TY - JOUR
T1 - Surveillance of hepatic late adverse effects in a large cohort of long-term survivors of childhood cancer
T2 - Prevalence and risk factors
AU - Mulder, Renée L.
AU - Kremer, Leontien C.M.
AU - Koot, Bart G.P.
AU - Benninga, Marc A.
AU - Knijnenburg, Sebastiaan L.
AU - Van Der Pal, Helena J.H.
AU - Koning, Caro C.E.
AU - Oldenburger, Foppe
AU - Wilde, James C.H.
AU - Taminiau, Jan A.J.M.
AU - Caron, Huib N.
AU - Van Dalen, Elvira C.
PY - 2013/1
Y1 - 2013/1
N2 - Background: Childhood cancer survivors (CCS) are a growing group of young individuals with a high risk of morbidity and mortality. We evaluated the prevalence and risk factors of hepatic late adverse effects, defined as elevated liver enzymes, in a large cohort of CCS. Methods: The cohort consisted of all five-year CCS treated in the EKZ/AMC between 1966 and 2003, without hepatitis virus infection and history of veno-occlusive disease (VOD). Liver enzyme tests included serum levels of alanine aminotransferase (ALT) for hepatocellular injury and gamma-glutamyltransferase (γGT) for biliary tract injury. We performed multivariable linear and logistic regression analyses. Results: The study population consisted of 1404 of 1795 eligible CCS, of whom 1362 performed liver enzyme tests at a median follow-up of 12 years after diagnosis. In total, 118 (8.7%) of 1362 CCS had hepatic late adverse effects defined as ALT or γGT above the upper limit of normal. Abnormal ALT and γGT levels were found in 5.8% and 5.3%, respectively. In multivariable regression analyses treatment with radiotherapy involving the liver, higher body mass index, higher alcohol intake and longer follow-up time were significantly associated with elevated ALT and γGT levels; older age at diagnosis was only significantly associated with elevated γGT levels (all p < 0.05). Conclusion: One in twelve CCS showed signs of hepatic late adverse effects after a median follow-up of 12 years. Several risk factors have been identified. Future studies should focus on the course of long-term liver related outcomes and on the influence of radiotherapy and chemotherapy dose.
AB - Background: Childhood cancer survivors (CCS) are a growing group of young individuals with a high risk of morbidity and mortality. We evaluated the prevalence and risk factors of hepatic late adverse effects, defined as elevated liver enzymes, in a large cohort of CCS. Methods: The cohort consisted of all five-year CCS treated in the EKZ/AMC between 1966 and 2003, without hepatitis virus infection and history of veno-occlusive disease (VOD). Liver enzyme tests included serum levels of alanine aminotransferase (ALT) for hepatocellular injury and gamma-glutamyltransferase (γGT) for biliary tract injury. We performed multivariable linear and logistic regression analyses. Results: The study population consisted of 1404 of 1795 eligible CCS, of whom 1362 performed liver enzyme tests at a median follow-up of 12 years after diagnosis. In total, 118 (8.7%) of 1362 CCS had hepatic late adverse effects defined as ALT or γGT above the upper limit of normal. Abnormal ALT and γGT levels were found in 5.8% and 5.3%, respectively. In multivariable regression analyses treatment with radiotherapy involving the liver, higher body mass index, higher alcohol intake and longer follow-up time were significantly associated with elevated ALT and γGT levels; older age at diagnosis was only significantly associated with elevated γGT levels (all p < 0.05). Conclusion: One in twelve CCS showed signs of hepatic late adverse effects after a median follow-up of 12 years. Several risk factors have been identified. Future studies should focus on the course of long-term liver related outcomes and on the influence of radiotherapy and chemotherapy dose.
KW - Childhood cancer survivors
KW - Hepatic late adverse effects
KW - Prevalence
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=84871432285&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2012.07.009
DO - 10.1016/j.ejca.2012.07.009
M3 - Article
C2 - 22901831
AN - SCOPUS:84871432285
SN - 0959-8049
VL - 49
SP - 185
EP - 193
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 1
ER -