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

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Authors: William Armando Mantilla, F. Canro, M. A. Bravo, P. Lopez, D. Rubio, Hernán Carranza, S. X. Franco
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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