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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05802420
Other study ID # K3378-01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2023
Est. completion date February 1, 2025

Study information

Verified date March 2023
Source Peking Union Medical College Hospital
Contact Chunmei Bai, MD
Phone 010-69158764
Email tangh160706@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to explore the value of molecular residual disease (MRD) monitoring based on ctDNA in advanced or metastatic pancreatic cancer. The main questions it aims to answer are: - prognostic value of baseline MRD; - the role of MRD dynamic changes after treatment in guiding treatment. Peripheral blood derived from participants will be obtained for MRD test before first-line chemotherapy initiation and at the first imaging assessment after chemotherapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date February 1, 2025
Est. primary completion date February 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients with histologically confirmed unresectable advanced or metastatic pancreatic cancer; - both sexes, age =18 years old; - ECOG performance status score =2; - the expected survival time was =3 months. Exclusion Criteria: - a known diagnosis of pancreatic cancer other than ductal adenocarcinoma; - treated with any systemic antitumor treatment before first-line chemotherapy onset; - died or lost to follow-up within one month after the initiation of first-line chemotherpay; - combined with other primary malignances.

Study Design


Intervention

Drug:
Later-line therapy
Another chemotherapy regimen, targeted therapy, or immunotherapy

Locations

Country Name City State
China Peking Union Medical College Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other The prognostic value of MRD The prognostic value of baseline MRD and dynamic MRD changes Baseline until death from any cause (up to approximately 24 months)
Other The prognostic role of targeted therapy selected based on MRD The prognostic role of targeted therapy selected based on MRD Baseline until death from any cause (up to approximately 24 months)
Primary Progression-free survival The date of first-line chemotherpay initiation to tumor progression or death due to any cause in the absence of progression. Baseline until death from any cause (up to approximately 24 months)
Secondary Overall survival The date of first-line chemotherpay initiation to death due to any cause. Baseline until death from any cause (up to approximately 24 months)
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