Evidence map›Paper›PMID 35681735›Full record

ArticleCancers2022

Long-Term Tubular Dysfunction in Childhood Cancer Survivors; DCCSS-LATER 2 Renal Study.

Esmee C M Kooijmans, Helena J H van der Pal, Saskia M F Pluijm, Margriet van der Heiden-van der Loo, Leontien C M Kremer, Dorine Bresters, Eline van Dulmen-den Broeder, Marry M van den Heuvel-Eibrink, Jacqueline J Loonen, Marloes Louwerens and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

18 authors at 8 institutions in 2 countries.

Esmee C M KooijmansDepartment of Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0001-6961-1684
Helena J H van der PalPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Saskia M F PluijmPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Margriet van der Heiden-van der LooPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Leontien C M KremerPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Dorine BrestersPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Eline van Dulmen-den BroederDepartment of Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
Marry M van den Heuvel-EibrinkPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Jacqueline J LoonenDepartment of Hematology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Marloes LouwerensDepartment of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Sebastian J C NeggersDepartment of Internal Medicine, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Cécile RonckersPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Wim J E TissingPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Andrica C H de VriesPrincess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Gertjan J L KaspersDepartment of Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0001-7716-8475
Arend BökenkampDepartment of Pediatric Nephrology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.ORCID 0000-0002-3492-2252
Margreet A VeeningDepartment of Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
On Behalf Of The Dutch Later Study Group
Emma Kinderziekenhuis · NLPrincess Máxima Center · NLLeiden University Medical Center · NLErasmus MC · NLRadboud University Nijmegen · NLStichting Kinderoncologie Nederland · NLUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NL

Funding

KWF Dutch Cancer Society 7889
6 · The paper itself

Abstract

The aim of this nationwide cross-sectional cohort study was to determine the prevalence of and risk factors for tubular dysfunction in childhood cancer survivors (CCS). In the DCCSS-LATER 2 Renal study, 1024 CCS (≥5 years after diagnosis), aged ≥ 18 years at study, treated between 1963 and 2001 with potentially nephrotoxic therapy (i.e., nephrectomy, abdominal radiotherapy, total body irradiation, cisplatin, carboplatin, ifosfamide, high-dose cyclophosphamide, or hematopoietic stem cell transplantation) participated, and 500 age- and sex-matched participants from Lifelines acted as controls. Tubular electrolyte loss was defined as low serum levels (magnesium < 0.7 mmol/L, phosphate < 0.7 mmol/L and potassium < 3.6 mmol/L) with increased renal excretion or supplementation. A α1-microglobulin:creatinine ratio > 1.7 mg/mmol was considered as low-molecular weight proteinuria (LMWP). Multivariable risk analyses were performed. After median 25.5 years follow-up, overall prevalence of electrolyte losses in CCS (magnesium 5.6%, potassium 4.5%, phosphate 5.5%) was not higher compared to controls. LMWP was more prevalent (CCS 20.1% versus controls 0.4%). LMWP and magnesium loss were associated with glomerular dysfunction. Ifosfamide was associated with potassium loss, phosphate loss (with cumulative dose > 42 g/m2) and LMWP. Cisplatin was associated with magnesium loss and a cumulative dose > 500 mg/m2 with potassium and phosphate loss. Carboplatin cumulative dose > 2800 mg/m2 was associated with potassium loss. In conclusion, long-term tubular dysfunction is infrequent. Yet, ifosfamide, cisplatin and carboplatin are risk factors.

Indexed as

childhood cancer survivornephrotoxicitytubular dysfunction

Identifiers

PMID35681735
PMCPMC9179377
OpenAlexW4281733315

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.