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A single-center, prospective, observational cohort study of chemoradiotherapy in elderly patients with locally advanced pancreatic cancer (70+).

A single-center, prospective, observational cohort study of chemoradiotherapy in elderly patients with locally advanced pancreatic cancer (70+).

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095520
Enrollment
Unknown
Registered
2025-01-08
Start date
2025-01-13
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Locally advanced pancreatic cancer

Interventions

Observation group:None

Sponsors

Zhongshan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
70 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate and sign the informed consent form; 2. Age 70-85 years old, life expectancy > 1 year. Gender is not limited; 3. ECOG physical state score=3.0 × 109/L; Absolute neutrophil count (ANC) >=1.5 × 109/L; Platelets (PLT) >=100 × 109/L; hemoglobin (Hgb) >=90 g/L; 9. Blood biochemical indexes: AST (SGOT), ALT (SGPT) <=2.5 × upper limit of normal value (ULN); Total bilirubin (TBIL) < = ULN; Serum creatinine (CRE) <=1.5 × ULN; 10. Coagulation function: prothrombin time (PT), international normalized ratio (INR) <=1.5 × ULN; 11. Able to comply with the requirements of the study visit plan and other programs. Note: ECOG score, Eastern Cooperative Oncology Group Physical Status Score.

Exclusion criteria

Exclusion criteria: 1. Accompanied by malignant tumors of other systems; 2. Received any form of anti-tumor therapy before treatment, including systemic chemotherapy, interventional chemotherapy, high-energy focused ultrasound, radiotherapy, immunotherapy, molecular targeted therapy, and anti-tumor traditional Chinese medicine therapy; 3. Have used any other non-anti-tumor research drugs within 4 weeks before treatment; 4. Combined with uncontrollable hypertension, diabetes, infection, etc.; 5. Poor compliance, unable or unwilling to sign informed consent; 6. Patients who are expected to be out of the observation period for 14 days or more during the treatment period.

Design outcomes

Primary

MeasureTime frame
1-year survival rate;

Secondary

MeasureTime frame
Overall survival,OS;Event-free survival, EFS;Objective Response Rate,ORR;Disease control rate,DCR;

Countries

China

Contacts

Public ContactWang Wenquan

Zhongshan Hospital Affiliated to Fudan University

wang.wenquan@zs-hospital.sh.cn+86 137 0187 4954

Outcome results

None listed

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