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Clinical research of multi-mode thermal ablation for the treatment of pancreatic cancer with liver metastasis

Clinical research of multi-mode thermal ablation for the treatment of pancreatic cancer with liver metastasis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074590
Enrollment
Unknown
Registered
2023-08-10
Start date
2023-08-08
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

pancreatic cancer liver metastasis

Interventions

multi-mode thermal ablation combined with intravenous anti-PD-1 and chemotherapy:1. multi-mode thermal ablation 2. Camrelizumab 200 mg IV D1 + Gemcitabine 1000mg/m2 IV + albumin-bound paclitaxel125mg/
for 6 circles.
intravenous anti-PD-1 and chemotherapy:Camrelizumab 200 mg IV D1 + Gemcitabine 1000mg/m2 IV + albumin-bound paclitaxel125mg/m2 IV D1.8 Q3W

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Ages 18-70 years. Can be male or female; 2. Histologically confirmed pancreatic cancer with liver metastasis and no extrahepatic metastasis; 3. Measurable liver metastasis in CT or MRI, can be punctured safely; 4. Less than 3 lesions per half liver and less than 3 cm each; 5. ECOG score =2, expected survival more than 3 month.

Exclusion criteria

Exclusion criteria: 1. Child_Pugh level C with serious jaundice, especially obstructive jaundice; 2. Excessive tumor volume , or ablation range up to one-third of liver volume; 3. Expected survival less than 3 month; 4. Severe disorders of the heart, lung, liver, or kidney function, irreversible coagulation disorder; 5. Other uncontrolled diseases, including hypertension or diabetes, active infection, mental illness, or a social condition that may affect the subject’s compliance; 6. Intractable ascites, pleural effusion, or cachexia; 7. Pregnant or lactating women; 8. Other factors that researchers think not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
overall survival;severe adverse event rate;

Secondary

MeasureTime frame
progression-free survival;objective response rate;disease control rate;

Countries

China

Contacts

Public ContactLong Jiang

Shanghai General Hospital

jiang.long@shgh.cn+86 180 1731 7460

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026