Clinical Trials Directory

Trials / Unknown

UnknownNCT05976932

Circulating Tumor DNA Monitoring in Platinum-resistant Ovarian Cancer

The Utility of Circulating Tumor DNA in Monitoring the Response to Pegylated Liposomal Doxorubicin in Platinum-resistant Ovarian Cancer

Status
Unknown
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This observational study is conducted to assess the utility of circulating tumor DNA in monitoring the response to pegylated liposomal doxorubicin in platinum-resistant ovarian cancer,and evaluate the consistency of circulating tumor DNA with imaging and CA125 in platinum-resistant ovarian cancer.

Detailed description

The goal of this study is to assess the utility of circulating tumor DNA in monitoring the response to pegylated liposomal doxorubicin in platinum-resistant ovarian cancer.This is a single-arm, single-center prospective clinical study. After enrollment, patients will receive standard treatment (pegylated liposomal doxorubicin)and follow-up strategy. Peripheral blood samples will be collected from all patients before treatment and 3 weeks after the first cycle of treatment,If necessary, Peripheral blood samples also be collected after 2 cycles of treatment.Peripheral blood ctDNA will be tested for genetic variation based on next-generation sequencing (NGS). Finally, this study will to evaluate the consistency of circulating tumor DNA with imaging and CA125 in platinum-resistant ovarian cancer.

Conditions

Interventions

TypeNameDescription
DRUGpegylated liposomal doxorubicinAll eligible subjects will receive the standard chemotherapy of pegylated liposomal doxorubicin monotherapy.

Timeline

Start date
2023-08-01
Primary completion
2024-04-01
Completion
2024-10-01
First posted
2023-08-04
Last updated
2023-08-04

Source: ClinicalTrials.gov record NCT05976932. Inclusion in this directory is not an endorsement.