共 24 条
A baseline tool for predicting response to peginterferon alfa-2a in HBeAg-positive patients with chronic hepatitis B
被引:39
作者:

Chan, H. L. Y.
论文数: 0 引用数: 0
h-index: 0
机构:
Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Messinger, D.
论文数: 0 引用数: 0
h-index: 0
机构:
Prometris GmbH, Mannheim, Germany Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Papatheodoridis, G. V.
论文数: 0 引用数: 0
h-index: 0
机构:
Natl & Kapodistrian Univ Athens, Med Sch, Athens, Greece Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Cornberg, M.
论文数: 0 引用数: 0
h-index: 0
机构:
Hannover Med Sch, Hannover, Germany Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Xie, Q.
论文数: 0 引用数: 0
h-index: 0
机构:
Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Shanghai, Peoples R China Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Piratvisuth, T.
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h-index: 0
机构:
Prince Songkla Univ, Hat Yai, Thailand Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Ren, H.
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h-index: 0
机构:
Chongqing Med Univ, Affiliated Hosp 2, Chongqing, Peoples R China Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Kennedy, P. T.
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h-index: 0
机构:
Barts & London Queen Marys Sch Med & Dent, London, England Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Thompson, A.
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h-index: 0
机构:
St Vincents Hosp Melbourne, Fitzroy, Vic, Australia Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Caputo, A.
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h-index: 0
机构:
Roche SpA, Monza, Italy Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Bakalos, G.
论文数: 0 引用数: 0
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机构:
F Hoffmann La Roche Ltd, Basel, Switzerland Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Pavlovic, V.
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h-index: 0
机构:
Roche Prod Ltd, Welwyn Garden City, Herts, England Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China

Lampertico, P.
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h-index: 0
机构:
Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol & Hepatol, CRC AM & A Migliavacca Ctr Liver Dis, Milan, Italy Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China
机构:
[1] Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China
[2] Prometris GmbH, Mannheim, Germany
[3] Natl & Kapodistrian Univ Athens, Med Sch, Athens, Greece
[4] Hannover Med Sch, Hannover, Germany
[5] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Shanghai, Peoples R China
[6] Prince Songkla Univ, Hat Yai, Thailand
[7] Chongqing Med Univ, Affiliated Hosp 2, Chongqing, Peoples R China
[8] Barts & London Queen Marys Sch Med & Dent, London, England
[9] St Vincents Hosp Melbourne, Fitzroy, Vic, Australia
[10] Roche SpA, Monza, Italy
[11] F Hoffmann La Roche Ltd, Basel, Switzerland
[12] Roche Prod Ltd, Welwyn Garden City, Herts, England
[13] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol & Hepatol, CRC AM & A Migliavacca Ctr Liver Dis, Milan, Italy
关键词:
CLINICAL-PRACTICE GUIDELINES;
SUSTAINED RESPONSE;
VIRUS GENOTYPES;
THERAPY;
COMBINATION;
MANAGEMENT;
LAMIVUDINE;
RISK;
D O I:
10.1111/apt.14862
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background: Peginterferon induces off-treatment responses in approximately one-third of patients with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B. Aim: To develop an easy-to-use baseline prediction score to identify hepatitis B virus (HBV) genotype B-/C-infected HBeAg-positive Asian patients likely to respond to peginterferon alfa-2a. Methods: Generalised additive models, multiple logistic regression (MLR) analysis and internal validation methods were applied to data from 647 HBeAg-positive patients from China, Hong Kong and Taiwan to develop a scoring system to predict response 24weeks after completing a 48-week course of peginterferon alfa-2a. Results: Five baseline factors (age, sex, alanine aminotransferase ratio, hepatitis B surface antigen (HBsAg) level and HBV DNA level) were retained in the final MLR for HBeAg seroconversion and used to develop a scoring system from 0 to 7. Among patients with scores of 0-1, 2-3, 4 or >= 5, HBeAg seroconversion was achieved in 6.4% (6/94), 23.0% (61/265), 36.4% (67/184) and 54.8% (57/104), respectively, and a combined response (HBeAg seroconversion plus HBV DNA >= 2000 IU/mL) in 5.3% (5/94), 12.8% (34/265), 25.0% (46/184) and 36.5% (38/104), respectively. Among patients with scores of 0-1, 2-3, 4 or 5, 57.0% (53/93), 12.3% (31/253), 3.4% (6/178) and 1.0% (1/100) had HBsAg >= 20000 IU/mL at treatment Week 12; only 3/91 (3.3%) with HBsAg >= 20000 IU/mL experienced a combined response at 24 weeks post-treatment (negative predictive value=97% [88/91]). Conclusion: A pre-treatment scoring system using readily available baseline characteristics identifies HBeAg-positive Asian patients likely to experience sustained HBeAg seroconversion after treatment with peginterferon alfa-2a.
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页码:547 / 555
页数:9
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