Cryoablation, Atezolizumab/Nab-paclitaxel for Locally Advanced or Metastatic Triple Negative Breast Cancer
NCT ID: NCT04249167
Last Updated: 2023-01-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
EARLY_PHASE1
INTERVENTIONAL
2020-01-23
2021-11-17
Brief Summary
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Detailed Description
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I. To determine the safety and feasibility of cryoablation of a primary breast tumor followed by PD-L1 blockade in patients with locally advanced or metastatic triple negative breast cancer (TNBC).
SCONDARY OBJECTIVE:
I. To evaluate the systemic immune response to cryoablation of a primary breast tumor and PD-L1 blockade.
OUTLINE:
Patients undergo cryoablation of the primary tumor over about 1 hour. After 2-3 weeks, patients receive atezolizumab intravenously (IV) on days 1 and 15 and nab-paclitaxel IV on days 1, 8, and 15. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 2-3 weeks post surgery and then periodically thereafter.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Treatment (cryoablation, atezolizumab, nab-paclitaxel)
Patients undergo cryoablation of the primary tumor over about 1 hour. After 2-3 weeks, patients receive atezolizumab IV on days 1 and 15 and nab-paclitaxel IV on days 1, 8, and 15. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Atezolizumab
Given IV
Cryosurgery
Undergo cryoablation of the primary tumor
Nab-paclitaxel
Given IV
Interventions
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Atezolizumab
Given IV
Cryosurgery
Undergo cryoablation of the primary tumor
Nab-paclitaxel
Given IV
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Presents with primary breast tumor lesion amenable to cryoablation
* Have at least one additional distant lesion feasible for biopsies
* Agreeable to start on atezolizumab and nab-paclitaxel as per standard of care
* Patients with locally advanced disease must be ineligible for curative surgery for any reason, including but not limited to comorbid status precluding surgery due to safety, unresectability, or patient refusal
* Patient may have received prior systemic chemotherapy regimens
Exclusion Criteria
* History of human immunodeficiency virus (HIV)
* Previous immune checkpoint targeting therapies
* No primary breast lesion amenable for cryoablation due to size (greater than 5 cm) or location (proximity of \< 0.5 cm to the skin or nipple-areola complex)
* Pregnancy
18 Years
FEMALE
No
Sponsors
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National Cancer Institute (NCI)
NIH
Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Emmanuel M Gabriel
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2020-00333
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
19-008704
Identifier Type: OTHER
Identifier Source: secondary_id
MC2031
Identifier Type: -
Identifier Source: org_study_id
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