Evidence map›Paper›PMID 35159118›Full record

ArticleCancers2022

Clinical Validity of Circulating Tumor DNA as Prognostic and Predictive Marker for Personalized Colorectal Cancer Patient Management.

Ariane Hallermayr, Verena Steinke-Lange, Holger Vogelsang, Markus Rentsch, Maike de Wit, Christopher Haberl, Elke Holinski-Feder, Julia M A Pickl

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Interpretable deep learning model of circulating genomics for quantitative survival prediction in advanced non-small cell lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

8 authors at 6 institutions in 1 country.

Ariane HallermayrMGZ-Medizinisch Genetisches Zentrum, 80335 Munich, Germany.ORCID 0000-0002-6503-1874
Verena Steinke-LangeMGZ-Medizinisch Genetisches Zentrum, 80335 Munich, Germany.ORCID 0000-0001-8491-3234
Holger VogelsangDepartment of General, Visceral, Thoracic and Endocrine Surgery, Klinikum Garmisch-Partenkirchen, Teaching Hospital, Ludwig Maximilian University Munich, 82467 Garmisch-Partenkirchen, Germany.ORCID 0000-0001-9750-8924
Markus RentschDepartment of General, Visceral and Thorax Surgery, Klinikum Ingolstadt, 85049 Ingolstadt, Germany.
Maike de WitDepartment of Haemaotology, Oncology and Palliative Medicine, Vivantes Klinikum Neukoelln, 12351 Berlin, Germany.
Christopher HaberlDepartment of Oncology and Hematology, Barmherzige Brüder, Klinikum St. Elisabeth, 94315 Straubing, Germany.
Elke Holinski-FederMGZ-Medizinisch Genetisches Zentrum, 80335 Munich, Germany.
Julia M A PicklMGZ-Medizinisch Genetisches Zentrum, 80335 Munich, Germany.ORCID 0000-0001-9269-5177
LMU Klinikum · DEAuguste-Viktoria-Klinik · DEBarmherzige Brüder Klinikum St. Elisabeth in Straubing · DEGarmisch-Partenkirchen Medical Center · DEKlinikum Ingolstadt · DEMedical Genetics Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor DNA (ctDNA) is a promising liquid biopsy (LB) marker to support clinical decisions in precision medicine. For implementation into routine clinical practice, clinicians need precise ctDNA level cutoffs for reporting residual disease and monitoring tumor burden changes during therapy. We clinically validated the limit of blank (LOB) and the limit of quantification (LOQ) of assays for the clinically most relevant somatic variants

Indexed as

cfDNAcolorectal cancerctDNAmonitoringresidual disease

Identifiers

PMID35159118
PMCPMC8834623
OpenAlexW4211044253

What OpenQuestion 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 OpenQuestion graph.