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Prednisolone withdrawal therapy enhances the effect of human lymphoblastoid interferon in chronic hepatitis B
被引:38
作者:
Krogsgaard, K
Marcellin, P
Trepo, C
Berthelot, P
SanchezTapias, JM
Bassendine, M
Tran, A
Ouzan, D
RingLarsen, H
Lindberg, J
Enriquez, J
Benhamou, JP
Bindslev, N
Bertet, S
Boyer, N
Brind, A
Civeira, MP
Housset, C
LundLaursen, A
Mas, A
Pol, S
Prieto, J
Quedens, J
Rampal, P
Schlichting, P
Soriano, G
Spacey, BEM
Hawley, S
Brand, C
Howe, I
机构:
[1] UNIV COPENHAGEN, RIGSHOSP, DEPT INFECT DIS, DK-2100 COPENHAGEN, DENMARK
[2] UNIV COPENHAGEN, RIGSHOSP, DEPT HEPATOL, DK-2100 COPENHAGEN, DENMARK
[3] UNIV COPENHAGEN, STAT RES UNIT, COPENHAGEN, DENMARK
[4] HOP BEAUJON, HEPATOL UNIT, CLICHY, FRANCE
[5] HOP HOTEL DIEU, HEPATOL UNIT, F-69288 LYON, FRANCE
[6] HOP NECKER ENFANTS MALAD, HEPATOL UNIT, PARIS, FRANCE
[7] HOSP & CLIN, LIVER UNIT, BARCELONA, SPAIN
[8] FREEMAN RD HOSP, GASTROENTEROL & LIVER UNIT, NEWCASTLE UPON TYNE, TYNE & WEAR, ENGLAND
[9] HOP ARCHET, GASTROENTEROL SERV, NICE, FRANCE
[10] INST ARNAUD TZANCK, ST LAURENT DU VAR, FRANCE
[11] OSTRA SJUKHUS, GOTHENBURG, SWEDEN
[12] HOSP SANTA CRUZ & SAN PABLO, LIVER UNIT, DEPT GASTROENTEROL, E-08025 BARCELONA, SPAIN
关键词:
chronic hepatitis B;
lymphoblastoid interferon;
prednisolone withdrawal therapy;
D O I:
10.1016/S0168-8278(96)80282-0
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background/Aims: The aim of this multicentre, randomised, controlled, clinical trial was to evaluate the effect of prednisolone followed by lymphoblastoid interferon treatment in chronic hepatitis B. Methods: Two hundred and thirteen patients with chronic hepatitis B were randomised to either prednisolone (2 weeks of 0.6 mg/kg/day, 1 week of 0.45 mg/kg/day and 1 week of 0.25 mg/kg/day) or matching placebo followed by a 2-week rest phase and then human lymphoblastoid interferon 10 MU daily for 5 days followed by 10 MU thrice weekly for 11 weeks. Of 200 evaluable patients, 33 (16.5%) were females, and 50 (25%) were male homosexuals. Thirty three patients (16.5%) had chronic persistent hepatitis, 145 (72.5%) had chronic active hepatitis and 22 (11%) had active cirrhosis. Results: Survival analysis disclosed statistically significant effects of prednisolone pre-treatment on both HBeAg disappearance and HBeAg to anti-HBe sereconversion (log-rank test statistics 5.43; p=0.02 and 4.75; p=0.03). Observed HBeAg disappearance and HBeAg to anti-HBe seroconversion rates (placebo vs. prednisolone patients) were 28% vs. 44% and 23% vs. 38%. Six months after stopping interferon, HBV DNA was negative in 51% of prednisolene patients vs. 28% of placebo patients (Chi-square test statistic 6.13; p=0.013). Prednisolone pre-treatment tended to be more effective in patients with higher transaminase levels and in patients with low levels of HBV DNA. Fifteen patients (7.5%) (13 within 1 year of follow-up) eventually lost HBsAg; 14 of these subsequently developed anti-HBs. Interferon treatment was modified in 102 patients (51%). Three out of 22 patients with cirrhosis (14%), one of whom received prednisolone pre-treatment, developed hepatic decompensation with a fatal outcome while on interferon treatment. Conclusions: Prednisolone pre-treatment significantly enhanced the treatment effect of lymphoblastoid interferon in terms of HBeAg clearance and seroconversion to anti-HBe. Treatment should be used with caution in patients with cirrhosis and avoided in patients showing signs, or with a history, of decompensated cirrhosis.
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页码:803 / 813
页数:11
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