Neoadjuvant Neratinib in Stage I-III HER2-Mutated Lobular Breast Cancers
Anatomic Stage I Breast Cancer, Anatomic Stage II Breast Cancer, Anatomic Stage III Breast Cancer
About this trial
This is an interventional treatment trial for Anatomic Stage I Breast Cancer
Eligibility Criteria
Inclusion Criteria: Each patient will be entered into this study only if all of these criteria are met: Subjects aged 18 years or older at signing of informed consent. New diagnosis of clinical stage I-III HR+ histologically-proven (i.e. absent or decreased e-cadherin expression) invasive lobular carcinoma Synchronous breast tumors are permitted as long as the synchronous tumor is ER+ and HER2-negative. ER+ disease defined as ≥1% estrogen receptor (ER) positive consistent with current American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) or European Society of Medical Oncology (ESMO) guidelines) At the time of screening, histologically confirmed cancers in patients with previously documented activating HER2 mutation (see Appendix A) confirmed by a Clinical Laboratory Improvement Amendments (CLIA)-certified or equivalent laboratory. Archival tissue availability (if not available a fresh tumor biopsy will be required) and subject must agree to submission of sample for central testing Minimum tumor size of ≥1.5 cm by US, mammogram, MRI imaging, or clinical breast exam ECOG performance status 0 or 1 Patients must have adequate hematologic, hepatic, and renal function. All laboratory tests must be obtained within 1 month of study entry. This includes: Estimated glomerular filtration rate of ≥50 mL/min Albumin ≥ 2.5 g/dL ANC ≥1500/mm^3 Platelet count ≥100,000/mm^3 HgB ≥ 9 g/dL Total serum bilirubin ≤ 1.5 x ULN (in patients with known Gilbert Syndrome, a total bilirubin ≤ 3.0 x ULN, with direct bilirubin ≤ 1.5 x ULN) AST and ALT ≤ 3 x ULN Pre-, peri-, or post-menopausal, confirmed by history or laboratory testing as needed Diagnostic biopsy tissue availability with sufficient tumor to permit NGS (if not available, a fresh biopsy will be required) No prior treatment for current diagnosis of breast cancer For patients who are not postmenopausal (women) or surgically sterile (absence of ovaries and/or uterus or vasectomy), agreement to remain abstinent or to use two adequate methods of contraception (e.g., condoms, diaphragm, vasectomy/vasectomized partner, tubal ligation), during the treatment period and for at least 30 days after the last dose of study treatment. Hormone based oral contraceptives are not allowed on study. Postmenopausal is defined as: Age ≥ 55 years Age ≤ 55 years and amenorrheic for 12 months in the absence of chemotherapy, tamoxifen, toremifene, or ovarian suppression; or follicle stimulating hormone and estradiol in the postmenopausal range. Exclusion Criteria: Evidence of distant metastatic disease Synchronous breast cancer that is estrogen receptor negative OR HER2-amplified OR requires treatment with neoadjuvant chemotherapy per the judgement of the treating physician Patients harboring ineligible somatic HER2 mutations, such as those that are subclonal in nature or those resulting in the expression of truncated proteins including alterations that result in premature stop codon or a change in reading frame (ie, frame shift mutations). Prior endocrine therapy for breast cancer within the last 2 years Women who are pregnant, are planning to become pregnant, or are breast-feeding Any investigational treatment for the current diagnosis of breast cancer HER2 amplification by FISH (HER2:CEP17 ratio >2.0) or IHC (HER2 (3+) Hepatic function impairment as defined by AST or ALT > 3x ULN OR total serum bilirubin > 1.5 (in patients with known Gilbert syndrome, a total bilirubin of > 3.0 x ULN or direct bilirubin > 1.5 x ULN) Significant chronic gastrointestinal disorder with diarrhea as a major symptom (eg, Crohn's disease, malabsorption, or Grade ≥2 National Cancer Institute [NCI] Common Terminology Criteria for Adverse Events Version 4.0 [CTCAE version 4.0] diarrhea of any etiology at baseline. Evidence of significant medical illness, abnormal laboratory finding, or psychiatric illness/social situations that could, in the Investigator's judgment, make the patient inappropriate for this study. Known hypersensitivity to any component of the investigational product, required combination therapy, or loperamide. Unable or unwilling to swallow tablets. Unable or unwilling to complete study procedures such as research biopsies or imaging Any medical condition that in the judgement of the co-investigator would impair the patient's ability to complete the planned study therapy
Sites / Locations
- Emory University/ Winship Cancer Institute
- University of Pittsburgh Medical Center
- Vanderbilt University/Ingram Cancer Center
- University of Texas, Southwestern
- Baylor College of Medicine
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Treatment A (endocrine therapy)
Treatment B (endocrine therapy, neratinib)
Patients receive standard of care endocrine therapy over 4 weeks for 1 cycle. Patients undergo breast tissue biopsy during the lead-in window/cycle 1. Patients then endocrine therapy and neratinib PO daily for 20 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo breast surgery during weeks 24-25. Patients undergo collection of blood samples every 4 weeks while on treatment, at weeks 4 and 24, and at time of surgery. Patients undergo mammogram, ultrasound, or breast MRI prior to surgery.
Patients receive standard of care endocrine therapy and neratinib PO over 4 weeks for 1 cycle. Patients undergo breast tissue biopsy during the lead-in window/cycle 1. Patients then continue endocrine therapy and neratinib PO daily for 20 weeks in the absence of disease progression or unacceptable toxicity. Patients undergo breast surgery during weeks 24-25. Patients undergo collection of blood samples every 4 weeks while on treatment, at weeks 4 and 24, and at time of surgery. Patients undergo mammogram, ultrasound, or breast MRI prior to surgery.