Evidence map›Paper›PMID 18954898›Full record

ArticleGynecologic oncology2009

Clinical significance of circulating tumor cells detected by an invasion assay in peripheral blood of patients with ovarian cancer.

Tina Fan, Qiang Zhao, John J Chen, Wen-Tien Chen, Michael L Pearl

Abstract read
In one paragraph

Article in Gynecologic oncology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 4 pooled it
–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

75 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Review
  9. Article
  10. Observational
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Recent Advances in Methods for Circulating Tumor Cell Detection.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review

15 more citing papers are in PubMed but not listed here.

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.

Tina FanDepartment of Medicine, Metastasis Research Laboratory, Stony Brook University, Stony Brook, NY 11794, USA.
Qiang Zhao
John J Chen
Wen-Tien Chen
Michael L Pearl

Funding

World Trade Center Worker and Volunteer Medical Screening ProgramM01RR010710 · NCRR · STATE UNIVERSITY NEW YORK STONY BROOK · PI GOLDSTEIN, RITA Z · 1998 to 2009
$17.6M
Cancer detection technologyR42CA108247 · NCI · VITATEX, INC. · PI CHEN, WEN-TIEN · 2004 to 2007
$2.2M
REGULATION OF TISSUE REPAIRR01EB002065 · NIBIB · STATE UNIVERSITY NEW YORK STONY BROOK · PI CHEN, WEN-TIEN · 2003 to 2008
$1.6M
MOLECULAR ULTRASTRUCTURE UNDERLYING CELL ADHESIONR01CA039077 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI CHEN, WEN-TIEN · 1985 to 2007
$1.6M
Gene Expression of Viable Ovarian Cancer CellsR41CA103467 · NCI · VITATEX, INC. · PI CHEN, WEN-TIEN · 2003 to 2003
$177k
NCI NIH HHS R01 CA039077NCI NIH HHS R41 CA103467NCI NIH HHS R42 CA108247NCRR NIH HHS M01 RR010710NIBIB NIH HHS R01 EB002065
6 · The paper itself

Abstract

objectivesThe invasive growth of circulating tumor cells (CTCs) propagates cancer metastasis. The aims of this study were to evaluate the association of invasive CTCs, detected by a novel cell invasion assay, with disease stage, CA-125 level and patient survival.

methodsPeripheral blood samples from 71 patients undergoing evaluation for ovarian malignancy were assessed for the presence of invasive CTCs using a cell invasion assay that enriches and identifies tumor cells with a cell adhesion matrix (CAM). Invasive CTCs were identified as cells exhibiting CAM invasion (CAM+) and expressing standard epithelial markers (Epi+).

results43 (60.6%) patients had detectable CTCs: 0/5 benign patients, 1/10 (10%) early stage, 39/52 (73.1%) late stage and 3/4 (75%) unstaged patients (p-value <0.001). CTC counts ranged from 0-149 CTCs/ml with stage III/IV patients exhibiting significantly higher mean counts (41.3 CTCs/ml) than stage I/II patients (6.0 CTCs/ml) and benign patients (0 CTCs/ml, p-value=0.001). A positive correlation between CTC count and CA-125 level was observed (Spearman correlation coefficient r=0.309, p-value=0.035). Kaplan-Meier curves revealed a significant decrease in disease-free survival in patients with detectable CTCs (median survival 15.0 months vs. 35.0 months, log-rank p-value=0.042). Tumor grade and tumor histology did not influence CTC detection.

conclusionsInvasive CTCs can be detected in a majority of epithelial ovarian cancer patients and may predict shorter disease-free survival. Furthermore, higher CTC counts may reflect later stage disease and higher CA-125 levels.

Indexed as

CA-125 AntigenCohort StudiesDisease-Free SurvivalFemaleHumansMiddle AgedNeoplasm InvasivenessNeoplasm MetastasisNeoplasm StagingNeoplastic Cells, CirculatingOvarian NeoplasmsPeritoneal NeoplasmsRetrospective StudiesSurvival RateCA-125 Antigen

Identifiers

PMID18954898
PMCPMC2606929

What OpenQuestion holds

Textmetadata
LicenceTDM
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.