Evidence map›Paper›PMID 37190081›Full record

ArticleCells2023

Prognostic Role of Circulating Tumor Cell Trajectories in Metastatic Colorectal Cancer.

Valentina Magri, Luca Marino, Chiara Nicolazzo, Angela Gradilone, Gianluigi De Renzi, Michela De Meo, Orietta Gandini, Arianna Sabatini, Daniele Santini, Enrico Cortesi and 1 more

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
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  6. Article
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  8. Clinical significances ofBiomedical reports · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Biomarkers in Colorectal Cancer: Actual and Future Perspectives.International journal of molecular sciences · 2024
    Review
  15. [Recent advances in responsive isolation, release and clinical application of circulating tumor cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Review
  16. Article
  17. Review
  18. Review
  19. 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

11 authors.

Valentina MagriDepartment of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.ORCID 0000-0001-7312-2904
Luca MarinoDepartment of Mechanical and Aerospace Engineering, Sapienza University of Rome, 00184 Rome, Italy.ORCID 0000-0001-7380-6222
Chiara NicolazzoDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.ORCID 0000-0002-2551-8979
Angela GradiloneDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Gianluigi De RenziDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Michela De MeoDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Orietta GandiniDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.ORCID 0000-0002-7867-1010
Arianna SabatiniDepartment of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
Daniele SantiniDepartment of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
Enrico CortesiDepartment of Pathology, Oncology and Radiology, Sapienza University of Rome, 00161 Rome, Italy.
Paola GazzanigaDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.ORCID 0000-0002-2325-2273

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA large amount of evidence from clinical studies has demonstrated that circulating tumor cells are strong predictors of outcomes in many cancers. However, the clinical significance of CTC enumeration in metastatic colorectal cancer is still questioned. The aim of this study was to evaluate the clinical value of CTC dynamics in mCRC patients receiving first-line treatments. MATERIALS AND

methodsSerial CTC data from 218 patients were used to identify CTC trajectory patterns during the course of treatment. CTCs were evaluated at baseline, at a first-time point check and at the radiological progression of the disease. CTC dynamics were correlated with clinical endpoints.

resultsUsing a cut-off of ≥1 CTC/7.5 mL, four prognostic trajectories were outlined. The best prognosis was obtained for patients with no evidence of CTCs at any timepoints, with a significant difference compared to all other groups. Lower PFS and OS were recognized in group 4 (CTCs always positive) at 7 and 16 months, respectively.

conclusionsWe confirmed the clinical value of CTC positivity, even with only one cell detected. CTC trajectories are better prognostic indicators than CTC enumeration at baseline. The reported prognostic groups might help to improve risk stratification, providing potential biomarkers to monitor first-line treatments.

Indexed as

Colorectal NeoplasmsNeoplastic Cells, CirculatingBiomarkers, TumorDisease-Free SurvivalHumansPrognosisBiomarkers, TumorCellSearch®circulating tumor cellscirculating tumor cell trajectoriesliquid biopsymetastatic colorectal cancerprecision medicineprognostic and predictive biomarkers

Identifiers

PMID37190081
PMCPMC10136568

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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.