Evidence map›Paper›PMID 39367702›Full record

ArticleMolecular oncology2025

Cellular liquid biopsy provides unique chances for disease monitoring, preclinical model generation and therapy adjustment in rare salivary gland cancer patients.

Nataša Stojanović Gužvić, Florian Lüke, Steffi Treitschke, Andrea Coluccio, Martin Hoffmann, Giancarlo Feliciello, Adithi Ravikumar Varadarajan, Xin Lu, Kathrin Weidele, Catherine Botteron and 22 more

Abstract read
In one paragraph

Article in Molecular oncology, 2025. 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. 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

32 authors.

Nataša Stojanović GužvićFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Florian LükeFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Steffi TreitschkeFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Andrea ColuccioFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Martin HoffmannFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Giancarlo FelicielloFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Adithi Ravikumar VaradarajanFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.ORCID https://orcid.org/0000-0002-9581-8598
Xin LuFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Kathrin WeideleFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.ORCID https://orcid.org/0009-0008-9313-5057
Catherine BotteronFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Silvia Materna-ReicheltFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Felix KeilBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Katja EvertBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Florian WeberFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Thomas SchambergerExperimental Medicine and Therapy Research, University of Regensburg, Germany.
Michael AlthammerExperimental Medicine and Therapy Research, University of Regensburg, Germany.
Jirka GrosseBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Dirk HellwigBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Christian SchulzBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Stephan SeitzBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Peter UgocsaiBavarian Cancer Research Center (BZKF), Regensburg, Germany.
Anke Schlenska-LangeDepartment of Oncology and Hematology, Hospital Barmherzige Brüder, Regensburg, Germany.
Roman MayrDepartment of Urology, Caritas St. Josef Medical Center, University of Regensburg, Germany.
Ulrich KaiserDepartment of Internal Medicine III, University Hospital Regensburg, Germany.
Wolfgang DietmaierInsitute for Pathology, University of Regensburg, Germany.
Bernhard PolzerFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Jens WarfsmannFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Kamran HonarnejadFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Tobias PukropFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.
Daniel HeudoblerDepartment of Internal Medicine III, University Hospital Regensburg, Germany.
Christoph A KleinFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.ORCID https://orcid.org/0000-0001-7128-1725
Christian WernoFraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.ORCID https://orcid.org/0009-0001-1647-4804

Funding

Bavarian ministry of economic affairs, energy and technology AZ 20-3410.1-1-1Deutsche Forschungsgemeinschaft SFB TRR 305 - A07Deutsche Forschungsgemeinschaft SFB TRR 305 - B13Deutsche Forschungsgemeinschaft SFB TRR 305 - Z02Deutsche Krebshilfe 70112504
6 · The paper itself

Abstract

While cell-free liquid biopsy (cfLB) approaches provide simple and inexpensive disease monitoring, cell-based liquid biopsy (cLB) may enable additional molecular genetic assessment of systemic disease heterogeneity and preclinical model development. We investigated 71 blood samples of 62 patients with various advanced cancer types and subjected enriched circulating tumor cells (CTCs) to organoid culture conditions. CTC-derived tumoroid models were characterized by DNA/RNA sequencing and immunohistochemistry, as well as functional drug testing. Results were linked to molecular features of primary tumors, metastases, and CTCs; CTC enumeration was linked to disease progression. Of 52 samples with positive CTC counts (≥1) from eight different cancer types, only CTCs from two salivary gland cancer (SGC) patients formed tumoroid cultures (P = 0.0005). Longitudinal CTC enumeration of one SGC patient closely reflected disease progression during treatment and revealed metastatic relapse earlier than clinical imaging. Multiomics analysis and functional in vitro drug testing identified potential resistance mechanisms and drug vulnerabilities. We conclude that cLB might add a functional dimension (to the genetic approaches) in the personalized management of rare, difficult-to-treat cancers such as SGC.

Indexed as

Salivary Gland NeoplasmsAdultAgedDisease ProgressionFemaleHumansLiquid BiopsyMaleMiddle AgedNeoplastic Cells, CirculatingOrganoidsCTCliquid biopsypersonalized tumor therapysalivary gland cancertumoroid culture

Identifiers

PMID39367702
PMCPMC12234380

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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.