Evidence map›Paper›PMID 25769657›Full record

ArticleGynecologic oncology2015

Treatment monitoring of patients with epithelial ovarian cancer using invasive circulating tumor cells (iCTCs).

Michael L Pearl, Huan Dong, Shaun Tulley, Qiang Zhao, Marc Golightly, Stanley Zucker, Wen-Tien Chen

Abstract read
In one paragraph

Article in Gynecologic oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Circulating tumor cells in the early detection of human cancers.International journal of biological sciences · 2022
    Review
  17. Article
  18. Article
  19. Review
  20. Combined detection and subclass characteristics analysis of CTCs and CTECs by SE-iFISH in ovarian cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2021
    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

7 authors.

Michael L PearlDivision of Gynecologic Oncology, Stony Brook Medicine, Stony Brook, NY 11794, USA.
Huan DongDivision of Gynecologic Oncology, Stony Brook Medicine, Stony Brook, NY 11794, USA; Vitatex Inc., 25 Health Sciences Drive, Stony Brook, NY 11790, USA.
Shaun TulleyDivision of Gynecologic Oncology, Stony Brook Medicine, Stony Brook, NY 11794, USA; Vitatex Inc., 25 Health Sciences Drive, Stony Brook, NY 11790, USA.
Qiang ZhaoDivision of Gynecologic Oncology, Stony Brook Medicine, Stony Brook, NY 11794, USA; Vitatex Inc., 25 Health Sciences Drive, Stony Brook, NY 11790, USA.
Marc GolightlyDepartment of Pathology, Stony Brook Medicine, Stony Brook, NY 11794, USA.
Stanley ZuckerDepartment of Medicine, Stony Brook Medicine, Stony Brook, NY 11794, USA; Department of Medicine and Research, Veterans Affairs Medical Center, Northport, NY 11768, USA.
Wen-Tien ChenDivision of Gynecologic Oncology, Stony Brook Medicine, Stony Brook, NY 11794, USA; Vitatex Inc., 25 Health Sciences Drive, Stony Brook, NY 11790, USA. Electronic address: wentien@vitatex.com.

Funding

Cancer Progeniyor Cell MarkersR44CA140047 · NCI · VITATEX, INC. · PI CHEN, WEN-TIEN · 2009 to 2012
$2.2M
NCI NIH HHS R44 CA140047NCI NIH HHS R44CA140047
6 · The paper itself

Abstract

goalsContemporary management of epithelial ovarian cancer (EOC) uses biomarkers to monitor response to therapy. This study evaluates the role of invasive circulating tumor cells (iCTCs) in monitoring EOC treatment in comparison with serum cancer antigen 125 (CA125).

methodsMolecular and microscopic analyses were used to identify seprase and CD44 as tumor progenitor (TP) markers. The iCTC flow cytometry assay was optimized using blood donated by 64 healthy donors, 49 patients with benign abdominal diseases and 123 EOC patients. Serial changes in iCTCs and CA125 were measured in 129 blood and 169 serum samples, respectively, from 31 EOC patients to assess their concordance during therapy and their relationship with risk of progressive disease (PD).

resultsThe assay had 97% specificity and 83% sensitivity for detecting iCTCs in blood of EOC patients. iCTCs were detected in each monitoring patient (31/31, 100%) and in 110 of the 129 blood samples (85.3%). The concordance between changes in iCTCs/CA125 levels and changes in the intervals associated with no evidence of disease (NED) were markedly stronger (specificity: CA125 93.8%; iCTCs 90.6%), whereas increases in iCTCs (79.5%) were more sensitive than increases in CA125 (67.6%) to predict PD or relapse. Among the six patients who had greater than 6 measurements, iCTCs but not CA125 antedated changes in clinical status from PD to NED during and after chemotherapy and predated relapse.

conclusionSerial measurements of iCTCs could predict therapeutic responsiveness in 31 EOC patients who underwent standard taxol/carboplatin therapy.

Indexed as

Biomarkers, TumorCA-125 AntigenCarcinoma, Ovarian EpithelialCase-Control StudiesCohort StudiesEnvironmental MonitoringFemaleFlow CytometryHumansHyaluronan ReceptorsMembrane ProteinsNeoplasm Recurrence, LocalNeoplasms, Glandular and EpithelialNeoplasm StagingNeoplastic Cells, CirculatingOvarian NeoplasmsBiomarkers, TumorCA-125 AntigenCD44 protein, humanHyaluronan ReceptorsMembrane ProteinsMUC16 protein, humanseprase, humanSerine EndopeptidasesCell invasionCirculating cancer cellsCTCMetastasis detectionOvarian cancerTreatment monitoring

Identifiers

PMID25769657
PMCPMC5568621

What OpenQuestion holds

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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.