Evidence map›Paper›PMID 40325791›Full record

ArticleActa oncologica (Stockholm, Sweden)2025

Patients with uHCC and Child-Pugh B8/9 also benefit from a combination of antiangiogenic agents and PD-1 inhibitors: a multicenter real-world study.

Xiaoyan Ding, Xue Yin, Linlin Zheng, Lin Zhou, Junke Hu, Wei Sun, Lei Sun, Yanjun Shen, Ying Teng, Yawen Xu and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Acta oncologica (Stockholm, Sweden), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

13 authors.

Xiaoyan Ding *Department of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xue Yin *Department of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Linlin ZhengJinan Eco-environmental Monitoring Center of Shandong Province, Jinan, Shandong Province, China.
Lin ZhouDepartment of Interventional Radiology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Junke HuDepartment of Pathology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Wei SunDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Lei SunDepartment of Pathology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yanjun ShenDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Ying TengDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yawen XuDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Wendong LiDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Mei LiuDepartment of Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China. liumei@ccmu.edn.cn.
Jinglong ChenDepartment of Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China. cjl6412@ccmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposePatients with unresectable hepatocellular carcinoma (uHCC) and Child-Pugh grade B face limited treatment options and poor outcomes. This study aims to evaluate whether the effect and safety of combining tyrosine kinase inhibitors (TKIs) with progressive disease (PD)-1 inhibitors in uHCC patients with Child-Pugh B7 (CP7) and B8/9 (CP8/9) differ.

methodsThis multicenter retrospective study included 179 uHCC patients with Child-Pugh B (CP7 group: n = 106; CP8/9 group: n = 73), receiving a combination of lenvatinib/sorafenib/other TKIs and PD-1 inhibitors between December 2020 and March 2023. Progression-free survival (PFS) and overall survival (OS) were defined as the primary endpoint. Secondary endpoints included the objective response rate (ORR) and safety.

resultsThe median PFS and OS for the entire cohort were 7.3 months (95% confidence intervals [CI]: 6.3-8.3) and 16.0 months (95% CI: 12.9-19.1), respectively. No statistically significant differences were observed between CP7 and CP8/9 groups in PFS (7.8 vs. 6.3 months, p = 0.28), OS (17.8 vs. 14.0 months, p = 0.20), ORR (33.0% vs. 27.4%, p = 0.42), or safety profiles. However, the CP8/9 group had significantly higher rates of TKI dose reductions (46.6% vs. 31.1%, p = 0.04) and discontinuations (57.5% vs. 24.5%, p < 0.001). Notably, 30.2% of patients maintained sustained radiographic responses despite advanced liver dysfunction.

interpretationCombining TKIs with PD-1 inhibitors is an effective and well-tolerated option for HCC patients with Child-Pugh B, including those with CP8/9.

Indexed as

Angiogenesis InhibitorsAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularImmune Checkpoint InhibitorsLiver NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPhenylurea CompoundsProgrammed Cell Death 1 ReceptorProgression-Free SurvivalProtein Kinase InhibitorsAngiogenesis InhibitorsImmune Checkpoint InhibitorslenvatinibPDCD1 protein, humanPhenylurea CompoundsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsQuinolinesSorafenib

Identifiers

PMID40325791
PMCPMC12067986

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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.