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Clinical Trials/NCT06129812
NCT06129812
Completed
Not Applicable

An Exploration of Candidates for Neoadjuvant Treatment in Resectable Pancreatic Cancer According to Tumor-vessel Relationship and CA 19-9 Levels

Seoul National University Hospital0 sites1,132 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Neoadjuvant treatment
Conditions
Pancreatic Cancer
Sponsor
Seoul National University Hospital
Enrollment
1132
Primary Endpoint
Overall survival
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

An Exploration of Candidates for Neoadjuvant Treatment in Resectable Pancreatic Cancer

Detailed Description

The 1,132 patients with resectable or borderline resectable PDAC who underwent surgery between 2007 and 2021 were retrospectively reviewed. Patients with resectable PDAC without contact of major vessels (R-no contact) (n=651), with contact of portal vein or superior mesenteric vein (PV/SMV) ≤180° (R-contact) (n=306), and borderline resectable PDAC without arterial involvement (BR-V) (n=175) were analyzed.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2021
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with resectable or borderline resectable pancreatic ductal adenocarcinoma (PDAC)
  • Between January 2007 and June 2021 at Seoul National University Hospital

Exclusion Criteria

  • Patients who had borderline resectable PDAC with arterial invasion
  • Patients who received chemotherapy as initial treatment and did not undergo surgery
  • Incomplete follow-up data for analysis

Arms & Interventions

resectable PDAC with no contact to major vessels (R-no contact)

Intervention: Neoadjuvant treatment

resectable PDAC with contact PV/SMV of ≤180° (R-contact)

Intervention: Neoadjuvant treatment

borderline resectable PDAC with PV/SMV contact >180° and without arterial involvement (BR-V)

Intervention: Neoadjuvant treatment

Outcomes

Primary Outcomes

Overall survival

Time Frame: From the date when biopsy results came out until the date of death from any cause or the date of the last visit, whichever came first, assessed up to 60 months

the time from diagnosis to death from any cause or the date of the last visit

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