Kadcyla And Neratinib for Interception of HER2+ Breast Cancer With Molecular Residual Disease

University Health Network, Toronto

Status and phase

Enrolling

Phase 2

Conditions

Breast Cancer

HER2-positive Breast Cancer

Treatments

Drug: Neratinib

Study type

Interventional

Funder types

Other

Identifiers

NCT05388149

KAN-HER2 MRD (Other Identifier)

22-5307

Details and patient eligibility

About

This is a Phase 2 study for patients with resected Stage I-III HER2+ breast cancer with detected molecular residual disease (MRD+) following standard neoadjuvant and locoregional therapy delivered with curative intent. In this study Patients will be treated with neratinib in addition to their standard T-DM1 adjuvant therapy. Neratinib will be administered orally at a dose of 160 mg daily for up to 12 months, or until the time of clinical recurrence, discontinuation due to toxicity, or withdrawal of consent. This study will have two stages, stage 1 would enroll up to 8 participants to clear the Minimal Residual Disease (MRD) and Stage 2 will enroll up to 5 participants. The purpose of this study is to determine if this study population would have a better outcome from adding neratinib to their standard T-DM1 adjuvant therapy.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female patients ≥ 18 years of age with histologically confirmed, resected HER2 positive stage I-III breast cancer, with residual invasive disease following prior neoadjuvant trastuzumab (+/- pertuzumab)-based chemotherapy.
Receiving adjuvant T-DM1, with evidence of MRD (positive test by Inivata RaDaR) after receiving 2-6 cycles of T-DM1
No contraindications to T-DM1 or neratinib
No clinical or radiographic evidence of recurrent or metastatic disease
Previous Therapy requirements:
- Received 2-6 cycles of trastuzumab-DM1 in the adjuvant setting
- Received min of 12 weeks of endocrine therapy (ER+ patients)
- Adjuvant radiation permitted (minimum 14-day washout required)
- No prior neratinib or other HER2 tyrosine kinase inhibitor
ECOG performance status 0-1.
Patient must have adequate organ function
WOCBP must have a negative serum [beta] HCG test result.
WOCBP must agree to use highly effective contraception
Male participants must agree to use highly effective contraception
Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up.
Signed informed consent

Exclusion criteria

Prior therapy with any HER2 tyrosine kinase inhibitor
Clinical or radiographic evidence of suspected or confirmed metastatic disease.
Previous or concurrent malignancy within 3 years of study entry, with exceptions
Impaired cardiovascular function or clinically significant cardiovascular diseases
Known positive serology for HIV that is not currently controlled with anti-retroviral therapy,
Has a known history of or is positive for active hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive) or hepatitis C (defined as HCV RNA [qualitative] is detected). HBV DNA must be undetectable and HBsAg negative at Screening Visit. Participants who have had definitive treatment for HCV are permitted if HCV RNA is undetectable at Screening Visit.
Impaired gastrointestinal function or disease that may significantly alter the absorption of neratinib
Medical, psychiatric, cognitive, or other conditions that may compromise the patient's ability to understand the patient information, give informed consent, comply with the study protocol, or complete the study.