No. 119 Zhuodaoquan South Road
Wuhan, Hubei, China
NCT Number: NCT07130643
This is a single arm, open label, phase 2 trial aimed to investigate the effects and safety of neoadjuvant CDK4/6 inhibitors in combination with endocrine for HR+/HER2- breast cancer. A total of 40 patients with stage II-III HR+/HER2- breast cancer will be enrolled. Six 4-week cycles of adjuvant therapy will be administrated.Premenopausal or perimenopausal patients should combine ovarian function suppression, including bilateral oophorectomy or treatment with gonadotropin-releasing hormone agonists.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
Female
Interventional
Phase 2
Wuhan, Hubei, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
3.Patients had to have histologically confirmed ER and (or PR>10%, HER2 -, early-stage invasive disease.
4.Intolerance or insensitivity to neoadjuvant chemotherapy: 2 cycles of neoadjuvant chemotherapy, PD/SD according to tumor evaluation, old age, and basic diseases can not tolerate chemotherapy.
8.Patients who had received neoadjuvant endocrine therapy were eligible if they were enrolled within 6 months of the initial histologic diagnosis and had completed no more than 2 months of neoadjuvant endocrine therapy.
Exclusion criteria
Patients who received any drugs or substances that were effective CYP3A isoenzyme inhibitors or inducers within 7 days of enrollment.
CDK4/6 inhibitors:dalpiciclib,palbociclib,abemaciclib,ribociclib
Time frame: up to 24 weeks
ORR is defined as proportion of patients demonstrating either a partial response (PR) or a complete response (CR)
Time frame: up to 24 weeks
change in Ki67 from baseline to end of treatment
Time frame: up to 4 weeks
The proportion of patients with Ki-67≤2.7% on day 15 of cycle 1 treatment
Time frame: up to 3 years
Time from adjuvant therapy to disease recurrence in patients with invasive disease
Xinhong Wu, PhD
Other
Single-arm Exploratory Study of Efficacy and Safety of CDK4/6 Inhibitors Combined With Endocrine Therapy in HR+/HER2- Neoadjuvant Therapy for Early Breast Cancer
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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