NCT06967233

Brief Summary

Pancreatic ductal adenocarcinoma (PDAC) remains a challenging malignancy, with over 300,000 patients diagnosed annually worldwide. Patients with metastatic pancreatic cancer (MPC) are generally not considered appropriate for operative management because it would not improve their prognosis. Developments in modern surgery and systemic treatment over the past decade have substantially improved the oncological outcomes for patients with PDAC. The prognosis can be further improved by using novel combined regimens. Systemic treatment is advantageous as it allows biological selection of patients and control of systemic lesions in patients with PDAC with only hepatic metastases (Hep-MPC), which may increase the likelihood of radical tumor resection and improved survival. Therefore, there is a strong need to reassess the value of surgery in Hep-MPC. Locoregional liver-directed treatments (LLDTs) are safe and efficient methodologies and have thus become the standard of care for patients with metastatic colorectal cancer (MCC) with liver-only or liver-dominant metastases. LLDT therapies include local liver resection, radiofrequency ablation (RFA), hepatic artery infusion pump chemotherapy (HAIP), stereotactic body radiation therapy (SBRT), and selective internal radiation therapy with yttrium-90 embolization (Y90). These therapies have been reported to influence the overall survival (OS), progression-free survival (PFS), and conversion to resection in patients with metastatic colorectal cancer. However, the data on the survival outcomes of conversion surgery and the clinical application of LLDT in Hep-MPC are sparse. Therefore, it remains unclear what types of treatment, based on the survival benefit, might actually be the optimal approach for Hep-MPC after effective systemic treatment. The present study aims to clarify the selection criteria of conversion surgery for Hep-MPC and explore the prognostic significance for its multimodal management, including surgical resection and/or LLDT.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
360

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2019

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2019

Completed
4.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 2, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

May 13, 2025

Completed
Last Updated

May 13, 2025

Status Verified

May 1, 2025

Enrollment Period

4.6 years

First QC Date

May 2, 2025

Last Update Submit

May 10, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Overall survival

    Calculated from the date of treatment initiation to the date of death or the last date of follow-up

    From the date of treatment initiation to the date of death or the last date of follow-up (up to 60 months)

Secondary Outcomes (1)

  • Progression free survival

    From the date of treatment initiation to the date of disease progression or death, whichever occurred first (up to 60 months).

Interventions

Surgical resection, locoregional liver-directed treatments and continuous systemic treatment in patients with liver metastatic pancreatic cancer

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients were cytologically or histologically diagnosed with pancreatic cancer, as well as with the primary tumor and liver metastasis. The primary and metastatic lesions were determined using CT and MRI.

You may qualify if:

  • Adult patients aged ≥18 years (at diagnosis).
  • Cytologically or histologically confirmed pancreatic adenocarcinoma.
  • Synchronous liver metastatic disease (at diagnosis).
  • No evidence of extrahepatic metastases (at diagnosis.)
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2.
  • Eligible for multimodal treatment.

You may not qualify if:

  • Multi-organ metastatic pancreatic cancer.
  • Contraindications to surgical resection or systemic treatment.
  • Inability to participate in follow-up assessments.
  • History of other malignancies.
  • Refusal of treatment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The first affiliated hospital, Zhejiang university school of medicine

Hangzhou, Zhejiang, 310000, China

Location

MeSH Terms

Conditions

Pancreatic Neoplasms

Interventions

Combined Modality Therapy

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsEndocrine Gland NeoplasmsDigestive System DiseasesPancreatic DiseasesEndocrine System Diseases

Intervention Hierarchy (Ancestors)

Therapeutics

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

May 2, 2025

First Posted

May 13, 2025

Study Start

June 1, 2019

Primary Completion

December 31, 2023

Study Completion

April 1, 2025

Last Updated

May 13, 2025

Record last verified: 2025-05

Locations