Evidence map›Paper›PMID 40281460›Full record

ArticleBMC cancer2025

The safety and efficacy of tyrosine kinase inhibitors and programmed cell death protein- 1 inhibitors combined with HAIC/TACE in the treatment of recurrent unresectable hepatocellular carcinoma.

Wei Deng, Jin Xie, Tao Wang, Laihui Luo, Guoqing Zhu, Yongqiang Xiao, Jiahao Tao, Liucong Lin, Xian Ge, Wu Wen and 7 more

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. 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

17 authors.

Wei Deng *Department of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.ORCID http://orcid.org/0009-0002-9468-9234
Jin Xie *Department of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Tao Wang *Department of Day Surgery Ward, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Laihui LuoDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.ORCID http://orcid.org/0000-0003-3351-2187
Guoqing ZhuDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Yongqiang XiaoDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.ORCID http://orcid.org/0000-0003-2626-9182
Jiahao TaoDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Liucong LinDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Xian GeDepartment of Pathology, Jiangxi Province, The First Affiliated Hospital of Nanchang University, Nanchang City, 330006, China.
Wu WenDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Minglong WangDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Bin YuDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Yu LiuDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Rongguang LuoDepartment of Medical Imaging and Interventional Radiology, Jiangxi Province, The First Affiliated Hospital of Nanchang University, Nanchang City, 330006, China.
Renhua WanDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China.
Zhigao HuDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China. 854189568@qq.com.
Renfeng ShanDepartment of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang City, Jiangxi Province, 330006, China. srf1978@126.com.ORCID http://orcid.org/0000-0001-5016-7448

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatocellular carcinoma (HCC) frequently recurs after surgical treatment, necessitating effective postoperative recurrence management for improved long-term patient outcomes. Currently, no standardized treatment approach exists for recurrent unresectable HCC. This study aims to investigate the safety and efficacy of combining tyrosine kinase inhibitors (TKIs) and programmed cell death protein-1 (PD-1) inhibitors with hepatic arterial infusion chemotherapy (HAIC) or transarterial chemoembolization (TACE) in the treatment of recurrent unresectable HCC.

methodsA retrospective analysis was conducted on clinical data from 83 patients diagnosed with unresectable recurrent HCC. Patients were categorized into three groups based on their treatment regimens: HAIC combined with TKIs and PD-1 inhibitors (HTP), TACE combined with TKIs and PD-1 inhibitors (TTP), and TACE alone. Treatment efficacy and safety were compared among these groups, and potential risk factors were identified.

resultsThe median progression-free survival (PFS) for patients in the HTP group, TTP group, and TACE alone group was found to be 13.7, 9.2, and 2.5 months (p = 0.001, p = 0.002). According to the mRECIST criteria, the disease control rates (DCR) in the HTP, TTP and TACE groups was 89.7%, 75.0%, 50.0% (p = 0.002); objective response rates (ORR) was 44.8%, 35%, 14.7% (p = 0.037); and complete response (CR) was 17.2%, 0, 0 (p = 0.005). No serious adverse reactions were observed in the HTP and TTP groups.

conclusionThe HTP and TTP groups were safe and effective compared to TACE alone for the treatment of recurrent unresectable hepatocellular carcinoma, and the HTP group demonstrated a superior CR.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularChemoembolization, TherapeuticImmune Checkpoint InhibitorsLiver NeoplasmsNeoplasm Recurrence, LocalProtein Kinase InhibitorsAdultAgedCombined Modality TherapyFemaleHumansInfusions, Intra-ArterialMaleMiddle AgedProgrammed Cell Death 1 ReceptorImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsTyrosine Kinase InhibitorsHepatic arterial infusion chemotherapyHepatocellular carcinomaProgrammed cell death protein- 1 inhibitorsTransarterial chemoembolizationTyrosine kinase inhibitorsUnresectable recurrence

Identifiers

PMID40281460
PMCPMC12032721

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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.