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Study identifier: NCT04716686 Synced from ClinicalTrials.gov · July 28, 2026
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Niraparib Monotherapy as Maintain and Recurrent Treatment of Endometrial Serous Carcinoma

Condition: Endometrial Carcinoma · Serous Carcinoma  ·  Sponsor: Shandong University

PhasePhase 2
Planned participants83
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Endometrial Serous carcinoma (ESC) has similar molecular characteristics to high-grade serous ovarian carcinoma (HGSOC) and basal cell-like breast cancer, such as similar Chromosomal instability, somatic copy number variation profiles and somatic mutations. The clinical treatment of ESC also refers to the treatment model of HGSOC. The PARP inhibitor niraparib used in this study, which was approved by FDA for the maintenance treatment of adult patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in complete or partial response to platinum-based chemotherapy on March 27, 2017. The homologous recombination related gene mutations in total endometrial cancer accounted for 22%. Homologous Recombination Repair Defect (HRD) +ARID1A accounted for 48%, and 53% of endometrial cancer cell lines were sensitive to PARP inhibitors. The incidence of HRD in endometrial cancer with high copy number (the pathological type is mainly ESC) is 50%, suggesting potential clinical applications of PARP inhibitors for the treatment of ESC.

This description comes directly from the study's public registry record.

Talk to the study team

Qing Zhang  ·  86-18560085996  ·  qiluqingzhang@sdu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Qilu Hospital of Shandong UniversityJinan, Shandong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04716686