- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06316466
Lipoprotein a is an Independent Risk Factor for Overall Survival in Patients With Pancreatic Cancer: a Propensity Score Matching Analysis
Background: This study aims to assess the prognostic significance of serum lipoprotein (a) [Lp (a)] levels on overall survival (OS) and progression free survival (PFS) in individuals diagnosed with pancreatic cancer through the utilization of propensity score matching (PSM).
Methods: A retrospective analysis was conducted on the clinicopathological data of 364 patients diagnosed with pancreatic cancer at the Affiliated Hospital of Qingdao University from January 2019 to December 2022. The cut-off value for Lp (a) was determined based on one-year survival rates after diagnosis. Patients were then categorized into the high and low Lp (a) groups. We applied PSM analysis to minimize selection bias. The study compared OS and PFS between two groups by Kaplan-Meier method and analyzed differences using the log-rank test. Additionally, univariate and multivariate Cox-regression analyses were performed to identify prognostic factors among patients.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Jinyue Liu
- Phone Number: 17854269227
- Email: liujinyue99@163.com
Study Locations
-
-
Shandong
-
Qingdao, Shandong, China
- Recruiting
- Affiliated Hospital of Qingdao University
-
Contact:
- Jinyue Liu
- Phone Number: 17854269227
- Email: liujinyue99@163.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patients aged over 18 years; (2) Patients with histologically confirmed pancreatic cancer through surgical or puncture procedures; (3) Complete lipid profiles available within one week prior to diagnosis.
Exclusion Criteria:
- (1) Presence of concurrent malignancies; (2) History of previous treatments such as pancreatectomy, chemotherapy, or radiation therapy; (3) Incomplete clinicopathological information.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
the high Lp (a) groups and the low Lp (a) groups
The cut-off value for Lp (a) was determined based on one-year survival rates after diagnosis.
Patients were then categorized into the high and low Lp (a) groups.
|
The cut-off value for Lp (a) was determined based on one-year survival rates after diagnosis.
Patients were then categorized into the high and low Lp (a) groups.
|
|
the low Lp (a) groups
The cut-off value for Lp (a) was determined based on one-year survival rates after diagnosis.
Patients were then categorized into the high and low Lp (a) groups.
|
The cut-off value for Lp (a) was determined based on one-year survival rates after diagnosis.
Patients were then categorized into the high and low Lp (a) groups.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
OS
Time Frame: 1-30months
|
The primary endpoint was overall survival (OS), defined as the time from pathological diagnosis to either death or the most recent follow-up.
|
1-30months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PFS
Time Frame: 1-10months
|
The secondary measure was the duration from the initial diagnosis to disease progression, referred to as progression-free survival (PFS).
Both are measured in months.
|
1-10months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- QYFYWZLL28521
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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