CtDNA as a Novel Biomarker of Treatment Efficacy in Patients With Ovarian Cancer

Recruiting now

Conditions studied: High-grade Serous Ovarian Cancer, Circulating Tumor DNA

In brief

This study is a prospective observational clinical trial. Patients who were diagnosed and treated for the first time were enrolled and their surgical pathology was confirmed to be high-grade serous ovarian cancer. At the same time, these patients will receive first-line maintenance treatment with PARP inhibitors after traditional chemotherapy. During the trial period, patients' plasma will be collected before surgery, after chemotherapy, during targeted maintenance therapy, and during disease progression, and ctDNA-specific genomes will be detected, and clinical data will be collected over the same period. It is expected that specific ctDNA can be used to predict the efficacy of PARP inhibitors in patients with ovarian cancer, and to detect the recurrence of the disease early.

Key facts

Study ID
NCT05027828
Run by
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
People needed
100
Starts
2021-09-01
Expected to finish
2027-09-30
Last updated by the study team
2026-04-24

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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