Evidence map›Paper›PMID 27160229›Full record

ArticleJournal of the National Comprehensive Cancer Network : JNCCN2016

Therapeutically Induced Changes in HER2, HER3, and EGFR Protein Expression for Treatment Guidance.

Shankar Sellappan, Adele Blackler, Wei-Li Liao, Emily O'Day, Peng Xu, Sheeno Thyparambil, Fabiola Cecchi, Todd Hembrough, Daniel V T Catenacci

Abstract readCase Reports
In one paragraph

Article in Journal of the National Comprehensive Cancer Network : JNCCN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Update on Gastroesophageal Adenocarcinoma Targeted Therapies.Hematology/oncology clinics of North America · 2017
    Review
  5. Novel Targeted Therapies for Esophagogastric Cancer.Surgical oncology clinics of North America · 2017
    Review
  6. 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

9 authors.

Shankar SellappanNantOmics, LLC, Rockville, Maryland
Adele BlacklerNantOmics, LLC, Rockville, Maryland
Wei-Li LiaoNantOmics, LLC, Rockville, Maryland
Emily O'DayUniversity of Chicago, Department of Medicine, Section of Hematology & Oncology, Chicago, Illinois
Peng XuUniversity of Chicago, Department of Medicine, Section of Hematology & Oncology, Chicago, Illinois
Sheeno ThyparambilNantOmics, LLC, Rockville, Maryland
Fabiola CecchiNantOmics, LLC, Rockville, Maryland
Todd HembroughNantOmics, LLC, Rockville, Maryland
Daniel V T CatenacciUniversity of Chicago, Department of Medicine, Section of Hematology & Oncology, Chicago, Illinois

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
PANGEA: Personalized Antibodies for GastroEsophageal Adenocarcinoma Pilot TrialK23CA178203 · NCI · UNIVERSITY OF CHICAGO · PI CATENACCI, DANIEL · 2014 to 2016
$507k
NCI NIH HHS K23 CA178203NCI NIH HHS P30 CA014599
6 · The paper itself

Abstract

Protein-targeted therapies are expected to selectively kill tumor cells that express the targeted protein biomarker. Although a tumor mass may initially respond to targeted therapies based on expression of the targeted protein, all cells within a tumor may not express the targeted protein above a critical threshold level; therefore, those cells that do not express, or that downregulate expression of, the targeted protein may not be responsive to therapy. The ability to monitor the dynamic expression of these protein biomarkers throughout the course of therapy may allow for treatment to be personalized in real-time in response to the evolving nature of the tumor. This report demonstrates, by monitoring a single patient through multiple therapies, how targeted mass spectrometry is an effective, quantitative method that provides real-time analysis of multiple therapeutically associated targeted proteins that can be used to personalize a patient's treatment strategy throughout the course of care.

Indexed as

AdultCell ProliferationErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansMaleSignal TransductionTreatment OutcomeErb-b2 Receptor Tyrosine KinasesErbB Receptors

Identifiers

PMID27160229
PMCPMC5889074

What OpenQuestion holds

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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.