Evidence map›Paper›PMID 10623654›Full record

ArticleThe American journal of pathology2000

Isolation by size of epithelial tumor cells : a new method for the immunomorphological and molecular characterization of circulatingtumor cells.

G Vona, A Sabile, M Louha, V Sitruk, S Romana, K Schütze, F Capron, D Franco, M Pazzagli, M Vekemans and 3 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 466 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
466citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% of its field
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.

NCT01725438 nacompletednot on this mapstarted 2012, after this paper: background citation

Clinical Validation of the ISET Method for the Non Invasive Prenatal Diagnosis of Trisomy 21 by Genetic Analysis of Circulating Trophoblastic Cells

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2012 to 2021Enrolled150ConditionsTrisomy 21Armssample blood
NCT03979339 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Feasibility of a New Technology for Isolating Circulating Tumour Cells in Selected Cancer Patients and Healthy Volunteers

TypeinterventionalSponsorCentre Oscar LambretRan2020 to 2023Enrolled76ConditionsHER2-positive Metastatic Breast Cancer, Ovarian Cancer, Hormone-resistant Prostate Cancer, Circulating Tumor CellArmsBlood sample collection
3 · Its place in the literature

Who cites it

466 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,053 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. From Tumour to Bloodstream: Advancing PD-L1 Testing With Liquid Biopsies in Non-Small Cell Lung Cancer.Cytopathology : official journal of the British Society for Clinical Cytology · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Circulating Tumor Cells for the Monitoring of Lung Cancer Therapies.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Review
  19. Review
  20. Review

406 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

13 authors at 5 institutions in 2 countries.

G VonaINSERM U 370,() Faculté Necker, Paris, France.
A Sabile
M Louha
V Sitruk
S Romana
K Schütze
F Capron
D Franco
M Pazzagli
M Vekemans
B Lacour
C Bréchot
P Paterlini-Bréchot
Hôpital Necker-Enfants Malades · FRInserm · FRHôpital Antoine-Béclère · FRHôpital Jean-Verdier · FRUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed a new assay, ISET (isolation by size of epithelial tumor cells), which allows the counting and the immunomorphological and molecular characterization of circulating tumor cells in patients with carcinoma, using peripheral blood sample volumes as small as 1 ml. Using this assay, epithelial tumor cells can be isolated individually by filtration because of their larger size when compared to peripheral blood leukocytes. ISET parameters were defined using peripheral blood spiked with tumor cell lines (HepG2, Hep3B, MCF-7, HeLa, and LNCaP). ISET can detect a single, micropipetted tumor cell, added to 1 ml of blood. We also demonstrate that fluorescence in situ hybridization can be used to perform chromosomal analyses on tumor cells collected using ISET. Polymerase chain reaction-based genetic analyses can be applied to ISET-isolated cells, and, as an example, we demonstrate homozygous p53 deletion in single Hep3B cells after filtration and laser microdissection. Finally, we provide evidence for the in vivo feasibility of ISET in patients with hepatocellular carcinoma undergoing tumor resection. ISET, but not reverse transcriptase-polymerase chain reaction, allowed analysis of cell morphology, counting of tumor cells, and demonstration of tumor microemboli spread into peripheral blood during surgery. Overall, ISET constitutes a novel approach that should open new perpectives in molecular medicine.

Indexed as

Carcinoma, HepatocellularCell SeparationCell SizeGene DeletionGenes, p53HumansImmunologic TechniquesIn Situ Hybridization, FluorescenceLiver NeoplasmsNeoplastic Cells, CirculatingSensitivity and SpecificityTumor Cells, Cultured

Identifiers

PMID10623654
PMCPMC1868645
OpenAlexW1558034062

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.