Evidence map›Paper›PMID 35025887›Full record

ArticlePloS one2022

Characteristics and outcome of children with renal tumors in the Netherlands: The first five-year's experience of national centralization.

Prakriti Roy, Sophie E van Peer, Martin M de Witte, Godelieve A M Tytgat, Henrike E Karim-Kos, Martine van Grotel, Cees P van de Ven, Annelies M C Mavinkurve-Groothuis, Johannes H M Merks, Roland P Kuiper and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.1field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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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

20 authors at 3 institutions in 1 country.

Prakriti RoyPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-0086-6691
Sophie E van PeerPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Martin M de WittePrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Godelieve A M TytgatPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Henrike E Karim-KosPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Martine van GrotelPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Cees P van de VenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Annelies M C Mavinkurve-GroothuisPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Roland P KuiperPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Janna A HolPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Geert O R JanssensPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Ronald R de KrijgerPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Marjolijn C J JongmansPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Jarno DrostPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Alida F W van der SteegPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Annemieke S LittooijPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Marc H W A WijnenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Harm van TinterenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-4626-8702
Marry M van den Heuvel-EibrinkPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Princess Máxima Center · NLUniversity Medical Center Utrecht · NLOncode Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Around 6% of all childhood malignancies represent renal tumors, of which a majority includes Wilms tumor (WT). Although survival rates have improved over the last decades, specific patients are still at risk for adverse outcome. In the Netherlands, since 2015, pediatric oncology care for renal tumors has been centralized in the Princess Máxima Center for Pediatric Oncology. Here, we describe experiences of the first 5 years of centralized care and explore whether this influences the epidemiological landscape by comparing data with the Netherlands Cancer Registry (NCR). We identified all patients <19 years with a renal mass diagnosed between 01-01-2015 and 31-12-2019 in the Princess Máxima Center. Epidemiology, characteristics and management were analyzed. We identified 164 patients (including 1 patient who refused consent for registration), in our center with a suspicion of a renal tumor. The remaining 163 cases included WT (n = 118)/cystic partially differentiated nephroblastoma (n = 2)/nephrogenic rests only (n = 6) and non-WT (n = 37). In this period, the NCR included 138 children, 1 17-year-old patient was not referred to the Princess Máxima Center. Central radiology review (before starting treatment) was performed in 121/163 patients, and central pathology review in 148/152 patients that underwent surgery. Treatment stratification, according to SIOP/EpSSG protocols was pursued based on multidisciplinary consensus. Preoperative chemotherapy was administered in 133 patients, whereas 19 patients underwent upfront surgery. Surgery was performed in 152 patients, and from 133 biomaterial was stored. Centralization of care for children with renal tumors led to referral of all but 1 new renal tumor cases in the Netherlands, and leads to referral of very rare subtypes not registered in the NCR, that benefit from high quality diagnostics and multidisciplinary decision making. National centralization of care led to enhanced development of molecular diagnostics and other innovation-based treatments for the future.

Indexed as

AdolescentAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolDactinomycinDisease-Free SurvivalHumansInfantKidney NeoplasmsNeoplasm StagingNetherlandsPrognosisTreatment OutcomeVincristineDactinomycinVincristine

Identifiers

PMID35025887
PMCPMC8757983
OpenAlexW4205557771

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.