RECRUITING

A Vaccine (MV-s-NAP) for the Treatment of Patients with Invasive Metastatic Breast Cancer

Conditions

Anatomic Stage IV Breast Cancer AJCC V8 Invasive Breast Carcinoma Metastatic Breast Adenocarcinoma Recurrent Breast Carcinoma Stage IV Breast Cancer AJCC V6 and V7

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This phase I trial investigates the side effects and best dose of using a modified measles virus, MV-s-NAP, in treating patients with invasive breast cancer that has spread to other places in the body (metastatic). Both the unmodified vaccination measles virus (MV-Edm) and this modified virus (MV-s-NAP) have been shown to multiply in and destroy breast cancer cells in the test tube and in research mice. MV-s-NAP has been altered by having an extra gene (piece of deoxyribonucleic acid \[DNA\]) so that virus can make a protein called helicobacter pylori neutrophil activating protein (NAP) which is normally expressed in inflammatory reactions. Monitoring blood, urine, tissue, and throat swab samples, and using imaging tests may help to determine whether MV-s-NAP has any impact on the amount of disease present in metastatic breast cancer patients.

Official Title

Phase I Trial of Intratumoral Administration of a Measles Virus Derivative Expressing the Helicobacter Pylori Neutrophil-Activating Protein (NAP) (MV-s-NAP) in Patients with Metastatic Breast Cancer

Quick Facts

Study Start:2020-09-23

Study Completion:2027-08-15

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT04521764

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Age \>= 18 years * COHORT 1 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented estrogen receptor (ER)/progesterone receptor (PR) /HER2 status and radiographic evidence of distant metastatic disease * COHORT 2 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented ER/PR/HER2 status and radiographic evidence of distant metastatic or recurrent disease * COHORT 1 ONLY: Radiographic evidence of distant metastatic disease (using 7th edition American Joint Committee on Cancer \[AJCC\] criteria) with two discrete sites of measurable disease * COHORT 2 ONLY: Radiographic evidence of distant metastatic or recurrent disease (using 8th edition AJCC criteria) with at least one site of measurable disease * Prior therapies: * Patients with ER/PR positive, HER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease and no longer be candidates for standard endocrine therapy or combination of endocrine therapy with other agents such as CDK4/6 inhibitors * Patients with HER2 positive breast cancer irrespective of ER/PR status must have received or no longer be candidates for HER2 directed therapy with trastuzumab or pertuzumab * Patients with ER/PR/HER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease * COHORT 1: At least one site of recurrent/metastatic disease that measures \> 1 cm in greatest dimension (\> 2 cm for lung lesions) and is amenable to safe percutaneous intratumoral administration of MV-s-NAP as determined by an interventional radiologist * COHORT 2: At least 1 site of recurrent/metastatic disease measuring \> 1 cm in greatest dimension \[\> 2 cm for lung lesions\] (Note that if the lesion injected in cycle 1 is not amenable to re-injection, another lesion could be selected for injection * Absolute neutrophil count (ANC) \>= 1500/uL (=\< 7 days prior to registration) * Platelets (PLT \>= 100,000/uL) (=\< 7 days prior to registration) * Total bilirubin =\< institutional upper limit of normal (=\< 7 days prior to registration) * Aspartate aminotransferase (AST) =\< 2 x upper limit of normal (ULN) (=\< 7 days prior to registration) * Creatinine =\< 1.5 x ULN (=\< 7 days prior to registration) * Hemoglobin \>= 9.0 g/dL (=\< 7 days prior to registration) * Negative pregnancy test done =\< 7 days prior to registration (for women of childbearing potential only) * Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2 * Ability to provide informed written consent * Willingness to return to the Mayo Clinic enrolling institution for follow-up * Willingness to provide biologic samples for correlative research purposes * Life expectancy \>= 12 weeks * Concomitant administration of a bone modifying agent (e.g., zoledronic acid or denosumab) is permitted for the prevention or management of skeletal related events in patients with bone metastases and documentation of tolerability with prior exposures	* Known standard therapy for the patient's disease that is potentially curative or definitely capable of extending life expectancy * Clinical or radiographic suspicion of impending visceral crisis due to invasion or compression by tumor * Active infection =\< 5 days prior to registration * History of other malignancy =\< 5 years except for non-melanoma skin cancer or carcinoma in situ of the cervix * Any of the following prior therapies: * Chemotherapy =\< 3 weeks prior to registration * Immunotherapy =\< 4 weeks prior to registration * HER2 directed therapy =\< 3 weeks prior to registration * Targeted therapy =\< 2 weeks prior to registration (e.g., CDK4/6 inhibitors, everolimus) * Investigational agent =\< 4 weeks prior to registration * Any viral or gene therapy prior to registration * Failure to fully recover from acute, reversible effects of prior systemic therapy regardless of interval since last treatment * New York Heart Association classification III or IV, known symptomatic coronary artery disease, or symptoms of coronary artery disease on systems review, or known cardiac arrhythmias (atrial fibrillation or supraventricular tachycardia \[SVT\]) * Untreated or progressive central nervous system (CNS) metastases * NOTE: Patients with a history of treated brain metastases (surgical resection, whole brain radiation, and/or stereotactic radiosurgery) are eligible only if they are asymptomatic and have stable MRI scans for 3 consecutive months, including \< 28 days of study entry * Standing requirement for blood product support * Human immunodeficiency virus (HIV) positive test result or history of other immunodeficiency * History of organ transplantation * History of chronic hepatitis B or C * Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (utilized for a non-Food and Drug Administration \[FDA\]-approved indication and in the context of a research investigation) * Any concurrent medications that the principal investigator determines could interfere with the trial * Treatment with oral/systemic corticosteroids, with the exception of topical or inhaled steroids * Exposure to household contacts =\< 15 months old or household contact with known immunodeficiency * Allergy to measles vaccine or history of severe reaction to prior measles vaccination * History of receiving the measles vaccination with the "killed vaccine" between 1963-1967 without subsequent re-immunization (2 doses) with the active, live vaccination."

Inclusion Criteria

Exclusion Criteria

* Age \>= 18 years
* COHORT 1 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented estrogen receptor (ER)/progesterone receptor (PR) /HER2 status and radiographic evidence of distant metastatic disease
* COHORT 2 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented ER/PR/HER2 status and radiographic evidence of distant metastatic or recurrent disease
* COHORT 1 ONLY: Radiographic evidence of distant metastatic disease (using 7th edition American Joint Committee on Cancer \[AJCC\] criteria) with two discrete sites of measurable disease
* COHORT 2 ONLY: Radiographic evidence of distant metastatic or recurrent disease (using 8th edition AJCC criteria) with at least one site of measurable disease
* Prior therapies:
* Patients with ER/PR positive, HER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease and no longer be candidates for standard endocrine therapy or combination of endocrine therapy with other agents such as CDK4/6 inhibitors
* Patients with HER2 positive breast cancer irrespective of ER/PR status must have received or no longer be candidates for HER2 directed therapy with trastuzumab or pertuzumab
* Patients with ER/PR/HER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease
* COHORT 1: At least one site of recurrent/metastatic disease that measures \> 1 cm in greatest dimension (\> 2 cm for lung lesions) and is amenable to safe percutaneous intratumoral administration of MV-s-NAP as determined by an interventional radiologist
* COHORT 2: At least 1 site of recurrent/metastatic disease measuring \> 1 cm in greatest dimension \[\> 2 cm for lung lesions\] (Note that if the lesion injected in cycle 1 is not amenable to re-injection, another lesion could be selected for injection
* Absolute neutrophil count (ANC) \>= 1500/uL (=\< 7 days prior to registration)
* Platelets (PLT \>= 100,000/uL) (=\< 7 days prior to registration)
* Total bilirubin =\< institutional upper limit of normal (=\< 7 days prior to registration)
* Aspartate aminotransferase (AST) =\< 2 x upper limit of normal (ULN) (=\< 7 days prior to registration)
* Creatinine =\< 1.5 x ULN (=\< 7 days prior to registration)
* Hemoglobin \>= 9.0 g/dL (=\< 7 days prior to registration)
* Negative pregnancy test done =\< 7 days prior to registration (for women of childbearing potential only)
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
* Ability to provide informed written consent
* Willingness to return to the Mayo Clinic enrolling institution for follow-up
* Willingness to provide biologic samples for correlative research purposes
* Life expectancy \>= 12 weeks
* Concomitant administration of a bone modifying agent (e.g., zoledronic acid or denosumab) is permitted for the prevention or management of skeletal related events in patients with bone metastases and documentation of tolerability with prior exposures

* Known standard therapy for the patient's disease that is potentially curative or definitely capable of extending life expectancy
* Clinical or radiographic suspicion of impending visceral crisis due to invasion or compression by tumor
* Active infection =\< 5 days prior to registration
* History of other malignancy =\< 5 years except for non-melanoma skin cancer or carcinoma in situ of the cervix
* Any of the following prior therapies:
* Chemotherapy =\< 3 weeks prior to registration
* Immunotherapy =\< 4 weeks prior to registration
* HER2 directed therapy =\< 3 weeks prior to registration
* Targeted therapy =\< 2 weeks prior to registration (e.g., CDK4/6 inhibitors, everolimus)
* Investigational agent =\< 4 weeks prior to registration
* Any viral or gene therapy prior to registration
* Failure to fully recover from acute, reversible effects of prior systemic therapy regardless of interval since last treatment
* New York Heart Association classification III or IV, known symptomatic coronary artery disease, or symptoms of coronary artery disease on systems review, or known cardiac arrhythmias (atrial fibrillation or supraventricular tachycardia \[SVT\])
* Untreated or progressive central nervous system (CNS) metastases
* NOTE: Patients with a history of treated brain metastases (surgical resection, whole brain radiation, and/or stereotactic radiosurgery) are eligible only if they are asymptomatic and have stable MRI scans for 3 consecutive months, including \< 28 days of study entry
* Standing requirement for blood product support
* Human immunodeficiency virus (HIV) positive test result or history of other immunodeficiency
* History of organ transplantation
* History of chronic hepatitis B or C
* Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (utilized for a non-Food and Drug Administration \[FDA\]-approved indication and in the context of a research investigation)
* Any concurrent medications that the principal investigator determines could interfere with the trial
* Treatment with oral/systemic corticosteroids, with the exception of topical or inhaled steroids
* Exposure to household contacts =\< 15 months old or household contact with known immunodeficiency
* Allergy to measles vaccine or history of severe reaction to prior measles vaccination
* History of receiving the measles vaccination with the "killed vaccine" between 1963-1967 without subsequent re-immunization (2 doses) with the active, live vaccination."

Contacts and Locations

Study Contact

Clinical Trials Referral Office

CONTACT

855-776-0015

mayocliniccancerstudies@mayo.edu

Principal Investigator

Siddhartha Yadav, MD

PRINCIPAL_INVESTIGATOR

Mayo Clinic in Rochester

Study Locations (Sites)

Mayo Clinic in Rochester

Rochester, Minnesota, 55905

United States

Collaborators and Investigators

Sponsor: Mayo Clinic

Siddhartha Yadav, MD, PRINCIPAL_INVESTIGATOR, Mayo Clinic in Rochester

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-09-23

Study Completion Date2027-08-15

Study Record Updates

Study Start Date2020-09-23

Study Completion Date2027-08-15

Terms related to this study

Additional Relevant MeSH Terms

Anatomic Stage IV Breast Cancer AJCC V8
Invasive Breast Carcinoma
Metastatic Breast Adenocarcinoma
Recurrent Breast Carcinoma
Stage IV Breast Cancer AJCC V6 and V7