RecruitingNCT06774027

Prospective Registry of ADC as First- and Second-line Treatment for Breast Cancer

ENCORE: Multicenter ProspectivE Registry of Sequential ANtibody Drug COnjugates (ADCs) in HER2 Negative Metastatic BREast Cancer (MBC)


Sponsor

University of California, San Francisco

Enrollment

100 participants

Start Date

Oct 8, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

Antibody-drug conjugates (ADCs) have demonstrated substantial improvement in progression free survival (PFS) and overall survival (OS) in phase III clinical trials in patients with metastatic triple negative breast cancer (mTNBC) and hormone receptor positive/HER2 negative (HR+/HER2-) metastatic breast cancer (MBC), offering an effective new treatment strategy. Several outstanding questions drive the decision to use ADC drugs clinically. This is a prospective, multi-site observational study of patients with metastatic breast cancer (mBC) who are being treated with FDA-approved antibody drug conjugates (ADCs) as part of routine care and aims to collect real-world data to evaluate the impact of ADC treatment as part of routine care.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This registry is tracking real-world outcomes for people with advanced breast cancer who are receiving a class of drugs called antibody-drug conjugates (ADCs) — targeted medicines that deliver chemotherapy directly to cancer cells. The study aims to understand how well these treatments work and in which patients. **You may be eligible if...** - You are 18 years or older with advanced (metastatic) breast cancer - You have hormone-receptor-positive/HER2-negative breast cancer, or triple-negative breast cancer - You are starting or continuing treatment with an FDA-approved ADC as part of standard care - You are willing to provide tumor tissue and blood samples at several points during the study - Your life expectancy is at least 3 months **You may NOT be eligible if...** - You are not receiving an ADC as part of your current treatment plan - You are unwilling or unable to provide tissue and blood samples Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURESpecimen collection

Blood specimens will be collected during regular clinical visits for correlative and exploratory analysis

DRUGNon-Investigational Antibody-Drug Conjugates (ADC)

ADC given under usual care for the treatment of cancer

OTHERMedical Record Review

Prospective and retrospective medical chart reviews will be conducted to obtain data for analysis.


Locations(1)

University of California, San Francisco

San Francisco, California, United States

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NCT06774027


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