Evidence map›Paper›PMID 33088925›Full record

ArticleHealth science reports2020

Prognostic value of plasminogen activator inhibitor-1 in biomarker exploration using multiplex immunoassay in patients with metastatic renal cell carcinoma treated with axitinib.

Naoko Honma, Takamitsu Inoue, Norihiko Tsuchiya, Atsushi Koizumi, Ryohei Yamamoto, Taketoshi Nara, Sohei Kanda, Mingguo Huang, Kazuyuki Numakura, Mitsuru Saito and 3 more

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In one paragraph

Article in Health science reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

13 authors at 2 institutions in 1 country.

Naoko HonmaDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Takamitsu InoueDepartment of Urology Akita University Graduate School of Medicine Akita Japan.ORCID https://orcid.org/0000-0002-1362-4344
Norihiko TsuchiyaDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Atsushi KoizumiDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Ryohei YamamotoDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Taketoshi NaraDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Sohei KandaDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Mingguo HuangDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Kazuyuki NumakuraDepartment of Urology Akita University Graduate School of Medicine Akita Japan.ORCID https://orcid.org/0000-0002-5899-1738
Mitsuru SaitoDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Shintaro NaritaDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Shigeru SatohCenter for Kidney Disease and Transplantation Akita University Hospital Akita Japan.
Tomonori HabuchiDepartment of Urology Akita University Graduate School of Medicine Akita Japan.
Akita University · JPYamagata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsVascular endothelial growth factor-directed therapies play a significant role in patients with metastatic renal cell carcinoma (mRCC). Biomarkers for predicting treatment efficacy and resistance are required to develop personalized medicine. We evaluated multiple serum cytokine levels in patients with mRCC treated with axitinib to explore predictive biomarkers.

methodsFrom September 2012 to October 2015, serum samples were collected from 44 patients with mRCC before treatment and 4 weeks after axitinib initiation. Bio-Plex Pro Human Cancer Biomarker Panels 1 and 2 were used to measure levels of 34 serum biomarkers related to angiogenesis and cell proliferation.

resultsPatients with partial response or stable disease had significantly decreased serum plasminogen activator inhibitor-1 (PAI-1) level from pre-treatment to 4 weeks after axitinib initiation compared with those with progressive disease (

conclusionsThe initial change in serum PAI-1 level in the early stage of axitinib treatment could be a useful prognostic biomarker in patients with mRCC.

Indexed as

metastatic renal cell carcinomamolecular‐targeted therapyplasminogen activator inhibitor‐1serum biomarker

Identifiers

PMID33088925
PMCPMC7559632
OpenAlexW3093245512

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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.