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NCT Number: NCT07130643

Efficacy and Safety of CDK4/6 Inhibitors Combined With Endocrine Therapy in HR+/HER2- Neoadjuvant Therapy for Early Breast Cancer

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

No. 119 Zhuodaoquan South Road

Wuhan, Hubei, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Age ≥18 years old.
  • Premenopausal and postmenopausal women or men with stage II-III disease (multifocal and/or multifocal early invasive breast cancer) if all tumors on histopathological examination meet the pathological criteria for ER and/or PR > 10% and HER2- (HER2 expression of 0 or 1+ or 2+ and negative FISH test).

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.

  • ECOG PS score 0-2.
  • Patients must be able and willing to swallow and retain oral medications.
  • In premenopausal women, a serum or urine pregnancy test had to be negative within 14 days of enrollment or in women who had been amenorrhea for less than 12 months at enrollment.

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.

  • Absolute neutrophil count ≥1500/µL, platelet ≥100000/mm3, hemoglobin ≥10g/dL

Exclusion criteria

  • 1. Prior treatment with any CDK4/6 inhibitor.
  • Inflammatory or stage IV or bilateral breast cancer.
  • History of allergic reactions caused by chemical or biological components similar to CDK4/6 inhibitors.

Patients who received any drugs or substances that were effective CYP3A isoenzyme inhibitors or inducers within 7 days of enrollment.

  • Uncontrolled coexisting medical conditions may limit adherence to study requirements.
  • Pregnant women with a negative pregnancy test within 14 days before admission or women of childbearing potential.
  • Patients with a history of any malignancy were not eligible.
  • Patients receiving endocrine therapy within 5 years before diagnosis of current malignancy.

Treatment and study plan

CDK4/6 inhibitors+Endocrine Therapy

Drug

CDK4/6 inhibitors:dalpiciclib,palbociclib,abemaciclib,ribociclib

Primary outcomes

  1. Objective Response Rate (ORR)

    Time frame: up to 24 weeks

    ORR is defined as proportion of patients demonstrating either a partial response (PR) or a complete response (CR)

Secondary outcomes

  1. change in Ki67

    Time frame: up to 24 weeks

    change in Ki67 from baseline to end of treatment

  2. complete cell cycle arrest

    Time frame: up to 4 weeks

    The proportion of patients with Ki-67≤2.7% on day 15 of cycle 1 treatment

  3. Invasive disease free survival(iDFS)

    Time frame: up to 3 years

    Time from adjuvant therapy to disease recurrence in patients with invasive disease

Sponsors and collaborators

Lead sponsor

Xinhong Wu, PhD

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Aug 19, 2025
Registry last updated
Aug 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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