Evidence map›Paper›PMID 27198655›Full record

ArticleInternational journal of cancer2016

Central nervous system relapse in patients with untreated HER2-positive esophageal or gastroesophageal junction adenocarcinoma.

Harry H Yoon, Mark A Lewis, Nathan R Foster, William R Sukov, Maliha Khan, Christopher A Sattler, Anne E Wiktor, Tsung-Teh Wu, Robert B Jenkins, Frank A Sinicrope

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
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  7. Enrichment ofThe oncologist · 2019
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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

10 authors at 4 institutions in 1 country.

Harry H YoonDepartment of Medical Oncology, Mayo Clinic, Rochester, MN.
Mark A LewisDepartment of Medical Oncology, MD Anderson Cancer Center, Houston, TX.
Nathan R FosterDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN.
William R SukovDepartment of Cytogenetics, Mayo Clinic, Rochester, MN.
Maliha KhanDepartment of Leukemia Department, MD Anderson Cancer Center, Houston, TX.
Christopher A SattlerDepartment of Cytogenetics, Mayo Clinic, Rochester, MN.
Anne E WiktorMayo Collaborative Services, Mayo Clinic, Rochester, MN.
Tsung-Teh WuAnatomic Pathology, Mayo Clinic, Rochester, MN.
Robert B JenkinsDepartment of Cytogenetics, Mayo Clinic, Rochester, MN.
Frank A SinicropeDepartment of Medical Oncology, Mayo Clinic, Rochester, MN.
Mayo Clinic in Arizona · USMayo Clinic in Florida · USThe University of Texas MD Anderson Cancer Center · USMayo Clinic · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
North Central Cancer Treatment Group (NCCTG) Biospecimen ResourceU24CA114740 · NCI · MAYO CLINIC ROCHESTER · PI BUCKNER, JAN C · 2005 to 2014
$8.6M
Translational Research in Colon Cancer Prevention & TreatmentK05CA142885 · NCI · MAYO CLINIC ROCHESTER · PI SINICROPE, FRANK A. · 2009 to 2013
$808k
NCATS NIH HHS UL1 TR000135NCI NIH HHS K05 CA142885NCI NIH HHS K12 CA090628NCI NIH HHS U24 CA114740
6 · The paper itself

Abstract

Although HER2-positive breast cancers demonstrate a propensity for central nervous system (CNS) metastasis, it is unknown whether other HER2-positive tumors, including adenocarcinomas of the esophagus/gastroesophageal junction (EAC), share this characteristic. Insight into this association may inform the development of HER2-targeted therapies that penetrate the blood-brain barrier. We examined HER2 overexpression and gene amplification in 708 patients with EAC who underwent curative-intent surgery during a time period (1980-1997) when no patient received HER2-targeted therapy. We identified patients whose site of first cancer recurrence was CNS and those who had a CNS relapse at any time. After a median follow-up of 61.2 months, 3.4% (24/708) of patients developed CNS relapse (all involved the brain). Patients with HER2-positive (vs -negative) primary tumors showed a higher 5-year cumulative incidence of CNS relapse as first recurrence (5.8% vs. 1.2%; p = 0.0058) and at any time (8.3% vs. 2.4%; p = 0.0062). In a multivariable model that included covariates previously associated with HER2 or with CNS relapse in breast cancer, HER2 positivity was the only variable that was statistically significantly associated with shorter time to CNS relapse as first recurrence (p = 0.0026) or at any time (hazard ratio 4.3 [95% confidence interval 1.8 to 10.3]; p = 0.001). These are the first data in a non-breast cancer to demonstrate an association between HER2 positivity and higher CNS relapse risk after surgery, and suggest that HER2-positive EACs have a predilection for CNS metastases.

Indexed as

AdenocarcinomaCentral Nervous System NeoplasmsErb-b2 Receptor Tyrosine KinasesEsophageal NeoplasmsEsophagogastric JunctionGene AmplificationHumansImmunohistochemistryMiddle AgedProportional Hazards ModelsStomach NeoplasmsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesbrainCNSgastroesophageal cancerHER2/ERBB2relapse

Identifiers

PMID27198655
PMCPMC6631306
OpenAlexW2399876438

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.