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Combined Immunotherapies in Metastatic ER+ Breast Cancer

NCT04563507

This study is recruiting at 3 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

Women with Hormone Receptor (HR)+ Human Epidermal growth factor Receptor (HER)2- metastatic breast cancer are eligible to a randomized trial. Patients receiving standard first line therapy for metastatic HR+ Breast cancer(BC) (letrozole+palbociclib) are randomly assigned to also receive Stereotactic Body Radiation Therapy(SBRT) to each metastatic lesion.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Breast Cancer

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 to 90 years
Sex
Female
Healthy volunteers
Not accepted
Sponsor
Weill Medical College of Cornell University
Last updated on ClinicalTrials.gov
December 15, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

New York · 3

  • Brooklyn Methodist Hospital - NewYork Presbyterian · New York, NY
  • New York Presbyterian Hospital - Queens · New York, NY
  • Weill Cornell Medicine · New York, NY

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.