UPCC 14825 GOG-3100: Collection of Biospecimens from Homologous Recombination Deficient (HRD) Test Negative High-Grade Serous Ovarian Cancer Patients
Brief description of study
Primary Objective
1. To explore genetic, proteomic, and molecular characteristics associated with recurrence less than six months following completion of frontline adjuvant combination platinum-based chemotherapy versus recurrence 18 months following completion of frontline adjuvant combination platinum-based chemotherapy.
2. To create a biorepository of tissue and blood that will be used in research studies designed to better understand the molecular biology of HRD test negative high-grade serous ovarian cancer. There are no statistical considerations for this study. Statistical justifications will be required for
all requests to utilize biospecimens collected as part of this study. The purpose of this study is to explore genetic, proteomic, and molecular characteristics associated with recurrence. This study will also create a biorepository.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 99 years or below
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Gender: All
TBD
Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.
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