Evidence map›Paper›PMID 35342935›Full record

ArticleInternational journal of cancer2022

White paper: Oncofertility in pediatric patients with Wilms tumor.

M E Madeleine van der Perk, Nicholas G Cost, Annelies M E Bos, Robert Brannigan, Tanzina Chowdhury, Andrew M Davidoff, Najat C Daw, Jeffrey S Dome, Peter Ehrlich, Norbert Graf and 14 more

Open access · bronzeAbstract readConsensus Statement
In one paragraph

Article in International journal of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

24 authors at 20 institutions in 6 countries.

M E Madeleine van der PerkPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-0782-5307
Nicholas G CostDepartment of Surgery, Division of Urology, University of Colorado School of Medicine and the Surgical Oncology Program of the Children's Hospital Colorado, Aurora, Colorado, USA.
Annelies M E BosReproductive Medicine and Gynaecology, University Medical Center Utrecht, Utrecht, The Netherlands.
Robert BranniganDepartment of Urology, Northwestern University, Chicago, Illinois, USA.
Tanzina ChowdhuryGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Andrew M DavidoffDepartment of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Najat C DawDepartment of Pediatrics-Patient Care, MD Anderson Cancer Center, Houston, Texas, USA.
Jeffrey S DomeDivision of Oncology at Children's National Hospital, Washington, District of Columbia, USA.
Peter EhrlichC.S. Mott Children's Hospital Section of Pediatric Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Norbert GrafDepartment for Pediatric Oncology and Hematology, Saarland University Medical Center, Homburg, Germany.
James GellerDivision of Pediatric Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.
John KalapurakalDepartment of Radiation Oncology, Northwestern University, Chicago, Illinois, USA.
Kathleen KieranDepartment of Urology, University of Washington, Seattle, Washington, USA.
Marcus MalekDivision of Pediatric General and Thoracic Surgery, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Mary F McAleerDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Elizabeth MullenDepartment of Pediatric Oncology, Children's Hospital Boston/Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Luke PaterDepartment of Radiation Oncology, University of Cincinnati, Cincinnati, Ohio, USA.
Angela PolancoNational Cancer Research Institute Children's Group Consumer Representative, London, UK.
Rodrigo RomaoDepartments of Surgery and Urology, IWK Health Centre, Dalhousie University, Halifax, Canada.
Amanda F SaltzmanDepartment of Urology, University of Kentucky, Lexington, Kentucky, USA.
Amy L WalzDivision of Hematology, Oncology, Neuro-Oncology, and Stem Cell Transplant, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Andrew D WoodsChildren's Cancer Therapy Development Institute, Beaverton, Oregon, USA.
Marry M van den Heuvel-EibrinkPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Conrad V FernandezDepartment of Pediatric Hematology/Oncology, IWK Health Centre and Dalhousie University, Halifax, Canada.
Dalhousie University · CANorthwestern University · USThe University of Texas MD Anderson Cancer Center · USChildren's Cancer Therapy Development Institute · USChildren's Hospital Colorado · USChildren's Hospital of Pittsburgh · USChildren's National · USChildren with Cancer UK · GBCincinnati Children's Hospital Medical Center · USDana-Farber Cancer Institute · USFirst Consulting Group (United States) · USGreat Ormond Street Hospital for Children NHS Foundation Trust · GBLurie Children's Hospital · USPrincess Máxima Center · NLSaarland University · DESeattle Children's Hospital · USSt. Jude Children's Research Hospital · USUniversity Medical Center Utrecht · NLUniversity of Cincinnati · USUniversity of Kentucky · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The survival of childhood Wilms tumor is currently around 90%, with many survivors reaching reproductive age. Chemotherapy and radiotherapy are established risk factors for gonadal damage and are used in both COG and SIOP Wilms tumor treatment protocols. The risk of infertility in Wilms tumor patients is low but increases with intensification of treatment including the use of alkylating agents, whole abdominal radiation or radiotherapy to the pelvis. Both COG and SIOP protocols aim to limit the use of gonadotoxic treatment, but unfortunately this cannot be avoided in all patients. Infertility is considered one of the most important late effects of childhood cancer treatment by patients and their families. Thus, timely discussion of gonadal damage risk and fertility preservation options is important. Additionally, irrespective of the choice for preservation, consultation with a fertility preservation (FP) team is associated with decreased patient and family regret and better quality of life. Current guidelines recommend early discussion of the impact of therapy on potential fertility. Since most patients with Wilms tumors are prepubertal, potential FP methods for this group are still considered experimental. There are no proven methods for FP for prepubertal males (testicular biopsy for cryopreservation is experimental), and there is just a single option for prepubertal females (ovarian tissue cryopreservation), posing both technical and ethical challenges. Identification of genetic markers of susceptibility to gonadotoxic therapy may help to stratify patient risk of gonadal damage and identify patients most likely to benefit from FP methods.

Indexed as

Fertility PreservationInfertilityKidney NeoplasmsNeoplasmsWilms TumorChildFemaleHumansMaleQuality of Lifefertility preservationgonadal damagepediatric cancerWilms tumor

Identifiers

PMID35342935
PMCPMC9541948
OpenAlexW4221084306

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.