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Clinical Trials/NCT05723978
NCT05723978
Completed
Not Applicable

Selective Extended Dissection in Different Types of Pancreatic Head Cancer: A Retrospective Cohort Study.

Tianjin Medical University Cancer Institute and Hospital1 site in 1 country520 target enrollmentJanuary 1, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carcinoma, Pancreatic Ductal
Sponsor
Tianjin Medical University Cancer Institute and Hospital
Enrollment
520
Locations
1
Primary Endpoint
Disease-free survival (DFS)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant tumor with relatively poor survival. Surgery is the first choice for the treatment of patients with early pancreatic cancer. However, the surgical approach and the extent of resection for patients with pancreatic cancer are controversial at present.

The investigators optimized the procedure of standard pancreaticoduodenectomy to selective extended dissection (SED), which is based on the extra-pancreatic nerve plexus (PLX) potentially invaded by tumor. The investigators retrospectively analyzed the clinicopathological data of patients with pancreatic adenocarcinoma who underwent radical surgery in our center from 2011 to 2020. Patients who underwent standard dissection (SD) were matched 2:1 to those who underwent SED using propensity score matching (PSM). The log-rank test and cox regression model were used to analyze survival data. In addition, statistical analyses were performed for the perioperative complications, postoperative pathology and recurrence pattern.

Registry
clinicaltrials.gov
Start Date
January 1, 2011
End Date
December 1, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed as resectable pancreatic cancer were pathologically diagnosed as PDAC after surgery.
  • Patients received radical surgery (R0) and had complete photos or videos of the operation.

Exclusion Criteria

  • The operation records as well as related photo or video data could not reflect the surgical approach and the extent of resection.
  • Patients with incomplete clinical, pathological, imaging and follow-up information.

Outcomes

Primary Outcomes

Disease-free survival (DFS)

Time Frame: From the day the patient received surgery to the time the patient was diagnosed with postoperative recurrence, assessed up to 36 months.

Study Sites (1)

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