BRCA Mutation, Epithelial Ovarian Cancer, Homologous Recombination Deficiency, Loss of Heterozygosity, Platinum Resistance, Prognosis
Conditions
Brief summary
A homologous recombination deficiency (HRD) scoring model based on loss of heterozygosity (LOH) is little explored in epithelial ovarian cancer (EOC) patients. This study would recruit 200 Chinese EOC patients with known BRCA1/2 mutation status and resistance to platinum-based chemotherapy. A LOH-HRD model is to be constructed based on the genetic testing in these patients. The mutated genes, HRD score model and their relationship with the prognosis, would provide a full description of for the Chinese EOC patients, and a potential explanation of platinum-resistance in such population.
Interventions
A homologous recombination deficiency (HRD) scoring model based on loss of heterozygosity (LOH)
Sponsors
Study design
Eligibility
Inclusion criteria
* Aged 18 years or older * Pathological confirmation of epithelial ovarian cancer * With available tumor tissues * Given consents to participate the study
Exclusion criteria
• Not meeting all of the inclusion criteria
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Homologous recombination deficiency (HRD) score | Two years | The HRD score for individual patient is a scale describing her HRD status. The score model is calculated by the analysis for loss of heterozygosity (LOH), and the minimum value is 0, but the maximun value is not available. Higher scores mean more sensitivity to poly-ADP-ribose polymerase inhibitor |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | Five years | Progression-free survival in recruited patients |
| Overall survival | Five years | Overall survival in recruited patients |
Countries
China