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. 2018 Aug 15;48(7):761–767. doi: 10.1111/apt.14939

Table 4.

Characteristics and treatment details of patients with AIH variants

Patient Diagnosis Age, gender Reason for prior AZA/MP failure Tioguanine therapy Biochemical response Drug survival Prednisone Comedication
mg/d Mo Baseline (mg/d) Last FU (mg/d)
1 AIH‐PSC 17, m Nonresponse, AZA/MP 21 3 Nonresponse No 20 20 UDCA (14 mg/kg)
2 AIH‐PSC 40, f Nonresponse, AZA 21 31 Incomplete Yes 10 7.5 UDCA (12 mg/kg, tacrolimus
3 AIH‐PSC 40, f Nonresponse, AZA/MP 24 97 Incomplete Noa 10 2.5 UDCA (14 mg/kg)
4 AIH‐PSC 51, m Nonresponse and intolerance, AZA 20 11 Complete Intolerant 30 5 UDCA (24 mg/kg)
5 AIH‐PSC 67, m Intolerance, AZA 10 3 Incomplete Yes 10
6 AIH‐PSC 29, m Intolerance, AZA 20 5 Complete Yes 10 UDCA (13 mg/kg)
7 AIH‐PBC 67, f Nonresponse and intolerance, MP 20 86 Complete Yes 30 10 UDCA (13 mg/kg), ciclosporin
8 AIH‐PBC 67, f Intolerance, AZA 20 93 Complete Yes UDCA (18 mg/kg)
9 AMA neg. AIH‐PBC 62, f Toxic levels and intolerance, AZA/MP 18 18 Complete Intolerant 10 10 UDCA (9 mg/kg), budesonideb
10 AMA neg. AIH‐PBC 27, f Toxic levels, AZA 24 80 Complete Noc 30 UDCA (19 mg/kg)

AZA: azathioprine; f: female; m: male; MP: mercaptopurine; UDCA: ursodeoxycholic acid.

a

Initially, nodular regenerative hyperplasia was suspected in histology, however, review of the histology by two hepatopathologists did not confirm this.

b

Budesonide (6 mg/d) was fully tapered.

c

A trial of withdrawal was offered after more than 2 years of complete biochemical remission on tioguanine monotherapy, according to recent guidelines.1