Background: Type II ovarian cancer (OC) is generally diagnosed at an advanced stage, translating into a poor survival rate. Current screening methods for OC have failed to demonstrate a reduction in mortality. The uterine lavage technique has been used to detect tumor-specific TP53 mutations from cells presumably shed from high-grade serous ovarian cancer (HGSOC). We aimed to pilot whether the detection of TP53 mutation in uterine cavity lavage can be used as a diagnostic method for HGSOC using an expanded gene panel. Methods: In this study 90, uterine lavage and 46 paired biopsy samples were analyzed using next-generation sequencing (NGS) targeting TP53 as well as five additional OC-related genes: BRCA1, BRCA2, PI3KCA, PTEN, and KRAS. Resu...
High-grade serous ovarian cancer (HGSOC) is the most common subtype of epithelial ovarian cancer and...
Background: Pathogenic variants in homologous recombination repair (HRR) genes other than BRCA1/2 ha...
The aim of this study was to estimate the contribution of deleterious mutations in BRCA1, BRCA2, MLH...
OBJECTIVE: Ovarian cancer is known for its poor prognosis, which is mainly due to the lack of early ...
Endometrial cancer is the most common gynecologic malignancy, and its incidence and associated morta...
Background: Germline BRCA1/2 mutations are identified in 13-15% of ovarian cancers, while an additio...
Several studies have been carried out to determine the complexity of ovarian cancer as a disease wit...
AbstractMicroinvasive carcinomas and high-grade intraepithelial neoplasms are commonly discovered wi...
OBJECTIVE: Approximately 25% of ovarian cancer (OC) cases are related to an inherited predisposition...
Ovarian cancer (OC) is the fifth most common type of cancer in women and the fourth most common caus...
Thesis (Master's)--University of Washington, 2022Individuals with germline BRCA1 and BRCA2 mutations...
Ovarian cancer, often called the silent killer due to its diffuse symptoms at early stage, poor prog...
Aim: To identify the frequency of somatic BRCA mutation in epithelial ovarian cancer (EOC), particul...
Ovarian carcinomas and carcinosarcomas often cause malignant effusions, an accumulation within serou...
Microinvasive carcinomas and high-grade intraepithelial neoplasms are commonly discovered within the...
High-grade serous ovarian cancer (HGSOC) is the most common subtype of epithelial ovarian cancer and...
Background: Pathogenic variants in homologous recombination repair (HRR) genes other than BRCA1/2 ha...
The aim of this study was to estimate the contribution of deleterious mutations in BRCA1, BRCA2, MLH...
OBJECTIVE: Ovarian cancer is known for its poor prognosis, which is mainly due to the lack of early ...
Endometrial cancer is the most common gynecologic malignancy, and its incidence and associated morta...
Background: Germline BRCA1/2 mutations are identified in 13-15% of ovarian cancers, while an additio...
Several studies have been carried out to determine the complexity of ovarian cancer as a disease wit...
AbstractMicroinvasive carcinomas and high-grade intraepithelial neoplasms are commonly discovered wi...
OBJECTIVE: Approximately 25% of ovarian cancer (OC) cases are related to an inherited predisposition...
Ovarian cancer (OC) is the fifth most common type of cancer in women and the fourth most common caus...
Thesis (Master's)--University of Washington, 2022Individuals with germline BRCA1 and BRCA2 mutations...
Ovarian cancer, often called the silent killer due to its diffuse symptoms at early stage, poor prog...
Aim: To identify the frequency of somatic BRCA mutation in epithelial ovarian cancer (EOC), particul...
Ovarian carcinomas and carcinosarcomas often cause malignant effusions, an accumulation within serou...
Microinvasive carcinomas and high-grade intraepithelial neoplasms are commonly discovered within the...
High-grade serous ovarian cancer (HGSOC) is the most common subtype of epithelial ovarian cancer and...
Background: Pathogenic variants in homologous recombination repair (HRR) genes other than BRCA1/2 ha...
The aim of this study was to estimate the contribution of deleterious mutations in BRCA1, BRCA2, MLH...