Systematic review: managing suboptimal treatment responses in autoimmune hepatitis with conventional and nonstandard drugs

被引:55
作者
Selvarajah, V. [1 ,2 ]
Montano-Loza, A. J. [1 ,2 ]
Czaja, A. J. [3 ]
机构
[1] Univ Alberta Hosp, Div Gastroenterol, Edmonton, AB T6G 2B7, Canada
[2] Univ Alberta Hosp, Liver Unit, Edmonton, AB T6G 2B7, Canada
[3] Mayo Clin, Coll Med, Div Gastroenterol & Hepatol, Rochester, MN USA
关键词
CHRONIC ACTIVE HEPATITIS; PRIMARY SCLEROSING CHOLANGITIS; THIOPURINE METHYLTRANSFERASE DEFICIENCY; LIVER ANTIGEN/LIVER PANCREAS; SOLID-ORGAN TRANSPLANTATION; INFLAMMATORY-BOWEL-DISEASE; PRIMARY BILIARY-CIRRHOSIS; OF-THE-LITERATURE; MYCOPHENOLATE-MOFETIL; CORTICOSTEROID-THERAPY;
D O I
10.1111/apt.12042
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Corticosteroid treatment for autoimmune hepatitis has been shown by randomised controlled clinical trials to ameliorate symptoms, normalise liver tests, improve histological findings and extend survival. Nevertheless, suboptimal responses to corticosteroid treatment still occur. Aim To describe the current definitions, frequencies, clinical relevance and treatment options for suboptimal responses, and to discuss alternative medications that have been used off-label for these occurrences. Methods Literature search was made for full-text papers published in English using the keyword autoimmune hepatitis. Authors' personal experience and investigational studies also helped to identify important contributions to the literature. Results Suboptimal responses to standard therapy include treatment failure (7%), incomplete response (14%), drug toxicity (13%) and relapse after drug withdrawal (5086%). The probability of a suboptimal response prior to treatment is higher in young patients and in patients with a severe presentation, jaundice, high MELD score at diagnosis, multilobular necrosis or cirrhosis, antibodies to soluble liver antigen, or inability to improve by clinical indices within two weeks or by MELD score within 7 days of conventional corticosteroid treatment. Management strategies have been developed for the adverse responses and nonstandard drugs, including mycophenolate mofetil, budesonide, ciclosporin, tacrolimus, sirolimus and rituximab, are emerging as rescue therapies or alternative frontline agents. Conclusions Once diagnosed, the suboptimal response should be treated by a highly individualised and well-monitored regimen, preferentially using first-line therapy. Nonstandard drugs warrant consideration as salvage or second-line therapies.
引用
收藏
页码:691 / 707
页数:17
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