Table 1.
Pre-LTx patients* | Post-LTx | |
---|---|---|
Number of patients | 45 | 49 |
Age [Median ± SD (range)] | 58 ± 9 (35–69) | 57 ± 11.5 (21–69) |
Gender (Male : Female) | 32 : 13 | 35 : 14 |
Race (% Caucasian) | 93% | 92% |
Diagnosis | ||
Alcoholic cirrhosis/hepatitis | 15 | 6 |
NASH | 6 | 5 |
Viral hepatitis | 2 | 5 |
PSC/PBC | 3 | 2 |
HCC# | 11 | 25 |
Other## | 8 | 6 |
Immunosuppressive Therapy | ||
Tac + MMF + P | 32 | |
Tac + MMF | 6 | |
Tac + Evr | 1 | |
Tac + P | 4 | |
Tac | 2 | |
CsA + MMF + P | 3 | |
CsA + Az + P | 1 | |
Time from LTx | ||
≤ 1month (30 days) | 15 | |
> 1 – 3 months (31–91 days) | 17 | |
≥ 3 – 8 months (92–244 days) | 14 | |
> 8 months | 3 |
One patient provided a pre and post-LTx sample.
HCC patients’ second diagnoses (if any): pre-LTX - NASH 5, alcoholic cirrhosis/hepatitis 3, viral hepatitis 1; post-LTx NASH 8, alcoholic cirrhosis/hepatitis 5, viral hepatitis 8, congenital biliary atresia 1
Other diagnosis: pre-LTx - cryptogenic 4, and 1 each lipodystrophy plus alpha1 antitrypsin deficiency, nodular regenerative hyperplasia, neuroendocrine tumor, substance abuse; post-LTx - 1 each cryptogenic, autoimmune hepatitis, Wilson’s disease, common variable immunodeficiency, cholangiocarcinoma, Waldenstrom’s macroglobulinemia
Abbr: Pre-LTx: pre liver transplant, post-LTx: post liver transplant, NASH: non-alcoholic steatohepatitis, PSC: primary sclerosing cholangitis; PBC: primary biliary cholangitis, HCC: hepatocellular carcinoma, Tac: tacrolimus, CsA: cyclosporine A, MMF: mycophenolate mofetil; P: prednisone, Az:azathioprine; Evr: everolimus