Neoadjuvant Endocrine Therapy in Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Node-Negative Breast Cancer

Medical College of Wisconsin

Status and phase: Completed; Phase 2

Conditions: Breast Cancer; Invasive Breast Cancer

Treatments: Drug: Letrozole; Drug: Tamoxifen; Drug: Exemestane; Drug: Anastrozole

Study type: Interventional

Funder types: Other

Identifiers

NCT03219476

PRO30178

Details and patient eligibility

About

This is an exploratory interventional study that initiates standard-of-care anti-estrogen treatment preoperatively for four weeks.

Full description

STUDY RATIONALE: Patients with hormone receptor (HR)+, HER2- node-negative breast cancers generally undergo surgical resection upfront, followed by adjuvant chemotherapy, if needed, in addition to adjuvant endocrine therapy. Because endocrine therapy is primarily delivered in the postoperative setting, the ability to assess the tumor response to this treatment modality is lost and very difficult to assess. This study offers the unique opportunity to assess the responsiveness of breast tumors to endocrine therapy while the tumors are still in vivo by treating patients with endocrine therapy before surgery and assessing molecular changes with treatment. By comparing pre- and post-treatment levels of molecular markers in individual tumors, the team expects to identify predictors of responsiveness to existing agents and identify new candidate therapeutic targets.

PRIMARY OBJECTIVE: The primary objective is to determine the frequency of increased HER family of receptor tyrosine kinases protein expression in tumors, following treatment with neoadjuvant endocrine therapy and their correlation with Ki-67 tumor responses. The team will measure cancer cell protein levels of growth factor receptors of the human epidermal growth factor receptor (HER) family before and after neoadjuvant endocrine therapy. The data will be used to inform a future randomized trial of combined endocrine and the most promising anti-HER targeted therapy.

Enrollment: 37 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Female; age ≥18 years.

• Pathologically proven diagnosis of invasive breast cancer, clinically stage I-II.

• Clinically lymph node negative, confirmed by clinical exam and/or ultrasound imaging.

• Estrogen- and/or progesterone-receptor-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.

• HER2/neu must be negative by immunohistochemistry (IHC) or fluorescence in situ hybridization (FISH).

• Eastern Cooperative Oncology Group (ECOG) performance status 0-2.

• Pretreatment evaluations (minimum diagnostic workup) within 28 days prior to study

• Qualify for anti-endocrine treatment (per medical oncologist).

• Informed consent provided.

• If history of contralateral breast cancer, patient completed all treatment two years prior

• No treatment for this breast cancer or any malignancy within two years (except non-melanomatous skin cancer, carcinoma in situ of the cervix and contralateral breast cancer)

• Using adequate methods of contraception; negative pregnancy test.

• No strong CYP2D6 inhibitors.

• Adequate organ function with baseline lab values.

  • Absolute neutrophil count (ANC) ≥ 1500/µL.
  • Hemoglobin (Hb) ≥ 9g/dL.
  • Platelet count ≥ 100,000/µL.
  • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3x upper limit of normal (ULN).
  • Serum bilirubin within ≤ 1.5 x ULN.

Exclusion criteria

• American Joint Committee on Cancer (AJCC) clinical T4, N1-3 or M1, breast cancer.
• Synchronous non-breast malignancy (exceptions include non-melanomatous skin cancer, carcinoma in situ of the cervix).
• Purely noninvasive breast cancer (i.e., ductal carcinoma in situ, lobular carcinoma in situ).
• Men with breast cancer.
• Medical, psychiatric or other condition that would prevent the patient from receiving the protocol therapy or providing informed consent.
• Pregnant or lactating women.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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37 participants in 1 patient group

Neoadjuvant endocrine therapy treatment (physician's choice)

Experimental group

Description:

Once enrolled, patients would be treated with the current standard-of-care endocrine therapy. Choice of endocrine therapy (aromatase inhibitors or tamoxifen) would be decided by medical oncologist, following a review of the patient's medical history and menstrual status. The patient would be treated with endocrine therapy in a neoadjuvant setting for four weeks, with dosing continuing until surgery.

Treatment:

Drug: Anastrozole

Drug: Exemestane

Drug: Tamoxifen

Drug: Letrozole