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Original Article
The Impact of Obesity on Treatment Outcomes in Patients with Hormone Receptor-Positive HER2-Negative Metastatic Breast Cancer Receiving CDK 4/6 Inhibitors
Yoo Bin Jung1orcid , Hee Kyung Ahn2, Hyun-Young Shin3, Ji Hyung Hong1orcid , Chai Hong Rim4,5orcid

DOI: https://doi.org/10.4143/crt.2025.110 [Accepted]
Published online: April 15, 2025
1Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea
2Department of Medicine, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul, Korea
3Department of Family Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
4Department of Radiation Oncology, Korea University Ansan Hospital, Korea University Medical College, Ansan, Korea
5CURE analytics, Korea
Corresponding author:  Ji Hyung Hong
Tel: 82-2-2258-6362 
Email: jhhong8107@gmail.com
Chai Hong Rim
Tel: 82-31-412-6850 
Email: crusion3@naver.com
Received: 25 January 2025   • Accepted: 13 April 2025
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Purpose
Guidelines from the aromatase inhibitor era for early breast cancer (EBC) treatment recommend maintaining a body mass index (BMI) below 25. In the current era of CDK 4/6 inhibitors, now standard in metastatic breast cancer (MBC), limited data exist on treatment outcomes in obese patients. This study investigates how adiposity affects the treatment outcome of CDK 4/6 inhibitors in patients with hormone receptor (HR)-positive, HER2-negative MBC.
Materials and Methods
We searched PubMed, MEDLINE, and Embase databases, assessing efficacy outcomes such as progression-free survival (PFS) based on obesity markers, including BMI and visceral adipose tissue (VAT) index.
Results
Twelve studies were reviewed, with seven studies and 1,812 patients included in a pooled meta-analysis. Among patients with BMI ≥25, modest improvement in PFS was observed, with a pooled hazard ratio (HR) of 0.944 (95% CI, 0.909-0.980; p = 0.003). Besides, add-on analysis using VAT to define obesity revealed a notable PFS improvement, with a pooled HR of 0.452 (95% CI, 0.256-0.798; p = 0.006).
Conclusion
While BMI-defined obesity showed slight PFS improvement with CDK 4/6 inhibitors and endocrine therapy, using VAT to define obesity revealed significant PFS gains. This highlights the need for further research on biomarker to clarify the role of adiposity in MBC, which may differ from its impact in EBC.

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