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Clinical Trial NCT07501650 for Head and Neck Cancer, Head and Neck Small Cell Carcinoma, Metastatic Head and Neck Cancer, Recurrent Head and Neck Cancer is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
Thomas Jefferson UniversityPembrolizumab Plus Ultrasound-Induced Microbubble Cavitation in Head and Neck Cancer Phase 1 6 Overall Survival
Feasibility Trial of Pembrolizumab Plus Ultrasound-Induced Microbubble Cavitation in Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma
- iRISID-2025-0984
- JT 45752 (Other Identifier) (JeffTrial Number)
Pembrolizumab
Pembro
Microbubble
Cavitation
| Participant Group/Arm | Intervention/Treatment |
|---|---|
ExperimentalArm 1: Pembro + Ultrasound-Induced Microbubble Cavitation Treatment will be administered on an outpatient basis. 200 mg Pembrolizumab + 3 mL Definity infusions will be administered by nurses at Thomas Jefferson University every 3 weeks for up to 3 cycles. The first cycle will take 60 minutes, while the subsequent infusions should take half an hour to complete. | Pembrolizumab Pembrolizumab will be administered intravenously at a dose of 200 mg every 3 weeks for up to 3 cycles Definity Definity will be administered intravenously during each treatment cycle to facilitate ultrasound-induced microbubble cavitation. Ultrasound-Induced Microbubble Cavitation Therapeutic Ultrasound will be applied to the tumor site during and following the Definity infusion to induce microbubble cavitation using modified ultrasound parameters. |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Number of Participants who complete all planned treatment cycles | The number of participants who completed trial procedures among at least 80 percent of patients, among patients with recurrent or metastatic head and neck squamous cell carcinoma. | Up to 9 weeks |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Number of Treatment-Related Adverse Events (TRAEs) | Number of adverse events related to study treatment, assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) v5.0. | Up to 6 months post-treatment |
Objective Response Rate using RECIST v1.1 | Objective Response Rate (ORR) will be assessed using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0). The number of participants who achieve a Complete Response (CR)-disappearance of all target lesions, Partial Response (PR)-at least a 30% reduction in tumor size from baseline, Progressive Disease (PD)--At least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study, and Stable Disease (SD)--Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, will be reported. ORR measured using the RECISTv1.1 criteria or assessment of clinical and pathologic response. | Up to 3 months after last treatment |
Overall Survival | Time from treatment start until death from any cause. | 90 days after last dose |
Disease-Free Survival | Time from treatment start until recurrence of disease or death from any cause, whichever occurs first. | 90 days after last dose |
Progression-Free Survival | Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions | 90 days after last dose |
Individuals must meet all of the following inclusion criteria in order to be eligible to participate in the study:
Pathologically confirmed, HPV-negative, R/M HNSCC per American Joint Committee on Cancer (AJCC) 8th Edition Staging Criteria, with CPS score > 1
The target lesion is ultrasound-accessible, biopsy-accessible, and measurable in at least one dimension, based on RECISTv1.1 criteria.
Male or female, aged ≥18 years of age
ECOG Performance status 0-2.
Must have a life expectancy of at least 6 months as judged by the treating physician.
Adequate organ function:
- Absolute neutrophil count 1500/μl or more;
- Platelets 100,000/μl or more,
- Hemoglobin 8 g/dl or more;
- Bilirubin less than or equal to 1.5 x the upper limit of normal (except subjects with Gilbert syndrome, who can have total bilirubin <3 mg/dl);
- AST and ALT less than or equal to 2.5x the upper limit of normal
Women of reproductive potential should have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG), which must also be confirmed as negative within 28 days of the start of study drugs.
Women of reproductive potential must use highly effective contraception methods to avoid pregnancy for 90 days after the last dose of study drugs. "Women of reproductive potential" is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy, tubal ligation, or bilateral oophorectomy) or who is not postmenopausal. Menopause is defined clinically as 12 months of amenorrhea in a woman over 45 in the absence of other biological or physiological causes. In addition, women under the age of 55 must have a documented serum follicle stimulating hormone (FSH) level less than 40 mIU/mL.
Men of reproductive potential who are sexually active with women of reproductive potential must use any contraceptive method with a failure rate of less than 1% per year. Men who are receiving the study medications will be instructed to adhere to contraception for 90 days after the last dose of study drugs. Men who are azoospermic do not require contraception.
Informed Consent: All subjects must be able to comprehend and sign a written informed consent document.
An individual who meets any of the following criteria will be excluded from participation in this study:
Patients with HPV-positive or p16-positive SCC
Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or antiCTLA-4 antibody
Any history of allergy to the study drug components, including to polyethyleneglycol or medications containing polyethylene glycol.
Patients with the following cardiac conditions or history:
- Patients with a known history of anatomic right-to-left, bi-directional, or transient right-to-left cardiac shunts
- Patients with NYHA class III or greater heart failure, unstable anginal syndrome, or experiencing active chest pain.
- Uncontrolled arterial hypertension (defined as systolic blood pressure ≥ 200 mmHg or diastolic blood pressure ≥ 110 mmHg) or arterial hypotension (defined as systolic blood pressure ≤ 90 mmHg)
- Patients who have experienced a STEMI or NSTEMI within the last 6 months
- QTc >500 as determined by Fridericia correction
- Patients with a history of ventricular arrhythmia that has not been corrected by placement of a PPM or ICD
Any concurrent malignancies: exceptions include- cutaneous basal cell carcinoma, chronic lymphocytic leukemia, melanoma in situ, squamous cell carcinoma of the skin of a secondary location, superficial bladder cancer or in situ cervical cancer that has undergone potentially curative therapy. Patients with a history of other prior malignancy must have been treated with curative intent and must have remained disease-free for 2 years post-diagnosis.
Any unresolved toxicity CTCAEv5.0 Grade ≥2 from previous anticancer therapy with the exception of alopecia, vitiligo, and the laboratory values defined in the inclusion criteria. Patients with Grade ≥2 neuropathy will be evaluated on a caseby-case basis after consultation with the Study Physician. Patients with irreversible toxicity not reasonably expected to be exacerbated by treatment with anti-PD-1 therapy may be included only after consultation with the Study Physician.
Any subjects with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 28 days of study drug administration., or a prior history of allogenic organ transplantation.
Any active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
Patients must not be receiving any other investigational agents; must not have participated in a study of an investigational agent or be using an investigational device within 4 weeks of the first dose of Pembrolizumab plus Definity.
Receipt of a live attenuated vaccine within 30 days prior to the first dose of drug on trial.
Uncontrolled intercurrent illness, including but not limited to, ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.
Patients must not be pregnant or breastfeeding.
Active infection including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and TB testing in line with local practice), hepatitis B (known positive HBV surface antigen (HBsAg) result), hepatitis C, or human immunodeficiency virus (positive HIV 1/2 antibodies). Patients with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody \[anti-HBc\]and absence of HBsAg) are eligible. Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCVRNA.
Any untreated metastasis(es) to the brain that may be considered active.
History of pneumonitis within the past 5 years.
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