Pembrolizumab, Decitabine, and Standard Chemotherapy before Surgery in Treating Patients with Locally Advanced HER2-Negative Breast Cancer
- Invasive adenocarcinoma of the breast diagnosed by core needle biopsy
- Breast cancer determined to be HER2-negative per current American Society of Clinical Oncologists/College of American Pathologists (ASCO/CAP) HER2 guidelines (if immunohistochemistry [IHC] was performed, IHC 0 or 1+; if fluorescence in situ hybridization [FISH] or other in situ hybridization test, dual probe HER2/CEP17 ratio < 2.0 with an average HER2 copy number < 4.0 signals/cell)
- Breast cancer determined to be hormone receptor-positive or hormone receptor-negative defined as follows: * Hormone receptor-positive: >= 10% staining by IHC for either estrogen receptor (ER) or progesterone receptor (PgR) * Hormone receptor-negative: < 10% staining by IHC for both ER and PgR
- Locally advanced breast cancer defined as any of the following per American Joint Committee on Cancer (AJCC) staging criteria: Note: imaging methods that may be used for tumor measurement to determine eligibility include breast ultrasound and breast magnetic resonance imaging (MRI); mammography may not be used * T2 based on tumor measurements by physical examination or imaging with clinically positive regional lymph nodes (cN1 or cN2), irrespective of hormone receptor status * Hormone receptor-negative patients with tumor size of 3-5 cm measured by physical examination or imaging with clinically negative regional lymph nodes (cN0) * Any T3 based on tumor measurements by physical examination or imaging, irrespective of hormone receptor status * Any T4 (including inflammatory breast cancer), irrespective of hormone receptor status
- Ipsilateral axillary lymph nodes must be evaluated by MRI or ultrasound within 12 weeks prior to study registration to determine clinical nodal status; if imaging is suspicious or abnormal, a fine needle aspiration (FNA) or core biopsy of the questionable node(s) on imaging is required; nodal status should be classified according to the following criteria: * Nodal status – negative ** Imaging of the axilla is negative; OR ** Imaging of the axilla is suspicious or abnormal AND FNA or core biopsy is negative * Nodal status – positive ** FNA or core biopsy of node(s) is cytologically or histologically suspicious or positive
- Breast imaging performed prior to study registration as follows: * Ipsilateral breast – within 12 weeks * Contralateral breast – within 24 weeks
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Absolute neutrophil count (ANC) >= 1,500/mm^3
- Platelet count >= 100,000/mm^3
- Hemoglobin >= 10.0 g/dL
- Serum creatinine =< upper limit of normal (ULN) for the lab or a calculated creatinine clearance >= 60 mL/min
- Total bilirubin =< ULN for the laboratory
- Aspartate aminotransferase (AST) =< 1.5 x ULN for the laboratory
- Alanine aminotransferase (ALT) =< 1.5 x ULN for the laboratory
- Alkaline phosphatase (ALP) =< 2.5 x ULN for the laboratory * Note: If ALP is > 1.5 x ULN, imaging to rule out bone and liver metastasis is required
- Left ventricular ejection fraction (LVEF) assessment (i.e., 2 dimensional [2-D] echocardiogram or multi-gated acquisition [MUGA] scan) performed within 12 weeks prior to study registration indicates an LVEF >= 50% regardless of the cardiac imaging facility’s lower limit of normal
- Women who are not postmenopausal or have not undergone hysterectomy must have a documented negative serum pregnancy test within 72 hours prior to initiating study treatment; Note: postmenopausal is defined as any of the following: * Age >= 60 years * Age < 60 years and amenorrheic for at least 1 year with follicle-stimulating hormone (FSH) and plasma estradiol levels in the postmenopausal range * Bilateral oophorectomy
- A female patient who is a woman of child-bearing potential (WCBP) and a male patient with a partner who is a WCBP must agree to use a medically accepted method for preventing pregnancy for the duration of immunotherapy and neoadjuvant chemotherapy and until after completion of breast surgery or, for patients who do not receive neoadjuvant chemotherapy, for a minimum of 6 months following the last dose of pembrolizumab or decitabine
- Ability to understand and willingness to sign the consent form
- Breast cancer treatment for the currently diagnosed breast cancer including radiation therapy, chemotherapy, targeted therapy, or endocrine therapy prior to study registration
- Administration of a live vaccine within 30 days prior to initiating study treatment; Note: seasonal influenza vaccines for injection are generally inactivated flu vaccines and are permitted; however, intranasal influenza vaccines (eg, Flu-Mist) are live attenuated vaccines, and are not allowed
- Administration of a monoclonal antibody within 4 weeks prior to initiating study treatment or has not recovered (i.e., =< grade 1 or at baseline) from adverse events (AEs) due to agents administered more than 4 weeks earlier
- Administration of any investigational agent within 4 weeks prior to initiating study treatment
- Evidence of metastatic disease that is extensive enough to preclude consideration of subsequent definitive surgery for the primary tumor
- History of ipsilateral invasive breast cancer or ipsilateral ductal carcinoma in situ (DCIS); Note: patients with history of ipsilateral lobular carcinoma in situ (LCIS) are eligible
- History of solid organ or allogeneic stem cell transplant
- Previous therapy for any malignancy with an anthracycline or taxane for Cohorts A and B and carboplatin for Cohort A
- Cardiac disease that would preclude administration of the drugs included in the study treatment regimen including, but not limited to: * Angina pectoris that requires the current use of anti-anginal medication * Ventricular arrhythmias except for benign premature ventricular contractions * Supraventricular and nodal arrhythmias requiring a pacemaker or not controlled with medication * Conduction abnormality requiring a pacemaker * Valvular disease with documented compromise in cardiac function; and symptomatic pericarditis
- Nervous system disorder (i.e., paresthesia, peripheral motor neuropathy, or peripheral sensory neuropathy) >= grade 2, per Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5.0
- Administration of or condition requiring administration of systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to initiating study treatment; Exception: patients with conditions that can be managed with steroids equivalent to or less than an oral prednisone dose of 10 mg daily would not be excluded from the study
- Previous therapy for this cancer with an anti-PD-1, anti-PD-L1, anti-PD-L2 agent, or any other immunomodulatory agent
- Known or presumed hypersensitivity to decitabine or pembrolizumab (or any of their excipients)
- Diagnosed immunodeficiency, eg, human immunodeficiency virus (HIV)
- Active autoimmune disease requiring systemic treatment within the past 2 years (i.e., with use of disease-modifying agents, corticosteroids, or immunosuppressive drugs) or a documented history of clinically severe autoimmune disease or a syndrome that requires systemic steroids or immunosuppressive agents; Note: patients with the conditions or medical history listed below are NOT excluded from this study * Vitiligo * Resolved childhood asthma/atopy * Requirement for intermittent use of bronchodilators or local steroid injections or topical steroids * Hypothyroidism stable on hormone replacement * Sjogren's syndrome
- Known history or evidence of interstitial lung disease or active, non-infectious pneumonitis
- Known history of active bacillus tuberculosis (TB)
- Active infection requiring systemic therapy
- Known active hepatitis B or C
- Pregnancy or breastfeeding
- Diagnosis or treatment for another malignancy within 5 years prior to study registration, with the following exceptions: complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, any in situ malignancy, and low-risk prostate cancer after curative therapy
- Medical, psychological, or social condition that, in the opinion of the investigator, may increase the patient’s risk or limit the patient’s adherence with study requirements
I. To determine and quantify if treatment with neoadjuvant decitabine followed by pembrolizumab increases lymphocyte infiltration into tumor and/or stroma in patients with locally advanced, HER2-negative breast cancer.
I. To evaluate the safety and toxicity of sequential decitabine plus pembrolizumab followed by dose-dense doxorubicin and cyclophosphamide (AC), weekly paclitaxel (or paclitaxel plus carboplatin) administered as neoadjuvant therapy.
II. To determine if the study treatment increases the proportion of tumors with >= 60% tumor or stromal area infiltrated with lymphocytes (i.e., lymphocyte-predominant breast cancer [LPBC]) in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab.
III. To determine the rate of pathologic complete response (pCR) in the breast and lymph nodes (pCR breast and nodes) in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
IV. To determine the rate of residual cancer burden (RCB) index value of 0-1 following all neoadjuvant therapy in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
V. To determine the rate of clinical complete response in the breast and lymph nodes (clinical complete response [cCR] breast and nodes) following all neoadjuvant therapy in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
VI. To characterize the alteration of T lymphocyte and other host cell infiltration and immune response gene signatures in breast cancers resulting from treatment with decitabine and pembrolizumab in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
VII. To evaluate the correlation of pre-existing and post-immunotherapy immune response signatures with response to neoadjuvant chemotherapy in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
VIII. To correlate the Merck proprietary PD-L1 assay results with response to therapy in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
IX. To evaluate the level of circulating myeloid-derived suppressor cell (MDSC) at baseline, following treatment with decitabine alone, and following treatment with pembrolizumab administered after decitabine in patients with locally advanced, HER2-negative breast cancer who have received neoadjuvant decitabine and pembrolizumab followed by a standard neoadjuvant chemotherapy regimen.
IMMUNOTHERAPY: All patients receive decitabine intravenously (IV) over 60 minutes on days 1-5 and pembrolizumab IV over 30 minutes on days 8 and 22.
NEOADJUVANT CHEMOTHERAPY: Patients are assigned to 1 of 2 cohorts.
COHORT A (TRIPLE NEGATIVE BREAST CANCER [TNBC]): Patients receive doxorubicin hydrochloride IV over 15 minutes and cyclophosphamide IV over 30-60 minutes once every 2 weeks for up to 4 cycles. Patients then receive paclitaxel IV over 60 minutes and carboplatin IV over 30-60 minutes once weekly for 12 weeks. At the treating medical oncologist’s discretion, the paclitaxel regimen may be administered first followed by doxorubicin and cyclophosphamide.
COHORT B (HER2-NEGATIVE, HORMONE RECEPTOR-POSITIVE TUMORS): Patients receive doxorubicin hydrochloride IV over 15 minutes and cyclophosphamide IV over 30-60 minutes once every 2 weeks for up to 4 cycles. Patients then receive paclitaxel IV over 60 minutes once weekly for 12 weeks. At the treating medical oncologist’s discretion, the paclitaxel regimen may be administered first followed by doxorubicin and cyclophosphamide.
SURGERY: Patients undergo either breast-conserving surgery or mastectomy.
After completion of study treatment, patients are followed up for 30 days.
Trial Phase Phase II
Trial Type Treatment
Virginia Commonwealth University / Massey Cancer Center
Harry Douglas Bear
- Primary ID MCC-15-11083
- Secondary IDs NCI-2016-01980, HM20008607
- Clinicaltrials.gov ID NCT02957968