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Clinical Trial Summary

The purpose of this study is to determine whether cytoreduction of bulky metastatic disease using ultra high dose SBRT in combination with immunotherapy is tolerable and feasible In patients who have exhausted SoC treatment options.


Clinical Trial Description

Patients that provide informed consent will undergo a 30-day screening period to determine eligibility for the trial. If eligible, patients will begin treatment on SBRT (delivered to metastases over 3-5 fractions within 1-2 weeks) with concurrent and adjuvant atezolizumab (1680 mg on Day 1 of each 28-day cycle) immunotherapy regimen for up to one year. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06416436
Study type Interventional
Source University of Kansas Medical Center
Contact Nurse Navigator
Phone 913-945-7552
Email CTNurseNav@kumc.edu
Status Not yet recruiting
Phase Phase 1
Start date May 23, 2024
Completion date July 1, 2027

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