Evidence map›Paper›PMID 31139312›Full record

ArticleWorld journal of gastrointestinal oncology2019

ADAMTS13 and von Willebrand factor are useful biomarkers for sorafenib treatment efficiency in patients with hepatocellular carcinoma.

Hiroaki Takaya, Tadashi Namisaki, Naotaka Shimozato, Kosuke Kaji, Mitsuteru Kitade, Kei Moriya, Shinya Sato, Hideto Kawaratani, Takemi Akahane, Masanori Matsumoto and 1 more

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Von Willebrand Factor as a Biomarker for Liver Disease - An Update.Journal of clinical and experimental hepatology
    Review
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

11 authors at 1 institution in 1 country.

Hiroaki TakayaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan. htky@naramed-u.ac.jp.
Tadashi NamisakiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Naotaka ShimozatoThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kosuke KajiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Mitsuteru KitadeThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kei MoriyaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Shinya SatoThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hideto KawarataniThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Takemi AkahaneThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Masanori MatsumotoDepartment of Blood Transfusion Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hitoshi YoshijiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Nara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany advanced hepatocellular carcinoma (HCC) patients are receiving sorafenib treatment. Sorafenib reportedly improves overall survival (OS) significantly in patients with HCC. Prediction of sorafenib response and prognosis in patients with HCC receiving sorafenib treatment are important due to the potentially serious side effects of sorafenib. A disintegrin-like and metalloproteinase with thrombospondin type-1 motifs 13 (ADAMTS13) and von Willebrand factor (VWF) are associated with the pathophysiology of liver cirrhosis and HCC through their roles in hypercoagulability; they are also associated with angiogenesis

aimTo investigate ADAMTS13 and VWF as potential biomarkers for sorafenib response and prognosis in patients with HCC receiving sorafenib treatment.

methodsForty-one patients with HCC receiving sorafenib treatment were included in this study. The initial daily sorafenib dose was 400 mg in all patients. ADAMTS13 activity (ADAMTS13:AC), VWF antigen (VWF:Ag), VEGF levels were determined by enzyme-linked immunosorbent assay. Univariate and multivariate analyses were used to determine predictive factors for sorafenib response and prognosis in patients with HCC receiving sorafenib treatment.

resultsADAMTS13:AC was significantly higher in patients with stable disease (SD), partial response (PR), and complete response (CR) than in those with progressive disease (PD) (

conclusionThe VWF:Ag/ADAMTS13:AC ratio and ADAMTS13:AC are potentially useful biomarkers for sorafenib response and prognosis, respectively, in patients with HCC receiving sorafenib treatment.

Indexed as

ADAMTS13BiomarkersHepatocellular carcinomaSorafenibVon Willebrand factor

Identifiers

PMID31139312
PMCPMC6522768
OpenAlexW2946383944

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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.