Abstract PS1-12-10: Real-world effectiveness of CDK4/6 inhibitors in HR+/HER2- advanced breast cancer with bone marrow involvement: A case series from a single institution
Abstract
Abstract Background: Bone marrow (BM) metastasis is a rare and challenging manifestation of advanced breast cancer (ABC), typically associated with high hematologic toxicity risk and poor outcomes. These patients are frequently excluded from clinical trials, limiting available evidence to guide treatment decisions. While chemotherapy is commonly recommended to achieve a rapid response, including hematologic recovery, CDK4/6 inhibitors (CDK4/6i) are increasingly used due to their efficacy in HR+/HER2- ABC. We aimed to assess the real-world (RW) efficacy of CDKis in this high-risk subgroup. Methods: We conducted a retrospective study of patients with HR+/HER2- ABC and BM involvement treated with CDK4/6i between 2022 and 2025 in a single institution located in Bogota, Colombia. Eligibility required histologic or smear-confirmed BM metastasis and receipt of at least one cycle of CDKi (palbociclib, ribociclib, or abemaciclib) in combination with endocrine therapy. Descriptive statistics were used to summarize clinicopathologic characteristics and hematologic outcomes. RW progression-free survival (rwPFS) was also described using the Kaplan-Meier method. Results: Fourteen patients were identified through retrospective chart review, two patients were excluded for being HER2-positive BC, two had HR positive BC but did not receive CDK4/6i, and one died before completion of the first treatment month with CDK4/6i. Nine patients were included (median age: 67 years). All were post menopausal with confirmed BM metastasis; De novo disease was present in 44.5% of the cases, and 8 Patients were ECOG
Fields of Study & Subjects
Advanced Breast Cancer Therapies
Breast Cancer Treatment Studies
PARP inhibition in cancer therapy
Publication details
- Journal / source
- Clinical Cancer Research
- Volume
- 32
- Issue
- 4_Supplement
- Pages
- PS1–12
- Publication date
- 17 February 2026
- Language
- EN