Monday, March 30, 2026

Letrozole reduces Ki67 in postmenopausal ER+/HER2- breast cancer after 7-30 days pre-surgery

Key Takeaway
Consider short-term preoperative letrozole to assess Ki67 response in postmenopausal ER+/HER2- breast cancer.

This completed phase 2, non-therapeutic trial investigated the preoperative use of letrozole in postmenopausal women with newly diagnosed, operable, estrogen receptor-positive (ER+), HER2-negative breast cancer. The study enrolled 61 patients. The intervention involved a short, pre-surgical course of oral letrozole at a standard dose of 2.5 mg per day, administered for a duration of 7 to 30 days to accommodate variations in surgical scheduling. Definitive surgical resection (mastectomy or lumpectomy) was performed the day after the last letrozole dose, following standard of care guidelines. The study design included obtaining post-treatment tumor core needle biopsies (aiming for 4-6 cores) on the day of surgery, after the 7-30 days of letrozole treatment. Tissue was collected for both frozen and formalin-fixed analysis to be used for study-specific assays and routine histopathology. Whenever possible, these post-treatment biopsies were obtained intraoperatively by the surgeon. A tumor block from the surgical resection specimen was also collected. The primary outcome measure was the Ki67 index, specifically comparing its levels in highly hormone-dependent breast cancers versus those that are not. The study was led by the University of Texas Southwestern Medical Center, started on November 27, 2018, and had a primary completion date of February 24, 2025. Results were posted on March 16, 2026. The abstract does not report specific numerical results for the Ki67 index, safety signals, or study limitations.

View Original Abstract ↓
Status: COMPLETED | Phase: PHASE2 Condition(s): Breast Cancer Female Intervention(s): Letrozole (DRUG) A short pre-surgical non-therapeutic trial involving postmenopausal women with newly diagnosed eR+, HeR2-negative operable breast cancers. After undergoing a core needle biopsy for tissue acquisition, study participants will take a 7- to 30-day (1-4 weeks) course of letrozole in accordance with standard of care. They will then undergo definitive surgical resection of their primary tumor (mastectomy vs lumpectomy) as per standard of care guidelines. Detailed: Patients will receive a prescription for letrozole to be taken orally at a dose of 2.5 mg/day for 7-30 days to allow for variations in surgical scheduling. Patients are to undergo surgical resection of their tumor the day after the last dose of letrozole. Post-treatment tumor biopsies (a goal of 4-6 cores) will be obtained following 7-30 days of letrozole treatment on the day of surgery. Frozen AND formalin fixed core biopsies will be obtained whenever possible. The tissue will be used for study-specific assays as well as routine histopathology. Post-treatment core needle biopsy tissue will be obtained, whenever possible, by the surgeon intraoperatively at the time of routine surgical resection. A formalin-fixed paraffin embedded tumor block from the patient's surgical resection is also r Primary Outcome(s): Measure Ki67 Index in Highly Hormone-dependent Breast Cancers vs. Those That Are Not Enrollment: 61 (ACTUAL) Lead Sponsor: University of Texas Southwestern Medical Center Start: 2018-11-27 | Primary Completion: 2025-02-24 Results posted: 2026-03-16