Hereditary Breast and Ovarian Cancer Screening Syndrome Profile in Women Diagnosed with Breast Cancer from Paraná State Southwest

Author:

Moura Juliana Batista de1ORCID,Ghedin Carla Camila1ORCID,Takakura Érika Tomie1ORCID,Scandolara Thalita Basso12ORCID,Rech Daniel3ORCID,Panis Carolina1ORCID

Affiliation:

1. Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil

2. Department of Genetics, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil

3. Center of Health Sciences, Francisco Beltrão Cancer Hospital, Francisco Beltrão, PR, Brazil

Abstract

Abstract Objective This study evaluated the risk of the hereditary breast and ovarian cancer (HBOC) syndrome in patients with breast cancer by using the Family History Screening 7 (FHS-7) tool, a validated low-cost questionnaire with high sensitivity able to screen the HBOC risk in the population. Methods Women diagnosed with breast cancer (n = 101) assisted by the Unified Health System at the 8th Regional Health Municipal Office of the state of Paraná answered the FHS-7, and the results were analyzed using IBM SPSS Statistics for Windows, Version 25.0. software (IBM Corp., Armonk, NY, USA). Results The risk of HBOC was 19.80% (n = 20). Patients at risk exhibited aggressive tumor characteristics, such as high-grade tumors (30%), presence of angiolymphatic emboli (35%), and premenopausal at diagnosis (50%). Significant associations between the prevalence of high-grade tumors were observed in women younger than 50 years at diagnosis with HBOC (p = 0.003). Conclusion Our findings suggest a possible family inheritance associated with worse clinical features in women with breast cancer in this population, indicating that HBOC investigation can be initially performed with low-cost instruments such as FHS-7.

Publisher

Georg Thieme Verlag KG

Subject

Obstetrics and Gynecology

Reference28 articles.

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