Ignite Creation Date:
2024-05-06 @ 7:49 PM
Last Modification Date:
2024-10-26 @ 3:15 PM
Study NCT ID:
NCT06154967
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-12-04
First Post:
2023-11-23
Brief Title:
To Explore the Effect of Immune-induced Stereotactic Body Radiotherapy SBRT on Reversing Immunoresistance in Stage IIIcIV Non-small Cell Lung Cancer NSCLC
Sponsor:
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Organization:
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Study Overview
Official Title:
To Explore the Effect of Immune-induced Stereotactic Body Radiotherapy SBRT on Reversing Immunoresistance in Stage IIIcIV Non-small Cell Lung Cancer NSCLC
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn about in describe participant population The main questions it aims to answer are
the outcomes of the efficacy ORR and safety adverse events including irAEs AE SAEs and laboratory indicators of continued immunotherapy in patients with immune-resistant IIIcIV metastatic NSCLC treated with immune-induced radiotherapy SBRT
Participants will be asked to accept the treatment of ICIs regimen and SBRT plan as follows
ICIs regimen tislelizumab 200mg every 3 weeks the first dose was given 7 days after the last SBRT treatment then the first day of each cycle 21 days as a cycle until disease progression
SBRT plan The radiation dose and fractionation of SBRT should be evaluated according to the size and location of the tumor
the outcomes of the efficacy ORR and safety adverse events including irAEs AE SAEs and laboratory indicators of continued immunotherapy in patients with immune-resistant IIIcIV metastatic NSCLC treated with immune-induced radiotherapy SBRT
Participants will be asked to accept the treatment of ICIs regimen and SBRT plan as follows
ICIs regimen tislelizumab 200mg every 3 weeks the first dose was given 7 days after the last SBRT treatment then the first day of each cycle 21 days as a cycle until disease progression
SBRT plan The radiation dose and fractionation of SBRT should be evaluated according to the size and location of the tumor
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None