Report of an international workshop: Roadmap for management of patients receiving oral therapy for chronic hepatitis B

被引:235
作者
Keeffe, Emmet B.
Zeuzem, Stefan
Koff, Raymond S.
Dieterich, Douglas T.
Esteban-Mur, Rafael
Gane, Edward J.
Jacobson, Ira M.
Lim, Seng G.
Naoumov, Nikolai
Marcellin, Patrick
Piratvisuth, Teerha
Zoulim, Fabien
机构
[1] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
[2] JW Goethe Univ Hosp, Frankfurt, Germany
[3] Univ Connecticut, Sch Med, Farmington, CT USA
[4] CUNY Mt Sinai Sch Med, New York, NY 10029 USA
[5] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
[6] Auckland Hosp, Auckland, New Zealand
[7] Cornell Univ, Weill Med Coll, New York, NY USA
[8] Natl Univ Singapore Hosp, Singapore 117548, Singapore
[9] UCL, Inst Hepatol, London, England
[10] Hop Beaujon, Clichy, France
[11] Songklanagarind Hosp, Hat Yai, Thailand
[12] Univ Lyon, INSERM, Lyon, France
[13] Liver Dept, Hotel Dieu, Lyon, France
关键词
D O I
10.1016/j.cgh.2007.05.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
An international group of experienced hepatologists and virologists conducted a single-day workshop to review the management of patients with chronic hepatitis B receiving treatment with oral nucleosides or nucleotides. Guidelines regarding on-treatment management and available published data on the importance of serum hepatitis B virus (HBV) DNA as a marker of outcomes were reviewed. On-treatment monitoring strategies to define early virologic responses that might be predictive of better outcomes and a reduced risk of viral resistance were proposed for further study. This treatment plan, labeled the roadmap concept, recommends monitoring of serum HBV DNA levels to identify outcomes of therapy. Primary treatment failure was defined as a reduction of serum HBV DNA levels by less than 1 log(10) IU/mL from baseline at week 12. Measurement of the HBV DNA level at week 24 was considered essential to characterize virologic responses as complete, partial, or inadequate. Complete virologic response was defined as negative HBV DNA by a sensitive assay (< 60 IU/mL or < 300 copies/mL); partial virologic response was defined as HBV DNA levels less than 2000 IU/mL (4 log(10) copies/mL), and inadequate virologic response was defined as HBV DNA levels of 2000 IU/mL or greater (4 log(10) copies/mL). Strategies are proposed for managing patients in each of these categories, depending in part on the rapidity with which HBV DNA suppression is achieved and the emergence of genotypic mutations that reduce the effectiveness of a specific drug. Future studies of the use of the roadmap concept in improving outcomes of chronic hepatitis B are warranted.
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页码:890 / 897
页数:8
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