# Prognostic Value of Baseline Sarcopenia and Adipose Tissue Indices in HR+/HER2− Metastatic Breast Cancer Treated with CDK4/6 Inhibitors: A Retrospective Cohort Study

**Authors:** Latif Karahan, Arif Akyildiz, Taha Koray Sahin, Mustafa Arda Batu, Cagatay Ersan, Mehmet Ruhi Onur, Sercan Aksoy, Deniz Can Guven

PMC · DOI: 10.3390/jcm15041623 · 2026-02-20

## TL;DR

This study finds that low muscle mass (sarcopenia) at diagnosis is linked to worse outcomes in breast cancer patients treated with CDK4/6 inhibitors.

## Contribution

The study is the first to show that non-sarcopenia and de novo metastasis predict better survival in CDK4/6 inhibitor-treated breast cancer patients.

## Key findings

- Patients with sarcopenia had shorter progression-free survival compared to non-sarcopenic patients.
- Non-sarcopenia and de novo metastatic disease were independent predictors of longer progression-free survival.
- Adipose tissue indices and BMI were not associated with survival outcomes.

## Abstract

Background/Objectives: Sarcopenia, defined by reduced skeletal muscle mass, may have prognostic relevance in metastatic breast cancer. Muscle quality, reflected by adipose tissue indices, could also influence outcomes, but evidence in CDK4/6 (cyclin-dependent kinase)-inhibitor-treated patients is limited. We therefore evaluated the prognostic impact of baseline sarcopenia and adipose tissue distribution indices in this population. Methods: We retrospectively analyzed 156 women with HR+/HER2− MBC (hormone-receptor-positive, Her2-negative metastatic breast cancer) who initiated ribociclib or palbociclib plus endocrine therapy between May 2020 and January 2024. Association between L3 computed tomography (CT)-derived skeletal muscle index (SMI) and adipose tissue indices was evaluated with univariable and multivariable analyses. Sarcopenia was defined as SMI < 41 cm2/m2. Results: Median age was 57.6 years; 75% of patients were postmenopausal, and 48% of the cohort were sarcopenic. Median progression-free survival (PFS) for the entire cohort was 24.7 months (95% CI: 20.3–29.2). Patients with baseline sarcopenia had substantially shorter PFS compared to those without sarcopenia (21.5 months (95% CI: 10.9–32.1), versus 27.1 months (95% CI: 15.2–39; p = 0.016). Multivariable Cox regression analyses identified two independent predictors of prolonged PFS: non-sarcopenia (SMI ≥ 41 cm2/m2) and de novo metastatic disease. BMI (body mass index) and all adipose indices were not associated with PFS. Conclusions: Baseline non-sarcopenia and de novo metastatic disease independently predict longer PFS on CDK4/6 inhibitors, whereas adiposity measures and BMI are not prognostic. Routine body composition assessment may refine risk stratification and identify candidates for supportive interventions. Prospective studies are needed to validate these findings.

## Linked entities

- **Proteins:** Cdk4 (Cyclin-dependent kinase 4), ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Chemicals:** ribociclib (PubChem CID 44631912), palbociclib (PubChem CID 5330286)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** TAT (tyrosine aminotransferase) [NCBI Gene 6898], NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** toxicity (MESH:D064420), endocrine (MESH:D004700), Stage IV disease (MESH:D007676), death (MESH:D003643), metastases (MESH:D009362), muscle loss (MESH:D009135), Breast Cancer (MESH:D001943), adiposity (MESH:D018205), metastatic disease (MESH:D000092182), Tumor (MESH:D009369), Diabetes mellitus (MESH:D003920), muscle depletion (MESH:D019042), inflammatory (MESH:D007249), muscle wasting (MESH:D009133), fatty (MESH:D008067), Sarcopenia (MESH:D055948), injury to (MESH:D014947), Low skeletal muscle mass (MESH:C536030), visceral adiposity (MESH:D007418), frailty (MESH:D000073496), SMI (MESH:D005207), cachexia (MESH:D002100), overweight (MESH:D050177), obese (MESH:D009765)
- **Chemicals:** letrozole (MESH:D000077289), CDK4/6 (-), Ribociclib (MESH:C000589651), palbociclib (MESH:C500026), fulvestrant (MESH:D000077267), abemaciclib (MESH:C000590451)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941785/full.md

---
Source: https://tomesphere.com/paper/PMC12941785