I125 Seed Implantation vs Stereotactic Radiotherapy for Pancreatic Cancer

NCT03964064 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2019-07-19

No results posted yet for this study

Summary

Data of 100 patients with locally advanced pancreatic cancer who received stereotactic radiotherapy or ct-guided radioactive 125I seed implantation in the multicenter of the research group from July 2019 to June 2021 were collected, as well as follow-up data.To evaluate the clinical efficacy of stereotactic radiotherapy and ct-guided 125I seed therapy with 3D printing template in pancreatic cancer;In addition, the local control rate and side effects of ct-guided radioactive 125I particles in the treatment of pancreatic cancer lesions were explored, and the efficacy and safety of different doses of stereotactic radiotherapy were determined.

Conditions

  • Pancreatic Cancer Non-resectable
  • Brachytherapy
  • Radiotherapy

Interventions

RADIATION

Stereotactic Radiotherapy

GTV: Combining localization and fusion images to delineate the tumors seen PTV = GTV + 0-10mm Target volume radiation dose: The range of BED value of radiotherapy was 80-100 when the distance between the tumor and gastrointestinal tract was more than 5 mm (alpha/beta=10) and 60-80 when the distance between the tumor and gastrointestinal tract was less than 5 mm (alpha/beta=10). Normal Tissue Limit: Reference to TG101 Report

RADIATION

3D-printing Template-assisted CT-guided I125 Seed Implantation

CT-guided radioactive 125I particle therapy with 3D printing template for pancreatic cancer Preoperative planning Design and fabrication of 3D-PNCT Particle implantation Postoperative dose assessment: CT scan was performed after operation, and the image was transmitted to BTPS for dose verification . The dosimetric parameters included tumor volume, D90, mPD, V100, V150 and V200.

Sponsors & Collaborators

  • Beijing 302 Hospital

    collaborator OTHER
  • Guangxi Ruikang Hospital

    collaborator OTHER
  • Tengzhou Central People's Hospital

    collaborator OTHER_GOV
  • Peking University Third Hospital

    lead OTHER

Principal Investigators

  • Junjie Wang, Chairman · Peking University Third Hospital

  • Fei Xu · Peking University Third Hospital

  • Xuezhang Duan, Director · Beijing 302 Hospital

  • Kaixian Zhang, Director · Tengzhou Central People's Hospital

  • Zuping Lian, Director · Guangxi Ruikang Hospital

  • Zhe Ji · Peking University Third Hospital

  • Jing Sun · Beijing 302 Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-11
Primary Completion
2021-05-31
Completion
2022-05-01

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03964064 on ClinicalTrials.gov