Evidence map›Paper›PMID 25879949›Full record

ArticleBMC cancer2015

Transcriptional expression of 8 genes predicts pathological response to first-line docetaxel + trastuzumab-based neoadjuvant chemotherapy.

Esther Schmitt, Frédérique Végran, Sandy Chevrier, Laura Burillier, Muriel Cadouot, Sarab Lizard-Nacol, Bruno Coudert, Pierre Fumoleau, Laurent Arnould, Romain Boidot

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 27% 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, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Guideline
  2. Review
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 1 institution in 1 country.

Esther SchmittMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. schmitt.esther1704@gmail.com.
Frédérique VégranMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. frederique.vegran@laposte.net.
Sandy ChevrierMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. schevrier@cgfl.fr.
Laura BurillierPathology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. lburillier@cgfl.fr.
Muriel CadouotMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. mcadouot@cgfl.fr.
Sarab Lizard-NacolMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. slizard@cgfl.fr.
Bruno CoudertDepartment of Oncology, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. bcoudert@cgfl.fr.
Pierre FumoleauDepartment of Oncology, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. pfumoleau@cgfl.fr.
Laurent ArnouldPathology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. larnould@cgfl.fr.
Romain BoidotMolecular Biology Unit, Centre Georges-François Leclerc, 1, rue du Professeur Marion, Dijon, 21079 Cedex, France. rboidot@cgfl.fr.
Centre Georges François Leclerc · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverexpression of HER2 is observed in 20 to 30% of breast carcinomas. The use of trastuzumab has improved the treatment of these patients, especially when it is associated with docetaxel. To optimize the use of this treatment, it seems important to select putative complete responders before treatment administration.

methodsIn this study, we analyzed by quantitative PCR the expression of 28 genes in HER2-overexpressing tumors treated with trastuzumab + docetaxel-based chemotherapy. We then correlated their expression profile with those of trastuzumab-sensitive and resistant cell lines to classify tumors as having a sensitive (pCR) or resistant (non-pCR) profile. Finally, we used public datasets from the GEO website to validate the reduced gene-expression profile obtained.

resultsWe identified an 8-gene-expression combination that predicted the response to treatment with an accuracy of 76%. Based on public microarray data, we showed that the expression profile was specific to first-line trastuzumab + docetaxel-based treatment with an accuracy of 85%.

conclusionsOur results showed that by profiling the expression of 8 genes it was possible to predict the response to first-line trastuzumab + docetaxel-based chemotherapy. The use of cancer cell lines as the reference allowed a proper fit with the specificity of different tissues, such as lung or gastric cancers, which could also be eligible to concomitant HER2 inhibition by treatment with trastuzumab or tyrosine kinase inhibitors and docetaxel.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsDatabases, GeneticDocetaxelErb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoadjuvant TherapyNeoplasm ProteinsNeoplasm StagingTaxoidsTrastuzumabDocetaxelERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesNeoplasm ProteinsTaxoidsTrastuzumab

Identifiers

PMID25879949
PMCPMC4417290
OpenAlexW1976352165

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.