Overview

Stereotactic Radiotherapy in Locally Advanced Pancreatic Cancer With Different Biological Effective Doses

Status:
Recruiting
Trial end date:
2023-10-01
Target enrollment:
0
Participant gender:
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/A
Accepts Healthy Volunteers?
No
Details
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