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The goal of this clinical trial is to compare the efficacy and safety of neoadjuvant Stereotactic Body Radiotherapy (SBRT) combined with immunochemotherapy versus neoadjuvant immunochemotherapy. The main questions it aims to answer are: Dose SBRT combined with immunochemotherapy improve event-free survival? Is SBRT combined with immunochemotherapy safe enough? Participants will: Receive neoadjuvant SBRT combined with immunochemotherapy or neoadjuvant immunochemotherapy. Tumor assessment will be performed prior to surgery. Surgery will be performed within 4 to 6 weeks (+ 7 days) after completion of the last cycle of immunochemotherapy.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
Start Date
October 15, 2024
Primary Completion Date
January 30, 2027
Completion Date
January 30, 2030
Last Updated
May 29, 2025
360
ESTIMATED participants
Stereotactic body radiotherapy (SBRT)
RADIATION
Tislelizumab
DRUG
Chemotherapy
DRUG
Lead Sponsor
Yang Hong
NCT07486219
NCT06305754
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06987890