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Variance of HRD From Paired Ovarian Cancer

Variance of HRD From Primary to Recurrent in High-grade Serous Ovarian Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05069818
Acronym
HOPEII
Enrollment
50
Registered
2021-10-06
Start date
2021-10-31
Completion date
2022-12-31
Last updated
2021-10-06

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

Conditions

HRD, Ovarian Cancer, Platinum-sensitive Ovarian Cancer

Brief summary

Homologous recombination deficiency (HRD) is an important biomarker of poly (ADP-ribose) polymerase inhibitor (PARPi) in patients with high-grade serous ovarian cancer (HGSOC). The stability of HRD in the recurrent HGSOC and its primary pair remains unknown.

Detailed description

This study intends to perform HRD testing of ovarian cancer in the recurrent HGSOC and its primary pair, furtherly correlate HRD status and clinical characteristics in the recurited population.

Interventions

None listed

Sponsors

Xiaoxiang Chen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. Subjects join the study voluntarily and sign informed consent; 2. Female subjects are older than 18 years; 3. ECOG(Eastern Cooperative Oncology Group) physical status score is 0-2; 4. Life expectancy≥3 months; 5. Histologically confirmed FIGO(International Federation of Gynecology and Obstetrics ) III/IV ovarian cancer, fallopian tube cancer, or primary peritoneal cancer; Participants must have high-grade serous histology

Exclusion criteria

1. Personnel involved in the formulation or implementation of the research plan; 2. The subjects had other malignant diseases in past 2 years, except skin squamous cell carcinoma, basal-like carcinoma, breast intraductal carcinoma in situ, or cervical carcinoma in situ;

Design outcomes

Primary

MeasureTime frameDescription
Loss of heterozygosity (LOH) score in the primary and recurrent ovarian cancerThrough study completion, an average of 1 year]The LOH score is a scale describing the genomic loss of heterozygosity status in the primary or recurrent tumor of an ovarian cancer patient. The score is determined by analyzing more than 3500 SNPs spaced at 1Mb intervals across the genome on the FoundationOne CDx test and extrapolating an LOH profile, excluding arm and chromosome-wide LOH segments. The score is summarized as the percentage of the genome with LOH regions.
Homologous recombination deficiency (HRD) statusThrough study completion, an average of 1 yearThe HRD status for primary or recurrent tumor in a patient is considered according to the LOH score and genomic mutation status of BRCA1 and BRCA2 genes in the sample. A sample with LOH≥16%,and/or with genomic mutation in BRCA1 or BRCA2 gene, is defined as HRD positive. Otherwise, a sample with LOH\<16% and wild type BRCA1/BRCA2 genes is defined as HRD negative.

Secondary

MeasureTime frameDescription
Progression-free survivalFrom the beginning of the patient's onset, an average of 1 yearProgression-free survival in recruited patients
Overall survivalFrom the beginning of the patient's onset, an average of 3 yearOverall survival in recruited patients

Countries

China

Contacts

Primary ContactJing Ni, MD
nijingwulin@126.com+86 13327833586
Backup ContactXiaoxiang Chen, MD,PhD

Outcome results

None listed

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