Evidence map›Paper›PMID 37452019›Full record

ArticleNPJ breast cancer2023

Tumor-agnostic ctDNA levels by mFAST-SeqS in first-line HR-positive, HER2 negative metastatic breast cancer patients as a biomarker for survival.

Noortje Verschoor, Vanja de Weerd, Mai N Van, Jaco Kraan, Marcel Smid, Joan B Heijns, Jan C Drooger, Johanna M Zuetenhorst, Annemieke van der Padt-Pruijsten, Agnes Jager and 3 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2023. 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
1.7field-weighted citation impact, top 15% of its field
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, 7 citations in OpenAlex.

  1. Article
  2. Article
  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

13 authors at 5 institutions in 1 country.

Noortje VerschoorDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. n.verschoor@erasmusmc.nl.ORCID http://orcid.org/0000-0003-4465-253X
Vanja de WeerdDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Mai N VanDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Jaco KraanDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Marcel SmidDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Joan B HeijnsDepartment of Medical Oncology, Amphia, Breda, The Netherlands.
Jan C DroogerDepartment of Medical Oncology, Breast Cancer Center South Holland South, Ikazia Hospital, Rotterdam, The Netherlands.
Johanna M ZuetenhorstDepartment of Medical Oncology, Franciscus Gasthuis & Vlietland, Rotterdam/ Schiedam, the Netherlands.
Annemieke van der Padt-PruijstenDepartment of Internal Medicine, Breast Cancer Center South Holland, Maasstad Hospital, Rotterdam, The Netherlands.
Agnes JagerDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Stefan SleijferDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
John W M MartensDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-3428-3366
Saskia M WiltingDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-2838-841X
Erasmus MC Cancer Institute · NLAmphia Ziekenhuis · NLIkazia Ziekenhuis · NLMaasstad Ziekenhuis · NLSint Franciscus Gasthuis · NL

Funding

KWF Kankerbestrijding (Dutch Cancer Society) 12481
6 · The paper itself

Abstract

This prospective cohort study reports aneuploidy score by mFast-SeqS as a strong prognostic marker in MBC patients. mFAST-SeqS is an affordable and easily implementable method for the assessment of total ctDNA levels and, as such, provides an alternative prognostic tool. One mixed cohort (cohort A, n = 45) starting any type of treatment in any line of therapy and one larger cohort (cohort B, n = 129) consisting of patients starting aromatase inhibitors (AI) as first-line therapy were used. mFAST-SeqS was performed using plasma of blood in which CTCs (CellSearch) were enumerated. The resulting aneuploidy score was correlated with categorized CTC count and associated with outcome. The aneuploidy score was significantly correlated with CTC count, but discordance was observed in 31.6% when applying cut-offs of 5. In both cohorts, aneuploidy score was a significant prognostic marker for both PFS and OS. In the Cox regression models, the HR for aneuploidy score for PFS was 2.52 (95% CI: 1.56-4.07), and the HR for OS was 2.37 (95% CI: 1.36-4.14). Results presented here warrant further investigations into the clinical utility of this marker in MBC patients.

Identifiers

PMID37452019
PMCPMC10349058
OpenAlexW4384397881

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.