Universal tumor DNA testing in epithelial ovarian cancer patients can function not only as an efficient prescreen for hereditary cancer testing, but may also guide treatment choices. This innovation, introduced as Tumor-First workflow, offers great opportunities, but ensuring optimal multidisciplinary collaboration is a challenge. We investigated factors that were relevant and important for large-scale implementation. In three multidisciplinary online focus groups, healthcare professionals (gynecologic oncologists, pathologists, clinical geneticists, and clinical laboratory specialists) were interviewed on factors critical for the implementation of the Tumor-First workflow. Recordings were transcribed for analysis in Atlas.ti according to t...
Background: Women with epithelial ovarian cancer (OC) have a higher chance to benefit from poly (ADP...
Background: NCCN guidelines recommend germline and somatic tumor testing for all women with invasive...
Background: BRCA1/2 mutation status has increasing relevance for ovarian cancer treatments, making t...
Universal tumor DNA testing in epithelial ovarian cancer patients can function not only as an effici...
We present findings of a cancer multidisciplinary-team (MDT) coordinated mainstreaming pathway of un...
Objective: Genetic testing in epithelial ovarian cancer (OC) is essential to identify a hereditary c...
We present findings of a cancer multidisciplinary-team (MDT) coordinated mainstreaming pathway of un...
The final publication is available at Springer via http://dx.doi.org/10.1007/s10897-017-0108-5Decrea...
According to current guidelines, all women with epithelial ovarian cancer are eligible for genetic t...
The majority of patients with ovarian cancer ultimately develop recurrent chemotherapy-resistant dis...
The aim of this PhD project was to evaluate alternative procedures for genetic testing and counselli...
Contains fulltext : 245251.pdf (Publisher’s version ) (Open Access
Funding: The study is funded by The Barts Charity, grant ECMG1B6R. Acknowledgments: D.G.E. is suppor...
Decreasing costs of genetic testing and advances in treatment for women with cancer with germline $\...
Objective: Pathogenic BRCA variants account for between 5.8-24.8% of ovarian cancers. The identifica...
Background: Women with epithelial ovarian cancer (OC) have a higher chance to benefit from poly (ADP...
Background: NCCN guidelines recommend germline and somatic tumor testing for all women with invasive...
Background: BRCA1/2 mutation status has increasing relevance for ovarian cancer treatments, making t...
Universal tumor DNA testing in epithelial ovarian cancer patients can function not only as an effici...
We present findings of a cancer multidisciplinary-team (MDT) coordinated mainstreaming pathway of un...
Objective: Genetic testing in epithelial ovarian cancer (OC) is essential to identify a hereditary c...
We present findings of a cancer multidisciplinary-team (MDT) coordinated mainstreaming pathway of un...
The final publication is available at Springer via http://dx.doi.org/10.1007/s10897-017-0108-5Decrea...
According to current guidelines, all women with epithelial ovarian cancer are eligible for genetic t...
The majority of patients with ovarian cancer ultimately develop recurrent chemotherapy-resistant dis...
The aim of this PhD project was to evaluate alternative procedures for genetic testing and counselli...
Contains fulltext : 245251.pdf (Publisher’s version ) (Open Access
Funding: The study is funded by The Barts Charity, grant ECMG1B6R. Acknowledgments: D.G.E. is suppor...
Decreasing costs of genetic testing and advances in treatment for women with cancer with germline $\...
Objective: Pathogenic BRCA variants account for between 5.8-24.8% of ovarian cancers. The identifica...
Background: Women with epithelial ovarian cancer (OC) have a higher chance to benefit from poly (ADP...
Background: NCCN guidelines recommend germline and somatic tumor testing for all women with invasive...
Background: BRCA1/2 mutation status has increasing relevance for ovarian cancer treatments, making t...