Evidence map›Paper›PMID 39482556›Full record

ArticleBreast cancer research and treatment2025

Cardiovascular disease risk after breast cancer treatment in patients with a BRCA1/2 pathogenic variant.

Lara Terra, Naomi B Boekel, Maartje H Hooning, Margriet Collee, Marjanka K Schmidt, Muriel A Adank, Marleen Kok, Berthe M P Aleman, Agnes Jager, Margriet G A Sattler and 3 more

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Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Lara TerraDivision of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066, Amsterdam, CX, The Netherlands.
Naomi B BoekelDivision of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066, Amsterdam, CX, The Netherlands.
Maartje H HooningDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Margriet ColleeDepartment of Clinical Genetics, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Marjanka K SchmidtDivision of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066, Amsterdam, CX, The Netherlands.
Muriel A AdankClinical Genetics Department, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marleen KokDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Berthe M P AlemanDepartment of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Agnes JagerDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Margriet G A SattlerDepartment of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
Angela H E M MaasDepartment of Cardiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Michael SchaapveldDivision of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066, Amsterdam, CX, The Netherlands.
Flora E van LeeuwenDivision of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066, Amsterdam, CX, The Netherlands. f.v.leeuwen@nki.nl.

Funding

KWF Kankerbestrijding 10164
6 · The paper itself

Abstract

purposeBreast cancer (BC) treatment can induce adverse events, such as cardiovascular disease (CVD). Defective DNA repair, as in carriers of BRCA1/2 pathogenic variants (BRCA1/2pv), may contribute to CVD risk. We aimed to study if female BRCA1/2pv carriers are more sensitive to develop CVD after BC treatment than BC patients without a known BRCA1/2pv.

methodsIn a hospital-based cohort of 17,300 female BC patients, we identified 509 BRCA1/2pv carriers. Cardiovascular morbidity and mortality were assessed through hospital charts and general practitioner questionnaires. We performed Cox regression analyses comparing BRCA1/2pv carriers with all other BC patients, adjusting for age, radiotherapy regimen, chemotherapy regimen, and smoking status.

resultsMedian follow-up time since BC treatment was 14 years. In total, 1108 women experienced ischemic heart disease (IHD), of whom 20 (1.8%) were BRCA1/2pv carriers. Heart failure (HF) was diagnosed in 638 women, of whom 10 (1.6%) were BRCA1/2pv carriers. BRCA1/2pv carriership was associated with a slight not statistically significant increase of IHD (adjHR 1.51, 95%CI 0.93; 2.42), but not with risk of HF (adjHR 0.86, 95%CI 0.44; 1.69). The association between radiotherapy and IHD risk was not significantly different between BRCA1/2pv carriers [HR 2.30 (95%CI 0.79; 6.66)] and other BC patients (HR 1.50, 95%CI 1.30; 1.73). Associations between anthracycline-based chemotherapy and HF risk also did not differ between carriers and other BC patients (HRs of 4.02 (95%CI 1.02; 15.77) and 2.31 (95%CI 1.77; 3.01), respectively).

conclusionsIn BRCA1/2pv BC patients, we found no evidence for a higher risk of BC treatment-related CVD than in other BC patients.

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCardiovascular DiseasesAdultAgedFemaleGenetic Predisposition to DiseaseHumansMiddle AgedMutationRisk FactorsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCA1/2 pathogenic variantBreast cancerChemotherapyHeart failureIschemic heart diseaseRadiotherapy

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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.