What this study is
Participants will have a confirmed diagnosis of metastatic breast cancer and will receive pembrolizumab in combination with ablation (cryoablation or histotripsy) OR pembrolizumab alone. Participants will be randomly assigned.
What's being tested
- Pembrolizumab
Intervention · DRUG
Participants will receive Pembrolizumab as part of standard of care treatment.
- Cryoablation
Intervention · DEVICE
Cryoablation is a type of thermal ablation that is a minimally invasive alternative technique to surgical resection.
- Histotripsy
Intervention · DEVICE
Histotripsy of the liver is a noninvasive, nonthermal ablation technique that employs high intensity focused ultrasound pulses to mechanically disrupt targeted hepatic tissues- typically liver tumors-via a process known as acoustic cavitation.
Study details
- Official title
- Does Ablation (Cryoablation or Histotripsy) Boost Immune Response Improving the Benefits of Pembrolizumab in Patients With Metastatic or Locally Advanced Triple Negative Breast Cancer?
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Conditions
- Metastatic Breast Cancer · Breast Cancer · Breast Cancer Stage IV · Triple Negative Breast Cancer · Triple Negative Breast Neoplasms · Metastatic Triple-Negative Breast Carcinoma · Locally Advanced Breast Cancer · Locally Advanced Triple-Negative Breast Carcinoma
- Enrolling
- 30 people
- Starts
- 2024-01-29
- Est. completion
- 2027-01-29
- Design
- Open-label, randomized, parallel groups, Phase 1
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Patients ≥ 18 years of age
- Confirmed histologic diagnosis of metastatic TNBC or locally advanced inoperable TNBC
- 1 site amenable cryoablation of at least 1.5 cm in size as determined by an Interventional Radiologist. Eligible cryoablation sites include (but not limited to) soft tissue, liver, lung, and bone as determined by an Interventional Radiologist to be safest and most feasible.
- Physically fit (clinically eligible) to undergo ablation as per usual clinical practice
- Per clinical guidelines, women of childbearing age should use effective contraception during treatment with pembrolizumab and for at least 4 months after the last dose of the drug, which will be assessed and monitored by, and the responsibility of, the patient's medical oncologist (not study investigators or research team) as pembrolizumab is standard of care. Memorial Sloan Kettering Cancer Center Pregnancy Standards will be followed prior to ablation. That is, female patients that are 11-50 years of age and of childbearing potential will undergo a pregnancy test within 2 weeks (15 days) before ablation. Pregnancy test will not be required in patients with bilateral oophorectomy, bilateral salpingectomy, bilateral salpingectomy-oophorectomy, hysterectomy, menopause (no menses ≥ 1 year prior to treatment or after completion of all treatment), or surgical sterilization (i.e. tubal ligation or blockage), with documentation of permanent exemptions in CIS ("Pregnancy Testing Exemption").
- Pembrolizumab therapy (200 mg every 3 weeks) planned as part of standard of care as first, second, or third line of therapy
- Eligible for PD-1 inhibitor per the patient's medical oncologist, with planned treatment with PD-1 inhibitor per the patient's medical oncologist. Additional systemic therapy is per the patient's medical oncologist. The following systemic therapy will be accepted (the timing of the systemic therapy relative to pembrolizumab and ablation is not restricted):; Capecitabine (Xeloda, available as a generic drug); Carboplatin (Paraplatin, available as a generic drug); Cisplatin (Platinol, available as a generic drug); Cyclophosphamide (Cytoxan, available as a generic drug); Docetaxel (Taxotere); Doxorubicin (Adriamycin, available as a generic drug); Pegylated liposomal doxorubicin (Doxil); Epirubicin (Ellence, available as a generic drug); Eribulin (Halaven); Fluorouracil (5-FU, Adrucil, available as a generic drug); Gemcitabine (Gemzar, available as a generic drug); Ixabepilone (Ixempra); Methotrexate (available as a general drug); Nab-paclitaxel (Abraxane); Paclitaxel (Taxol, available as a generic drug); Vinorelbine (Navelbine, available as a generic drug)
You can't join if
- Patient not eligible for PD-1 inhibitor per the patient's medical oncologist
- No disease amenable for ablation
- Pembrolizumab therapy not planned as part of standard of care
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (7)
7 openContact for every open site
- Yolanda Bryce, MD · Contact212-639-6530
Memorial Sloan Kettering Cancer Center at Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey, United States
RecruitingMemorial Sloan Kettering Monmouth (Limited protocol activities)
Middletown, New Jersey, United States
RecruitingMemorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey, United States
RecruitingMemorial Sloan Kettering Suffolk-Commack (Limited Protocol Activities )
Commack, New York, United States
RecruitingMemorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York, United States
RecruitingMemorial Sloan Kettering Cancer Center (All protocol activites)
New York, New York, United States
RecruitingMemorial Sloan Kettering Nassau (Limited Protocol Activites)
Rockville Centre, New York, United States
Recruiting
Study team
Sponsor
Memorial Sloan Kettering Cancer Center
Study ID 23-390
Principal investigator
Yolanda Bryce, MD
Memorial Sloan Kettering Cancer Center
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.