Evidence map›Paper›PMID 39380101›Full record

ArticleJournal of translational medicine2024

Monocyte subsets in breast cancer patients under treatment with aromatase inhibitor and mucin-1 cancer vaccine.

Viktoria Knöbl, Lukas Maier, Stefan Grasl, Carmen Kratzer, Felix Winkler, Vanessa Eder, Hubert Hayden, Maria Amparo Sahagun Cortez, Monika Sachet, Rudolf Oehler and 10 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. 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.

  1. Article
  2. Review
  3. Article
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

20 authors.

Viktoria KnöblDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Lukas MaierDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Stefan GraslDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Carmen KratzerDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Felix WinklerDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Vanessa EderDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Hubert HaydenDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Maria Amparo Sahagun CortezDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Monika SachetDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Rudolf OehlerDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Sophie FrantalAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Christian FeslAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Karin ZehetnerAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Georg PfeilerAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Rupert BartschAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Florian FitzalDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria.
Christian F SingerAustrian Breast & Colorectal Cancer Study Group (ABCSG), Vienna, Austria.
Martin FilipitsComprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Michael GnantComprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Christine BrostjanDivision of Vascular Surgery, Department of General Surgery, Medical University of Vienna, University Hospital Vienna, Vienna, Austria. christine.brostjan@meduniwien.ac.at.ORCID 0000-0003-1462-5397

Funding

Oesterreichische Nationalbank 15104
6 · The paper itself

Abstract

backgroundMonocytes comprise subsets of classical, intermediate and non-classical monocytes with distinct anti- or pro-tumor effects in breast cancer (BC). They are modulated by estrogen, and can contribute to BC control by endocrine therapy in preclinical models.

methodsTo elucidate whether changes in monocyte subsets are associated with treatment and response, we investigated peripheral blood samples of 73 postmenopausal women with estrogen receptor (ER) positive BC, who received aromatase inhibitor therapy with or without the mucin-1 vaccine tecemotide in the ABCSG34 trial. Blood was retrieved at baseline, midterm and end of therapy, and was analyzed for the distribution and ER expression of monocyte subsets by flow cytometry.

resultsWhen 40 healthy, age-matched women were compared with BC patients before treatment start, ER levels of monocytes did not differ, yet patients presented with a higher frequency of classical and fewer non-classical monocytes. Endocrine therapy triggered a significant increase in ER levels in all monocyte subsets, without affecting subset distribution. Vaccination had no overall impact on subset frequency and ER expression. Yet, a shift from intermediate to classical monocytes during therapy correlated with changes in plasma cytokines and chemokines and was significantly associated with low residual cancer burden in vaccinated patients. Without tecemotide, baseline ER levels in classical monocytes were significantly higher in women with good response to endocrine therapy.

conclusionsThis study identified classical monocytes to be associated with ER positive BC and with patient response to neoadjuvant endocrine treatment and cancer vaccination.

Indexed as

Aromatase InhibitorsBreast NeoplasmsCancer VaccinesMonocytesMucin-1AgedFemaleHumansMiddle AgedReceptors, EstrogenAromatase InhibitorsCancer VaccinesMucin-1Receptors, EstrogenAromatase inhibitorBreast cancerEstrogen receptorLetrozoleMonocyteStimuvaxTecemotide

Identifiers

PMID39380101
PMCPMC11460172

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.