Clinical Trial

Adjuvant Intensification for LAR

Study acronym: POLARIS
Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
This study enrolled patients with early-stage triple-negative breast cancer who had undergone radical surgery. The postoperative pathology met the TNM staging criteria of pT1c-3N0-3M0, and immunohistochemistry (IHC) results confirmed ER-negative status (IHC showed \<1% of tumor cells positive for ER), PR-negative status (IHC showed \<1% of tumor cells positive for PR), and HER2-negative status (IHC intensity of 0 or 1+; or IHC intensity of 2+ but with negative in situ hybridization results). Additionally, patients either exhibited high AR expression (IHC showing AR ≥10%) or were classified as the LAR subtype based on digital pathology. This study plans to prospectively enroll 904 subjects, who will be randomized in a 1:1 ratio after completing standard chemotherapy. They will be allocated to either the standard-of-care (SOC) chemotherapy followed by everolimus group or the SOC-alone group. The study aims to evaluate the efficacy of SOC chemotherapy followed by everolimus versus SOC chemotherapy alone as adjuvant therapy for patients with early-stage radically resected triple-negative breast cancer of the LAR subtype, with the primary endpoint being 3-year invasive disease-free survival (iDFS).
Trial Details
NCT Number NCT07407517
Lead Sponsor Fudan University
Conditions Breast Cancer Females, Triple Negative Breast Cancer (TNBC)
Enrollment 904 participants
Start Date 2026-02-01
Primary Completion 2033-02-01 (estimated)
Study Completion 2033-02-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-12