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PD-1 inhibitor combined with second-line chemotherapy for advanced pancreatic cancer

Efficacy of PD-1 inhibitor combined with second-line chemotherapy in the treatment of advanced pancreatic cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038730
Enrollment
Unknown
Registered
2020-09-29
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-12-14

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

Conditions

Advanced pancreatic cancer

Interventions

Experimental group:PD-1 inhibitor combined with chemotherapy

Sponsors

Chizhou people's Hospital, Anhui Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Patients with unresectable, recurrent and / or metastatic pancreatic cancer confirmed by cytology or histology; 3. Have at least one evaluable lesion judged according to rrecist version 1.1 (spiral CT scan length of measurable lesion >=10mm or short diameter of enlarged lymph node >=15mm according to RECIST version 1.1); 4. ECoG PS The following criteria should be met: (1) HB >=80 g/L; ANC >=1.5 x 10^9/L; PLT >=80 x 10^9/L; (2) biochemical examination should meet the following criteria: TBIL 45 ml / min (Cockcroft Gault formula); 7. ECG is basically normal; 8. Patients have good compliance, can understand the situation of this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who have received local treatment for target lesions (including local radiotherapy, interventional therapy, ultrasonic scalpel, etc.); 2. Pregnant and lactating women, or women with fertility but without contraceptive measures; 3. Severe acute infection that has not been controlled; or purulent and chronic infection, delayed wound healing; 4. Organ transplantation due to autoimmune system; 5. Patients with mental illness and AIDS; 6. Severe autoimmune diseases; 7. Those who have participated in the clinical trials of other drugs in the past 3 months; 8. The researchers think that they are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Measurable tumor focus;PFS, OS;

Countries

China

Contacts

Public ContactXu Jinfa

Department of oncology, Chizhou people's Hospital

jinfaxu@163.com+86 15339668787

Outcome results

None listed

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