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The Significance and Indications of Surgery for Synchronous Liver Metastatic Pancreatic Cancer

Liver Metastasis of Pancreatic Cancer:Chinese Surgical Study Group

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06873178
Acronym
PCLM:CSSG
Enrollment
50
Registered
2025-03-12
Start date
2024-08-23
Completion date
2026-06-30
Last updated
2025-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adjuvant Therapy, Liver Metastases, Pancreatic Cancer, Surgery

Brief summary

To explore the clinical characteristics of pancreatic cancer patients with liver metastases who can benefit from surgery, and to develop evaluation criteria for surgical indications, so as to provide basis for comprehensive treatment strategies for advanced pancreatic cancer patients.

Detailed description

Initial Systemic Treatment: Subjects who meet the inclusion criteria will first undergo systemic treatment. The primary treatment regimens will follow the NCCN guideline-recommended first-line chemotherapy options, including the AG regimen, FOLFIRINOX regimen, and the NALIRIFOX regimen. Periodic Assessments: Every 4 treatment cycles, laboratory tests (including blood routine, coagulation function, liver and kidney function, and tumor markers) and imaging studies (enhanced CT or MRI, with PET-CT if necessary) will be conducted. After 4-6 cycles, imaging and tumor marker assessments will be performed to evaluate the patient's disease status. A multidisciplinary discussion will determine if patients with a good response to systemic treatment are eligible for radical surgery. Treatment Adjustment and Surgical Intervention: For patients assessed as having disease progression during the first evaluation, the treatment plan will be adjusted, and assessments will be conducted every 2 cycles. Patients showing a good response may still be considered for radical surgery. For pancreatic lesions, surgical procedures such as pancreaticoduodenectomy or distal pancreatectomy with splenectomy will be performed based on the lesion's location, with total pancreatectomy considered if necessary. For liver lesions, the surgical approach will depend on the number, size, and location of the lesions. During surgery, tumor and adjacent tissue samples (approximately 100mg, the size of a soybean) will be collected for research purposes, provided it does not affect diagnosis. Postoperative discarded specimens (approximately 500mg) will also be collected and preserved. Postoperative Monitoring: Laboratory tests, including but not limited to blood routine, coagulation, liver, kidney, and pancreatic function, will be collected on postoperative days 1, 3, 5, 7, and 30. Adjuvant Treatment and Complication Monitoring: Postoperative adjuvant treatment will continue according to the original regimen. Any postoperative complications and adverse reactions during chemotherapy will be recorded. Trial Progress Tracking: The progress of each subject will be documented. If a subject withdraws or drops out, the reason and the date of the last medication will be recorded. Follow-Up: After the completion of treatment, patients will be followed up monthly until death.

Interventions

None listed

Sponsors

Peking University First Hospital
CollaboratorOTHER
Chongqing General Hospital
CollaboratorOTHER
Tongji Hospital
CollaboratorOTHER
Zhejiang Provincial People's Hospital
CollaboratorOTHER
China-Japan Friendship Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-75 years old * Pancreatic cancer was diagnosed as pancreatic ductal adenocarcinoma by biopsy of primary/metastases * Physical Condition Score (ECOG)0-1 * Simultaneous/prior discovery of liver metastases and primary lesions was defined as simultaneous liver metastases * Enhanced CT/MRI can detect liver metastases (if the diseases not detected by enhanced CT/MRI during screening are not included in the number calculation) * The patient's liver, kidney and bone marrow function is good

Exclusion criteria

* The primary lesions of pancreatic cancer are acinar cell carcinoma of pancreas, neuroendocrine carcinoma of pancreas and other pathological types * there are other metastases outside the liver * Had other malignant tumors within 5 years * History of central nervous system disease, mental illness, unstable angina pectoris, congestive heart failure, severe arrhythmia and other serious diseases * Active or chronic hepatitis B/C virus infection * Allergy to iodine, unable to perform enhanced imaging * Previous anti-tumor therapy for pancreatic cancer (surgery/ radiotherapy/ chemotherapy/ ablation/ targeted therapy/ immunotherapy)

Design outcomes

Primary

MeasureTime frameDescription
OSthrough study completion, an average of 2 yearOverall Survival

Secondary

MeasureTime frameDescription
RFSthrough study completion, an average of 2 yearRecurrence free survival

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026