Re-irradiation With Stereotactic Body Radiotherapy for Relapsed Pancreatic Cancer
Primary Purpose
Pancreatic Cancer
Status
Active
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Re-irradiation with SBRT
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cancer
Eligibility Criteria
Inclusion Criteria:
- Age≥18
- KPS≥70
- Pancreatic malignancy need to be confirmed by histological or cytological valuation or clinical diagnosis (MDT with typical clinical manifestations, radiological features of pancreatic cancer via MRI and PET-CT).
- Patients were previously treated with SBRT in Shanghai Changhai hospital
- The time from the end of prior SBRT to local recurrence is more than 6 months
- In-field recurrences of pancreatic cancer confirmed by Imaging examinations.
- Blood routine examination: Absolute neutrophil count (ANC) ≥ 1.5 ×10^9/L, leukocyte count≥ 3.5 ×10^9/L, platelets ≥ 70×10^9/L, hemoglobin ≥ 80 g/L
- Blood routine examination: Absolute neutrophil count (ANC) ≥ 1.5 ×10^9/L, leukocyte count≥ 3.5 ×10^9/L, platelets ≥ 70×10^9/L, hemoglobin ≥ 80 g/L
- INR < 2 (0.9-1.1), PPT <1.5 × ULN
- Ability of the research subject or authorized legal representative to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Age<18
- KPS<70
- Prior anti-tumor treatment (surgery, chemotherapy, radiation etc.) for the relapsed pancreatic cancer.
- Evidences of metastatic disease or invasion of the stomach or duodenum confirmed by Imaging examinations.
- The time from the end of prior SBRT to local recurrence is less than 6 months
- Patients with active inflammatory bowel diseases or peptic ulcer
- Gastrointestinal bleeding or perforation within 6 months
- Abnormal results of blood routine examinations and liver and kidney tests
- Female who is pregnant or nursing, or is of childbearing potential and not using a reliable method of contraception
- Patients with a history of any other malignancy (except basal cell carcinoma and carcinoma in situ of cervix)
- Contraindication to SBRT
- Inability of the research subject or authorized legal representative to understand and the willingness to sign a written informed consent document
Sites / Locations
- Huojun Zhang
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Re-irradiation with SBRT
Arm Description
Patients with relapsed pancreatic cancer meeting all inclusion criteria will receive re-irradiation with SBRT.
Outcomes
Primary Outcome Measures
The toxicities following SBRT will be determined.
The toxicities following SBRT will be assessed by CTCAE v4.0
Secondary Outcome Measures
Overall survival
The median survival time will be determined.
Local recurrence-free survival
The local recurrence-free survival will be determined.
Objective response rates
The rate is the ratio of the number of patients with complete remission and partial remission to the total number of enrolled patients.
The quality of life will be analyzed.
The analysis of quality of life is based on QLQ-C30.
The quality of life will be analyzed.
The analysis of quality of life is based on QLQ-PAN26.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02745847
Brief Title
Re-irradiation With Stereotactic Body Radiotherapy for Relapsed Pancreatic Cancer
Official Title
The Safety and Efficacy of Re-irradiation With Stereotactic Body Radiotherapy for Relapsed Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 2016 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Changhai Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The safety and efficacy of re-irradiation with stereotactic body radiotherapy for relapsed pancreatic cancer will be evaluated.
Detailed Description
Pancreatic cancer is one of the most lethal malignant tumors, probably attributable to local recurrence deemed as a predominant factor influencing patients' prognosis and quality of life. Only 15%-20% patients are suitable for surgeries among those first diagnosed with pancreatic cancer and the 5-year survival rate of those patients with R0 resection is still less than 20%. Therefore, radiotherapy is becoming a promising method to improve survival. However, due to adjacent organs at risk, conventional external beam radiotherapy, besides long courses, sometimes results in severe radiation-induced toxicity, delaying the initial of thereafter treatment, such as chemotherapy, which reduces clinical benefits.
A single-fraction dose in the gross tumor volume could be increased stereotactic body radiotherapy (SBRT). Furthermore, doses of organs at risk could also be reduced, thus effectively improving local control rates and reducing radiation related toxicity. Compared with conventional external beam radiotherapy, SBRT is proved to provide longer progression free survival and safe with combination of chemotherapy. Moreover, owing to short courses and low toxicity of SBRT, quality of life is largely improved.
However, it was reported that progression usually occurred 2 years after the initial treatment. The most common failure pattern was local recurrence. Chemotherapy and supportive treatment were commonly used in relapsed pancreatic cancer but with unfavored outcomes. Palliative surgeries are performed in patients with recurrent pancreatic cancer in some studies. Nevertheless, because of bad medical conditions and high complication rates, many patients could not endure surgeries. Therefore, whether patients previously treated with SBRT could be re-irradiated is another challenge in the treatment of pancreatic cancer.
Some studies have confirmed that improved quality of life and longer survival could be available with re-irradiation via SBRT in patients with relapsed pancreatic cancer. Real-time guiding and synchronous tracing of SBRT increase the doses of tumor volumes but decrease doses of organs at risk and toxicity, rendering SBRT as an alternative treatment for relapsed pancreatic cancer. Chris et al. demonstrated that 1-year local control rate was 70% after re-irradiation with SBRT in 14 patients and the toxicity was mild. Nergiz Dagoglu et al. showed that the median overall survival was 14 months and no grade 3, 4 and 5 toxicities occurred.
From 2013-2015, we retrospectively reviewed medical records of 14 patients with relapsed pancreatic cancer re-irradiated with SBRT. All of their tumor markers and pain scores decreased and quality of life improved 3 months after re-irradiation. Hence, based on our experience, we attempt to prospectively evaluate the safety and efficacy of re-irradiation with SBRT for relapsed pancreatic cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Re-irradiation with SBRT
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Re-irradiation with SBRT
Arm Type
Experimental
Arm Description
Patients with relapsed pancreatic cancer meeting all inclusion criteria will receive re-irradiation with SBRT.
Intervention Type
Radiation
Intervention Name(s)
Re-irradiation with SBRT
Intervention Description
Patients previously treated with SBRT with relapsed pancreatic cancer will be re-irradiated with SBRT.
Primary Outcome Measure Information:
Title
The toxicities following SBRT will be determined.
Description
The toxicities following SBRT will be assessed by CTCAE v4.0
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Overall survival
Description
The median survival time will be determined.
Time Frame
3 years
Title
Local recurrence-free survival
Description
The local recurrence-free survival will be determined.
Time Frame
3 years
Title
Objective response rates
Description
The rate is the ratio of the number of patients with complete remission and partial remission to the total number of enrolled patients.
Time Frame
3 years
Title
The quality of life will be analyzed.
Description
The analysis of quality of life is based on QLQ-C30.
Time Frame
3 years
Title
The quality of life will be analyzed.
Description
The analysis of quality of life is based on QLQ-PAN26.
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age≥18
KPS≥70
Pancreatic malignancy need to be confirmed by histological or cytological valuation or clinical diagnosis (MDT with typical clinical manifestations, radiological features of pancreatic cancer via MRI and PET-CT).
Patients were previously treated with SBRT in Shanghai Changhai hospital
The time from the end of prior SBRT to local recurrence is more than 6 months
In-field recurrences of pancreatic cancer confirmed by Imaging examinations.
Blood routine examination: Absolute neutrophil count (ANC) ≥ 1.5 ×10^9/L, leukocyte count≥ 3.5 ×10^9/L, platelets ≥ 70×10^9/L, hemoglobin ≥ 80 g/L
Blood routine examination: Absolute neutrophil count (ANC) ≥ 1.5 ×10^9/L, leukocyte count≥ 3.5 ×10^9/L, platelets ≥ 70×10^9/L, hemoglobin ≥ 80 g/L
INR < 2 (0.9-1.1), PPT <1.5 × ULN
Ability of the research subject or authorized legal representative to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
Age<18
KPS<70
Prior anti-tumor treatment (surgery, chemotherapy, radiation etc.) for the relapsed pancreatic cancer.
Evidences of metastatic disease or invasion of the stomach or duodenum confirmed by Imaging examinations.
The time from the end of prior SBRT to local recurrence is less than 6 months
Patients with active inflammatory bowel diseases or peptic ulcer
Gastrointestinal bleeding or perforation within 6 months
Abnormal results of blood routine examinations and liver and kidney tests
Female who is pregnant or nursing, or is of childbearing potential and not using a reliable method of contraception
Patients with a history of any other malignancy (except basal cell carcinoma and carcinoma in situ of cervix)
Contraindication to SBRT
Inability of the research subject or authorized legal representative to understand and the willingness to sign a written informed consent document
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huo Jun Zhang, MD., PH.D
Organizational Affiliation
Changhai Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Huojun Zhang
City
Shanghai
State/Province
Shanghai
Country
China
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Re-irradiation With Stereotactic Body Radiotherapy for Relapsed Pancreatic Cancer
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