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An Exploratory Study of HRD Score in Chinese Ovarian Cancer Patients Benefiting From PARP Inhibitor Targeted Therapy

An Exploratory Study of HRD Score in Chinese Ovarian Cancer Patients Benefiting From PARP Inhibitor Targeted Therapy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05255861
Enrollment
300
Registered
2022-02-25
Start date
2022-03-01
Completion date
2024-12-31
Last updated
2022-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian Cancer

Keywords

Homologous Recombination Deficiency Score

Brief summary

This project intends to evaluate the sensitivity of different Homologous Recombination Deficiency (HRD) score to Poly(ADP-ribose) polymerase inhibitor (PARPi) by retrospectively analyzing the tissue samples of patients with ovarian cancer using PARPi, and to determine the cut off value of the HRD score algorithm suitable for the Chinese population, so as to provide evidence for the role of PARPi in ovarian cancer. The screening of the beneficiaries of maintenance therapy provides precise guidance and can be used as a reference for other cancer types.

Interventions

None listed

Sponsors

Xin Wu
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. age ≥ 18 years; 2. high-grade serous/endometrioid epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer; 3. FIGO stage III or IV; 4. at least 6 cycles and no more than 9 cycles First-line platinum-containing chemotherapy; 5. CR or PR after chemotherapy; 6. ECOG 0-1; 7. sufficient biological samples for HRD score detection; 8. patients signed informed consent; 9. good bone marrow function.

Exclusion criteria

1. incomplete follow-up records of survival information; 2. unqualified biological sample quality control

Design outcomes

Primary

MeasureTime frameDescription
Homologous Recombination Deficiency scoreAfter the ovarian tissue is obtained, an average of 3 yearOptimize the Homologous Recombination Deficiency scoring algorithm to calculate the Homologous Recombination Deficiency score of each patient's ovarian cancer tissue

Countries

China

Contacts

Primary ContactXin Wu, PHD
wuxin_fc@fudan.edu.cn(021)33189900-6529
Backup ContactLing Qiu, MD
QiuLingpang@163.com(021)33189900-6529

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026