio