About this trial

This study is being done to investigate clonal hematopoiesis and therapy-emergent myeloid neoplasms in patients with ovarian or other solid cancers. Researchers want to identify risk factors for developing these blood cancers as well as if there is/are a genetic/environmental component(s) to developing blood cancer.

Eligibility criteria

Qualifiers

Have completed or plan to complete at least 5 cycles of platinum-based chemotherapy

At least 4 months of exposure to a PARP inhibitor

Diagnosis of a blood disorder including, but not limited to, clonal hematopoiesis of indeterminate potential, cytopenia of unknown significance, or therapy-related myeloid neoplasm

Disqualifiers

Individuals with a life expectancy of less than 6 months

Trial design

Treatments tested in this trial

  • Non-Interventional Study

Treatment groups

2,000 Participants
are divided into 1 treatment group

Locations

1
Fred Hutch/University of Washington Cancer Consortium98109, SeattleWashington, United States

Sponsors and collaborators

University of Washington

Lead sponsor

National Cancer Institute (NCI)

Collaborator