| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Magaton, Isotta |
| dc.contributor.author | Linn, Sabine |
| dc.contributor.author | peccatori, fedro |
| dc.contributor.author | Blondeaux, Eva |
| dc.contributor.author | HAMY, Anne-Sophie |
| dc.contributor.author | Bernstein Molho, Rinat |
| dc.contributor.author | Carrasco Lopez, Estela |
| dc.date.accessioned | 2025-05-22T08:54:23Z |
| dc.date.available | 2025-05-22T08:54:23Z |
| dc.date.issued | 2025-06-03 |
| dc.identifier.citation | Magaton 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.issn | 0959-8049 |
| dc.identifier.uri | http://hdl.handle.net/11351/13122 |
| dc.description | Assisted reproductive technology; Breast cancer; Germline BRCA1/2 pathogenic variants |
| dc.description.abstract | Introduction
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.iso | eng |
| dc.publisher | Elsevier |
| dc.relation.ispartofseries | European Journal of Cancer;222 |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Mama - Càncer - Tractament |
| dc.subject | Mama - Càncer - Aspectes genètics |
| dc.subject | Embaràs |
| dc.subject | Antioncogens |
| dc.subject.mesh | Reproductive Techniques, Assisted |
| dc.subject.mesh | Pregnancy |
| dc.subject.mesh | Breast Neoplasms |
| dc.subject.mesh | /therapy |
| dc.subject.mesh | Breast Neoplasms |
| dc.subject.mesh | /genetics |
| dc.subject.mesh | Genes, BRCA1 |
| dc.title | Assisted reproductive technology in young BRCA carriers with a pregnancy after breast cancer: An international cohort study |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1016/j.ejca.2025.115434 |
| dc.subject.decs | técnicas reproductivas asistidas |
| dc.subject.decs | embarazo |
| dc.subject.decs | neoplasias de la mama |
| dc.subject.decs | /terapia |
| dc.subject.decs | neoplasias de la mama |
| dc.subject.decs | /genética |
| dc.subject.decs | genes BRCA1 |
| dc.relation.publishversion | https://doi.org/10.1016/j.ejca.2025.115434 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut 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.pmid | 40300260 |
| dc.identifier.wos | 001485669700001 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |