Evidence map›Paper›PMID 28228136›Full record

ArticleJournal of translational medicine2017

Circulating tumor cells capture disease evolution in advanced prostate cancer.

Justin Lack, Marc Gillard, Maggie Cam, Gladell P Paner, David J VanderWeele

Abstract read
In one paragraph

Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Liquid biopsy approach in the management of prostate cancer.Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  12. Review
  13. 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

5 authors.

Justin LackCenter for Cancer Research Collaborative Bioinformatics Resource, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Marc GillardDepartment of Surgery, University of Chicago, Chicago, IL, 60615, USA.
Maggie CamCenter for Cancer Research Collaborative Bioinformatics Resource, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Gladell P PanerDepartment of Pathology, University of Chicago, Chicago, IL, 60615, USA.
David J VanderWeeleLaboratory for Genitourinary Pathogenesis, Center for Cancer Research, National Cancer Institute, 37 Convent Drive, Rm 1066A, Bethesda, MD, 20892, USA. david.vanderweele@nih.gov.ORCID 0000-0003-4576-5034

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Evolution of prostate cancer genomeZIABC011770 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI VANDERWEELE, DAVID · 2017 to 2017
$43k
NCI NIH HHS P30 CA014599
6 · The paper itself

Abstract

backgroundGenetic analysis of advanced cancer is limited by availability of representative tissue. Biopsies of prostate cancer metastasized to bone are invasive with low quantity of tumor tissue. The prostate cancer genome is dynamic, however, with temporal heterogeneity requiring repeated evaluation as the disease evolves. Circulating tumor cells (CTCs) offer an alternative, "liquid biopsy", though single CTC sequencing efforts are laborious with high failure rates.

methodsWe performed exome sequencing of matched treatment-naïve tumor tissue, castrate resistant tumor tissue, and pooled CTC samples, and compared mutations identified in each.

resultsThirty-seven percent of CTC mutations were private to CTCs, one mutation was shared with treatment-naïve disease alone, and 62% of mutations were shared with castrate-resistant disease, either alone or with treatment-naïve disease. An acquired nonsense mutation in the Retinoblastoma gene, which is associated with progression to small cell cancer, was identified in castrate resistant and CTC samples, but not treatment-naïve disease. This timecourse correlated with the tumor acquiring neuroendocrine features and a change to neuroendocrine-specific therapy.

conclusionsThese data support the use of pooled CTCs to facilitate the genetic analysis of late stage prostate cancer.

Indexed as

Disease ProgressionAgedHumansMaleMutationNeoplasm StagingNeoplastic Cells, CirculatingProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantRetinoblastoma ProteinRetinoblastoma ProteinCastrate resistant prostate cancerCirculating tumor cellsNeuroendocrine prostate cancerTumor evolution

Identifiers

PMID28228136
PMCPMC5322599

What OpenQuestion holds

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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.