Overview
Stereotactic Radiotherapy in Locally Advanced Pancreatic Cancer With Different Biological Effective Doses
Status:
Recruiting
Recruiting
Trial end date:
2023-10-01
2023-10-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of this study is to compare the safety and efficacy of SBRT in LAPC with different biological effective dose (BED) (60-70Gy Vs.>70Gy ) , to identify a dose range that could achieve better survival benefit and minimize the toxicity of radiotherapy.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Changhai Hospital
Criteria
Inclusion Criteria:- 18≤Age≤75 years
- Cytologically or histologically verified pancreatic adenocarcinoma or clinically
diagnosed as pancreatic cancer by multidisciplinary consultation
- locally advanced pancreatic cancer (LAPC)
- SBRT was not preceded by any targeted antitumor therapy
- ECOG 0-1
- Written informed consent according to ICH/GCP regulations before registration and
prior to any trial specific procedures
Exclusion Criteria:
- Patients who have previously received related treatment because of pancreatic
adenocarcinoma, such as radiotherapy, chemotherapy or focal treatment
- Patients with severe liver or kidney dysfunction
- Patients with obstructive jaundice
- Patients with mass ascites
- Patients participated in other clinical trials for less than three months
- Patients with other malignancies, or acute or other severe infections, with ulcerative
colitis, inflammatory bowel disease, ect
- Unsuitable to participate in this clinical trial judged by the investigator