Publication:
Cohort-based association study of germline genetic variants with acute and chronic health complications of childhood cancer and its treatment: Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study protocol.

cris.virtual.author-orcid0000-0001-5016-9822
cris.virtualsource.author-orcidd15960e0-11a9-420b-9007-f6c8da4fb3e0
cris.virtualsource.author-orcidb8932f53-2bfb-4049-bd8c-402bf013be7d
cris.virtualsource.author-orcidcaf970b7-1acc-4c13-9fa2-dd48be5beabc
cris.virtualsource.author-orcidf6c3549a-a8a5-4ea9-8d92-e7a0c4aa7609
cris.virtualsource.author-orcida65a1ccb-d060-4e23-87a5-0c9297d23a3d
cris.virtualsource.author-orcid3857e2d3-2b7f-42b6-878d-ce868ac1673c
datacite.rightsopen.access
dc.contributor.authorWaespe Laredo, Nicolas Thomas
dc.contributor.authorStrebel, Sven
dc.contributor.authorNava, Tiago
dc.contributor.authorUppugunduri, Chakradhara Rao S
dc.contributor.authorMarino, Denis
dc.contributor.authorMattiello, Veneranda
dc.contributor.authorOtth, Maria
dc.contributor.authorGumy-Pause, Fabienne
dc.contributor.authorVon Bueren, André O
dc.contributor.authorBaleydier, Frederic
dc.contributor.authorMader, Luzius Adrian
dc.contributor.authorSpörri, Adrian
dc.contributor.authorKühni, Claudia
dc.contributor.authorAnsari, Marc
dc.date.accessioned2024-10-09T16:48:18Z
dc.date.available2024-10-09T16:48:18Z
dc.date.issued2022-01-24
dc.description.abstractINTRODUCTION Childhood cancer and its treatment may lead to various health complications. Related impairment in quality of life, excess in deaths and accumulated healthcare costs are relevant. Genetic variations are suggested to contribute to the wide inter-individual variability of complications but have been used only rarely to risk-stratify treatment and follow-up care. This study aims to identify germline genetic variants associated with acute and late complications of childhood cancer. METHODS AND ANALYSIS The Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study is a nationwide cohort study. Eligible are patients and survivors who were diagnosed with childhood cancers or Langerhans cell histiocytosis before age 21 years, were registered in the Swiss Childhood Cancer Registry (SCCR) since 1976 and have consented to the Paediatric Biobank for Research in Haematology and Oncology, Geneva, host of the national Germline DNA Biobank Switzerland for Childhood Cancer and Blood Disorders (BISKIDS).GECCOS uses demographic and clinical data from the SCCR and the associated Swiss Childhood Cancer Survivor Study. Clinical outcome data consists of organ function testing, health conditions diagnosed by physicians, second primary neoplasms and self-reported information from participants. Germline genetic samples and sequencing data are collected in BISKIDS. We will perform association analyses using primarily whole-exome or whole-genome sequencing to identify genetic variants associated with specified health conditions. We will use clustering and machine-learning techniques and assess multiple health conditions in different models. DISCUSSION GECCOS will improve knowledge of germline genetic variants associated with childhood cancer-associated health conditions and help to further individualise cancer treatment and follow-up care, potentially resulting in improved efficacy and reduced side effects. ETHICS AND DISSEMINATION The Geneva Cantonal Commission for Research Ethics has approved the GECCOS study.Research findings will be disseminated through national and international conferences, publications in peer-reviewed journals and in lay language online. TRIAL REGISTRATION NUMBER NCT04702321.
dc.description.numberOfPages15
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.description.sponsorshipUniversitätsklinik für Kinderheilkunde
dc.identifier.doi10.48350/165128
dc.identifier.pmid35074812
dc.identifier.publisherDOI10.1136/bmjopen-2021-052131
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/67197
dc.language.isoen
dc.publisherBMJ Publishing Group
dc.relation.ispartofBMJ open
dc.relation.issn2044-6055
dc.relation.organizationDCD5A442BADAE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BB22E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.relation.schoolDCD5A442C27BE17DE0405C82790C4DE2
dc.relation.schoolDCD5A442C3E5E17DE0405C82790C4DE2
dc.subjectadverse events cancer genetics clinical pharmacology genetics paediatric clinical genetics & dysmorphology paediatric oncology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleCohort-based association study of germline genetic variants with acute and chronic health complications of childhood cancer and its treatment: Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study protocol.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPagee052131
oaire.citation.volume12
oairecerif.author.affiliationUniversitätsklinik für Kinderheilkunde
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliation2Institut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliation2Universitätsklinik für Kinderheilkunde
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unibe.date.licenseChanged2022-02-14 21:11:30
unibe.description.ispublishedpub
unibe.eprints.legacyId165128
unibe.journal.abbrevTitleBMJ Open
unibe.refereedtrue
unibe.subtype.articlecontribution

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