Skip to content

Application of precision neoadjuvant chemotherapy in the surgical treatment of pancreatic cancer

Application of precision neoadjuvant chemotherapy in the surgical treatment of pancreatic cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082320
Enrollment
Unknown
Registered
2024-03-26
Start date
2023-06-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Pancreatic cancer

Interventions

Experimental group:Organoid establishment According to the results of drug sensitivity to organoids, a more sensitive drug regimen was adopted

Sponsors

Department of hepatobiliary Surgery, 13th floor, main ward building, Xinqiao Zhengjie, Xinqiao Hospital, Shapingba District, Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Patients aged 18-75 years old, both male and female; ? The ECOG score is 0-2; ? Patients with clinically determined borderline resectable pancreatic cancer who are scheduled for neoadjuvant therapy; ? Fresh tissue specimens sufficient for organoid establishment can be obtained by puncture; ? Patients with pancreatic ductal adenocarcinoma confirmed by histopathology and/or cytology; ? The patients voluntarily joined the study and signed the informed consent, with good compliance and follow-up

Exclusion criteria

Exclusion criteria: ? Patients who have previously received systemic therapy for pancreatic cancer ? Patients with clinically determined resectable pancreatic cancer, locally advanced pancreatic cancer, and metastatic pancreatic cancer ? Patients who have had other malignant tumors within 5 years, except skin cancer that has been cured; Patients who have had clinically important (i.e. active) heart disease (e.g. congestive heart failure, symptomatic coronary artery disease, arrhythmia, etc.) or myocardial infarction within the past 12 months; ? Patients who have a history of psychotropic drug abuse and cannot quit or have mental disorders;

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Disease-free survival;

Countries

China

Contacts

Public ContactHuang Xiaobin

the Second Affiliated Hospital of the PLA Army Military Medical University

13372618116@163.com+86 133 7261 8116

Outcome results

None listed

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