Evidence map›Paper›PMID 37056288›Full record

ArticleFrontiers in genetics2023

Case Report: Potential role of selective venous sampling for liquid biopsy in complex clinical settings: Three case presentations.

Vladimira Tichà, Gianluigi Patelli, Gianpaolo Basso, Aurelio Prino, Elena Repetti, Maria Grugni, Bruno Damascelli

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 1 country.

Vladimira TichàDepartment of Interventional Oncology, EMO GVM Centrocuore Columbus, Milan, Italy.
Gianluigi PatelliDepartment of Radiology, ASST Bergamo Est-Bolognini Hospital, Seriate, Italy.
Gianpaolo BassoSchool of Medicine and Surgery, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.
Aurelio PrinoPalliative Care Department and Hospice, University Hospital Maggiore Della Carità, Novara, Italy.
Elena RepettiTOMA Advanced Biomedical Assays S.p.A, Busto Arsizio, Varese, Italy.
Maria GrugniTOMA Advanced Biomedical Assays S.p.A, Busto Arsizio, Varese, Italy.
Bruno DamascelliDepartment of Interventional Oncology, EMO GVM Centrocuore Columbus, Milan, Italy.
EMO GVM Centro Cuore Columbus · ITAzienda Ospedaliera Bolognini Seriate · ITUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor mutation profiling from a blood sample, known as liquid biopsy, is a reality that has already been approved for some cancers. This molecular diagnostic method complements tissue biopsy but is less invasive and therefore more easily applied, especially during tumor evolution. Its use should allow detection of residual disease, evaluation of treatment response or resistance, and selection of targeted treatments. However, implementation of liquid biopsy in routine clinical practice is hindered by unsolved issues, one of which is the scarcity of circulating tumor DNA in blood samples drawn from peripheral veins. To address this problem, we propose minimally invasive selective venous sampling from the region of interest, as used for some hormonal studies and for mapping of endocrine tumors. Intuitively, selective sampling should improve the sensitivity of liquid biopsy by avoiding the dilution of tumor biomarkers that occurs in the peripheral circulation. We report three cases that illustrate the potential utility of selective liquid biopsy in complex clinical settings, providing implications for diagnosis and treatment as well as for monitoring over time, disease localization, identification of drug resistance, and differential diagnosis.

Indexed as

ctDNAglioblastomaLiquid biopsypancreatic cancerprostate cancervenous sampling

Identifiers

PMID37056288
PMCPMC10086121
OpenAlexW4361205144

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.