Evidence map›Paper›PMID 26123742›Full record

Trial reportBMC cancer2015

PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study.

Nicole C M Visser, Johan Bulten, Anneke A M van der Wurff, Erik A Boss, Carolien M Bronkhorst, Harrie W H Feijen, Joke E Haartsen, Hilde A D M van Herk, Ineke M de Kievit, Paul J J M Klinkhamer and 8 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  5. Review
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  8. Observational
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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

18 authors.

Nicole C M VisserDept. Pathology, Radboud university medical centre, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands. nicole.visser@radboudumc.nl.
Johan BultenDept. Pathology, Radboud university medical centre, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands. Hans.Bulten@radboudumc.nl.
Anneke A M van der WurffDept. Pathology, St Elisabeth Hospital, Tilburg, The Netherlands. a.vd.wurff@elisabeth.nl.
Erik A BossDept. Obstetrics and Gynaecology, Maxima Medical Centre, Veldhoven and Eindhoven, The Netherlands. e.boss@mmc.nl.
Carolien M BronkhorstDept. Pathology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands. c.bronkhorst@jbz.nl.
Harrie W H FeijenDept. Obstetrics and Gynaecology, Amphia Hospital, Breda, The Netherlands. HFeijen@Amphia.nl.
Joke E HaartsenDept. Obstetrics and Gynaecology, Elkerliek Hospital, Helmond, The Netherlands. jhaartsen@elkerliek.nl.
Hilde A D M van HerkDept. Pathology, Elkerliek Hospital, Helmond, The Netherlands. hvherk@elkerliek.nl.
Ineke M de KievitDept. Pathology, Canisius Wilhemina Hospital, Nijmegen, The Netherlands. i.d.kievit@cwz.nl.
Paul J J M KlinkhamerDept. Pathology, PAMM, Eindhoven, The Netherlands. P.Klinkhamer@pamm.nl.
Brenda M PijlmanDept. Obstetrics and Gynaecology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands. B.Pijlman@jbz.nl.
Marc P M L SnijdersDept. Obstetrics and Gynaecology, Canisius Wilhemina Hospital, Nijmegen, The Netherlands. m.snijders@cwz.nl.
Ingrid VandenputDept. Obstetrics and Gynaecology, Catharina Hospital, Eindhoven, The Netherlands. ingrid.vandenput@catharinaziekenhuis.nl.
M Caroline VosDept. Obstetrics and Gynaecology, St Elisabeth Hospital, Tilburg, The Netherlands. c.vos@elisabeth.nl.
Peter E J de WitDept. Pathology, Amphia Hospital, Breda, The Netherlands. pdwit@amphia.nl.
Lonneke V van de Poll-FranseDept. of Medical and Clinical Psychology, Tilburg University, Tilburg, The Netherlands. L.vd.Poll@ikz.nl.
Leon F A G MassugerDept. Obstetrics and Gynaecology, Radboud university medical centre, Nijmegen, The Netherlands. Leon.Massuger@radboudumc.nl.
Johanna M A PijnenborgDept. Obstetrics and Gynaecology, TweeSteden Hospital, Tilburg, The Netherlands. hpijnenborg@tsz.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndometrial carcinoma is the most common gynaecologic malignancy in industrialised countries and the incidence is still rising. Primary treatment is based on preoperative risk classification and consists in most cases of hysterectomy with bilateral salpingo-oophorectomy. In patients with serous and clear cell histology a complete surgical staging is mandatory. However, in routine clinical practice final histology regularly does not correspond with the preoperative histological diagnosis. This results in both over and under treatment. METHODS/

designThe aim of this multicentre, prospective cohort study is to select a panel of prognostic biomarkers to improve preoperative diagnosis of endometrial carcinoma in order to identify those patients that need extended surgery and/or additional treatment. Additionally, we will determine whether incorporation of cervical cytology and comorbidity could improve this preoperative risk classification. All patients treated for endometrial carcinoma in the participating hospitals from September 2011 till December 2013 are included. Patient characteristics, as well as comorbidity are registered. Patients without preoperative histology, history of hysterectomy and/or endometrial carcinoma or no surgical treatment including hysterectomy are excluded. The preoperative histology and final pathology will be reviewed and compared by expert pathologists. Additional immunohistochemical analysis of IMP3, p53, ER, PR, MLH1, PTEN, beta-catenin, p16, Ki-67, stathmin, ARID1A and L1CAM will be performed. Preoperative histology will be compared with the final pathology results. Follow-up will be at least 24 months to determine risk factors for recurrence and outcome. DISCUSSION: This study is designed to improve surgical treatment of endometrial carcinoma patients. A total of 432 endometrial carcinoma patients were enrolled between 2011 and 2013. Follow-up will be completed in 2015. Preoperative histology will be evaluated systematically and background endometrium will be classified. This is the first study incorporating immunohistochemistry, cervical cytology and comorbidity to define the optimal panel of prognostic biomarkers that contribute in clinical decision making in the management of endometrial carcinoma.

trial registrationNetherlands Trial Register number NTR3503.

Indexed as

PrognosisAdultAgedAged, 80 and overBiopsyCohort StudiesDisease-Free SurvivalEndometrial NeoplasmsFemaleHumansHysterectomyMiddle AgedNeoplasm ProteinsNeoplasm Recurrence, LocalProspective StudiesNeoplasm Proteins

Identifiers

PMID26123742
PMCPMC4485884

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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.