Investigation of the Optimal Duration of Neoadjuvant Therapy for Resectable Pancreatic Cancer
Completed
- Conditions
- Pancreatic Cancer Resectable
- Registration Number
- NCT06809374
- Lead Sponsor
- Kochi University
- Brief Summary
Investigating the Optimal Duration of Neoadjuvant Chemotherapy for Resectable Pancreatic Cancer to Determine the True Surgical Indication.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- radiologically resectable pancreatic cancer patients
Exclusion Criteria
- a body weight loss of greater than 10% during the six months prior to surgery, the presence of distant metastases, or seriously impaired function of vital organs due to respiratory, renal, or heart disease
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Investigating the Presence of Occult Metastatic Lesions Detected During Neoadjuvant Therapy. within 6 months
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
How does neoadjuvant chemotherapy duration impact KRAS mutation status in resectable pancreatic cancer (NCT06809374)?
What comparative effectiveness data exist for FOLFIRINOX vs. gemcitabine-based neoadjuvant durations in pancreatic cancer?
Which biomarkers predict response to neoadjuvant therapy duration in resectable pancreatic cancer (NCT06809374)?
What adverse events are associated with extended neoadjuvant chemotherapy for pancreatic cancer and management strategies?
How do PARP inhibitors or immunotherapy combinations compare to standard neoadjuvant approaches in resectable pancreatic cancer?