Evidence map›Paper›PMID 26296970›Full record

ArticleOncotarget2015

Detection of soluble EpCAM (sEpCAM) in malignant ascites predicts poor overall survival in patients treated with catumaxomab.

Andreas Seeber, Ioana Braicu, Gerold Untergasser, Mani Nassir, Dominic Fong, Laura Botta, Guenther Gastl, Heidi Fiegl, Alain Zeimet, Jalid Sehouli and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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.

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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Shedding light on the EpCAM: An overview.Journal of cellular physiology · 2019
    Review
  7. Article
  8. Review
  9. Advances in ovarian cancer therapy.Cancer chemotherapy and pharmacology · 2018
    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

11 authors at 4 institutions in 3 countries.

Andreas SeeberDepartment of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Ioana BraicuEuropean Competence Center for Ovarian Cancer, Charité Berlin, Berlin, Germany.
Gerold UntergasserDepartment of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Mani NassirEuropean Competence Center for Ovarian Cancer, Charité Berlin, Berlin, Germany.
Dominic FongDepartment of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Laura BottaEvaluative Epidemiology Unit, Fondazione IRCSS "Istituto Nazionale dei Tumori", Milan, Italy.
Guenther GastlDepartment of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Heidi FieglDepartment of Gynaecology and Obstetrics, Innsbruck Medical University, Innsbruck, Austria.
Alain ZeimetDepartment of Gynaecology and Obstetrics, Innsbruck Medical University, Innsbruck, Austria.
Jalid SehouliEuropean Competence Center for Ovarian Cancer, Charité Berlin, Berlin, Germany.
Gilbert SpizzoDepartment of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
Innsbruck Medical University · ATCharité - Universitätsmedizin Berlin · DETyrolean Cancer Research Institute · ATFondazione IRCCS Istituto Nazionale dei Tumori · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EpCAM is an attractive target for cancer therapy and the EpCAM-specific antibody catumaxomab has been used for intraperitoneal treatment of EpCAM-positive cancer patients with malignant ascites. New prognostic markers are necessary to select patients that mostly benefit from catumaxomab. Recent data showed that soluble EpCAM (sEpCAM) is capable to block the effect of catumaxomab in vitro. This exploratory retrospective analysis was performed on archived ascites samples to evaluate the predictive role of sEpCAM in catumaxomab-treated patients. Sixty-six catumaxomab-treated patients with an available archived ascites sample were included in this study and tested for sEpCAM by sandwich ELISA. All probes were sampled before treatment start and all patients received at least one catumaxomab infusion. Overall survival, puncture-free survival and time to next puncture were compared between sEpCAM-positive and -negative patients. We detected sEpCAM in ascites samples of 9 patients (13.6%). These patients showed a significantly shorter overall survival. The prognostic significance of sEpCAM in ascites was particularly strong in patients with ovarian cancer. Puncture-free survival and time to next puncture were not significantly different between sEpCAM-positive and -negative patients. We propose sEpCAM in malignant ascites as a potential predictive marker in cancer patients treated with catumaxomab. Prospective studies with larger patients samples are urgently needed to confirm these findings and studies testing dose-intensified catumaxomab in patients with sEpCAM-positive ascites should be envisaged.

Indexed as

Antibodies, BispecificAntigens, NeoplasmAscitesBiomarkers, TumorCell Adhesion MoleculesEnzyme-Linked Immunosorbent AssayEpithelial Cell Adhesion MoleculeFemaleFollow-Up StudiesHumansKaplan-Meier EstimateMaleMiddle AgedOvarian NeoplasmsPredictive Value of TestsPrognosisAntibodies, BispecificAntigens, NeoplasmBiomarkers, TumorcatumaxomabCell Adhesion MoleculesEPCAM protein, humanEpithelial Cell Adhesion MoleculeascitescatumaxomabEpCAMovarian cancersoluble EpCAM

Identifiers

PMID26296970
PMCPMC4694811
OpenAlexW1893025524

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.