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Study identifier: NCT03808337 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Investigating the Effectiveness of Stereotactic Body Radiotherapy (SBRT) in Addition to Standard of Care Treatment for Cancer That Has Spread Beyond the Original Site of Disease

Condition: Triple Negative Breast Cancer · Non Small Cell Lung Cancer · Metastatic Breast Cancer  ·  Sponsor: Memorial Sloan Kettering Cancer Center

PhasePhase 2
Planned participants145
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is being done to determine if stereotactic body radiotherapy (SBRT) when delivered to all sites of disease in participants with 1-5 metastases will increase the length of time before participants' disease gets worse.

This description comes directly from the study's public registry record.

Talk to the study team

Amy Xu, MD, PhD  ·  646-888-6863  ·  xua@mskcc.org

Wanqing Zhi, MD, PhD  ·  631-623-4246  ·  zhiw@mskcc.org

Always discuss trial participation with your own doctor first.

Locations (12)

Natera, Inc. (Data and Specimen Analysis Only)San Carlos, California, United StatesNot Yet Recruiting
Hartford HealthcareHartford, Connecticut, United StatesRecruiting
WCHN Norwalk Hospital - Data CollectionNorwalk, Connecticut, United StatesRecruiting
Baptist Alliance - McIMiami, Florida, United StatesRecruiting
Memorial Sloan Kettering Basking RidgeBasking Ridge, New Jersey, United StatesRecruiting
Memorial Sloan Kettering MonmouthMiddletown, New Jersey, United StatesRecruiting
Memorial Sloan Kettering BergenMontvale, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Cancer Center @ CommackCommack, New York, United StatesRecruiting
Memorial Sloan Kettering WestchesterHarrison, New York, United StatesRecruiting
Memorial Sloan Kettering Cancer CenterNew York, New York, United StatesRecruiting
Memorial Sloan Kettering NassauUniondale, New York, United StatesRecruiting
Lehigh Valley Health NetworkAllentown, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT03808337