Evidence map›Paper›PMID 26079252›Full record

ReviewCritical reviews in clinical laboratory sciences2015

Using circulating tumor cells to inform on prostate cancer biology and clinical utility.

Jing Li, Simon G Gregory, Mariano A Garcia-Blanco, Andrew J Armstrong

Abstract readReview
In one paragraph

Review in Critical reviews in clinical laboratory sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Toward a New Era for the Management of Circulating Tumor Cells.Advances in experimental medicine and biology · 2021
    Review
  9. Article
  10. Liquid Biopsy Potential Biomarkers in Prostate Cancer.Diagnostics (Basel, Switzerland) · 2018
    Article
  11. Association of urinary and plasma DNA in early breast cancer patients and its links to disease relapse.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Article
  12. Article
  13. Review
  14. Article
  15. Single-Cell Analysis of Circulating Tumor Cells as a Window into Tumor Heterogeneity.Cold Spring Harbor symposia on quantitative biology · 2016
    Review
  16. Review
  17. 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

4 authors.

Jing Lia Duke Cancer Institute, Duke University Medical Center , Durham , NC , USA .
Simon G Gregory
Mariano A Garcia-Blanco
Andrew J Armstrong

Funding

Regulation of Alternative Splicing of FGFR2 pre-mRNAR01GM063090 · NIGMS · DUKE UNIVERSITY · PI GARCIA-BLANCO, MARIANO A. · 2001 to 2008
$2.3M
Alternative splicing and epithelial-mesenchymal plasticity in prostate tumorsR01CA127727 · NCI · DUKE UNIVERSITY · PI GARCIA-BLANCO, MARIANO A. · 2009 to 2013
$1.6M
NCI NIH HHS R01 CA127727NIGMS NIH HHS R01 GM063090NIGMS NIH HHS R01 GM63090
6 · The paper itself

Abstract

Substantial advances in the molecular biology of prostate cancer have led to the approval of multiple new systemic agents to treat men with metastatic castration-resistant prostate cancer (mCRPC). These treatments encompass androgen receptor directed therapies, immunotherapies, bone targeting radiopharmaceuticals and cytotoxic chemotherapies. There is, however, great heterogeneity in the degree of patient benefit with these agents, thus fueling the need to develop predictive biomarkers that are able to rationally guide therapy. Circulating tumor cells (CTCs) have the potential to provide an assessment of tumor-specific biomarkers through a non-invasive, repeatable "liquid biopsy" of a patient's cancer at a given point in time. CTCs have been extensively studied in men with mCRPC, where CTC enumeration using the Cellsearch® method has been validated and FDA approved to be used in conjunction with other clinical parameters as a prognostic biomarker in metastatic prostate cancer. In addition to enumeration, more sophisticated molecular profiling of CTCs is now feasible and may provide more clinical utility as it may reflect tumor evolution within an individual particularly under the pressure of systemic therapies. Here, we review technologies used to detect and characterize CTCs, and the potential biological and clinical utility of CTC molecular profiling in men with metastatic prostate cancer.

Indexed as

Biomarkers, TumorNeoplastic Cells, CirculatingProstatic Neoplasms, Castration-ResistantHumansMaleReceptors, AndrogenAR protein, humanBiomarkers, TumorReceptors, AndrogenAndrogen receptorbiomarkercastration resistant prostate cancerEpCAMliquid biopsymicrofluidicPSA

Identifiers

PMID26079252
PMCPMC4808585

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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.