Evidence map›Paper›PMID 36103864›Full record

ArticleOncology2023

The Impact of Lenvatinib on Tumor Blood Vessel Shrinkage of Hepatocellular Carcinoma during Treatment: An Imaging-Based Analysis.

Nozomu Muraishi, Yusuke Kawamura, Norio Akuta, Junichi Shindoh, Masaru Matsumura, Satoshi Okubo, Shunichiro Fujiyama, Tetsuya Hosaka, Satoshi Saitoh, Hitomi Sezaki and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  4. Review
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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

17 authors at 2 institutions in 1 country.

Nozomu MuraishiDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan, nonmoment@gmail.com.
Yusuke KawamuraDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Norio AkutaDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Junichi ShindohOkinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Masaru MatsumuraOkinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Satoshi OkuboOkinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Shunichiro FujiyamaDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Tetsuya HosakaDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Satoshi SaitohDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Hitomi SezakiDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Fumitaka SuzukiDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Yoshiyuki SuzukiDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Kenji IkedaDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Yasuji AraseDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Masaji HashimotoOkinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Ichiro YasudaDepartment of Gastroenterology, Toyama University Hospital, Toyama, Japan.
Hiromitsu KumadaDepartment of Hepatology, Toranomon Hospital, Tokyo, Japan.
Toranomon Hospital · JPToyama University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWhen lenvatinib is administered to people with hepatocellular carcinoma (HCC), tumor blood flow is reduced due to the inhibition of the vascular endothelial growth factor receptor (VEGFR) and fibroblast growth factor receptor (FGFR). Few studies have examined the decrease in tumor blood flow with respect to changes in tumor blood vessels (TBVs) in clinical practice. We investigated the mechanism of tumor blood flow control by investigating changes in the diameter of relatively large TBVs in large-sized lesions with high blood flow.

methodsFrom January 2011 to October 2021, patients receiving lenvatinib for unresectable intrahepatic HCC at Toranomon Hospital, Tokyo, Japan, were considered for inclusion. We investigated the TBV diameter in the arterial phase of dynamic computed tomography before treatment and its change over time (2-12 weeks after lenvatinib initiation). The relationship between changes in TBV diameter and prognosis was also examined.

resultsOf 114 patients treated with lenvatinib for HCC, 26 patients who had intrahepatic lesions with a tumor diameter of 30 mm or more enrolled in the study. The median tumor and TBV diameters before treatment were 58 mm and 2.55 mm, respectively. Twenty-five patients (96%) had a shrinkage in TBV diameter 2-12 weeks after lenvatinib administration. The maximum TBV diameter shrinkage of 20% or more was observed in 19 patients (73%), and progression-free survival was prolonged in these patients compared to the group with less than 20% TBV diameter shrinkage (p = 0.039). DISCUSSION/

conclusionDue to the antiangiogenic effect of lenvatinib, a shrinkage in the TBV diameter of HCC was observed. The shrinkage of TBV may be regarded as a process of normalization of TBVs. The shrinkage of TBVs in imaging analysis may be associated with improved prognosis; however, additional studies are still required.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularLiver NeoplasmsHumansPhenylurea CompoundsQuinolinesVascular Endothelial Growth Factor AAntineoplastic AgentslenvatinibPhenylurea CompoundsQuinolinesVascular Endothelial Growth Factor AHepatocellular carcinomaLenvatinibNormalization of tumor blood vesselsTumor blood vessels

Identifiers

PMID36103864
PMCPMC9932824
OpenAlexW4295791158

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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.