Evidence map›Paper›PMID 24558399›Full record

ArticlePloS one2014

Breast cancer subtype specific classifiers of response to neoadjuvant chemotherapy do not outperform classifiers trained on all subtypes.

Jorma J de Ronde, Marc Jan Bonder, Esther H Lips, Sjoerd Rodenhuis, Lodewyk F A Wessels

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

5 authors.

Jorma J de RondeDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands ; Department of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marc Jan BonderDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Esther H LipsDepartment of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands ; Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Sjoerd RodenhuisDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Lodewyk F A WesselsDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands ; Faculty of EEMCS, Delft University of Technology, Delft, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite continuous efforts, not a single predictor of breast cancer chemotherapy resistance has made it into the clinic yet. However, it has become clear in recent years that breast cancer is a collection of molecularly distinct diseases. With ever increasing amounts of breast cancer data becoming available, we set out to study if gene expression based predictors of chemotherapy resistance that are specific for breast cancer subtypes can improve upon the performance of generic predictors.

methodsWe trained predictors of resistance that were specific for a subtype and generic predictors that were not specific for a particular subtype, i.e. trained on all subtypes simultaneously. Through a rigorous double-loop cross-validation we compared the performance of these two types of predictors on the different subtypes on a large set of tumors all profiled on the same expression platform (n = 394). We evaluated predictors based on either mRNA gene expression or clinical features.

resultsFor HER2+, ER- breast cancer, subtype specific predictor based on clinical features outperformed the generic, non-specific predictor. This can be explained by the fact that the generic predictor included HER2 and ER status, features that are predictive over the whole set, but not within this subtype. In all other scenarios the generic predictors outperformed the subtype specific predictors or showed equal performance.

conclusionsSince it depends on the specific context which type of predictor - subtype specific or generic- performed better, it is highly recommended to evaluate both specific and generic predictors when attempting to predict treatment response in breast cancer.

Indexed as

AlgorithmsAntineoplastic AgentsArea Under CurveBreast NeoplasmsChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesEstrogen Receptor alphaFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLogistic ModelsNeoadjuvant TherapyOligonucleotide Array Sequence AnalysisPredictive Value of TestsRNA, MessengerAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesESR1 protein, humanEstrogen Receptor alphaRNA, Messenger

Identifiers

PMID24558399
PMCPMC3928239

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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.