Evidence map›Paper›PMID 37723998›Full record

ArticleTechnology in cancer research & treatment

TACE Combined with Lenvatinib and Camrelizumab for Unresectable Multiple Nodular and Large Hepatocellular Carcinoma (>5 cm).

Zhanwang Xiang, Guohong Li, Luwen Mu, Haofan Wang, Churen Zhou, Huzheng Yan, Mingsheng Huang

Abstract read
In one paragraph

Article in Technology in cancer research & treatment. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 5 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

16 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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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

7 authors.

Zhanwang XiangDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Guohong LiDepartment of Radiology, Guangdong Second Provincial General Hospital, Guangdong Provincial Emergency Hospital, Middle, Guangzhou, China.
Luwen MuDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Haofan WangDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Churen ZhouDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Huzheng YanDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Mingsheng HuangDepartment of Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0003-4749-4231

Funding

National Natural Science Foundation of China 82072035
6 · The paper itself

Abstract

backgroundThe incidence and mortality of hepatocellular carcinoma (HCC) had increased globally over the past decades. Previous studies found that transarterial chemoembolization (TACE) combined with lenvatinib had also shown efficacy in the unresectable HCC. We aimed to evaluate the safety and efficacy of TACE combined with lenvatinib and camrelizumab to treat unresectable multiple nodular and large HCC (>5 cm). MATERIALS AND

methodsBetween November 2018 and June 2021, we retrospectively recruited 82 patients with unresectable multiple nodular and large HCC (BCLC stage B or C with a single nodular diameter of >5 cm). Of the patients who had not previously been treated, 33 patients received TACE + lenvatinib + camrelizumab (group A, TLC), and 49 patients treated with TACE + lenvatinib (group B, TLB) as the initial treatment. Related efficacy and safety results were recorded and assessed.

resultsThe median follow-up periods of groups A and B were 14.5 ± 7.9 months (range, 3-36) and 12.5 ± 8.2 months (range, 3-32), respectively (P = 0.799). The progression-free survival (PFS) of groups A and B was 9.4 months and 5.9 months (P < 0.01), respectively, and overall survival (OS) was significantly longer in group A (16.4 months vs 11.0 months, P < 0.01). In group A, the local response rate (LRR) and disease control rate (DCR) were 51.5% and 81.8%, respectively, which was higher than the corresponding 46.9% and 77.6% observed in group B (P = 0.233; 0.429). Patients with BCLC B stage had better PFS and OS (P < 0.05). The BCLC stage was an independent factor that affected PFS and OS. There were no massive bleeding or treatment-related deaths.

conclusionsIn patients with unresectable multiple nodular and large HCC (single nodular diameter of >5 cm), TACE combined with target therapy and immunotherapy is safe and effective.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticLiver NeoplasmsAntibodies, Monoclonal, HumanizedHumansPhenylurea CompoundsQuinolinesRetrospective StudiesAntibodies, Monoclonal, HumanizedcamrelizumablenvatinibPhenylurea CompoundsQuinolinescamrelizumabefficacyhepatocellular carcinomalenvatinibsafetyTACE

Identifiers

PMID37723998
PMCPMC10510362

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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.