Patients who survive hematopoietic cell transplantation (HCT) have multiple
risk factors for chronic liver disease, including hepatitis virus infectio
n, iron overload, and chronic graft-versus-host disease (GVHD). We studied
3,721 patients who had survived 1 or more years after HCT at a single cente
r and identified patients with histologic or clinical evidence of cirrhosis
. Risk factors for the development of cirrhosis were evaluated and compared
with a group of matched control subjects. Cirrhosis was identified in 31 o
f 3,721 patients surviving 1 or more years after HCT, 23 of 1,850 patients
surviving 5 or more years, and in 19 of 860 patients surviving 10 or more y
ears. Cumulative incidence after 10 years was estimated to be 0.6% and afte
r 20 years was 3.8%. The median time from HCT to the diagnosis of cirrhosis
was 10.1 years (range, 1.2 to 24.9 years). Twenty-three patients presented
with complications of portal hyper-tension, and 1 presented with hepatocel
lular carcinoma. Thirteen patients have died from complications of liver di
sease, and 2 died of other causes. Three patients have undergone orthotopic
liver transplantation. Hepatitis C virus infection was present in 25 of 31
(81%) of patients with cirrhosis and in 14 of 31 (45%) of controls (P = .0
1). Cirrhosis was attibutable to hepatitis C infection in 15 of 16 patients
presenting more than 10 years after HCT. There was no difference in the pr
evalence of acute or chronic GVHD, duration of posttransplant immunosuppres
sion, or posttransplant marrow iron stores between cases and controls. Cirr
hosis is an important late complication of hematopoietic cell transplantati
on and in most cases is due to chronic hepatitis C. Long-term survivors sho
uld be evaluated for the presence of abnormal liver function and hepatitis
virus infection. (C) 1999 by The American Society of Hematology.