Evidence map›Paper›PMID 28794448›Full record

ArticleScientific reports2017

Prognostic impact of CD133 expression in Endometrial Cancer Patients.

G Mancebo, J M Sole-Sedeno, O Pino, E Miralpeix, S Mojal, L Garrigos, B Lloveras, P Navarro, J Gibert, M Lorenzo and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Epithelial Ovarian Cancer and Cancer Stem Cells.Advances in experimental medicine and biology · 2021
    Article
  6. Article
  7. Article
  8. 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

13 authors.

G ManceboObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain. gmancebo@hospitaldelmar.cat.ORCID 0000-0001-5859-7936
J M Sole-SedenoObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
O PinoUniversitat Autónoma de Barcelona, Plaza Cívica, Campus de la UAB, 08193, Bellaterra, Catalonia, Spain.
E MiralpeixObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
S MojalDepartment of Statistics, IMIM-Hospital del Mar Medical Research Institute, Doctor Aiguader, 88, 08003, Barcelona, Catalonia, Spain.
L GarrigosOncology Department of Hospital Universitari de la Vall d'Hebron, Passeig de la Vall d'Hebron, 119-129, 08035, Barcelona, Catalonia, Spain.
B LloverasPathology Department of Hospital Universitari del Mar., Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
P NavarroCancer Research Programme, IMIM-Hospital del Mar Medical Research Institute, Doctor Aiguader, 88, 08003, Barcelona, Catalonia, Spain.
J GibertCancer Research Programme, IMIM-Hospital del Mar Medical Research Institute, Doctor Aiguader, 88, 08003, Barcelona, Catalonia, Spain.
M LorenzoObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
I AranObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
R CarrerasObstetrics and Gynaecology Department of Hospital Universitari del Mar, Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.
F AlamedaPathology Department of Hospital Universitari del Mar., Passeig Marítim, 25-29, 08003, Barcelona, Catalonia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To assess the impact of CD133 expression on the prognosis of endometrioid endometrial carcinoma (EEC). We retrospectively assessed CD133 expression in tissue microarray of 116 surgically treated FIGO I-III EEC. Tumors with ≥10% of CD133-expressing cells were considered CD133-positive (CD133+). On the basis of CD133 expression, clinical and pathological parameters, progression-free survival (PFS) and overall survival (OS) were evaluated. Of the EEC studied 85.2% showed CD133-expressing cells. Only 61% (n = 66) of EEC presented ≥10% of CD133 expressing cells and were considered CD133+. The mean OS for CD133+ tumour patients was 161 months (95% CI, 154-168) as compared with 146 months (95% CI, 123-160) for those with CD133- tumors (p = 0.012). The mean PFS for CD133+ tumour was 159 months (95% CI, 149-168) as compared with 147 months (95% CI, 132-161) in those with a CD133-tumour (p = 0.014). CD133+ tumours were less likely to have vascular invasion (p = 0.010) and more likely to be well differentiated (p = 0.034). C133+ tumours predicted favorable OS and PFS of EEC patients, with a Hazard Ratio 4.731 (95% CI, 1.251-17.89; p = 0.022). CD133+ tumor status correlates with favorable prognosis of EEC. Our findings are in agreement with studies addressing brain and colorectal tumours.

Indexed as

Biomarkers, TumorGene Expression Regulation, NeoplasticAC133 AntigenAgedAged, 80 and overEndometrial NeoplasmsFemaleFollow-Up StudiesHumansImmunohistochemistryMiddle AgedNeoplasm GradingNeoplasm StagingPrognosisProportional Hazards ModelsROC CurveAC133 AntigenBiomarkers, TumorPROM1 protein, human

Identifiers

PMID28794448
PMCPMC5550511

What OpenQuestion holds

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Registered trials

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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.