No longer is histology solely predictive of cancer treatment and outcome. There is an increasing influence of tumor genomic characteristics on therapeutic options. Both breast and ovarian cancers are at higher risk of development in patients with BRCA 1/2-germline mutations. Recent data from The Cancer Genome Atlas and others have shown a number of genomic similarities between triple negative breast cancers (TNBCs) and ovarian cancers. Recently, poly (ADP-ribose) polymerase (PARP) inhibitors have shown promising activity in hereditary BRCA 1/2-mutated and sporadic breast and ovarian cancers. In this review, we will summarize the current literature regarding the genomic and phenotypic similarities between BRCA 1/2-mutation related cancers, s...
The standard of treatment for advanced ovarian cancer is represented by optimal surgical debulking p...
In order to adequately evaluate the clinical relevance of genetic testing in sporadic breast and ova...
The importance of proper mutational analysis of BRCA1/2 in individuals at risk for hereditary breast...
No longer is histology solely predictive of cancer treatment and outcome. There is an increasing inf...
Hereditary breast and ovarian cancer is caused by a germline mutation in BRCA1 or BRCA2 genes. The f...
Approximately 9000 women are diagnosed with ovarian cancer in Germany each year. The most common sub...
Patients with inherited germline mutations in BRCA1/2 carry a drastically increased risk of early-on...
Context Most hereditary ovarian cancers are associated with germline mutations in BRCA1 or BRCA2. At...
AbstractAbout 10% to 15% of ovarian cancers are linked to genetic abnormalities, including breast ca...
Abstract Germline mutations in BRCA1 and BRCA2 (BRCA) genes confer high risk of developing cancer, e...
Mutations in BRCA1/2 increase the risk of developing breast and ovarian cancer. Germline BRCA1/2 mut...
Mutations in BRCA1 and BRCA2 cause tumor development in Hereditary Breast and Ovarian Cancer syndrom...
Mutations in BRCA1/2 increase the risk of developing breast and ovarian cancer. Germline BRCA1/2 mut...
Ovarian cancer is a heterogeneous disease that encompasses a number of different cellular subtypes, ...
BRCA1 mutations, although implicated in disease predisposition in a major part of the hereditary bre...
The standard of treatment for advanced ovarian cancer is represented by optimal surgical debulking p...
In order to adequately evaluate the clinical relevance of genetic testing in sporadic breast and ova...
The importance of proper mutational analysis of BRCA1/2 in individuals at risk for hereditary breast...
No longer is histology solely predictive of cancer treatment and outcome. There is an increasing inf...
Hereditary breast and ovarian cancer is caused by a germline mutation in BRCA1 or BRCA2 genes. The f...
Approximately 9000 women are diagnosed with ovarian cancer in Germany each year. The most common sub...
Patients with inherited germline mutations in BRCA1/2 carry a drastically increased risk of early-on...
Context Most hereditary ovarian cancers are associated with germline mutations in BRCA1 or BRCA2. At...
AbstractAbout 10% to 15% of ovarian cancers are linked to genetic abnormalities, including breast ca...
Abstract Germline mutations in BRCA1 and BRCA2 (BRCA) genes confer high risk of developing cancer, e...
Mutations in BRCA1/2 increase the risk of developing breast and ovarian cancer. Germline BRCA1/2 mut...
Mutations in BRCA1 and BRCA2 cause tumor development in Hereditary Breast and Ovarian Cancer syndrom...
Mutations in BRCA1/2 increase the risk of developing breast and ovarian cancer. Germline BRCA1/2 mut...
Ovarian cancer is a heterogeneous disease that encompasses a number of different cellular subtypes, ...
BRCA1 mutations, although implicated in disease predisposition in a major part of the hereditary bre...
The standard of treatment for advanced ovarian cancer is represented by optimal surgical debulking p...
In order to adequately evaluate the clinical relevance of genetic testing in sporadic breast and ova...
The importance of proper mutational analysis of BRCA1/2 in individuals at risk for hereditary breast...