Aims: Phase III studies investigating CDK 4/6 inhibitors have failed to identify significant predictive or prognostic markers that aid clinicians in therapeutic decision-making. Given the complex treatment landscape in breast cancer, identifying patient and tumor characteristics that optimize the utilization of CDK 4/6 inhibitors across diverse therapeutic approaches is crucial. In our study, we aimed to evaluate the predictive role of progesterone receptor (PR) expression levels in patients with estrogen receptor
(ER)-positive and human epidermal growth factor receptor 2 (HER2)-negative advanced-stage breast cancer treated with CDK 4/6 inhibitors.
Methods: This study retrospectively evaluated 244 patients who received a combination of CDK 4/6 inhibitors and endocrine therapy as their first-line treatment. Those with PR levels below 20% were designated as low PR expression patients, and those with levels of 20% or above were classified as high PR expression patients. These two groups were compared in terms of demographic characteristics and progression-free survival (PFS).
Results: Progression events occurred in 37 of 83 patients in the low PR expression group and 55 of 161 patients in the high PR expression group. Patients with low PR expression demonstrated a significantly shorter median PFS of 23.13 months (95% CI, 15.67-30.59) compared to those with high PR expression, who exhibited a median PFS of 34.66 months (95% CI, 24.2745.05) (p=0.002). This significant difference in mPFS was observed consistently across both ribociclib (p=0.034) and palbociclib (p=0.024) treatment groups.
Conclusion: This study suggests that PR expression may also predict disease progression in patients initiating CDK 4/6 inhibitors and endocrine therapy in addition to ER levels. While these findings are promising, further research is warranted to validate them in more extensive, prospective studies.
Advanced stage breast cancer biomarker CDK 4/6 inhibitors endocrine therapy progesterone receptor
This retrospective study was conducted in accordance with recognized ethical standards, including the principles of the Declaration of Helsinki, and received approval from the Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital Non-Interventional Clinical Research Ethics Committee (Approval No: 2024-02/04). The Ethics Committee waived the requirement for informed consent, as the study was retrospective and non-interventional, and deemed that obtaining consent was unnecessary in accordance with national regulations.
Primary Language | English |
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Subjects | Clinical Oncology |
Journal Section | Research Articles |
Authors | |
Publication Date | May 30, 2025 |
Submission Date | April 5, 2025 |
Acceptance Date | May 29, 2025 |
Published in Issue | Year 2025 Volume: 7 Issue: 3 |
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