Evidence map›Paper›PMID 41212151›Full record

ArticleCancer research communications2025

Stand-alone Transcriptional Immune Response Prediction in Primary Triple-Negative Breast Cancer.

Suze Roostee, Fredrika Killander, Hani Saghir, Deborah F Nacer, Jari Häkkinen, Iñaki Sasiain, Srinivas Veerla, Johan Vallon-Christersson, Niklas Loman, Mattias Ohlsson and 1 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. 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

11 authors.

Suze RoosteeDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-3908-7417
Fredrika KillanderDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0001-6266-0459
Hani SaghirDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0009-0004-2666-2798
Deborah F NacerDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-7117-1371
Jari HäkkinenDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0002-8466-9179
Iñaki SasiainDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0009-0007-6177-0155
Srinivas VeerlaDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0001-7328-6239
Johan Vallon-ChristerssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0002-2195-0385
Niklas LomanDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0003-1425-5189
Mattias OhlssonComputational Science for Health and Environment, Centre for Environmental and Climate Science, Lund University, Lund, Sweden.ORCID 0000-0003-1145-4297
Johan StaafDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0001-5254-5115

Funding

BCF ViktoriaCancerfonden (Swedish Cancer Society) CAN 2021/1407Cancerfonden (Swedish Cancer Society) CAN 2024/3591Fru Berta Kamprads Stiftelse (Mrs. Berta Kamprad Foundation) FBKS-2024-14Magnus Bergvalls Stiftelse (Magnus Bergvall Foundation)Swedish Breast Cancer AssociationSwedish governmental funding (ALF) 2022/0021Vetenskapsrdet (VR) 2021-01800
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) accounts for 10% to 20% of primary breast cancers and often has early relapses and aggressive progression. An activated tumor immune response can be prognostic in patients with treatment-naïve and chemotherapy-treated TNBC and may be assessed using gene expression data. We derived a stand-alone predictor for a proposed immunomodulatory transcriptional TNBC subtype in a training cohort of 235 patients with primary disease based on random forest modeling of RNA sequencing data. Validation in independent TNBC cohorts totaling more than 1,200 patients demonstrated that the classifier recapitulates the immunomodulatory mRNA subtype classification, is associated with elevated immune expression and diversity of T-cell receptor genes, is associated with response to neoadjuvant chemotherapy, and can separate patients into subgroups with better or worse prognosis after adjuvant chemotherapy. The availability of stand-alone classifiers for mRNA-based prediction may further enhance RNA sequencing's usability in a more routine clinical context and for translational endpoints in clinical trials. SIGNIFICANCE: Tumor immune response has prognostic and treatment predictive value in TNBC and can be estimated by, e.g., mRNA profiling. Translating this association into classifications for single patients requires stand-alone predictors. We have developed one such mRNA classifier that could be applied in future clinical contexts and clinical trials.

Indexed as

Biomarkers, TumorTriple Negative Breast NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMiddle AgedNeoadjuvant TherapyPrognosisRNA, MessengerBiomarkers, TumorRNA, Messenger

Identifiers

PMID41212151
PMCPMC12703016

What Socratic 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 Socratic graph.