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A Real-World Study of Lerociclib in Patients with HR-Positive/HER2-Negative Advanced Breast Cancer

A Real-World Study of Lerociclib in Patients with HR-Positive/HER2-Negative Advanced Breast Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118047
Enrollment
Unknown
Registered
2026-02-01
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HR-positive, HER2-negative breast carcinoma

Interventions

The observation group of breast malignant tumors with HR positive and HER-2 negative:None

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who visited the hospital from January 1, 2026 to December 31, 2028; 1. Patients with HR+/HER2- advanced breast cancer who have not received or have received at most one line of CDK4/6i treatment; 2. Patients for whom the investigator plans to administer lorlatinib treatment; 3. ECOG PS (Eastern Cooperative Oncology Group Performance Status): 0-2 points;

Exclusion criteria

Exclusion criteria: 1.Patients with known active brain metastases; 2.Patients with advanced, symptomatic visceral metastases at risk of developing life-threatening complications in the short term; 3.Patients with significant comorbidities. 4.Patients deemed ineligible for enrollment by the investigators.

Design outcomes

Primary

MeasureTime frame
The progression-free survival period utilized by Lorus for patients with advanced breast cancer of HR+/HER2- type;The progression-free survival period utilized by Lorusi for patients with advanced breast cancer of HR+/HER2- type in the second line treatment stage;

Secondary

MeasureTime frame
Therapeutic model;The safety of patients receiving treatment at Roselli Hospital;

Countries

China

Contacts

Public ContactXiaojia Wang

Zhejiang Cancer Hospital

wxiaojia0803@163.com+86 571 88122078

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026