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. 2022 Aug 2;12:816198. doi: 10.3389/fonc.2022.816198

Table 2.

Subgroup analysis of clinical response.

Items, No. (%) ORR Non-ORR P-value DCR Non-DCR P-value
Age 0.963 0.680
 ≤65 years 37 (57.8) 27 (42.2) 55 (85.9) 9 (14.1)
 >65 years 8 (57.1) 6 (42.9) 13 (92.9) 1 (7.1)
Gender 1.000 1.000
 Female 4 (57.1) 3 (42.9) 6 (85.7) 1 (14.3)
 Male 41 (57.7) 30 (42.3) 62 (87.3) 9 (12.7)
HBV 0.224 0.107
 No 12 (70.6) 5 (29.4) 17 (100.0) 0 (0.0)
 Yes 33 (54.1) 28 (45.9) 51 (83.6) 10 (16.4)
ECOG PS score 0.673 0.348
 0 13 (59.1) 9 (40.9) 21 (95.5) 1 (4.5)
 1 31 (56.4) 24 (43.6) 46 (83.6) 9 (16.4)
 2 1 (100.0) 0 (0.0) 1 (100.0) 0 (0.0)
Child–Pugh class 0.608 1.000
 A 35 (59.3) 24 (40.7) 51 (86.4) 8 (13.6)
 B 10 (52.6) 9 (47.4) 17 (89.5) 2 (10.5)
Extrahepatic metastasis 0.522 0.172
 No 21 (61.8) 13 (38.2) 32 (94.1) 2 (5.9)
 Yes 24 (54.5) 20 (45.5) 36 (81.8) 8 (18.2)
Vascular invasion 0.630 0.086
 No 27 (60.0) 18 (40.0) 42 (93.3) 3 (6.7)
 Yes 18 (54.5) 15 (45.5) 26 (78.8) 7 (21.2)
BCLC stage 0.777 0.155
 B 15 (60.0) 10 (40.0) 24 (96.0) 1 (4.0)
 C 30 (56.6) 23 (43.4) 44 (83.0) 9 (17.0)
CNLC stage 0.788 0.518
 Ib 1 (100.0) 0 (0.0) 1 (100.0) 0 (0.0)
 IIa 1 (100.0) 0 (0.0) 1 (100.0) 0 (0.0)
 IIb 7 (53.8) 6 (46.2) 13 (100.0) 0 (0.0)
 IIIa 11 (61.1) 7 (38.9) 16 (88.9) 2 (11.1)
 IIIb 25 (55.6) 20 (44.4) 37 (82.2) 8 (17.8)
AFP 0.070 0.290
 <400 ng/ml 31 (66.0) 16 (34.0) 43 (91.5) 4 (8.5)
 ≥400 ng/ml 13 (44.8) 16 (55.2) 24 (82.8) 5 (17.2)
 UK 1 (50.0) 1 (50.0) 1 (50.0) 1 (50.0)
Hepatectomy 0.384 1.000
 No 30 (54.5) 25 (45.5) 48 (87.3) 7 (12.7)
 Yes 15 (65.2) 8 (34.8) 20 (87.0) 3 (13.0)
Times of previous TACE 0.617 0.490
 0 12 (57.1) 9 (42.9) 18 (85.7) 3 (14.3)
 1 16 (61.5) 10 (38.5) 23 (88.5) 3 (11.5)
 2 9 (64.3) 5 (35.7) 13 (92.9) 1 (7.1)
 3 4 (66.7) 2 (33.3) 6 (100.0) 0 (0.0)
 >3 4 (36.4) 7 (63.6) 8 (72.7) 3 (27.3)
Previous treatment lines 0.577 0.538
 First-line 37 (58.7) 26 (41.3) 56 (88.9) 7 (11.1)
 Second-line 7 (50.0) 7 (50.0) 11 (78.6) 3 (21.4)
 > Second-line 1 (100.0) 0 (0.0) 1 (100.0) 0 (0.0)
Times of TACE, No. (%) 0.356 0.199
 ≤3 36 (55.4) 29 (44.6) 55 (84.6) 10 (15.4)
 >3 9 (69.2) 4 (30.8) 13 (100.0) 0 (0.0)
Timing of camrelizumab administration, No. (%) 1.000 0.574
 Before TACE 4 (66.7) 2 (33.3) 5 (83.3) 1 (16.7)
 After TACE 41 (56.9) 31 (43.1) 63 (87.5) 9 (12.5)
Treatment cycle of camrelizumab 0.176 1.000
 Q2W 0 (0.0) 2 (100.0) 2 (100.0) 0 (0.0)
 Q3W 45 (59.2) 31 (40.8) 66 (86.8) 10 (13.2)
Cycles of camrelizumab, No. (%) 0.023 0.080
 ≤2 2 (25.0) 6 (75.0) 8 (100.0) 0 (0.0)
 3–4 11 (45.8) 13 (54.2) 18 (75.0) 6 (25.0)
 >4 32 (69.6) 14 (30.4) 42 (91.3) 4 (8.7)
Interval between TACE and camrelizumab administration 0.454 0.658
 Within 7 days 40 (59.7) 27 (40.3) 58 (86.6) 9 (13.4)
 Within 8 to 14 days 3 (60.0) 2 (40.0) 5 (100.0) 0 (0.0)
 Within 15 to 28 days 2 (33.3) 4 (66.7) 5 (83.3) 1 (16.7)
Treatment regimen 0.341 1.000
 Monotherapy of camrelizumab 21 (52.5) 19 (47.5) 35 (87.5) 5 (12.5)
 Combination therapy with TKI 24 (63.2) 14 (36.8) 33 (86.8) 5 (13.2)

ORR, objective response rate; DCR, disease control rate; HBV, hepatitis B virus; ECOG PS, Eastern Cooperative Oncology Group Performance Status; BCLC, Barcelona Clinic Liver Cancer; CNLC, China liver cancer; AFP, alpha-fetoprotein; UK, unknown; TACE, transarterial chemoembolization; Q2W, every 2 weeks; Q3W, every 3 weeks; TKI, tyrosine kinase inhibitors. The bold values indicate the comparison with statistical significance.