ETHAN - ET for Male BC

Jose Pablo Leone

Status and phase: Enrolling; Phase 2

Conditions: Male Breast Cancer; Hormone Receptor-positive Breast Cancer; Hormone Receptor Negative Breast Carcinoma

Treatments: Drug: Tamoxifen; Drug: Anastrozole; Drug: Degarelix; Drug: Abemaciclib

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05501704

22-225

Details and patient eligibility

About

This research study is looking to see how well male breast cancer responds to preoperative treatment with endocrine therapy and which endocrine therapy regimen is the most effective treatment for male breast cancer.

The drugs used in this study are:

• Tamoxifen
• Anastrozole
• Degarelix
• Abemaciclib

Full description

This is an open-label, multicenter, randomized trial for men with stage I-III hormone receptor-positive (HR+)/HER2-negative breast cancer. The trial will have two phases: A 3-week window phase containing endocrine therapy followed by a 4-month treatment phase where participants are treated with one of four endocrine therapy treatment combinations.

Tamoxifen is the standard of care for the treatment of breast cancer in men. Anastrozole is a standard treatment in women with breast cancer and works more effectively than tamoxifen. This study hopes to learn if anastrozole may also be effective in men. Given that gonadal suppression and CDK 4/6 inhibitors have both improved treatment in women with breast cancer, the study hopes to learn how the addition of Degarelix (gonadal suppression) and Abemaciclib (CDK 4/6 inhibitors) work in comparison to standard of care tamoxifen.

The research study procedures include screening for eligibility and study treatment including laboratory evaluations and quality of life questionnaires.

After completion of treatment, participants will be followed for up to 10 years

It is expected that about 60 men will take part in this research study.

Eli Lilly, a pharmaceutical company, is supporting this research study by providing one of the study drugs. This study is also being supported by Johns Hopkins University on behalf of the Translational Breast Cancer Research Consortium (TBCRC).

Enrollment: 60 estimated patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Men aged 18 years or older, with diagnosis of invasive breast cancer who have not undergone surgical resection of the primary tumor and axillary nodes.

• Stage I, II, or III per American Joint Committee on Cancer (AJCC) staging 8th edition (112).

• Breast cancer must be hormone receptor-positive and HER2-negative according to definition below assessed by local pathology.

  • Hormone receptor-positive is defined as: positivity for at least one of the hormone receptors (estrogen receptor [ER] or progesterone receptor [PR]) by IHC. ER and PR assays are considered positive if there are > 1% positive tumor nuclei in the samples.
  • HER2-negative is defined per the current American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline (113).

• Patients with multifocal or multicentric disease are eligible if the treating investigator has determined the patient should be treated as ER-positive and HER2-negative.

• Bilateral breast cancers are allowed if the treating investigator has determined the patient should be treated as ER-positive and HER2-negative.

• Patients with a history of ipsilateral or contralateral DCIS or LCIS are eligible.

• ECOG performance status ≤ 2.

• Required laboratory values demonstrating adequate organ function:

  • ANC ≥ 1000/mm3
  • Hemoglobin ≥ 8 g/dl
  • Platelets ≥ 50,000/mm3
  • Serum creatinine ≤ 3.0 x ULN (institutional)
  • Total bilirubin ≤ 2.0 x ULN (institutional).
  • AST and ALT ≤ 5.0 x ULN (institutional)

• Men with partners of childbearing potential must be willing to use one highly effective form of non-hormonal contraception or two effective forms of non-hormonal contraception by the patient and/or partner and continue its use for the duration of the study treatment and for 6 months after the last dose of study treatment.

• Non-English-speaking patients are eligible but will be exempt from patient-completed questionnaires.

• Willing and able to sign informed consent.

• Willing to undergo breast biopsy after completion of window phase.

• Patient is able to swallow oral medications.

Exclusion criteria

• Prior endocrine therapy, chemotherapy, radiation therapy, or investigational therapy for the current breast cancer diagnosis.
• Prior endocrine therapy, systemic therapy, radiation therapy, or investigational therapy for any other malignancy within the past 12 months.
• Diagnosis of inflammatory breast cancer (T4d).
• Other concurrent serious diseases that may interfere with planned treatment, including severe cardiac disease, congestive heart failure (CHF) of New York Heart Association (NYHA) Class III or higher, severe pulmonary conditions/illness, uncontrolled infections.
• The patient has serious and/or uncontrolled preexisting medical condition(s) that, in the judgment of the investigator, would preclude participation in this study (for example, interstitial lung disease, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment [e.g. estimated creatinine clearance <30ml/min], history of major surgical resection involving the stomach or small bowel, or preexisting Crohn's disease or ulcerative colitis or a preexisting chronic condition resulting in baseline Grade 2 or higher diarrhea).
• The patient has active systemic bacterial infection (requiring intravenous [IV] antibiotics at time of initiating study treatment), fungal infection, or detectable viral infection (such as known human immunodeficiency virus positivity or with known active hepatitis B or C [for example, hepatitis B surface antigen positive]. Screening is not required for enrollment.
• The patient has a personal history of any of the following conditions: syncope of cardiovascular etiology, ventricular arrhythmia of pathological origin (including, but not limited to, ventricular tachycardia and ventricular fibrillation), or sudden cardiac arrest.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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60 participants in 7 patient groups

Window Phase Arm A: Tamoxifen

Experimental group

Description:

Participants will be randomly assigned to receive Tamoxifen 1x daily for 3 weeks (21days).

Treatment:

Drug: Tamoxifen

Window Phase Arm B: Anastrozole

Experimental group

Description:

Participants will be randomly assigned to receive Anastrozole 1x daily for 3 weeks (21days).

Treatment:

Drug: Anastrozole

Window Phase Arm C: Anastrozole + Degarelix

Experimental group

Description:

Participants will be randomly assigned to receive Anastrozole 1x daily for 3 weeks (21days) and Degarelix on day 1 only.

Treatment:

Drug: Degarelix

Drug: Anastrozole

Neoadjuvant Phase Arm D: Tamoxifen

Experimental group

Description:

Participants will be randomly assigned to receive Tamoxifen 1x daily for 4 cycles (4 months); each study cycle is 28 days.

Treatment:

Drug: Tamoxifen

Neoadjuvant Phase Arm E: Tamoxifen + Abemaciclib

Experimental group

Description:

Participants will be randomly assigned to receive Tamoxifen 1x daily and Abemaciclib 2x daily for 4 cycles (4 months); each study cycle is 28 days.

Treatment:

Drug: Abemaciclib

Drug: Tamoxifen

Neoadjuvant Phase Arm F: Anastrozole and Degarelix

Experimental group

Description:

Participants will be randomly assigned to receive Anastrozole 1x daily and Degarelix on day 1 of each cycle for 4 cycles (4 months); each study cycle is 28 days.

Treatment:

Drug: Degarelix

Drug: Anastrozole

Neoadjuvant Phase Arm G: Anastrozole + Degarelix + Abemaciclib

Experimental group

Description:

Participants will be randomly assigned to receive Anastrozole 1x daily, Degarelix on day 1 of each cycle and Abemaciclib 2x daily for 4 cycles (4 months); each study cycle is 28 days.

Treatment:

Drug: Abemaciclib

Drug: Degarelix

Drug: Anastrozole