Endocrine Therapy in Treating Patients With HER2 Negative, Low Risk Breast Cancer

Fred Hutchinson Cancer Center (FHCC)

Status and phase

Withdrawn

Phase 4

Conditions

Invasive Breast Carcinoma

HER2/Neu Negative

Postmenopausal

Stage IA Breast Cancer

Stage 0 Breast Cancer

Treatments

Other: Quality-of-Life Assessment

Drug: Exemestane

Drug: Tamoxifen Citrate

Other: Questionnaire Administration

Drug: Anastrozole

Other: Laboratory Biomarker Analysis

Drug: Letrozole

Drug: Toremifene Citrate

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT03238703

9764 (Other Identifier)

P30CA015704 (U.S. NIH Grant/Contract)

NCI-2017-00724 (Registry Identifier)

Details and patient eligibility

About

This pilot clinical trial studies how well endocrine therapy works in treating patients with HER2 negative, low risk breast cancer. Estrogen can cause the growth of breast cancer cells. Endocrine therapies such as aromatase inhibitors and selective estrogen receptor modulators may lessen the amount of estrogen made by the body.

Full description

PRIMARY OBJECTIVES:

I. To estimate the conversion rate from a standard low-toxicity approach to guideline-directed therapy which includes surgery +/- radiation therapy as a result of progression of disease or patient/provider choice.

II. To examine factors that might differ between those who convert from the low-toxicity approach to the guideline-directed therapy and those do not convert.

SECONDARY OBJECTIVES:

I. To measure the safety and clinical effectiveness of systemic endocrine therapy used in a prolonged neoadjuvant fashion.

II. To evaluate the impact of risk-stratified care in Quality-Adjusted Life Years (QALY) and QALY gains.

III. To estimate the cost savings of indefinitely delaying surgery and radiation in favor of systemic endocrine therapy alone.

OUTLINE:

Patients receive exemestane orally (PO) once daily (QD), anastrozole PO QD, letrozole PO QD, tamoxifen citrate PO QD, or toremifene citrate PO QD at the discretion of the treating physician. Treatment continues in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up periodically.

Sex

Female

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Able to provide written informed consent
A diagnosis of invasive breast cancer, with or without an in situ component, that is:
- Originally identified by screening mammography
- Characterized by standard diagnostic mammography +/- breast ultrasound
- Clinically node negative
- Confirmed by breast magnetic resonance imaging (MRI) in a facility that maintains active American College of Radiology (ACR) accreditation to be of low clinical stage (=< 2 cm, node negative, unifocal invasive)
- Estrogen receptor (ER) and progesterone receptor (PR) Allred scored, each > 5/8
- Her2 negative using American Society of Clinical Oncology (ASCO)-College of American Pathologists (CAP) guidelines
- ki-67 proliferation scored, < 20%
- Clinical Nottingham grade 1 or 2
- Scored on the MammaPrint 70-gene breast cancer recurrence assay as low risk
Prior to the discovery of the breast cancer, clinically post-menopausal as defined as: i) one or more years from last menses; or ii) history of oophorectomy; or iii) follicle stimulating hormone (FSH) test result in the post-menopause reference range
Willing to accept oral endocrine therapy with a third generation aromatase inhibitor (AI) or selective estrogen receptor modifier (SERM)
Willing to undergo routine surveillance with breast ultrasound and/or mammography

Exclusion criteria

Known contraindication to aromatase inhibitor or SERM therapy
Pregnant at time of or within prior year of diagnosis
Clinically detected or palpable disease prior to biopsy in either breast or ipsilateral axilla
Prior history of invasive breast cancer or ductal breast carcinoma in situ (DCIS)
Prior use of aromatase inhibitor therapy apart from assisted reproduction
Prior use of SERM
Unmanaged/uncontrolled mental health disorder
Life expectancy < 6 months (m) for any cause
Biopsy confirmed multifocal, multicentric, or contralateral disease that is invasive or non-invasive
DCIS with focal invasion

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Treatment (AI, SERM)

Experimental group

Description:

Patients receive exemestane PO QD, anastrozole PO QD, letrozole PO QD, tamoxifen citrate PO QD, or toremifene citrate PO QD at the discretion of the treating physician. Treatment continues in the absence of disease progression or unacceptable toxicity.

Treatment: