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Table 2 Summary of efficacy outcomes

From: Efficacy and safety of radiotherapy plus anti-PD1 versus transcatheter arterial chemoembolization plus sorafenib for advanced hepatocellular carcinoma: a real-world study

Variables

RT + PD1, N = 37 (%)

TACE + Sorafenib, N = 41(%)

P value

According to RECIST 1.1

Confirmed objective response

20 (54.05%)

5(12.20%)

 < 0.001

Time to response, months, (IQR)

1.80(1.57–2.00)

2.87(1.407–6.86)

0.467

Disease control

26(70.27%)

19(46.34%)

0.041

Best overall response

  CR

0(0)

0(0)

1.000

  PR

20 (54.05%)

5(12.20%)

 < 0.001

  SD

6(16.22%)

14(34.15%)

0.118

  PD

11(29.73%)

22(53.66%)

0.041

Progression-free survival, months, median, (95% CI)

5.86(3.19–8.53)

3.70(2.60–4.80)

0.017

According to mRECIST

Confirmed objective response

21(56.76%)

13(31.71%)

0.039

Time to response, months, (IQR)

1.85(1.60–2.98)

1.47(0.80–2.60)

0.061

Disease control

26(70.27%)

19(46.34%)

0.041

Best overall response

  CR

1(2.70%)

1(2.44%)

1.000

  PR

20 (54.05%)

12(29.27%)

0.038

  SD

5(13.51%)

6(14.63%)

0.774

  PD

11(29.73%)

22(53.66%)

0.041

Progression-free survival, months, median, (95% CI)

5.86(3.19–8.53)

3.70(2.60–4.80)

0.019

Overall survival

3-month, %

97.30%

92.30%

 < 0.001

6-month, %

91.90%

68.60%

 < 0.001

9-month, %

75.50%

60.60%

 < 0.001

12-month, %

52.20%

47.5%

0.061

Overall survival, months, median, (95% CI)

17.40 (8.69–26.11)

11.90 (6.35–17.45)

0.146

  1. Data are N (%; 95% CI), unless indicated
  2. RT Radiotherapy; PD1 The monoclonal antibody against programmed cell death 1; TACE Transcatheter arterial chemoembolization; RECIST 1.1 Response Evaluation Criteria in Solid Tumors 1.1; mRECIST Modified Response Evaluation Criteria in Solid Tumors; CR Complete response; PR Partial response; SD Stable disease; PD Progressive disease