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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMagaton, Isotta
dc.contributor.authorLinn, Sabine
dc.contributor.authorpeccatori, fedro
dc.contributor.authorBlondeaux, Eva
dc.contributor.authorHAMY, Anne-Sophie
dc.contributor.authorBernstein Molho, Rinat
dc.contributor.authorCarrasco Lopez, Estela
dc.date.accessioned2025-05-22T08:54:23Z
dc.date.available2025-05-22T08:54:23Z
dc.date.issued2025-06-03
dc.identifier.citationMagaton IM, Blondeaux E, Hamy AS, Linn S, Bernstein-Molho R, Peccatori FA, et al. Assisted reproductive technology in young BRCA carriers with a pregnancy after breast cancer: an international cohort study. Eur J Cancer. 2025 Jun 3;222:115434.
dc.identifier.issn0959-8049
dc.identifier.urihttp://hdl.handle.net/11351/13122
dc.descriptionAssisted reproductive technology; Breast cancer; Germline BRCA1/2 pathogenic variants
dc.description.abstractIntroduction Very limited data exist on assisted reproductive technology (ART) use in BRCA1/2 carriers conceiving after breast cancer. This study aimed to investigate the safety of ART to achieve a pregnancy after breast cancer in BRCA1/2 carriers. Methods This is an international, hospital-based, retrospective cohort study including BRCA1/2 carriers with a pregnancy after prior breast cancer diagnosis at ≤ 40 years of age between 2000 and 2020. Outcomes were compared between young BRCA1/2 carriers who conceived using ART and those who conceived spontaneously. Results Among 543 BRCA1/2 carriers with a pregnancy after breast cancer, 436 conceived spontaneously and 107 using ART. Of 107 pregnancies achieved with ART, 45 (42.1 %) were obtained using oocytes/embryo cryopreserved at diagnosis, 33 (30.8 %) after controlled ovarian stimulation for in-vitro-fertilization/intracytoplasmic sperm injection or ovulation induction for intrauterine insemination or planned intercourse after anticancer treatments, 21 (19.6 %) after oocyte donation, while for 8 (7.5 %) patients type of ART was missing. Compared to patients in the no-ART group, those in the ART group were older at the time of conception, had more frequently hormone receptor-positive breast cancer and a longer median time from cancer diagnosis to conception. At a median follow-up of 5.2 years after conception, no apparent detrimental effect of ART on disease-free survival was observed (adjusted HR=0.72, 95 % CI 0.39–1.34). Conclusion In young BRCA1/2 carriers with a pregnancy after breast cancer, ART use did not appear to be associated with increased risk of DFS events.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesEuropean Journal of Cancer;222
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectMama - Càncer - Tractament
dc.subjectMama - Càncer - Aspectes genètics
dc.subjectEmbaràs
dc.subjectAntioncogens
dc.subject.meshReproductive Techniques, Assisted
dc.subject.meshPregnancy
dc.subject.meshBreast Neoplasms
dc.subject.mesh/therapy
dc.subject.meshBreast Neoplasms
dc.subject.mesh/genetics
dc.subject.meshGenes, BRCA1
dc.titleAssisted reproductive technology in young BRCA carriers with a pregnancy after breast cancer: An international cohort study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ejca.2025.115434
dc.subject.decstécnicas reproductivas asistidas
dc.subject.decsembarazo
dc.subject.decsneoplasias de la mama
dc.subject.decs/terapia
dc.subject.decsneoplasias de la mama
dc.subject.decs/genética
dc.subject.decsgenes BRCA1
dc.relation.publishversionhttps://doi.org/10.1016/j.ejca.2025.115434
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Magaton IM] Medical Oncology Department, U.O.C. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy. University Women’s Hospital, Inselspital, Bern, Switzerland. [Blondeaux E] U.O. Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Genova, Italy. [Hamy AS] Department of Medical Oncology, Université Paris Cité, Institut Curie, Paris, France. [Linn S] Department of Molecular Pathology, Netherlands Cancer Institute (NKI), Amsterdam, the Netherlands and Deptment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands. [Bernstein-Molho R] Susanne Levy Gertner Oncogenetics Unit, Danek Gertner Institute of Human Genetics, Chaim Sheba Medical Centre affiliated to Tel Aviv University, Tel Hashomer, Israel. [Peccatori FA] Gynaecology Oncology Program, European Institute of Oncology (IRCCS), Milan, Italy. [Carrasco E] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Hereditary Cancer Genetics Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid40300260
dc.identifier.wos001485669700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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