Last updated: June 12, 2023
Sponsor: Zhejiang University
Overall Status: Active - Recruiting
Phase
3
Condition
Pancreatitis
Pancreatic Cancer
Digestive System Neoplasms
Treatment
Anti-PD-1 monoclonal antibody
Clinical Study ID
NCT03983057
CISPD-4
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Pathologically (histologically or cytologically) confirmed pancreatic ductaladenocarcinoma (PDAC).
- No evidence of distant metastasis (such as liver, peritoneum, lung) evaluated byabdominal contrast-enhanced CT, MRI, and chest CT. PET/CT or other imagingexaminations would be used if necessary.
- Initial assessment for definitive borderline resectable or locally advanced tumors (resectability judgment is based on CT enhanced scan or magnetic resonance imaging,NCCN2019 first edition standard).
- ECOG score 0 or 1.
- Serum creatinine level is normal, and serum total bilirubin level is less than 1.5 xULN.
- ALT and AST are less than 2 x ULN.
- If biliary obstruction is observed, biliary decompression should be performed when thepatient is randomly assigned to receive neoadjuvant chemotherapy.
- Leukocyte count (> 3.5 x 10^6 /mL), neutrophil count (> 1.5 x 10^6 /mL), plateletcount (> 80 x 10^6 /mL), hemoglobin (> 9 g/dL).
- Signed informed consent.
Exclusion
Exclusion Criteria:
- History of malignance treatment in the past, excluding basal and cutaneous squamouscell carcinoma, cervical carcinoma in situ, papillary thyroid carcinoma
- History of participation of other clinical trails within 4 weeks
- History of immunotherapy within 4 weeks
- History of receiving chemotherapy, radiotherapy and molecular target therapy within 2weeks
- Tumor is a local recurrent lesion.
- Imaging confirmed severe portal hypertension / cavernous transformation.
- Ascites
- Gastric outlet obstruction
- Respiratory failure requires supplementation of oxygen.
- Immune deficiency syndrome, such as active tuberculosis and HIV infection.
- Hematological precancerous diseases, such as myelodysplastic syndromes.
- Major cardiovascular diseases (including myocardial infarction, unstable angina,congestive heart failure, severe uncontrolled arrhythmia) during the past six monthsof enrollment.
- Evidence of clinical-related or previous interstitial lung disease, such asnoninfectious pneumonia or pulmonary fibrosis, or baseline chest CT scan or chestX-ray findings
- Previous or physical findings of central nervous system disease, except for adequatelytreated (e.g. primary brain tumors, uncontrolled seizures or strokes with standardmedications)
- Preexisting neuropathy > 1 (NCI CTCAE).
- Allograft requires immunosuppressive therapy or other major immunosuppressivetherapies.
- Severe serious wounds, ulcers or fractures.
- Confirmed coagulant disease.
- Clinical evaluation is unacceptable.
Study Design
Total Participants: 830
Treatment Group(s): 1
Primary Treatment: Anti-PD-1 monoclonal antibody
Phase: 3
Study Start date:
April 01, 2019
Estimated Completion Date:
December 01, 2024
Study Description
Connect with a study center
the First Affiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang 310003
ChinaActive - Recruiting

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