RecruitingPhase 4NCT05809024

Select the Appropriate Population for Adding CDK4/6i to Neoadjuvant Endocrine Therapy

Select the Appropriate Population for Adding CDK4/6i to Neoadjuvant Endocrine Therapy in High Risk Early HR+/HER2-breast Cancer Based on Molecular Marker


Sponsor

Yongsheng Wang

Enrollment

100 participants

Start Date

Mar 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Select the appropriate population for adding CDK4/6 inhibitors therapy in high risk early HR+/HER2-breast cancer based on molecular detection


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether adding a CDK4/6 inhibitor (a type of targeted drug that slows cancer cell growth) to standard hormone-blocking therapy before surgery helps shrink hormone-receptor-positive, HER2-negative breast cancer more effectively. **You may be eligible if...** - You are a woman aged 18–75 with newly diagnosed breast cancer - Your cancer is hormone receptor-positive and HER2-negative (confirmed by pathology) - Your primary tumor is larger than 2 cm - Your cancer is classified as stage II or III (has not spread to distant organs) - You have not yet started treatment **You may NOT be eligible if...** - You have HER2-positive or triple-negative breast cancer - Your cancer has spread to distant parts of the body - You are older than 75 or under 18 - You have significant other health conditions 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.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGletrozole

Hormone receptor positive,HER2 negative participants will receive letrozole as neoadjuvant endocrine therapy,if don't work, CDK4/6 Inhibitor was added.


Locations(1)

Breast Cancer Center, Shandong Cancer Hospital and Institute

Jinan, Shandong, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05809024


Related Trials