PD-1 +/- IL-4 Inhibition in ER+ Breast Cancer

Trial Title: PD-1 +/- IL-4 Inhibition in ER+ Breast Cancer

NCT ID: NCT05967884

Condition: Breast Cancer

Conditions: Official terms:
Breast Neoplasms
Cemiplimab

Conditions: Keywords:
Window of Opportunity Clinical Trials
cemiplimab
dupilumab

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Arm A: Cemiplimab, Arm B: Cemiplimab + Dupilumab
Description: Arm A: Cemiplimab: 350mg IV x 1 dose administered prior to surgery Arm B: Cemiplimab + Dupilumab: Cemiplimab 350mg IV x 1 dose + Dupilumab 600 mg SC x 1 dose administered prior to surgery
Arm group label: Arm A: Cemiplimab
Arm group label: Arm B: Cemiplimab + Dupilumab

Summary: This proposal is for a Window of Opportunity (WOO) clinical trial using a novel combination of two Health Canada approved agents, cemiplimab (Libtayo) and dupilumab (Dupixent), for off label use in early-stage estrogen receptor positive (ER+) breast cancer.

Detailed description: This is a phase II, open-label, randomized window of opportunity trial evaluating the immunologic effects within the tumour, microenvironment, and host blood of patients treated with either - Arm A: Cemiplimab (n=10) - Arm B: Cemiplimab + Dupilumab (n=10) administered prior to surgery. Randomization will be at 1:1 ratio in patients newly diagnosed with primary operable ER+* HER2- invasive breast cancer awaiting surgery in the next 4-6 weeks who are not planned for neoadjuvant therapy. Primary Hypothesis: In ER+ breast cancer, blockade of IL-4 signalling using dupilumab enhances anti-tumor immunity (through reduced Th2 skewing) when used in combination with PD-1 inhibitors (Cemiplimab) compared to PD-1 inhibition alone in ER+ breast cancer Primary Objective: • To determine whether addition of dupilumab to cemiplimab reduces TH2 skewing of the tumor, tumor microenvironment (TME) and blood in patients with ER+ breast cancer Secondary Objectives: - To evaluate dynamic changes in immune cell populations as measured by in situ proteomics - To characterize the safety of a short-term duration of the combination of dupilumab with cemiplimab in patients with ER+ breast cancer awaiting surgery Exploratory Objective: • To test the effect of tumor PD-1 gene expression and its effect on the immune response in treated and untreated patients This is a window of opportunity trial which will require administration of cemiplimab or combination of cemiplimab + dupilumab prior to surgery. Surgery will be a minimum of 96 hours to 2 weeks after the cemiplimab. Patient follow-up after surgery will be for a period of 30 days post-surgery. Target: 20 patients (10 in Arm A and 10 in Arm B). Accounting for screen failures and withdrawals (20%), 24 patients will be accrued.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Female patients with newly diagnosed histologically confirmed primary invasive breast cancer currently not undergoing any treatment while awaiting surgery. 2. Invasive ductal or lobular carcinoma, invasive carcinoma Not Otherwise Specified (NOS) 3. ER+ breast cancer (1-10%*) of any size. ER positive tumor defined ≥1% positively staining cells by immunohistochemistry, according to the current American Society of Clinical Oncology (ASCO) / College of American Pathologists (CAP) guidelines. 4. The participant is eligible for surgery within the next 4-6 weeks. 5. HER2/neu must be negative by immunohistochemistry (IHC) defined as IHC 0 or 1+ or fluorescence in situ hybridization (FISH) or other ISH methods with a ratio of < 2 according to current ASCO (American Society of Clinical Oncology)/CAP guidelines. 6. Eastern Cooperative Oncology Group (ECOG) performance status 0 to 2. 7. Age ≥18 years. 8. The participant (or legally acceptable representative if applicable) is able to provide written informed consent for the study. Exclusion Criteria: 1. Known or suspected breast cancer metastasized to distant organ (lung, liver, bone, brain, abdomen) 2. Prior therapy with any chemotherapy or endocrine for breast cancer or other cancers within last 3 months 3. Pre-dominant histology other than invasive ductal or lobular carcinoma or invasive carcinoma NOS. 4. Patients with an active infection or an absolute neutrophil count < 1.5 x 10^9/L. 6. Patients with pre-existing renal impairment, Creatinine clearance calculated by Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation of less than 50 mL/min/1.73m2. 7. Known or current history of pneumonitis or interstitial lung disease (e.g., idiopathic pulmonary fibrosis) or pneumonia in past month 8. Has known HIV or active Hepatitis B (e.g., HBV detected by PCR, presence of HBsAg surface antigen and/or Anti-HBc core antigen) or active Hepatitis C (e.g., HCV RNA [qualitative] is detected). Presence of Anti-HBs alone suggesting immunity to Hepatis B is eligible. 9. Any serious known immediate or delayed hypersensitivity reaction(s) to dupilumab and or cemiplimab. 10. Concurrent medical condition requiring the use of systemic immunosuppressive medications, or systemic corticosteroids at doses of greater than 10 mg Prednisone-equivalent. Topical steroids and other localized corticosteroids are permitted. Patients who have received acute, low-dose, systemic immunosuppressant medications equivalent to ≤ 10mg of prednisone within the 7 days prior to study entry (small dose of dexamethasone for nausea, short course for upper respiratory tract infection etc.) may be enrolled in the study. Use of steroids as prophylactic treatment for subjects with contrast allergies to diagnostic imaging contrast dyes will be permitted. 11. Concurrent use or planned use of any forbidden medications within 4 weeks prior to study drug administration, which include chemotherapy, immunotherapy (tumor vaccine, cytokine, or growth factor given to control cancers), other biologic therapy, investigational therapy, or hormonal therapy. 12. Confirmed pregnancy (by pregnancy test) if patient is of childbearing age or breast feeding. 13. Subjects with signs/symptoms suggestive of COVID-19 and confirmed positive COVID-19 test. 14. Eastern Cooperative Oncology Group (ECOG) performance status ≥3 (see Appendix) 15. Any underlying medical condition that, in the Principal Investigator's opinion, will make the administration of study drug hazardous or obscure the interpretation of toxicity determination or adverse events, or renders the patient ineligible to be on study.

Gender: Female

Minimum age: 18 Years

Maximum age: 90 Years

Healthy volunteers: No

Locations:

Facility:
Name: The Ottawa Hospital Research Institute and Cancer Center

Address:
City: Ottawa
Zip: K1Y 4E9
Country: Canada

Contact:
Last name: Angel Arnaout, MD

Phone: 613-798-5555

Phone ext: 79622
Email: aarnaout@toh.on.ca

Facility:
Name: Ontario Institute for Cancer Research

Address:
City: Toronto
Zip: M5G 0A3
Country: Canada

Contact:
Last name: Melanie Spears, PhD
Email: melanie.spears@oicr.on.ca

Investigator:
Last name: Angel Arnaout, MD
Email: Principal Investigator

Start date: August 4, 2023

Completion date: August 1, 2024

Lead sponsor:
Agency: Ottawa Hospital Research Institute
Agency class: Other

Collaborator:
Agency: Ontario Institute for Cancer Research
Agency class: Other

Source: Ottawa Hospital Research Institute

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05967884