Evidence mapPaperPMID 41331053Full record

ArticleScientific reports2025

Evaluation of predictive biomarkers for late radiation toxicity in breast cancer patients.

Ángela Solana-Peña, Monica Pujol-Canadell, Miquel Macià, Evelyn Martínez Pérez, Isabel Linares, Milica Stefanovic, Héctor Pérez-Montero, Javier González-Viguera, Marina Arangüena Peñacoba, Montse Ventura and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Ángela Solana-PeñaUnit of Biological Anthropology, Department of Animal Biology, Plant Biology and Ecology, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Cerdanyola del Vallès, 08193, Spain.
Monica Pujol-CanadellUnit of Biological Anthropology, Department of Animal Biology, Plant Biology and Ecology, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Cerdanyola del Vallès, 08193, Spain.
Miquel MaciàRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Evelyn Martínez PérezRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Isabel LinaresRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Milica StefanovicRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Héctor Pérez-MonteroRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Javier González-VigueraRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Marina Arangüena PeñacobaRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Montse VenturaRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Ferran GuedeaRadiobiology and Cancer, Institut d'Investigació Biomèdica de Bellvitge (ONCOBELL-IDIBELL), Hospital Duran i Reynals, Gran Via de l'Hospitalet, 199- 203, Hospitalet de Llobregat, Barcelona, 08908, Spain.
Nadina ErillAtrys Health, Provenza 392, Barcelona, 08025, Spain.
Víctor González-RumayorAtrys Health, Príncipe de Vergara 132, Madrid, 28002, Spain.
Gemma ArmengolUnit of Biological Anthropology, Department of Animal Biology, Plant Biology and Ecology, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Cerdanyola del Vallès, 08193, Spain.
Joan Francesc Barquinero EstruchUnit of Biological Anthropology, Department of Animal Biology, Plant Biology and Ecology, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Cerdanyola del Vallès, 08193, Spain. Francesc.Barquinero@uab.cat.

Funding

Ministerio de Ciencia e Innovación CPP2021-008368
6 · The paper itself

Abstract

Radiotherapy is administered to 70% of breast cancer patients, but late complications such as breast fibrosis remain a significant clinical concern. Individual variability significantly influences radiosensitivity, underscoring the need for predictive biomarkers suitable for clinical application. We evaluated five assays using blood samples from 22 matched pairs of treated breast cancer patients, including one female who developed fibrosis grade II or higher and a female who did not. Matching was performed accounting for treatment type, tumor characteristics, and other variables. The assays included γ-H2AX detection, radiation-induced apoptosis evaluation, and cytogenetic analysis by chromosomal instability testing, and assessment of radiation-induced damage in G0- and G2- phase lymphocytes. The results indicated that patients who developed fibrosis presented significantly lower values in the G2 assay and higher values in the chromosomal instability test. The G2 assay evaluates the integrity of the G2/M checkpoint, while the chromosomal instability test measures chromosomal instability through crosslink sensitivity. In contrast, the other evaluated tests did not discriminate between groups. Considering the cohort and the variability in all tests, our results suggest that G2 assay and chromosomal instability test would be robust predictors of radiotherapy-induced breast fibrosis. Validation in a larger retrospective or prospective study is necessary.

Indexed as

Biomarkers, TumorBreast NeoplasmsRadiation InjuriesAdultAgedApoptosisBiomarkersChromosomal InstabilityFemaleFibrosisHistonesHumansMiddle AgedBiomarkersBiomarkers, TumorH2AX protein, humanHistones

Identifiers

PMID41331053
PMCPMC12796360

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.