Evidence map›Paper›PMID 41144783›Full record

ArticleInternational journal of cancer2026

Fast enrichment and detection of circulating tumor cells from large volumes of whole blood of breast cancer patients utilizing a functionalized bioaffinity CTC filtration membrane.

Leonie F Ott, Laura Keller, Nathan Bentley, Hümeyra Husseini-Wüsthoff, René Werner, Marc Zinggeler, Jakoba Heidler, Parinaz Mossahebi Mohammadi, Cornelia Coith, Anne Pradines and 17 more

Abstract read
In one paragraph

Article in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

27 authors.

Leonie F OttInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID https://orcid.org/0000-0002-6308-0242
Laura KellerInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID https://orcid.org/0000-0002-1786-9760
Nathan BentleyLaboratory for Chemistry and Physics of Interfaces, Department of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg im Breisgau, Germany.
Hümeyra Husseini-WüsthoffDepartment of Applied Medical Informatics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
René WernerDepartment of Applied Medical Informatics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Marc ZinggelerCentre Suisse d'électronique et de Microtechnique SA (CSEM), Muttenz, Switzerland.
Jakoba HeidlerCentre Suisse d'électronique et de Microtechnique SA (CSEM), Muttenz, Switzerland.
Parinaz Mossahebi MohammadiInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Cornelia CoithInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Anne PradinesLaboratoire de Biologie Medicale Oncologique, Oncopole Claudius Regaud, Toulouse, France.ORCID https://orcid.org/0000-0002-2449-678X
Nikolas H StoeckleinDepartment for General, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Malte LöptienInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sven PeineDepartment of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Maria GeffkenDepartment of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Corinna GüsmerDepartment of Transfusion Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mina Netkova-HeintzenDepartment of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Volkmar MüllerDepartment of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Elena LaakmannDepartment of Gynecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Verena ThewesDivision of Stem Cells and Cancer, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
Thomas M DeutschDepartment of Obstetrics and Gynecology, Heidelberg University Hospital, Heidelberg, Germany.
Laura L MichelNational Center for Tumor Diseases, Heidelberg University Hospital, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Andreas SchneeweissNational Center for Tumor Diseases, Heidelberg University Hospital, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Andreas TrumppDivision of Stem Cells and Cancer, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
Jürgen RüheLaboratory for Chemistry and Physics of Interfaces, Department of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg im Breisgau, Germany.
Thomas BrandtstetterLaboratory for Chemistry and Physics of Interfaces, Department of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg im Breisgau, Germany.
Sabine RiethdorfInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Klaus PantelInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Funding

Bundesministerium für Bildung und Forschung 161B0843DDeutsche Krebshilfe 70114705Erich und Gertrud Roggenbuck-Stiftung
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) are valuable liquid biopsy analytes as they facilitate an in-depth characterization of disseminated tumors by a simple blood draw. Most CTC assays can only process limited blood volumes, potentially hampering the detection of cells of very low frequency, such as CTCs. Here, we introduce a novel, functionalized nickel filtration membrane, facilitating rapid enrichment of CTCs from various volumes of blood up to 40 mL and leukapheresis products. We validated this assay with different cancer cell lines and compared the performance of our new assay with that of the FDA-cleared CellSearch® system. Performing a comparative analysis of 20 blood samples from patients with metastatic breast cancer, CTCs were found in 19/20 patients (95%), combining the results of both CTC enrichment assays. CTC counts/7.5 mL of blood ranged from 0 to 7280 (CTC filtration membrane) and 0 to 17,190 (CellSearch®). Applying the clinically relevant cut-off of ≥5 CTCs/7.5 mL of blood, 19/20 samples processed with our CTC filter were categorized identically to those analyzed with the CellSearch® system. Furthermore, the filtration time of 40 s for 7.5 mL of blood represents an important advantage of our system, compared to other systems. Importantly, we also demonstrated the feasibility of processing blood samples of up to 40 mL or 2 × 10

Indexed as

Breast NeoplasmsCell SeparationFiltrationNeoplastic Cells, CirculatingCell Line, TumorFemaleHumansLiquid BiopsyMiddle Agedbioaffinity filter membranehigh‐volume samplesliquid biopsyrapid CTC enrichment

Identifiers

PMID41144783
PMCPMC12811197

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.