Evidence map›Paper›PMID 42144789›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2026

Prognostic Value of Pathological Response After Conversion Therapy and Salvage Surgery in Unresectable Hepatocellular Carcinoma.

Qi-Yu Chi, Xiao-Di Gao, Mi Wang, Quan-Yuan Liu, Yong-Yi Zeng, Lan-Fang Yang, Zi-Jian Liu, Shuang-Jia Wang, Shan-Geng Weng, Zhi-Bo Zhang

Abstract readMulticenter Study
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. Prognostic Value of Pathological Response After Conversion Therapy and Salvage Surgery in Unresectable Hepatocellular Carcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
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.

Qi-Yu ChiDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Xiao-Di GaoDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Mi WangDepartment of Pathology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
Quan-Yuan LiuDepartment of Hepatobiliary Surgery, The Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
Yong-Yi ZengDepartment of Hepatopancreatobiliary Surgery, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, China.
Lan-Fang YangDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Zi-Jian LiuDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Shuang-Jia WangDepartment of Hepato-Biliary-Pancreatic and Vascular Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Shan-Geng WengDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Zhi-Bo ZhangDepartment of Hepatopancreatobiliary Surgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou, China.

Funding

Fujian Provincial Health Technology Project 2023CXA029The Natural Science Foundation of Fujian Province 2026J001500
6 · The paper itself

Abstract

BACKGROUND AND

aimsTo evaluate the prognostic significance of pathological response in patients with initially unresectable hepatocellular carcinoma (uHCC) who underwent salvage resection after successful conversion with lenvatinib, anti-PD-1 antibodies, and locoregional therapy (LPLRT).

methodsThis multicenter retrospective study included 102 uHCC patients who achieved curative resection after LPLRT across four tertiary centers in China. Residual viable tumour (pRVT) ratio was used to assess pathological response. Optimal pRVT cutoffs for overall survival (OS) and recurrence-free survival (RFS) were identified using X-tile (a statistical tool that identifies optimal prognostic cutoff values for continuous variables by systematically maximizing the log-rank statistic). Survival was analysed by Kaplan-Meier and log-rank tests, and prognostic factors by Cox regression analyses.

resultsAmong 102 patients, 25 (24.5%) achieved pathological complete response (pCR). X-tile identified pRVT thresholds of 10% and 35% as optimal for predicting OS and RFS, respectively. Patients with pRVT ≤ 10% had superior OS (1-, 2-, 3 year: 96.6%, 89.8%, 82.5%) compared with pRVT > 10% (95.5%, 73.0%, 49.4%; p = 0.002). pRVT ≤ 35% was associated with longer RFS (1-, 2 year: 60.5%, 47.1% vs. 24.0%, 10.0%; p < 0.001). Similar trends persisted after excluding pCR cases. On multivariate analysis, NLR < 2.6, adjuvant therapy, and pRVT ≤ 10% independently predicted improved OS, while age < 60 years was adverse for RFS, and NLR < 2.6 and pRVT ≤ 35% were independently associated with prolonged RFS. No clinical variables predicted pRVT thresholds.

conclusionspRVT refines postoperative prognostic assessment in uHCC after multimodal conversion therapy. Thresholds of ≤ 10% for OS and ≤ 35% for RFS serve as practical cutoffs for postoperative risk stratification.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsSalvage TherapyAdultAgedChinaFemaleHepatectomyHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm, ResidualPathologic Complete ResponsePhenylurea CompoundsPrognosisPhenylurea CompoundsConversion therapypathological responseprognosissalvage surgeryunresectable hepatocellular carcinoma

Identifiers

PMID42144789
PMCPMC13181223

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.