Evidence map›Paper›PMID 40693263›Full record

ArticleImmunoTargets and therapy2025

Comparative Effectiveness and Safety of Molecular Targeted Therapy Plus PD-(L)1 with or without TACE in Unresectable Hepatocellular Carcinoma: A Retrospective Study.

Jiangtao Liu, Yan Wang, Li Cui, Yan Nie, Chao Li, Wenle Tan, Ye Li, Yanhua Bai, Tao Wan, Bingyang Hu and 4 more

Abstract read
In one paragraph

Article in ImmunoTargets and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

14 authors.

Jiangtao Liu *Department of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.
Yan Wang *Department of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.
Li CuiDepartment of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.ORCID 0000-0001-6161-6958
Yan NieDepartment of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.
Chao LiDepartment of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.
Wenle TanDepartment of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.ORCID 0000-0001-5933-2833
Ye LiDepartment of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.
Yanhua BaiDepartment of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.
Tao WanFaculty of Hepato-Biliary-Pancreatic Surgery, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.
Bingyang HuFaculty of Hepato-Biliary-Pancreatic Surgery, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.
Zhe LiuFaculty of Hepato-Biliary-Pancreatic Surgery, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.
Minggen HuFaculty of Hepato-Biliary-Pancreatic Surgery, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.
Maoqiang WangDepartment of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.ORCID 0000-0002-0299-5289
Feng DuanDepartment of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aims to compare the effectiveness and safety of TACE combined with molecular targeted therapy (MTT) plus Programmed death-ligand 1 (PD-(L)1) antibodies versus MTT plus PD-(L)1 antibodies for HCC patients. Methods: Data from HCC patients who received either MTT plus PD-(L)1 (systemic therapy group) or TACE combined with MTT plus PD-(L)1 (combination therapy group) were retrospectively analyzed. The primary outcome was the objective reaction rate (ORR) at the initial assessment post-treatment initiation. Secondary outcomes included progressive free survival (PFS), overall survival (OS) and grade-3 or higher adverse events. Results: A total of 222 HCC patients were included (109 in the systemic therapy group, 113 in the combination therapy group). Propensity score matching yielded 80 patients per group. The odds ratio for ORR in the combination therapy group was 1.29 (95% CI: 0.64-2.60; p=0.479). Subgroup analysis revealed significantly higher ORR for patients with AFP≤200 ng/mL in the combination therapy group (OR=3.54, p=0.016). For patients without PVTT, the ORR odds were slightly higher with combination therapy (OR=5.33, p=0.068). Multivariate Cox regression analysis showed no significant differences in PFS (HR=0.68, p=0.131) or OS (HR=0.86, p=0.674) between the two groups. Higher baseline AFP (>200 ng/mL) was associated with worse PFS (HR=1.68, p=0.012) and OS (HR=2.33, p=0.021). Surgical resection improved PFS (HR=0.42, p<0.001) and OS (HR=0.31, p=0.004). Grade 3 or higher adverse events were more common in the combination therapy group (52% vs 15%, p<0.0001). Conclusion: No significant benefits were observed for combining TACE with MTT and PD-(L)1 in unresectable HCC patients. However, TACE may offer advantages for patients with AFP≤200 ng/mL or without PVTT.

Indexed as

hepatocellular carcinomamolecular targeted therapyPD-(L)1transarterial chemoembolization

Identifiers

PMID40693263
PMCPMC12278979

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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.