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. 2020 Jan 5;50(1):15–46. doi: 10.1111/hepr.13438

Table 12.

Transcatheter arterial chemoembolization

Hepatocellular carcinoma

n (%)

Intrahepatic cholangiocarcinoma

n (%)

Combined hepatocellular cholangiocarcinoma

n (%)

Transarterial therapy n = 16 920 n = 76 n = 115
Not performed 8586 (50.7) 697 (91.6) 74 (64.3)
Performed 8334 (49.3) 64 (8.4) 41 (35.7)
Transcatheter arterial chemoembolization n = 8283 n = 63 n = 41
Not performed 729 (8.8) 24 (38.1) 11 (26.8)
Performed 7554 (91.2) 39 (61.9) 30 (73.2)
Therapy through implanted catheter system n = 7102 n = 56 n = 41
Not performed 6488 (91.4) 42 (75.0) 32 (78.0)
Performed 614 (8.6) 14 (25.0) 9 (22.0)
Embolic agent n = 7012 n = 33 n = 30
Lipiodol alone 1125 (16.0) 8 (24.2) 10 (33.3)
Gelatin sponge alone 157 (2.2) 1 (3.0) 2 (6.7)
Lipiodol + gelatin sponge 5518 (78.7) 22 (66.7) 17 (56.7)
Other 212 (3.0) 2 (6.1) 1 (3.3)
Lipiodol dose n = 5250 n = 18 n = 20
Not used 2 (0.0) 0 (0.0) 0 (0.0)
0.1–1.0 440 (8.4) 0 (0.0) 1 (5.0)
1.1–3.0 2002 (38.1) 5 (27.8) 4 (20.0)
3.1–5.0 1439 (27.4) 7 (38.9) 10 (50.0)
5.1–7.0 559 (10.6) 3 (16.7) 2 (10.0)
7.1–10.0 662 (12.6) 3 (16.7) 3 (15.0)
>10 146 (2.8) 0 (0.0) 0 (0.0)
Combination with chemotherapy agents n = 7804 n = 38 n = 30
Doxorubicin 399 2 0
Epirubicin 4281 16 19
Mitomycin 1008 4 3
Cisplatin 1416 10 6
SMANCS 203 3 1
Miriplatin 131 0 0
5FU 97 1 1
Interferon 17 1 0
Other 252 1 0
Percentages not calculated as multiple choices were allowed
Area of embolization n = 6385 n = 33 n = 24
<1 segment 2339 (36.6) 10 (30.3) 3 (12.5)
≥1 segment to <1 lobe 2574 (40.3) 12 (36.4) 10 (41.7)
≥1 lobe to < entire liver 1058 (16.6) 9 (27.3) 8 (33.3)
Entire liver 414 (6.5) 2 (6.1) 3 (12.5)
Complications n = 241 n = 2 n = 0
Acute cholecystitis 26 1 0
Biloma 10 0 0
Hepatic abscess 27 0 0
Hepatic infarction 11 0 0
Liver failure 48 0 0
Tumor rupture 9 0 0
Gastrointestinal hemorrhage 10 0 0
Pulmonary infarction 0 0 0
Spinal cord injury 0 0 0
Other 100 1 0
Percentages not calculated as multiple choices were allowed
Direct response assessment n = 5602 n = 28 n = 22
TE4a 1134 (20.2) 5 (17.9) 1 (4.5)
TE4b 1494 (26.7) 3 (10.7) 4 (18.2)
TE3 1459 (26.0) 9 (32.1) 6 (27.3)
TE2 1053 (18.8) 6 (21.4 7 (31.8)
TE1 325 (5.8) 3 (10.7) 2 (9.1)
Overall response at 3 months n = 5128 n = 23 n = 19
CR 2100 (41.0) 7 (30.4) 3 (15.8)
PR 1118 (21.8) 5 (21.7) 4 (21.1)
SD 803 (15.7) 5 (21.7) 6 (31.6)
PD 1107 (21.6) 6 (26.1) 6 (31.6)
Overall response at 6 months n = 4505 n = 21 n = 16
CR 1806 (40.1) 5 (23.8) 2 (12.5)
PR 781 (17.3) 5 (23.8) 3 (18.8)
SD 545 (12.1) 2 (9.5) 3 (18.8)
PD 1373 (30.5) 9 (42.9) 8 (50.0)

For all parameters, n is the total number of patients, excluding those in the “unknown” category, and (%) is the percentage of n.

5FU, fluorouracil; CR, complete response; PD, progressive disease; PR, partial response; SD, stable disease; SMANCS, styrene maleic acid neocarzinostatin; TE1, treatment effect in target lesion (progressive disease); TE2, treatment effect in target lesion (partial response); TE3, treatment effect in target lesion (partial response); TE4a; treatment effect in target lesion (complete response with ablative margin); TE4b, treatment effect in target lesion (complete response without ablative margin).