ArticleBreast cancer research : BCR2026
Plasma extracellular vesicles reflect response and prognosis in patients with breast cancer undergoing neoadjuvant treatment.
Article in Breast cancer research : BCR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundExtracellular vesicles (EVs) are emerging as non-invasive biomarkers in cancer, but their role in monitoring the response to neoadjuvant systemic treatment (NST) in patients with breast cancer remains unclear. This study aimed to assess whether EV concentration and surface marker profiles in plasma reflect treatment response and clinical outcome in patients with early-stage breast cancer receiving NST.
methodsPlasma samples were collected from 59 patients with luminal B-like, HER2-positive, or triple-negative breast cancer before and after NST. EVs were isolated by size exclusion chromatography and characterized by nanoparticle tracking analysis, electron microscopy, Western blotting, and MACSPlex surface marker profiling. Paired samples were available for 29 patients, allowing longitudinal analysis.
resultsPatients who achieved pathological complete response (pCR) had significantly lower baseline EV concentrations than those with residual disease. Post-treatment EV levels were also lower in patients who remained free from distant metastasis and had improved breast cancer-specific survival. EV surface marker profiling revealed that CD69, CD29, and CD49e were reduced after NST, whereas CD44 was increased. Notably, EpCAM levels increased specifically in non-PCR patients, suggesting persistent tumor-derived EV release, whereas SSEA-4 levels increased only in patients who achieved pCR. Although EV concentrations and markers differed by subtype and outcome, changes in EV levels following NST were not independently predictive of prognosis.
conclusionsThese findings support the potential of plasma-derived EVs as dynamic biomarkers of treatment response, and suggest possible prognostic relevance in breast cancer. Validation in larger, independent cohorts is needed to assess their clinical applicability.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.