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. 2022 May 16;43(1):127–138. doi: 10.1111/liv.15286

TABLE 3.

Treatment, surveillance and follow‐up among patients who developed hepatobiliary cancer or dysplasia

Variable Cholangio‐carcinoma (N = 122) High‐grade dysplasia (N = 8) Low‐grade dysplasia (N = 51) Gallbladder cancer (N = 21) Hepatocellular carcinoma (N = 32)
Frequency of cancer/dysplasia 4.1% (122/2978) 0.3% (8/2978) 1.7% (51/2978) 0.7% (21/2978) 1.1% (32/2978)
Symptoms a at diagnosis of CCA/dysplasia
Yes 84 (68.9%) 6 (75.0%) 2 (3.9%) NA NA
No 31 (25.4%) 1 (12.5%) 2 (3.9%)
Unknown/Missing 7 (5.7%) 1 (12.5%) 47 (92.2%)
Frequency of cancer/dysplasia per type of surveillance
None 7.7% (27/350) 0% (0/350) 0% (0/350) 0.6% (2/350) 2.9% (10/350)
MRI and/or US 3.3% (63/1900) 0.4% (8/1900) 0.8% (16/1900) 0.8% (15/1900) 0.8% (16/1900)
Including ERCP 4.4% (32/728) 0% (0/728) 4.8% (35/728) 0.5% (4/728) 0.8% (6/728)
First treatment for CCA/dysplasia
LTx 31 (25.4%) 3 (37.5%) 2 (3.9%) NA NA
Resection 35 (28.7%) 2 (25.0%) 1 (2.0%)
Chemotherapy 23 (18.9%) 0 0
LTx and neoadjuvant brachy‐chemotherapy 1 (0.8%) 0 0
Other 5 (4.1%) 1 (12.5%) 1 (2.0%)
Best supportive care 17 (13.9%) 0 0
Unknown/missing 10 (8.2%) 2 (25.0%) 47 (92.2%)
Follow‐up b (years)
Mean (SD) 1.5 (2.5) 2.9 (2.9) 4.1 (3.4) 2.8 (2.7) 3.1 (3.4)
Median (IQR) 0.6 (0.2–1.7) 1.5 (1.1–6.6) 4.3 (0.6–6.7) 2.4 (0.9–3.6) 1.4 (0.5–5.7)
Range, min‐max 0.0–17.9 0.2–7.4 0.0–10.9 0.0–11.4 0.0–13.5
Categories, n (%)
<1y 76 (62.3%) 1 (12.5%) 13 (25.5%) 7 (33.3%) 12 (37.5%)
1–<5y 33 (27.0%) 4 (50.0%) 17 (33.3%) 9 (42.9%) 9 (28.1%)
5–<10y 10 (8.2%) 2 (25.0%) 19 (37.3%) 1 (4.8%) 7 (21.9%)
10–<20y 2 (1.6%) 0 2 (3.9%) 1 (4.8%) 1 (3.1%)
Missing cancer date 1 (0.8%) 1 (12.5%) 0 3 (14.3%) 3 (9.4%)

Abbreviations: CCA, cholangiocarcinoma; ERCP, endoscopic retrograde cholangiopancreatography; IQR, interquartile range; MRI, Magnetic resonance imaging; NA, Not available; SD, standard deviation; US, ultrasound.

a

Weight loss, recurrent cholangitis, jaundice, pruritus, or other suspicious PSC/cancer‐related symptom.

b

From first cancer diagnosis to death or last of follow‐up alive.