Evidence map›Paper›PMID 42218678›Full record

ReviewMagyar onkologia2026

Premedication with steroids in breast cancer - supportive treatment or tumour growth promotion?

Henriett Butz, Anna Oláh, Attila Patócs

Abstract readReview
In one paragraph

Review in Magyar onkologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Henriett ButzDepartment of Molecular Genetics and National Tumor Biology Laboratory, National Institute of Oncology, Budapest, Hungary. butz.henriett@oncol.hu.
Anna OláhDepartment of Molecular Genetics and National Tumor Biology Laboratory, National Institute of Oncology, Budapest, Hungary. butz.henriett@oncol.hu.
Attila PatócsDepartment of Molecular Genetics and National Tumor Biology Laboratory, National Institute of Oncology, Budapest, Hungary. butz.henriett@oncol.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoids, most commonly dexamethasone, are widely used alongside breast cancer therapy to alleviate adverse effects of chemotherapy, particularly allergic reactions and nausea. However, growing evidence shows that the activation of the glucocorticoid receptor (GR) has context-dependent effects on tumour biology, with both tumour-suppressive and tumour-promoting consequences. This review summarises the molecular basis of GR signalling in breast cancer and its prognostic relevance across molecular subtypes. Particular emphasis is placed on ligand-dependent and ligand-independent GR activation, crosstalk with the oestrogen receptor and GR-regulated transcriptional programmes associated with tumour cell migration and therapy resistance. Overall, the available evidence suggests that the use of glucocorticoids in triple-negative breast cancer is not biologically neutral. Assessment of GR using methods such as routine immunohistochemistry may add future value for patient's stratification for GR-targeted therapy and could inform more personalised supportive treatment and follow-up strategies; however, these approaches require prospective validation before clinical implementation.

Indexed as

Breast NeoplasmsDexamethasoneGlucocorticoidsReceptors, GlucocorticoidTriple Negative Breast NeoplasmsFemaleHumansPrognosisReceptors, EstrogenSignal TransductionDexamethasoneGlucocorticoidsReceptors, EstrogenReceptors, Glucocorticoid

Identifiers

PMID42218678
PMCPMC13233022

What OpenQuestion holds

Textmetadata
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.