SBRT and Anti-programmed Cell Death Protein 1(Anti-PD-1) in Late Stage or Recurrent Pancreatic Cancer Patients (CISPD-2)
Study on the Safety and Therapeutic Effect of Stereotactic Body Radiotherapy and Anti-PD-1 Antibody in Late Stage or Recurrent Pancreatic Cancer Patients Who Failed in Second-line Chemotherapy
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Contact
Study Contact
- Name: Yiwen Chen, MD
- Phone Number: +8615088682641
- Email: cherry0705@zju.edu.cn
Study Contact Backup
- Name: Qi Zhang, MD
- Phone Number: +8613858108798
- Email: zhangqi86@gmail.com
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China, 310000
- The Second Affiliated Hospital of Zhejiang University
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 1.≥18 years.
- 2.Histopathology or cytology confirmed pancreatic cancer.
- 3.Patients failed in second-line chemotherapy: patients have failed in gemcitabine-based chemotherapy and also failed in fluorouracil-based chemotherapy (like FOLFIRINOX), failed in combination of chemotherapy and radiotherapy; patients may have failed in immune therapy (including anti-PD-1 antibody).
- 4. Eastern cooperative oncology group physical fitness score was 0~2.
5. The main organs are functional and meet the following criteria (Routine blood tests were in accordance with the following criteria):
- White blood cell (WBC) ≥3.5 x 10^6 /L, neutrophil >1.5 x10^9/L,
- platelet (PLT) ≥50 x10^9/L,
- hemoglobin (HB) ≥80 g/L,
- total bilirubin (TB) ≤1.5 x ULN (upper limit of normal value). 5)Alanine transaminase (ALT) and aspartate aminotransferase (AST) ≤ 2 x ULN (upper limit of normal value) (if there is liver metastasis, ≤ 5 x ULN).
6) Serum creatinine (Scr) ≤ 1.5 x ULN 7) Albumin (ALB) ≥ 3 g/dL.
- 6. Patients will be informed consent, and understand and are willing to cooperate with the trial and sign related documents.
Exclusion Criteria:
- 1. In the first 4 weeks before the start of the study, they took part in other drug clinical trials.
- 2. Before the start of the study, they were diagnosed as immune deficiency diseases or need systemic steroid therapy.
- 3. In the first 4 weeks before the start of the study, they took anti-tumor immune therapy; or didn't recovery from the adverse effects caused by the anti-tumor immune therapy.
- 4. In the first 2 weeks before the start of the study, they took chemotherapy, small molecule targeting therapy, and radiotherapy; or didn't recovery from the adverse effects caused by these therapies.
- 5. Has had active tuberculosis before.
- 6. Has a history of malignant tumor, except for basal and skin squamous cell carcinoma, cervical carcinoma in situ and papillary thyroid carcinoma.
- 7. Has central nervous system metastasis or meningeal metastasis.
- 8. Has serious and uncontrollable internal diseases such as severe diabetes, severe hypertension, serious infection, congestive heart failure, ventricular fibrillation, coronary heart disease with obvious symptoms or myocardial infarction in the past 6 months.
- 9. Has blood precancerous diseases, such as myelodysplastic syndrome.
- 10. Has clinically relevant or preexisting interstitial lung diseases, such as noncommunicable pneumonia or pulmonary fibrosis, or evidence of interstitial lung diseases on baseline chest CT scans or chest x-rays.
- 11. Past or physical examinations have found diseases of the central nervous system, with the exception of those that have been adequately treated (such as primary brain tumors, uncontrolled seizures or strokes with standard medication).
- 12. Has preexisting neuropathy at > level 1 (NCI CTCAE).
- 13. Allotransplantation requires immunosuppression therapy or other major immunosuppression therapy.
- 14. Has a severe open wound, ulcer, or fracture.
- 15. Systemic treatment is required for autoimmune diseases that have been active for the past 2 years.Alternative therapies are not systemic treatments.
- 16. Has a history of non-infectious pneumonia requiring steroid therapy or active pneumonia.Has interstitial lung disease.
- 17. Patients with active infections require systemic treatment.
- 18. Patients with active hepatitis b or c are not included in liver lesions SBRT.
- 19. Has vaccinate within 30 days before treatment.Including intranasal influenza vaccines, except seasonal influenza vaccines
- 20. Others: allergic history of similar drugs, pregnancy or lactation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: SBRT and PD-1
Stereotactic body radiotherapy, radiation dose is 40-50 Gy in total.
Intravenous drug of anti-PD-1 antibody, 200mg, once a time, every three weeks.
|
SBRT radiation dose is 40-50 Gy in total.
Other Names:
Intravenous drug of anti-PD-1 antibody, 200mg, once a time, every three weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
overall survival
Time Frame: Up to approximately 12 months
|
The percentage of people still alive for a given period of time after diagnosis
|
Up to approximately 12 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Disease control rate
Time Frame: Up to approximately 12 months
|
Percentage of patients whose cancer doesn't progress after treatment
|
Up to approximately 12 months
|
|
Objective response rate
Time Frame: Up to approximately 12 months
|
Percentage of patients whose cancer shrinks or disappears after treatment
|
Up to approximately 12 months
|
|
Progression-free survival
Time Frame: Up to approximately 12 months
|
The percentage of people does not get worse for a period of time after diagnosis
|
Up to approximately 12 months
|
|
Common Toxicity Criteria for Adverse Effects
Time Frame: Up to approximately 12 months
|
According to Common Toxicity Criteria for Adverse Effects version 4
|
Up to approximately 12 months
|
|
EORTC quality of life questionnaire (QLQ)
Time Frame: Up to approximately 12 months
|
Assessed by the European Organization for Research and Treatment of Cancer Quality of Life
|
Up to approximately 12 months
|
|
Related tumor markers
Time Frame: Up to approximately 12 months
|
Serum level of related tumor markers (like carbohydrate antigen19-9, carcinoembryonic antigen and so on)
|
Up to approximately 12 months
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Tingbo Liang, MD PhD, Second Affiliated Hospital, Zhejiang University School of Medicine
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- CISPD-2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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