Evidence map›Paper›PMID 23300545›Full record

ArticlePloS one2012

Elevation in inflammatory serum biomarkers predicts response to trastuzumab-containing therapy.

Ahmed A Alkhateeb, Kim Leitzel, Suhail M Ali, Cynthia Campbell-Baird, Matthew Evans, Eva-Maria Fuchs, Wolfgang J Köstler, Allan Lipton, James Connor

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
–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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  16. Obesity-associated cancer risk: the role of intestinal microbiota in the etiology of the host proinflammatory state.Translational research : the journal of laboratory and clinical medicine · 2017
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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.

Ahmed A AlkhateebDepartment of Neurosurgery, The Pennsylvania State University Hershey Medical Center, Hershey, PA, USA.
Kim Leitzel
Suhail M Ali
Cynthia Campbell-Baird
Matthew Evans
Eva-Maria Fuchs
Wolfgang J Köstler
Allan Lipton
James Connor

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately half of all HER2/neu-overexpressing breast cancer patients do not respond to trastuzumab-containing therapy. Therefore, there remains an urgent and unmet clinical need for the development of predictive biomarkers for trastuzumab response. Recently, several lines of evidence have demonstrated that the inflammatory tumor microenvironment is a major contributor to therapy resistance in breast cancer. In order to explore the predictive value of inflammation in breast cancer patients, we measured the inflammatory biomarkers serum ferritin and C-reactive protein (CRP) in 66 patients immediately before undergoing trastuzumab-containing therapy and evaluated their progression-free and overall survival. The elevation in pre-treatment serum ferritin (>250 ng/ml) or CRP (>7.25 mg/l) was a significant predictor of reduced progression-free survival and shorter overall survival. When patients were stratified based on their serum ferritin and CRP levels, patients with elevation in both inflammatory biomarkers had a markedly poorer response to trastuzumab-containing therapy. Therefore, the elevation in inflammatory serum biomarkers may reflect a pathological state that decreases the clinical efficacy of this therapy. Anti-inflammatory drugs and life-style changes to decrease inflammation in cancer patients should be explored as possible strategies to sensitize patients to anti-cancer therapeutics.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic AgentsBiomarkersBreast NeoplasmsC-Reactive ProteinDisease-Free SurvivalDisease ProgressionEnzyme-Linked Immunosorbent AssayErb-b2 Receptor Tyrosine KinasesFemaleFerritinsHumansInflammationInflammation MediatorsMiddle AgedSurvival RateAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBiomarkersC-Reactive ProteinErb-b2 Receptor Tyrosine KinasesFerritinsInflammation MediatorsTrastuzumab

Identifiers

PMID23300545
PMCPMC3530544

What OpenQuestion holds

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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.