Evidence map›Paper›PMID 29097253›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2018

BRMS1 Expression in Surgically Resected Lung Adenocarcinoma Predicts Future Metastases and Is Associated with a Poor Prognosis.

Peter R Bucciarelli, Kay See Tan, Neel P Chudgar, Whitney Brandt, Joseph Montecalvo, Takashi Eguchi, Yuan Liu, Rania Aly, William D Travis, Prasad S Adusumilli and 1 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
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  11. Prognostic significance of BZW2 expression in lung adenocarcinoma patients.International journal of clinical and experimental pathology · 2019
    Article
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  13. Article
  14. Translational lung cancer research · 2018
    Article
4 · The record

Corrections and comments

  • Commented on by
    2018
  • Erratum issued
5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Peter R BucciarelliDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Kay See TanDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Neel P ChudgarDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Whitney BrandtDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Joseph MontecalvoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Takashi EguchiDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Yuan LiuDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Rania AlyDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
William D TravisDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Prasad S AdusumilliDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
David R JonesDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: jonesd2@mskcc.org.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Training and Career Development and Education CoreU54CA137788 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ADRIANA ESPINOSA, FRANCESCA M GANY · 2008 to 2026
$28.1M
SURGICAL ONCOLOGY RESEARCH TRAINING PROGRAMT32CA009501 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Babak J Mehrara · 1985 to 2026
$7.7M
BRMS1-mediated suppression of metastases in p53 mutant lung adenocarcinomaR01CA217169 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONES, DAVID R · 2018 to 2022
$2.5M
Epigenetic and post-translational regulation of the metastasis suppressor BRMS1R01CA136705 · NCI · UNIVERSITY OF VIRGINIA · PI JONES, DAVID R · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA136705NCI NIH HHS R01 CA217169NCI NIH HHS T32 CA009501NCI NIH HHS U54 CA137788
6 · The paper itself

Abstract

introductionExpression of breast cancer metastasis suppressor 1 gene (BRMS1) is decreased in NSCLC cells and tumors. We hypothesized that intratumoral breast cancer metastasis suppressor 1 (BRMS1) expression is associated with lung adenocarcinoma (LUAD) histologic subtypes and overall survival (OS) and disease-free survival (DFS) in patients undergoing resection for early-stage LUAD.

methodsPatients (N = 1030) who underwent complete resection for LUAD with tissue available for histologic evaluation were identified. Tissue microarrays were constructed, and immunostaining was performed and scored for intensity of BRMS1 expression. OS and DFS were estimated (by the Kaplan-Meier method) and compared between groups (by the log-rank test), stratified by stage. Hazard ratios (HRs) for hazard of death and recurrence were estimated using univariable and multivariable Cox proportional hazards models. OS and DFS nomograms were created, and model performance was examined.

resultsIntratumoral BRMS1 expression was high in 632 patients (61%) and low in 398 (39%). Low BRMS1 expression was associated with higher pathologic T stage (p = 0.001), larger tumor size (p ≤ 0.0001), greater lymphatic (p = 0.032) and vascular (p = 0.001) invasion, LUAD histologic subtype (p = 0.001), and intermediate and high architectural tumor grade (p = 0.003). Low BRMS1 expression was an independent predictor of worse OS (HR = 1.35, 95% confidence interval: 1.10-1.65, p = 0.004) and DFS (HR = 1.27, 95% confidence interval: 1.05-1.54, p = 0.012). OS and DFS nomograms showed excellent predictive performance based on discrimination and calibration.

conclusionsAmong patients with surgically resected LUAD, OS and DFS were significantly worse in cases with low intratumoral BRMS1 expression. Our findings suggest that BRMS1 is an independent biomarker with prognostic significance in surgically resected LUAD.

Indexed as

AdenocarcinomaAgedBiomarkers, TumorFemaleFollow-Up StudiesHumansLung NeoplasmsLymphatic MetastasisMaleMiddle AgedNeoplasm InvasivenessNeoplasm Recurrence, LocalPrognosisRepressor ProteinsSurvival RateBiomarkers, TumorBRMS1 protein, humanRepressor ProteinsBiomarkerBreast cancer metastasis suppressor 1Histologic subtypeLung adenocarcinomaMetastasis

Identifiers

PMID29097253
PMCPMC5738269
OpenAlexW2765183501

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.