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NCT06246968RecruitingPhase 1

A Study of Pembrolizumab and Ablation (Cryoablation or Histotripsy) in People With Breast Cancer

Does Ablation (Cryoablation or Histotripsy) Boost Immune Response Improving the Benefits of Pembrolizumab in Patients With Metastatic or Locally Advanced Triple Negative Breast Cancer?

Source: ClinicalTrials.gov · Last updated 14 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
First submitted
30 Jan 2024
Start date
29 Jan 2024
Primary completion date
29 Jan 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT06246968

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 30
  • From 29 Jan 2024 to the primary completion date, 29 Jan 2027
  • 7 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.

Prior treatment

  • Patient not eligible for PD-1 inhibitor per the patient's medical oncologist
  • Pembrolizumab therapy not planned as part of standard of care

Other illness

  • No disease amenable for ablation

Who the study is looking for

  • 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)

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

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering Cancer Center at Basking Ridge (Limited Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Memorial Sloan Kettering Suffolk - Commack (Limited Protocol Activities)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activites)
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Memorial Sloan Kettering Nassau (Limited Protocol Activites)
Coordinator of this site? Confirm its status
Rockville CentreUnited StatesRecruiting

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