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NCT06838429Not yet recruiting

PARPi and Ovarian Cancer Survival

Effect of PARP Inhibitors Maintenance Therapy on the Survival Rate of Advanced or Relapsed Epitherlial Ovarian Cancer: an Observational Cohort Study

Source: ClinicalTrials.gov · Last updated 20 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

With the widespread use of PARP inhibitors (PARPi) as maintenance therapy in ovarian cancer, there is still a lack of real-world data from large samples regarding their impact on survival outcomes in advanced and recurrent ovarian cancer. This study aims to conduct a pragmatic cohort study to evaluate the impact of first-line and second-line maintenance treatment with PARPi on survival rates in patients with advanced and recurrent ovarian cancer. The genetic status, different PARPi drugs, and the use of anti-angiogenic inhibitor maintenance therapy or not is used as confounding factors.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
6000 (estimated)
First submitted
17 Feb 2025
Start date
Mar 2025
Primary completion date
Mar 2026
Lead sponsor
Shanghai Gynecologic Oncology Group
NCT number
NCT06838429

What you commit to

  • Study type: Observational
  • Planned participants: 6000
  • From Mar 2025 to the primary completion date, Mar 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Platinum-resistant patients, such as those who had disease progression during chemotherapy or within 6 months after platinum-based chemotherapy.

Other

  • Group 1:
  • Non-epithelial tumors, borderline tumors, clear cell carcinoma, mucinous carcinoma.
  • Missing first-line or follow-up data.
    • Group 2:
  • Non-epithelial tumors, borderline tumors, clear cell carcinoma, mucinous carcinoma.
  • Patients with second relapse.
  • Missing second-line or follow-up data.

Who the study is looking for

  • Group 1:
  • Patients newly diagnosed with stage IIIC or IV primary epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer between December 2013 and December 2024.
  • Complete data on first-line treatment and maintenance therapy.
  • Availability of follow-up data.
    • Group 2:
  • Patients with platinum-sensitive first recurrence of any stage of epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer, diagnosed between December 2013 and December 2024.
  • Disease progression occurring at least 6 months after the completion of the last platinum-based chemotherapy regimen.
  • Complete data on second-line treatment and maintenance therapy.
  • Availability of follow-up data.

Age in the registry: 18 years to 80 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.