Evidence map›Paper›PMID 42257955›Full record

ArticleSurgical endoscopy2026

Effect of adjuvant transarterial chemoembolization on survival in hepatocellular carcinoma with microvascular invasion: a landmark analysis.

Tian-Chen Zhang, Wei-Li Jia, Yu Cao, Chen Feng, Zhen-Qi Li, Shuai Xu, Yi-Lin Hu, Fan Zhang, Xiong Chen, Nian-Xin Xia and 5 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Surgical endoscopy, 2026. 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

15 authors.

Tian-Chen ZhangThe First School of Clinical Medicine, First Affiliated Hospital of Lanzhou University, Lanzhou, China.
Wei-Li JiaThe First School of Clinical Medicine, First Affiliated Hospital of Lanzhou University, Lanzhou, China.
Yu CaoSenior Department of Hepato-Pancreato-Biliary Surgery, The First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Chen FengSenior Department of Hepato-Pancreato-Biliary Surgery, The First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Zhen-Qi LiSenior Department of Hepato-Pancreato-Biliary Surgery, The First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Shuai XuDepartment of Liver Transplantation and Hepatobiliary Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Yi-Lin HuDepartment of General Surgery, General Hospital of Central Theater Command, Wuhan, China.
Fan ZhangDepartment of Hepatobiliary Pancreatic Surgery, Affiliated Hospital of Binzhou Medical College, Binzhou, China.
Xiong ChenDepartment of Hepatobiliary Surgery, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
Nian-Xin XiaFaculty of Hepato-Pancreato-Biliary Surgery, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Wen-Chao ZhaoFaculty of Hepato-Pancreato-Biliary Surgery, the Sixth Medical Center of PLA General Hospital, Beijing, China.
Ming-Gen HuSenior Department of Hepato-Pancreato-Biliary Surgery, The First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Shu-Qun ChengDepartment of Hepatic Surgery, the Eastern Hepatobiliary Surgery Hospital, Navy Military Medical University, 225 Changhai Road, Shanghai, 200433, China. chengshuqun@aliyun.com.
Xiu-Ping ZhangSenior Department of Hepato-Pancreato-Biliary Surgery, The First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Beijing, 100853, China. xiupingzhang@aliyun.com.
Rong LiuThe First School of Clinical Medicine, First Affiliated Hospital of Lanzhou University, Lanzhou, China. liurong301@126.com.ORCID http://orcid.org/0000-0001-5170-6474

Funding

Beijing Nova Program 20230484372Beijing Nova Program 20250484809Capital Health Research and Development of Special Fund CFH 2024-4-5026Natural Science Foundation of Beijing Municipality F252053Natural Science Foundation of Beijing Municipality L242144Young Elite Scientists Sponsorship Program by BAST BYESS2024001Young Elite Scientists Sponsorship Program by CAST 2023QNRC001
6 · The paper itself

Abstract

backgroundThe prognostic significance of adjuvant transarterial chemoembolization (TACE) in hepatocellular carcinoma (HCC) patients with microvascular invasion (MVI) remains controversial. Furthermore, current literature often overlooks the treatment timing, and conventional survival analyses fail to address the immortal time bias introduced by delayed TACE initiation. This study aimed to evaluate the true clinical value of adjuvant TACE after adjusting for this bias.

methodsThis retrospective multicenter study included 512 HCC patients with MVI who underwent curative hepatectomy with or without adjuvant TACE between 2018 and 2024. Propensity score matching (PSM) was used to balance baseline characteristics. To rigorously adjust for immortal time bias, landmark analysis at 2-, 4-, 6-, and 12-month after surgery, along with time-dependent Cox regression (TDC) analysis, was performed.

resultsIn the entire cohort, conventional Kaplan-Meier analysis showed better overall survival (OS) and recurrence-free survival (RFS) in the TACE group than in the NO-TACE group (all p < 0.05). However, landmark analysis showed improved OS at the 4-, 6-, and 12-month landmarks (HR 0.68, 0.70, 0.69, respectively), whereas RFS differed significantly only at the 6-month landmark (p = 0.020). TDC analysis showed that adjuvant TACE was associated with improved OS (HR 0.63, 95% CI 0.47-0.85, p = 0.002) but not RFS. In the subgroup with tumor size ≥ 5 cm, landmark analysis showed significant advantages in both OS and RFS (all p < 0.05), and TDC analysis further revealed that adjuvant TACE was linked to improved OS (HR 0.46, 95% CI 0.30-0.69, p < 0.001) and RFS (HR 0.66, 95% CI 0.47-0.92, p = 0.014).

conclusionAdjuvant TACE was associated with improved OS in HCC patients with MVI, particularly in high-risk patients with tumor size ≥ 5 cm, who showed consistent improvements in both OS and RFS. The potential benefit of adjuvant TACE may extend beyond the conventional early postoperative period in MVI patients with tumor size ≥ 5 cm.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticLiver NeoplasmsAgedChemotherapy, AdjuvantFemaleHepatectomyHumansMaleMicrovesselsMiddle AgedNeoplasm InvasivenessPrognosisRetrospective StudiesAdjuvant transarterial chemoembolizationHepatocellular carcinomaImmortal time biasLandmark analysisMicrovascular invasion

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Registered trials

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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.