Evidence map›Paper›PMID 25806288›Full record

ArticleTranslational lung cancer research2014

Individual profiling of circulating tumor cell composition in patients with non-small cell lung cancer receiving platinum based treatment.

Ivonne Nel, Ulrich Jehn, Thomas Gauler, Andreas-Claudius Hoffmann

Abstract read
In one paragraph

Article in Translational lung cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 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, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Circulating tumour cells in patients with lung cancer universally indicate poor prognosis.European respiratory review : an official journal of the European Respiratory Society · 2022
    Pooled it
  3. Implications of Heterotypic Cell Fusion in Cancer.Advances in experimental medicine and biology · 2026
    Review
  4. Review
  5. The Hallmarks of Circulating Hybrid Cells.Results and problems in cell differentiation · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Circulating cancer stem cells: an interesting niche to explore.Exploration of targeted anti-tumor therapy · 2020
    Article
  20. 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.

Ivonne Nel1 Molecular Oncology Risk-Profile Evaluation, Department of Medical Oncology, West German Cancer Center, 2 Department of Radiotherapy, 3 Department of Medical Oncology, West German Cancer Center, University Duisburg-Essen, 45122 Essen, Germany.
Ulrich Jehn1 Molecular Oncology Risk-Profile Evaluation, Department of Medical Oncology, West German Cancer Center, 2 Department of Radiotherapy, 3 Department of Medical Oncology, West German Cancer Center, University Duisburg-Essen, 45122 Essen, Germany.
Thomas Gauler1 Molecular Oncology Risk-Profile Evaluation, Department of Medical Oncology, West German Cancer Center, 2 Department of Radiotherapy, 3 Department of Medical Oncology, West German Cancer Center, University Duisburg-Essen, 45122 Essen, Germany.
Andreas-Claudius Hoffmann1 Molecular Oncology Risk-Profile Evaluation, Department of Medical Oncology, West German Cancer Center, 2 Department of Radiotherapy, 3 Department of Medical Oncology, West German Cancer Center, University Duisburg-Essen, 45122 Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCirculating tumor cells (CTC) could serve as a "liquid biopsy" for individualizing and monitoring treatment in patients with solid tumors as recently shown by our group. We assessed which non-hematopoietic cell types are identifiable in the peripheral blood of patients with non-small cell lung cancer (NSCLC) and correlated those to clinical characteristics.

methodsBlood from NSCLC patients (n=43) was processed as previously described. For subtype analyses CTC were negatively enriched by hematopoietic cell depletion. The remaining cell suspension included pre-enriched tumor cells and was spun onto glass slides and further characterized by multi-immunofluorescence staining against epithelial markers pan-cytokeratin (CK) and epithelial cell adhesion molecule (EpCAM), mesenchymal marker N-cadherin, stem cell marker CD133, hematopoietic marker CD45 and nuclear counterstain DAPI. Individual cell type profiles were analyzed and correlated to therapeutic outcome.

resultsAmong other associations of CTC subtypes with clinical parameters Kaplan-Meier test revealed that an increased CD133-positive to pan-CK-positive cell type ratio (stem cell like to epithelial ratio) and the presence of mesenchymal N-cadherin+ cells, both were significantly associated to shortened PFS (2 vs. 8 months, P=0.003, HR =4.43; 5 vs. 8 months, P=0.03, HR =2.63).

conclusionsOur data suggest that different CTC populations are identifiable in peripheral blood and that these individual cell type profiles might be used to predict outcome to platinum based systemic therapies in lung cancer patients.

Indexed as

Circulating tumor cells (CTC)epithelial cellsmesenchymal cellsstem cell-like

Identifiers

PMID25806288
PMCPMC4367657

What OpenQuestion holds

Textmetadata
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.