Chemokine Modulation Therapy and Pembrolizumab in Treating Participants With Metastatic Triple-Negative Breast Cancer
Primary Purpose
Triple -Negative Breast Cancer, Estrogen Receptor Negative, HER2/Neu Negative
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Biopsy
Chemokine Modulation Therapy
Celecoxib
Recombinant Interferon Alfa-2b
Rintatolimod
Pembrolizumab
Sponsored by
About this trial
This is an interventional treatment trial for Triple -Negative Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Have pathologically confirmed diagnosis of unresectable or metastatic TNBC with no curative treatment options
- Have been informed of other treatment options
- Patient has lesion that can be biopsied and is willing to undergo the procedure as part of the protocol
- Have an Eastern Cooperative Oncology Group (ECOG) performance status of =< 1
- Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately
- Ability to swallow and retain oral medication
- Have measurable disease per RECIST 1.1 criteria present
- Any line of therapy allowed, radiologically confirmed progression on prior therapy
- No cancer-directed therapy for at least 3 weeks prior to study treatment (bone-directed therapies are allowed)
- Platelets >= 100,000/uL
- Hemoglobin >= 9.0 g/dL
- Absolute neutrophil count (ANC) >= 1500/uL
- Total bilirubin =< institutional upper limit of normal (ULN)
- Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x institutional ULN
- Creatinine < ULN OR creatinine clearance >= 50 mL/min per Cockcroft-Gault Equation for patients with creatinine levels greater than ULN
- Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
Exclusion Criteria:
- Patients currently treated with systemic immunosuppressive agents, including steroids (> than equivalent of 10 mg daily of prednisone), are ineligible until 3 weeks after removal from immunosuppressive treatment (inhaled steroids are allowed)
- Patients with active autoimmune disease or history of transplantation
- Pregnant or nursing female participants
- Unwilling or unable to follow protocol requirements
- Patients with known serious mood disorders (Major depression diagnosis is an exclusion. Other stable mood disorders on stable therapy for > 6 months or not requiring therapy may be allowed after consultation with PI
- Cardiac risk factors including:
- Patients experiencing cardiac event(s) (acute coronary syndrome, myocardial infarction, or ischemia) within 3 months of signing consent
- Patients with a New York Heart Association classification of III or IV
- History of upper gastrointestinal ulceration, upper gastrointestinal bleeding, or upper gastrointestinal perforation within the past 3 years
- Prior allergic reaction or hypersensitivity to nonsteroidal antiinflammatory drugs (NSAIDs) or any drugs administered on protocol
- Prior immunotherapy with anti-PD1/PDL1 therapy for the mTNBC
- Any condition which in the Investigator's opinion deems the participant an unsuitable candidate to receive study drug
- Any patients with a positive Antinuclear Antibodies test will be excluded from study
Sites / Locations
- Roswell Park Cancer Institute
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment (chemokine modulation therapy)
Arm Description
Participants undergo pre-treatment biopsy. Participants then undergo chemokine modulation therapy consisting of celecoxib PO BID, recombinant interferon alfa-2b IV over 20 minutes, and rintatolimod IV over 30-60 minutes on days -11 to -9, and -4 to -2. Participants then undergo additional biopsy. Following biopsy and chemokine modulation therapy, participants receive pembrolizumab IV over 30 minutes on day 1. Courses repeat every 3 weeks for up to 24 months in the absence of disease progression or unacceptable toxicity.
Outcomes
Primary Outcome Measures
Overall response rate (ORR) as measured by immune-related Response Evaluation Criteria in Solid Tumors (irRECIST) criteria 1.1
Will be assessed using a Simon two-stage minimax design.
Secondary Outcome Measures
Progression-free survival (PFS) as measured by irRECIST 1.1 criteria
Will be assessed using a Simon two-stage minimax design
Overall survival (OS) as measured by irRECIST 1.1 criteria
Disease control rate (DCR) as measured by irRECIST 1.1 criteria
Will be assessed using a Simon two-stage minimax design
Incidence of adverse events graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Adverse events (AEs), serious AEs (SAEs), and toxicities will be summarized by attribution (overall and related/unrelated to treatment) and grade using frequencies and relative frequencies
Full Information
NCT ID
NCT03599453
First Posted
July 16, 2018
Last Updated
July 17, 2023
Sponsor
Roswell Park Cancer Institute
Collaborators
AIM ImmunoTech Inc.
1. Study Identification
Unique Protocol Identification Number
NCT03599453
Brief Title
Chemokine Modulation Therapy and Pembrolizumab in Treating Participants With Metastatic Triple-Negative Breast Cancer
Official Title
Pilot Open Label Clinical Trial Evaluating the Safety and Efficacy of Chemokine Modulation to Enhance the Effectiveness of Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
January 9, 2019 (Actual)
Primary Completion Date
September 2, 2020 (Actual)
Study Completion Date
March 21, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Roswell Park Cancer Institute
Collaborators
AIM ImmunoTech Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot trial studies how well chemokine modulation therapy works when given prior to pembrolizumab in treating participants with triple-negative breast cancer that has spread to other places in the body. Drugs used in chemokine modulation therapy, such as celecoxib, recombinant interferon alfa-2b, and rintatolimod, work by unleashing or enhancing the cancer immune responses that already exist by either blocking inhibitory molecules or by activating stimulatory molecules. Monoclonal antibodies, such as pembrolizumab, may interfere with the ability of tumor cells to grow and spread. Giving chemokine modulation therapy before pembrolizumab may work better in treating participants with metastatic triple-negative breast cancer
Detailed Description
PRIMARY OBJECTIVES:
-To evaluate the increase of CD8+ infiltration into tumor microenvironment after pre-treatment CKM regime
SECONDARY OBJECTIVES:
To evaluate the overall response rate (ORR) to the combination therapy per RECIST v1.1
To evaluate the efficacy of the chemokine modulation (CKM) in combination with pembrolizumab in patients with metastatic triple negative breast cancer (mTNBC) as compared to historic outcomes of pembrolizumab and other anti-PD1/PD-L1 therapies alone, as determined by secondary measures of efficacy including progression-free survival (PFS), overall survival (OS), and disease control rate (DCR).
To evaluate the safety profile of CKM regimen given as pre-treatment to pembrolizumab therapy in metastatic breast cancer patients using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
EXPLORATORY OBJECTIVES:
Examine the immune analysis profile of CKM and pembrolizumab combination.
Examine the relationship of infiltrating CD4+ and CD8+ T cells and other immune and genetic markers, and their associated PD-1, CD45RA or CD45RO levels.
Correlate PD-L1 expression within both neoplastic and nonneoplastic stromal elements of the tumor microenvironment to PFS, OS, ORR and adverse events (AEs).
Correlate Immune Panel results with ORR, PFS, OS and AEs.
Comparison of response assessment criteria for a prospective analysis
OUTLINE:
Participants undergo pre-treatment biopsy. Participants then undergo chemokine modulation therapy consisting of celecoxib orally (PO) twice daily (BID), recombinant interferon alfa-2b intravenously (IV) over 20 minutes, and rintatolimod IV over 30-60 minutes on days -11 to -9, and -4 to -2. Participants then undergo additional biopsy. Following biopsy and chemokine modulation therapy, participants receive pembrolizumab IV over 30 minutes on day 1. After completion of study treatment, participants are followed up for 90 days and then every 6 months for up to 2 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Triple -Negative Breast Cancer, Estrogen Receptor Negative, HER2/Neu Negative, Anatomic Stage IV Breast Cancer AJCC, Progesterone Receptor Negative
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment (chemokine modulation therapy)
Arm Type
Experimental
Arm Description
Participants undergo pre-treatment biopsy. Participants then undergo chemokine modulation therapy consisting of celecoxib PO BID, recombinant interferon alfa-2b IV over 20 minutes, and rintatolimod IV over 30-60 minutes on days -11 to -9, and -4 to -2. Participants then undergo additional biopsy. Following biopsy and chemokine modulation therapy, participants receive pembrolizumab IV over 30 minutes on day 1. Courses repeat every 3 weeks for up to 24 months in the absence of disease progression or unacceptable toxicity.
Intervention Type
Procedure
Intervention Name(s)
Biopsy
Intervention Description
Undergo Biopsy
Intervention Type
Procedure
Intervention Name(s)
Chemokine Modulation Therapy
Intervention Description
Undergo chemokine modulation therapy
Intervention Type
Drug
Intervention Name(s)
Celecoxib
Other Intervention Name(s)
Celebrex, YM 177, Benzenesulfonamide
Intervention Description
Given by mouth
Intervention Type
Biological
Intervention Name(s)
Recombinant Interferon Alfa-2b
Other Intervention Name(s)
Alfatronol, Glucoferon, Heberon Alfa, IFN alpha-2B, Interferon alfa 2b, Intron A, recombinant interferon alfa-2b, Recombinant Interferon Alfa-2b, Sch
Intervention Description
Given intravenously
Intervention Type
Drug
Intervention Name(s)
Rintatolimod
Other Intervention Name(s)
38640-92-5, 616524, Ampligen, Ampligen, Atvogen, Poly(I).Poly(c12,U), Poly(Inosinic Acid) Poly(Cytidylic(12), Uridylic)Acid, RINTATOLIMOD, Rintatolimod
Intervention Description
Given intravenously
Intervention Type
Biological
Intervention Name(s)
Pembrolizumab
Other Intervention Name(s)
Immunoglobulin G4,Keytruda, Lambrolizumab
Intervention Description
Given intravenously
Primary Outcome Measure Information:
Title
Overall response rate (ORR) as measured by immune-related Response Evaluation Criteria in Solid Tumors (irRECIST) criteria 1.1
Description
Will be assessed using a Simon two-stage minimax design.
Time Frame
Up to 2 years
Secondary Outcome Measure Information:
Title
Progression-free survival (PFS) as measured by irRECIST 1.1 criteria
Description
Will be assessed using a Simon two-stage minimax design
Time Frame
Up to 2 years
Title
Overall survival (OS) as measured by irRECIST 1.1 criteria
Time Frame
Up to 2 years
Title
Disease control rate (DCR) as measured by irRECIST 1.1 criteria
Description
Will be assessed using a Simon two-stage minimax design
Time Frame
Up to 2 years
Title
Incidence of adverse events graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Description
Adverse events (AEs), serious AEs (SAEs), and toxicities will be summarized by attribution (overall and related/unrelated to treatment) and grade using frequencies and relative frequencies
Time Frame
Up to 2 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Have pathologically confirmed diagnosis of unresectable or metastatic TNBC with no curative treatment options
Have been informed of other treatment options
Patient has lesion that can be biopsied and is willing to undergo the procedure as part of the protocol
Have an Eastern Cooperative Oncology Group (ECOG) performance status of =< 1
Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately
Ability to swallow and retain oral medication
Have measurable disease per RECIST 1.1 criteria present
Any line of therapy allowed, radiologically confirmed progression on prior therapy
No cancer-directed therapy for at least 3 weeks prior to study treatment (bone-directed therapies are allowed)
Platelets >= 100,000/uL
Hemoglobin >= 9.0 g/dL
Absolute neutrophil count (ANC) >= 1500/uL
Total bilirubin =< institutional upper limit of normal (ULN)
Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x institutional ULN
Creatinine < ULN OR creatinine clearance >= 50 mL/min per Cockcroft-Gault Equation for patients with creatinine levels greater than ULN
Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
Exclusion Criteria:
Patients currently treated with systemic immunosuppressive agents, including steroids (> than equivalent of 10 mg daily of prednisone), are ineligible until 3 weeks after removal from immunosuppressive treatment (inhaled steroids are allowed)
Patients with active autoimmune disease or history of transplantation
Pregnant or nursing female participants
Unwilling or unable to follow protocol requirements
Patients with known serious mood disorders (Major depression diagnosis is an exclusion. Other stable mood disorders on stable therapy for > 6 months or not requiring therapy may be allowed after consultation with PI
Cardiac risk factors including:
Patients experiencing cardiac event(s) (acute coronary syndrome, myocardial infarction, or ischemia) within 3 months of signing consent
Patients with a New York Heart Association classification of III or IV
History of upper gastrointestinal ulceration, upper gastrointestinal bleeding, or upper gastrointestinal perforation within the past 3 years
Prior allergic reaction or hypersensitivity to nonsteroidal antiinflammatory drugs (NSAIDs) or any drugs administered on protocol
Prior immunotherapy with anti-PD1/PDL1 therapy for the mTNBC
Any condition which in the Investigator's opinion deems the participant an unsuitable candidate to receive study drug
Any patients with a positive Antinuclear Antibodies test will be excluded from study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shipra Gandhi, MD
Organizational Affiliation
Roswell Park Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Roswell Park Cancer Institute
City
Buffalo
State/Province
New York
ZIP/Postal Code
14263
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Chemokine Modulation Therapy and Pembrolizumab in Treating Participants With Metastatic Triple-Negative Breast Cancer
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