Evidence map›Paper›PMID 35467121›Full record

ArticleArchives of gynecology and obstetrics2022

How previous treatment changes the metabolomic profile in patients with metastatic breast cancer.

Juliane Nees, Simon Schafferer, Baowen Yuan, Quiqong Tang, Matthias Scheffler, Andreas Hartkopf, Michael Golatta, Andreas Schneeweiß, Barbara Burwinkel, Markus Wallwiener

Abstract read
In one paragraph

Article in Archives of gynecology and obstetrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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  5. 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

10 authors.

Juliane NeesDepartment of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany. Juliane.Nees@med.uni-heidelberg.de.ORCID 0000-0003-4886-9808
Simon SchaffererBIOCRATES Life Sciences AG, 6020, Innsbruck, Austria.
Baowen YuanMolecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, 69120, Heidelberg, Germany.
Quiqong TangMolecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, 69120, Heidelberg, Germany.
Matthias SchefflerBIOCRATES Life Sciences AG, 6020, Innsbruck, Austria.
Andreas HartkopfDepartment of Women's Health, University of Tübingen, 72076, Tübingen, Germany.ORCID 0000-0003-1227-1118
Michael GolattaDepartment of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.ORCID 0000-0002-2605-0060
Andreas SchneeweißNational Center for Tumor Diseases (NCT), 69120, Heidelberg, Germany.ORCID 0000-0002-2429-4512
Barbara Burwinkel *Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, 69120, Heidelberg, Germany.ORCID 0000-0002-6752-2589
Markus Wallwiener *Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.ORCID 0000-0002-4139-9340

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMetabolites are in the spotlight of attention as promising novel breast cancer biomarkers. However, no study has been conducted concerning changes in the metabolomics profile of metastatic breast cancer patients according to previous therapy.

methodsWe performed a retrospective, single-center, nonrandomized, partially blinded, treatment-based study. Metastatic breast cancer (MBC) patients were enrolled between 03/2010 and 09/2016 at the beginning of a new systemic therapy. The endogenous metabolites in the plasma samples were analyzed using the AbsoluteIDQ

resultsWe included 178 patients in our study. Upon dividing the study population according to therapy before study inclusion, we found the following: 4 patients had received no therapy, 165 chemotherapy, and 135 anti-hormonal therapy, 30 with anti-Her2 therapy and 38 had received treatment with bevacizumab. Two metabolites were found to be significantly different, depending on the further therapy of the patients: methionine and serine. Whereas methionine levels were higher in the blood of patients who received an anti-Her2-therapy, serine was lower in patients with endocrine therapy only.

conclusionWe identified two metabolites for which concentrations differed significantly depending on previous therapies, which could help to choose the next therapy in patients who have already received numerous different treatments.

Indexed as

Breast NeoplasmsNeoplastic Cells, CirculatingBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansMethionineRetrospective StudiesSerineBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesMethionineSerineCirculating tumor cellsMetabolomicsMetastatic breast cancerMethionineSerine

Identifiers

PMID35467121
PMCPMC9633507

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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.