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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorLee, Soo Chin
dc.contributor.authorsinger, christian
dc.contributor.authorDent, Rebecca
dc.contributor.authorTan, Veronique Kiak Mien
dc.contributor.authorPark, Yeon Hee
dc.contributor.authorBalmaña, Judith
dc.date.accessioned2025-10-09T07:40:52Z
dc.date.available2025-10-09T07:40:52Z
dc.date.issued2025-06-23
dc.identifier.citationPark YH, Lee SC, Singer CF, Balmaña J, Dent RA, Tan VKM, et al. Part II: consensus statements and expert recommendations for BRCA-associated breast cancer in the Asia-Pacific region: clinical management. Front Oncol. 2025 Jun 23;15:1507840.
dc.identifier.issn2234-943X
dc.identifier.urihttp://hdl.handle.net/11351/13809
dc.descriptionBRCA germline; PARP Inhibitors; Breast cancer
dc.description.abstractIntroduction: Existing guidelines have practical gaps in decision and treatment sequencing for BRCA germline pathogenic variant breast cancers. This paper aims to develop clinical-practice consensus guidelines to address these gaps in the clinical management of BRCA germline pathogenic variants-associated breast cancer in the Asia-Pacific region. Methods: An expert panel of 16 medical oncologists, geneticists, and breast cancer surgeons from the Asia-Pacific region arrived at 25 statements. The high level of consensus of statements was considered at ≥75%. A survey of 134 healthcare practitioners, breast cancer surgeons, geneticists, oncologists, molecular biologists/pathologists explored the real- world practices in the Asia-Pacific region. Results: A consensus was reached for 80% of the statements (20/25) and aligned with the international guidelines. A significant gap was observed between real-world practices and the recommendations of the steering committee members in discussing contralateral risk reducing mastectomy with the patients as a part of standard practice, considering poly ADP-ribose polymerase inhibitor (PARPi) + immunotherapy for early triple negative breast cancer (eTNBC) patients with BRCA variants who don’t achieve pathological complete response after neoadjuvant chemotherapy + immunotherapy, use of adjuvant PARPi in patients with BRCA germline pathogenic variants in eTNBC who have achieved pathological complete response from neoadjuvant therapy, and preference for endocrine therapy + PARPi over endocrine therapy + cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) as escalated adjuvant treatment for BRCA pathogenic variants with high-risk hormone receptor positive/human epidermal growth factor receptor 2 negative (HR+/HER2-negative) early breast cancer. Conclusion: Testing for BRCA germline pathogenic variants should be expanded to include all young patients with breast cancer. Patients with BRCA germline pathogenic variants should undergo genetic testing before surgery as it can impact surgical intervention decisions and further systemic treatment. The use of neoadjuvant platinum agents in chemotherapy increases the pathological complete response rate. Adjuvant PARPi is preferred over CDK4/6i as escalated treatment in patients who are HR+/HER2-negative.
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesFrontiers in Oncology;15
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectDecisió, Presa de
dc.subjectMama - Càncer - Tractament
dc.subjectEnzims - Inhibidors - Ús terapèutic
dc.subject.meshPoly(ADP-ribose) Polymerase Inhibitors
dc.subject.meshBreast Neoplasms
dc.subject.mesh/therapy
dc.subject.meshConsensus
dc.titlePart II: consensus statements and expert recommendations for BRCA-associated breast cancer in the Asia-Pacific region: clinical management
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fonc.2025.1507840
dc.subject.decsinhibidores de poli(ADP-ribosa) polimerasas
dc.subject.decsneoplasias de la mama
dc.subject.decs/terapia
dc.subject.decsconsenso
dc.relation.publishversionhttps://doi.org/10.3389/fonc.2025.1507840
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Park YH] Division of Haematology-Oncology, Department of Medicine, Samsung Medical Centre, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea. [Lee SC] Department of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore. [Singer CF] Department of Obstetrics and Gynaecology, Comprehensive Cancer Centre, Medical University of Vienna, Vienna, Austria. [Balmaña J] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Dent RA] Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore. [Tan VKM] Department of Breast Surgery, Division of Surgery and Surgical Oncology, National Cancer Centre Singapore, Singapore, Singapore
dc.identifier.pmid40626017
dc.identifier.wos001523638000001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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