Evidence map›Paper›PMID 31637868›Full record

ArticleThoracic cancer2019

Psf3 as a possible biomarker of postoperative chemotherapy for patients with early pulmonary adenocarcinoma.

Kenji Kimura, Yugo Tanaka, Shunsuke Tauchi, Yoshitaka Kitamura, Wataru Nishio, Yasuhiro Sakai, Yoshitake Hayashi, Masahiro Yoshimura, Yoshimasa Maniwa

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Kenji KimuraDivision of Thoracic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID 0000-0002-2617-6384
Yugo TanakaDivision of Thoracic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID 0000-0002-6541-1754
Shunsuke TauchiDivision of Thoracic Surgery, Akashi Medical Center, Akashi, Japan.
Yoshitaka KitamuraDivision of Thoracic Surgery, Hyogo Cancer Center, Akashi, Japan.
Wataru NishioDivision of Thoracic Surgery, Hyogo Cancer Center, Akashi, Japan.
Yasuhiro SakaiDivision of Pathology, Hyogo Cancer Center, Akashi, Japan.
Yoshitake HayashiDivision of Molecular and Medical Genetics, Department of Pathology, Kobe University Graduate School of Medicine, Kobe, Japan.
Masahiro YoshimuraDivision of Thoracic Surgery, Hyogo Cancer Center, Akashi, Japan.
Yoshimasa ManiwaDivision of Thoracic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Hyogo Prefectural Cancer Center · JPKobe University · JPAkashi Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPartner of Sld five 3 (Psf3) is a member of the heterotetrameric complex that consists of SLD5, Psf1, Psf2, and Psf3. We have shown in previous studies that high Psf3 expression was a poor prognostic marker for pulmonary adenocarcinoma. Here, we statistically evaluated the relationship between clinicopathologic factors and Psf3 expression in stage I pulmonary adenocarcinoma.

methodsA total of 583 patients who had undergone complete resection of stage I pulmonary adenocarcinoma from January 2002 to December 2009 were included in the study. Tissue microarrays were performed, and the resected tumors were divided into groups according to Psf3 expression.

resultsOf 583 patients, high expression of Psf3 was observed in 211 (36.2%) and low expression of Psf3 observed in 372 (63.8%) patients. Among stage I patients, the five-year survival rate was 76.7% in the Psf3 high expression group and 90.9% in the Psf3 low expression group (P < 0.0001). On multivariate analysis, Psf3 was found to be the independent prognostic factor. Among stage I patients in the Psf3 high expression group, a significantly greater five-year survival rate was observed in patients who received postoperative chemotherapy with tegafur-uracil than in those who underwent surgery alone (P < 0.0001). In contrast, among stage I patients in the Psf3 low expression group, no difference was found in the five-year survival, regardless of the presence or absence of tegafur-uracil (P = 0.873).

conclusionThe Psf3 expression was an independent prognostic factor and could be a biomarker of adjuvant tegafur-uracil for stage I pulmonary adenocarcinoma. KEY POINTS: Significant findings of the study: The Psf3 expression could be a biomarker of adjuvant tegafur-uracil administration for stage I pulmonary adenocarcinoma. WHAT THIS STUDY ADDS: Appropriate patients of adjuvant chemotherapy for stage I pulmonary adenocarcinoma using Psf3 expression could be selected.

Indexed as

Biomarkers, TumorAdenocarcinoma of LungAdultAgedAged, 80 and overChemotherapy, AdjuvantChromosomal Proteins, Non-HistoneFemaleHumansMaleMiddle AgedPostoperative CarePrognosisProportional Hazards ModelsTreatment OutcomeBiomarkers, TumorChromosomal Proteins, Non-HistoneGINS3 protein, humanAdjuvant chemotherapybiomarkerlung cancer

Identifiers

PMID31637868
PMCPMC6885426
OpenAlexW2981808360

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LicenceCC BY
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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.