Evidence map›Paper›PMID 41877798›Full record

ArticleFrontiers in medicine2026

Ishak stage 6 fibrosis is more likely to regress than stage 5 in CHB patients undergoing entecavir therapy.

Mengjie Li, Xiaogang Hao, Yuanyuan Li, Chao Zhang, Yongping Chen, Zujiang Yu, Qin Li, Lin Tan, Dedong Xiang, Qinghua Shang and 15 more

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01965418 (A Clinical Evaluation on Traditional Chinese Medicine Diagnosis and Treatment Program Blocking and Reversing Hepatitis B-related Liver Fibrosis - a Randomized, Controlled, Double-blind, Multi-center Clinical Trial), which is not on this map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01965418 phase4unknown statusnot on this map

A Clinical Evaluation on Traditional Chinese Medicine Diagnosis and Treatment Program Blocking and Reversing Hepatitis B-related Liver Fibrosis - a Randomized, Controlled, Double-blind, Multi-center Clinical Trial

TypeinterventionalSponsorBeijing 302 HospitalRan2013Enrolled1,000ConditionsLiver Fibrosis, Chronic Hepatitis BArmsFufang Biejia Ruangan Tablet, Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Mengjie Li *School of Pharmaceutical Sciences, Shandong University of Traditional Chinese Medicine, Jinan, China.
Xiaogang Hao *Department of Inpatient and Medical Record Management, Chinese PLA General Hospital, Beijing, China.
Yuanyuan Li *Department of Phase I Clinical Trial Ward, Senior Department of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Chao Zhang *Department of Infectious Diseases, Chinese PLA General Hospital, Beijing, China.
Yongping Chen *Department of Infectious and Liver Diseases, Liver Research Center, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Zujiang Yu *Department of Infectious Disease, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Qin Li *Fuzhou Infectious Diseases Hospital, Fuzhou, Fujian, China.
Lin TanDepartment of Liver Disease, Fuyang 2nd People's Hospital, Fuyang, Anhui, China.
Dedong XiangDepartment of Infectious Diseases, Southwest Hospital, the Third Military Medical University, Chongqing, China.
Qinghua ShangTherapeutic Center for Liver Disease, the 960th Hospital of PLA, Taian, Shandong, China.
Chunliang LeiGuangzhou 8th People's Hospital, Guangzhou, Guangdong Province, China.
Liang ChenDepartment of Hepatic Diseases, Shanghai Public Health Clinical Center, Shanghai, China.
Xiaoyu HuNational Integrative Medicine Clinical Base for Infectious Diseases and Department of Infectious Diseases, Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Jing WangAffiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Huabao LiuTraditional Chinese Medicine Hospital of Chongqing, Chongqing, China.
Wei LuTianjin Second People's Hospital, Tianjin Institute of Hepatology, Tianjin, China.
Yan ChenDepartment of Liver Diseases, Chinese PLA General Hospital, Beijing, China.
Zheng DongDepartment of Liver Diseases, Chinese PLA General Hospital, Beijing, China.
Wenlin BaiDepartment of Liver Diseases, Chinese PLA General Hospital, Beijing, China.
Eric M YoshidaDivision of Gastroenterology, Vancouver General Hospital, Vancouver, BC, Canada.
Nahum Mendez-SanchezLiver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico.
Ke-Qin HuDivision of Gastroenterology and Hepatology, University of California, Irvine, School of Medicine, Irvine, CA, United States.
Xingshun QiDepartment of Gastroenterology, General Hospital of Northern Theater Command (formerly General Hospital of Shenyang Military Area), Shenyang, Liaoning, China.
Yongping YangDepartment of Liver Diseases, Chinese PLA General Hospital, Beijing, China.
Jingfeng BiDepartment of Phase I Clinical Trial Ward, Senior Department of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic hepatitis B (CHB) patients with milder baseline fibrosis have traditionally been considered more likely to achieve histological improvement after antiviral therapy. However, our previous finding suggests that patients with Ishak stage 6 may have greater potential for fibrosis regression than those with stage 5. This study aimed to evaluate whether CHB patients with Ishak stage 6 are more likely to achieve fibrosis regression than those with stage 5 after entecavir (ETV) monotherapy or ETV in combination with Biejia-Ruangan (ETV + BR) therapy. Methods: Baseline Ishak fibrosis stage served as the main analytic variable, while the use of concomitant traditional Chinese medicine was included as a stratification factor. Demographic characteristics, viral markers, and baseline laboratory parameters were incorporated as covariates. A logistic regression model was applied to evaluate the association between baseline Ishak stage and fibrosis regression. Based on this model, a sensitivity analysis was further performed in the subgroup of patients with baseline Ishak stage 5 or 6 to assess the robustness of the findings. A generalized additive model (GAM) was additionally applied to explore potential non-linear stage-related patterns. Results: A total of 705 patients had paired biopsy data. The fibrosis regression rate was 50.21% in stage 6 versus 45.58% in stage 5. In the multivariable logistic regression analysis, baseline Ishak stage 6 was associated with a higher likelihood of fibrosis regression compared with stage 5 ( Conclusion: Among CHB patients treated with ETV, those with baseline Ishak stage 6 were more likely to achieve histological fibrosis regression than those with stage 5. Clinical trial registration: Identifier NCT01965418.

Indexed as

chronic hepatitis Bentecavirfibrosis regressionIshak stagelogistic regression

Identifiers

PMID41877798
PMCPMC13006690

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.