Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06751303

Patient Preferences for Precision Medicine: Determining Optimal Patient Quality of Life Using PARPi's

Patient Preferences for Precision Medicine

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University of Saskatchewan · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Patients with ovarian cancer with defective DNA repair mechanisms derive substantial benefit from PARP inhibitor (PARPi) maintenance therapy. Both niraparib and olaparib are effective inhibitors of PARP, which exploit already defective DNA repair mechanisms (e.g., via BRCA mutations), particularly those with homologous recombination deficiency (HRD). These two PARPis have notably different toxicity profiles, with niraparib showing many more severe side effects. In this Ovarian Cancer Canada funded study, we will implement perform HRD testing for ovarian cancer patients in Saskatchewan with response to platinum-based chemotherapy. This information will provide personalized and precision estimates about the amount of benefit that can be expected from taking a PARPi. We will evaluate both treatment outcomes and quality of life in a real-world study setting, to inform future decision-making regarding efficacy, quality of life and cost-effectiveness of PARPi therapy, specifically for niraparib. We hypothesize that for patients who are homologous recombinant proficient (HRP), the median 32.7-month incremental benefit (in delaying cancer progression) from taking a PARPi (niraparib is the only PARPi approved in this setting) will not be seen as being value-add when balanced by the decreased quality of life that accompanies the first 6-12 weeks of therapy. We also hypothesize that for women who are HRP, that PARPi therapy will not be cost-efficient.

Conditions

Interventions

TypeNameDescription
OTHERPatients that are HRP are given a decision aid for PARPi useStudy created patient decision aid if the first for HRD tested Ovarian Cancer patients

Timeline

Start date
2023-09-17
Primary completion
2026-09-16
Completion
2027-09-16
First posted
2024-12-27
Last updated
2024-12-27

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06751303. Inclusion in this directory is not an endorsement.