Evidence map›Paper›PMID 34541832›Full record

ArticleCancer reports (Hoboken, N.J.)2022

The Norwegian childhood cancer biobank.

Johanne U Hermansen, Dorota M Wojcik, Nina Robinson, Jens Pahnke, Hans Kristian Haugland, Ann Helen Jamtøy, Trond Flaegstad, Hanne Halvorsen, Bendik Lund, Lars O Baumbusch and 1 more

Abstract readCase Reports
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Reduced abundance ofFrontiers in microbiomes · 2023
    Article
  4. The Norwegian childhood cancer biobank.Cancer reports (Hoboken, N.J.) · 2022
    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

11 authors.

Johanne U HermansenDepartment of Oncology, Division of Pediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.ORCID 0000-0003-3830-2277
Dorota M WojcikDepartment of Pediatrics, Haukeland University Hospital, Bergen, Norway.
Nina RobinsonDepartment of Oncology, Division of Pediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Jens PahnkeDepartment of Pathology, Section for Neuropathology, Oslo University Hospital, Oslo, Norway.
Hans Kristian HauglandDepartment of Pathology, Haukeland University Hospital, Bergen, Norway.
Ann Helen JamtøyDepartment of Pathology, St. Olavs Hospital, Trondheim, Norway.
Trond FlaegstadDepartment of Pediatrics, University Hospital of North-Norway, Tromsø, Norway.
Hanne HalvorsenDepartment of Pathology, University Hospital of North-Norway, Tromsø, Norway.
Bendik LundDepartment of Pediatrics, St. Olavs Hospital, Trondheim, Norway.
Lars O BaumbuschDepartment of Pediatric Research, Division of Pediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Monica C Munthe-KaasDepartment of Oncology, Division of Pediatric and Adolescent Medicine, Oslo University Hospital Rikshospitalet, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rapidly expanding era of "omics" research is highly dependent on the availability of quality-proven biological material, especially for rare conditions such as pediatric malignancies. Professional biobanks provide such material, focusing on standardized collection and handling procedures, distinctive quality measurements, traceability of storage conditions, and accessibility. For pediatric malignancies, traditional tumor biobanking is challenging due to the rareness and limited amount of tissue and blood samples. The higher molecular heterogeneity, lower mutation rates, and unique genomic landscapes, however, renders biobanking of this tissue even more crucial.

aimThe aim of this study was to test and establish methods for a prospective and centralized biobank for infants, children, and adolescents up to 18 years of age diagnosed with cancer in Norway.

methodsObtain judicial and ethical approvals and administration through a consortium, steering committee, and advisory board. Develop pipelines including SOPs for all aspects in the biobank process, including collection, processing and storing of samples and data, as well of quality controlling, safeguarding, distributing, and transport.

resultsThe childhood cancer biobanking started at Oslo University Hospital in March 2017 and was from 2019 run as a national Norwegian Childhood Cancer Biobank. Informed consent and biological samples are collected regionally and stored centrally. Approximately 12 000 samples from 510 patients and have been included by January 1, 2021, representing a 96% consent and participation rate among our newly diagnosed patients.

conclusionA well-functioning nationwide collection and centralized biobank with standardized procedures and national storage for pediatric malignancies has been established with a high acceptance among families.

Indexed as

Biological Specimen BanksNeoplasmsAdolescentChildGenomicsHumansNorwayProspective Studiesbiobankcancerpediatric tumorsprospectivetissue collection

Identifiers

PMID34541832
PMCPMC9351664

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.