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NCT07578116RecruitingPhase 3

Adding Surgery and Radiation to the Usual Treatment for HER2-Positive Breast Cancer That Had Already Spread at Diagnosis

Randomized Phase III Trial of Multimodality Therapy Versus Standard of Care Systemic Therapy in HER2 Positive (HER2+) De Novo (AJCC Stage IV) Oligometastatic Breast Cancer With Response to Initial Chemotherapy

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

This phase III trial evaluates the effect of adding locoregional therapy (surgery and radiation) and metastasis-directed stereotactic body radiation therapy (SBRT) to standard systemic therapy following standard HER2-targeted systemic therapy, compared to standard systemic therapy alone, in treating patients with HER2-positive stage IV breast cancer that has spread from where it first started (primary site) to other places in the body (metastatic) or to a limited number of sites (oligometastatic). The usual approach for patients with (oligo)metastatic HER2-positive breast cancer is systemic drug treatment, which means medicines that travel through the whole body to treat both the breast and any areas where the cancer has spread. There are a number of approved HER2-targeted systemic therapy regimens available to patients. These typically include immunotherapy and/or chemotherapy. Immunotherapy drugs may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Unlike systemic therapy, locoregional therapies like surgery and radiation are focused treatments at the site of disease, delivered with the intent of sparing healthy tissues. Breast surgeries such as breast conserving therapy or total mastectomy are procedures in which the cancerous breast tissue (and healthy breast tissue in the case of total mastectomy) are surgically removed from the body. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors. SBRT is a type of external radiation therapy that uses special equipment to position a patient and precisely deliver radiation to tumors in the body (except the brain). The total dose of radiation is divided into smaller doses given over several days. This type of radiation therapy helps spare normal tissue. Adding locoregional therapy, as well as metastasis-directed SBRT, to standard systemic therapy may help patients with (oligo)metastatic, HER2-positive stage IV breast cancer live longer overall or before their cancer progresses, and may help more patients achieve no evidence of disease, when compared to standard systemic therapy alone.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
562 (estimated)
First submitted
4 May 2026
Start date
Mar 2027
Primary completion date
May 2032
Lead sponsor
SWOG Cancer Research Network
NCT number
NCT07578116

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 562
  • From Mar 2027 to the primary completion date, May 2032
  • 59 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • REGISTRATION STEP 1 - SCREENING \& INITIAL TREATMENT:
  • Participants must have histologically confirmed de novo metastatic (i.e. American Joint Committee on Cancer \[AJCC\] stage IV, no prior history of breast cancer) HER2+ breast cancer with 1 to 5 distant metastatic lesions (oligometastatic). Metastatic breast cancer must be histologically confirmed through biopsy of a distant metastatic lesion unless it is not feasible or safe to biopsy a metastatic lesion, then there must be unequivocal evidence of metastasis on imaging and laboratory studies. HER2+ status must be confirmed in the breast tumor and distant metastatic site as defined per NCCN guidelines version 4.2025
    • NOTE: If HER2 positivity at metastatic site is equivocal due to limitations in HER2 analysis in bone, or it is not feasible or safe to biopsy the metastatic lesion, then HER2 positivity based on breast tumor only is acceptable. If there is no breast lesion, HER2+ must be confirmed in at least one metastatic site
  • Participants with brain metastases are eligible if they meet all of the following criteria at baseline:
    • There are 5 or fewer intracranial lesions
    • Each intracranial lesions is no larger than 2cm in longest dimension
    • NOTE: The brain is counted as 1 distant site towards the oligometastatic definition. Brain imaging is not required for participants who have no neurological signs or symptoms suggestive of central nervous system (CNS) involvement; however, assessment of neurological symptoms and brain MRI is strongly encouraged to rule out CNS disease
  • Participants must have no known leptomeningeal disease
  • Participants must meet one of the following criteria prior to Step 1 registration:
    • Treatment naïve and planning to initiate standard of care systemic HER2+ targeted treatment OR
    • Have already initiated standard of care systemic HER2+ targeted treatment and have completed at least one (≥ 1) but no more than three (≤ 3) cycles prior to enrollment, without progression
    • NOTE: Standard of care scans for baseline disease assessment must have been performed within 28 days prior to initiation of treatment
  • Participants must not be receiving or planning to receive any investigational systemic therapy during study before disease progression
  • Participants must not have received whole brain irradiation
    • NOTE: Participants with up to five brain metastases may have received SRS/SRT either before or after initiation of systemic therapy. If lesions are small and asymptomatic and the participant is receiving CNS penetration they may be managed with observation
  • Participants must be ≥ 18 years old at the time of registration
  • Participants must have Zubrod performance status of 0-2
  • Participants with known human immunodeficiency virus (HIV)-infection must be on effective anti-retroviral therapy and have undetectable viral load test on the most recent test results obtained within 6 months prior to registration
  • Participants must be able to safely receive the physician's choice of standard of care systemic HER2+ targeted treatment per the current Food and Drug Administration (FDA)-approved package insert(s), treating physician's discretion, and institutional guidelines
  • Participants must be candidates for definitive surgical and radiotherapeutic management of locoregional disease opinion per the discretion of the treating physician
  • Participants must be able to receive ablative dose stereotactic body radiation therapy (SBRT) to all metastatic lesions identified at baseline, in the opinion of the treating physician
  • Participants must be offered the opportunity to participate in specimen banking
  • NOTE: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system
    • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines For participants with impaired decision-making capabilities, legally authorized representatives may sign and give informed consent on behalf of study participants in accordance with applicable federal, local, and CIRB regulations
  • REGISTRATION STEP 2 - COHORT ASSIGNMENT AND RANDOMIZATION:
  • COHORT A: Participants must be registered to Step 2 within 14 days of staging scans performed after completing Step 1 systemic therapy
  • COHORT A: Participants must have standard of care (SOC) staging scans and breast imaging performed following 12-24 weeks (minimum of 4 cycles) of initial systemic therapy and within 14 days prior to Step 2 registration
  • COHORT A: Participants must have experienced partial or complete response in the breast (in the opinion of the treating physician) following 12-24 weeks of initial systemic therapy based on staging scans performed within 14 days prior to Step 2 registration
    • Participants with breast lesion(s) at diagnosis must have a clinical response on breast imaging per the treating physician
    • Metastatic lesions, as assessed by Response Evaluation Criteria in Solid Tumors (RECIST) and bone response criteria, must have at least stable disease
    • Brain metastases treated with SRS/SRT must have at least stable disease as per Response Assessment in Neuro-Oncology Brain Metastases (RANO BM) and must not require steroid treatment
    • Participants with no known breast lesions at diagnosis must have at least partial response in the metastatic sites as assessed by RECIST and bone response criteria
    • NOTE: The same imaging modality must be used as in Step 1
  • COHORT A: Participants must be eligible for definitive surgical and radiotherapeutic management of locoregional disease per the discretion of the treating physician
  • COHORT A: Participants must not have metastatic lesions that are not amenable to ablative dose stereotactic body radiation therapy (SBRT)
    • Lung lesions that completely resolve after systemic therapy will not be targeted with SBRT, as it is not possible to achieve dose build-up
    • The development of new sclerotic bone lesions after systemic therapy is not to be interpreted as disease progression, and all such lesions should be targeted with SBRT
  • COHORT B: Participants must be registered to Step 2 within 14 days of staging scans performed after completing Step 1 systemic therapy
  • COHORT B: Participants must have standard of care (SOC) staging and breast imaging performed following 12-24 weeks (minimum of 4 cycles) of initial systemic therapy and within 14 days prior to Step 2 registration
  • COHORT B: Participants must experience clinically stable disease or progression following 12-24 weeks (minimum of 4 cycles) of initial systemic therapy and within 14 days prior to Step 2 registration
    • Participants must have progression in metastatic lesions as assessed by RECIST and bone response criteria or may have stable disease in metastatic lesions by RECIST and bone response criteria if there is progression or no clinical response in the breast
    • Participants with known breast lesion must have progression or no clinical response on breast imaging as per the treating physician
    • NOTE: The same modality must be used as in Step 1

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (59)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesRecruiting
OSF Saint Joseph Medical Center
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BloomingtonUnited StatesRecruiting
Illinois CancerCare-Canton
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CantonUnited StatesRecruiting
Saint Francis Medical Center
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Cape GirardeauUnited StatesRecruiting
Illinois CancerCare-Carthage
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CarthageUnited StatesRecruiting
Mercy Cancer Center-West Lakes
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CliveUnited StatesRecruiting
Baptist Memorial Hospital and Cancer Center-Collierville
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ColliervilleUnited StatesRecruiting
Baptist Memorial Hospital and Cancer Center-Golden Triangle
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ColumbusUnited StatesRecruiting
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesRecruiting
Decatur Memorial Hospital
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DecaturUnited StatesRecruiting
Smilow Cancer Hospital-Derby Care Center
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DerbyUnited StatesRecruiting
Mercy Medical Center - Des Moines
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Des MoinesUnited StatesRecruiting
Iowa Methodist Medical Center
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Des MoinesUnited StatesRecruiting
Broadlawns Medical Center
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Des MoinesUnited StatesRecruiting
Illinois CancerCare-Eureka
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EurekaUnited StatesRecruiting
Smilow Cancer Hospital Care Center-Fairfield
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FairfieldUnited StatesRecruiting
Illinois CancerCare-Galesburg
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GalesburgUnited StatesRecruiting
Smilow Cancer Hospital Care Center at Greenwich
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GreenwichUnited StatesRecruiting
Baptist Cancer Center-Grenada
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GrenadaUnited StatesRecruiting
Smilow Cancer Hospital Care Center - Guilford
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GuilfordUnited StatesRecruiting
Smilow Cancer Hospital-Hamden Care Center
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HamdenUnited StatesRecruiting
NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro
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JonesboroUnited StatesRecruiting
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesRecruiting
Illinois CancerCare-Macomb
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MacombUnited StatesRecruiting
Bon Secours Memorial Regional Medical Center
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MechanicsvilleUnited StatesRecruiting
Baptist Memorial Hospital and Cancer Center-Memphis
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MemphisUnited StatesRecruiting
Bon Secours Saint Francis Medical Center
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MidlothianUnited StatesRecruiting
Baptist Memorial Hospital and Cancer Center-Union County
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New AlbanyUnited StatesRecruiting
Smilow Cancer Center/Yale-New Haven Hospital
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New HavenUnited StatesRecruiting
Yale University
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New HavenUnited StatesRecruiting
Yale-New Haven Hospital North Haven Medical Center
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North HavenUnited StatesRecruiting
Cancer Care Center of O'Fallon
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O'FallonUnited StatesRecruiting
HSHS Saint Elizabeth's Hospital
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O'FallonUnited StatesRecruiting
Orlando Health Cancer Institute
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OrlandoUnited StatesRecruiting
Illinois CancerCare-Ottawa Clinic
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OttawaUnited StatesRecruiting
Baptist Memorial Hospital and Cancer Center-Oxford
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OxfordUnited StatesRecruiting
Illinois CancerCare-Pekin
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PekinUnited StatesRecruiting
Illinois CancerCare-Peoria
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PeoriaUnited StatesRecruiting
OSF Saint Francis Radiation Oncology at Peoria Cancer Center
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PeoriaUnited StatesRecruiting
OSF Saint Francis Medical Center
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PeoriaUnited StatesRecruiting
Illinois CancerCare-Peru
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PeruUnited StatesRecruiting
Thomas Jefferson University Hospital
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PhiladelphiaUnited StatesRecruiting
Illinois CancerCare-Princeton
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PrincetonUnited StatesRecruiting
Bon Secours Saint Mary's Hospital
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RichmondUnited StatesRecruiting
Bon Secours Cancer Institute at Reynolds Crossing
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RichmondUnited StatesRecruiting
Springfield Clinic
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SpringfieldUnited StatesRecruiting
Southern Illinois University School of Medicine
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SpringfieldUnited StatesRecruiting
Springfield Memorial Hospital
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SpringfieldUnited StatesRecruiting
Smilow Cancer Hospital Care Center at Long Ridge
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StamfordUnited StatesRecruiting
Smilow Cancer Hospital-Torrington Care Center
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TorringtonUnited StatesRecruiting
Smilow Cancer Hospital Care Center-Trumbull
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TrumbullUnited StatesRecruiting
Illinois CancerCare - Washington
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WashingtonUnited StatesRecruiting
Smilow Cancer Hospital-Waterbury Care Center
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WaterburyUnited StatesRecruiting
Smilow Cancer Hospital Care Center - Waterford
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WaterfordUnited StatesRecruiting
Lexington Health
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West ColumbiaUnited StatesRecruiting
Mercy Medical Center-West Lakes
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West Des MoinesUnited StatesRecruiting
Smilow Cancer Hospital Care Center - Westerly
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WesterlyUnited StatesRecruiting
Ascension Via Christi Hospitals Wichita
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WichitaUnited StatesRecruiting
Asplundh Cancer Pavilion
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Willow GroveUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.