Phase I, II study of neoadjuvant chemotherapy with gemcitabine and nab-paclitaxel for resectable pancreatic cancer
- Conditions
- pancreatic ductal cancer
- Registration Number
- JPRN-jRCTs021200003
- Lead Sponsor
- Ishido Keinosuke
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
1. Pathologically adenocarcinoma or adenosquamous carcinoma is confirmed.
2. No distant metastasis except for the positive case of intraoerative abdominal cytology.
3. Resectable pancreatic cancer according to the Japan Classification of pancreatic cancer 7th edition.
4. Patients who are tolerable for radical surgery,
5. Patients who had not treated for pancreatic cancer.
6. Over 20 y.o.
7. ECOG PS, 0-1
8. In cases with obstructive jaundice, proper drainage is performed.
9. Cases in which functions of major organs (bone marrow, liver, kidney, lung, etc.) are retained.
10. The informed consent has been obtained from the patient concerning the participation in the document.
1. Patients who had treated with gemcitabine and nab-paclitaxel.
2. Patients who are judged that R2 resection is anticipated.
3. Severe diarrhea
4. Patients who have sever ascitis fluid and pleural effusion.
5. Patients who have active malignant disease but pancreatic cancer.
6. Patients who have sever co-morbidity.
7. Patients who have active infection except type B and C viral hepatitis.
8. Patients who have either significant abnormality of ECG or sever heart disease.
9. Patients who have sever psychiatric disease.
10. Pregnant women, nursing women and cases who are likely to be pregnant or willing, men who wish to be pregnant by partner.
11. Patients that have experienced severe drug allergies in the past
12. Cases receiving continuous systemic administration of corticosteroids.
13. Patients where administration of gemcitabine and nab-paclitaxel is contraindicated.
14. Other cases that the doctor in charge judged unsuitable for safely carrying out this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relapse-free survival time
- Secondary Outcome Measures
Name Time Method 1. over-all survival time<br>2. Treatment completion rate of 4 courses of chemotherapy<br>3. down-staging rate<br>4. R0 resectrion rate<br>5. Adverse event rate<br>6. Response rate