Evidence map›Paper›PMID 41800186›Full record

ArticleJHEP reports : innovation in hepatology2026

Prognostic implications of tumour number in intrahepatic cholangiocarcinoma.

Brandon Lok-Hang Chan, Yan Li, YoungJae Kim, Alex Chi-Fung Wong, Dorothy Cheuk-Yan Yiu, Landon Long Chan, Cheuk Man Chu, Changhoon Yoo, Hui-Chuan Sun, Stephen Lam Chan

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Brandon Lok-Hang ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Yan LiDepartment of Hepatobiliary Surgery and Liver Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.
YoungJae KimDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Alex Chi-Fung WongDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Dorothy Cheuk-Yan YiuDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Landon Long ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Cheuk Man ChuDepartment of Imaging and Interventional Radiology, Prince of Wales Hospital, Hong Kong.
Changhoon YooDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Hui-Chuan SunDepartment of Hepatobiliary Surgery and Liver Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.
Stephen Lam ChanDepartment of Clinical Oncology, Sir YK Pao Centre for Cancer, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Intrahepatic cholangiocarcinoma (ICC) with multiple liver tumours is staged as T2 disease in the 8 Methods: Patients who were diagnosed with ICC with solitary liver tumours or multiple liver tumours between May 2008 and December 2019 at three tertiary referral centres in Hong Kong, Seoul and Shanghai were enrolled. Kaplan-Meier analyses and multivariable Cox proportional hazards models were used to analyse the association between tumour multiplicity and overall survival (OS). Results: A total of 849 patients were included in the analysis. Among the 563 patients without distant metastasis, 434 (77.1%) and 129 (22.9%) had solitary and multiple liver tumours at baseline, respectively. The median follow-up period was 91.9 months (IQR 69.6-131.5). Median OS for patients with a solitary liver tumour, multiple liver tumours, and distant metastasis was 39.5 months (95% CI 34.4-49.2), 14.8 months (11.4-20.3), and 7.1 months (95% CI 6.1-8.3), respectively (log-rank Conclusions: Tumour multiplicity in ICC is associated with inferior OS compared with solitary liver tumours, particularly in patients with ≥4 tumours. Future ICC staging systems should consider the prognostic significance of tumour number. Impact and implications: Our research provides critical insights into the prognosis of intrahepatic cholangiocarcinoma (ICC) with multiple liver tumours, highlighting the significant impact of tumour multiplicity on survival outcomes. This work addresses the gap in the current staging system, which does not adequately reflect the poor prognosis associated with multiple tumours, especially with the presence of ≥4 tumours. Incorporating these insights into clinical practice could aid in treatment decision-making, risk stratification, and potentially improve patient care and outcomes in ICC management.

Indexed as

Biliary tract cancerMetastasesStagingSurvival

Identifiers

PMID41800186
PMCPMC12962086

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