Finding studies
Finding studies
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Bin Li Bin Li, PhD
CONTACT
Lead
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
This study is a single-arm, interventional, open-label, prospective clinical trial. Patients with advanced epithelial ovarian cancer (Federation of International of Gynecologists and Obstetricians,FIGO stage III-IV), who are not eligible for R0 resection or unable to tolerate surgery based on radiological assessment (Suidan score) or laparoscopic assessment (Fagotti score), and who are Homologous recombination deficiency (HRD)positive, will receive neoadjuvant therapy with fuzuloparib and apatinib for two cycles (28 days per cycle). After neoadjuvant treatment, patients who achieve complete or partial response according to radiological assessment will proceed to the surgical treatment phase.
Age
18–70
Sex
FEMALE
Healthy volunteers
Not accepted
