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Peer-reviewedCC BYCurrent oncology (Toronto, Ont.)

Lactate Dehydrogenase-to-Albumin Ratio and Glasgow Prognostic Score as Prognostic Markers in Metastatic Breast Cancer Treated with CDK4/6 Inhibitors.

  1. 1Division of Medical Oncology, Faculty of Medicine, Celal Bayar University, 45030 Manisa, Turkey.

Abstract

Background: CDK4/6 inhibitors with endocrine therapy are standard first-line treatment for hormone receptor-positive, HER2-negative metastatic breast cancer, yet simple pretreatment prognostic markers are lacking. The LDH-to-albumin ratio (LAR) and the Glasgow Prognostic Score (GPS) both incorporate serum albumin and are each reported as prognostic, but have not been compared within a single cohort, and LAR has not been examined during CDK4/6 inhibitor therapy. This study evaluated both indices in this setting. Methods: Consecutive patients (n = 139) receiving palbociclib or ribociclib plus endocrine therapy (2020-2025) were analysed retrospectively. LAR was modelled continuously on the logarithmic scale, with hazard ratios per doubling; an external cut-off (46.27) served for Kaplan-Meier illustration only. GPS was calculated in its original form. As both contain albumin, each entered a separate multivariable Cox model with identical covariates. Endpoints were overall survival (OS) and progression-free survival (PFS). Results: Over a median follow-up of 50.0 months, 72 deaths and 110 progression events occurred. LAR was independently associated with OS (adjusted HR 2.87 per doubling, 95% CI 1.78-4.62, p < 0.001) and PFS (2.21, 1.45-3.35, p < 0.001). GPS was independently associated with OS (1.72, 1.05-2.82, p = 0.032) but not PFS (1.32, 0.88-1.98, p = 0.187). LAR-based models had lower Akaike information criterion values (ΔAIC 12.3 and 10.9), but concordance did not differ significantly between the indices (ΔC ≈ 0.04, p > 0.20). Conclusions: Baseline LAR, an inexpensive routine index, was associated with both endpoints, whereas GPS was associated with overall survival alone. Discrimination was modest for both indices (C-index ≤ 0.61) and did not differ significantly between them. External validation is required.

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BibTeX
@article{hafizoglu2026lactate,
  title = {{Lactate Dehydrogenase-to-Albumin Ratio and Glasgow Prognostic Score as Prognostic Markers in Metastatic Breast Cancer Treated with CDK4/6 Inhibitors.}},
  author = {Ece Sahin Hafizoglu and Ferhat Ekinci and Mustafa Sahbazlar and Atike Pinar Erdogan},
  journal = {Current oncology (Toronto, Ont.)},
  year = {2026},
  month = sep,
  doi = {10.3390/curroncol33100582},
  url = {https://europepmc.org/article/MED/42930149},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Lactate Dehydrogenase-to-Albumin Ratio and Glasgow Prognostic Score as Prognostic Markers in Metastatic Breast Cancer Treated with CDK4/6 Inhibitors.
AU  - Ece Sahin Hafizoglu
AU  - Ferhat Ekinci
AU  - Mustafa Sahbazlar
AU  - Atike Pinar Erdogan
PY  - 2026
DA  - 2026/09/29
JO  - Current oncology (Toronto, Ont.)
DO  - 10.3390/curroncol33100582
UR  - https://europepmc.org/article/MED/42930149
AB  - Background: CDK4/6 inhibitors with endocrine therapy are standard first-line treatment for hormone receptor-positive, HER2-negative metastatic breast cancer, yet simple pretreatment prognostic markers are lacking. The LDH-to-albumin ratio (LAR) and the Glasgow Prognostic Score (GPS) both incorporate serum albumin and are each reported as prognostic, but have not been compared within a single cohort, and LAR has not been examined during CDK4/6 inhibitor therapy. This study evaluated both indices in this setting. Methods: Consecutive patients (n = 139) receiving palbociclib or ribociclib plus endocrine therapy (2020-2025) were analysed retrospectively. LAR was modelled continuously on the logarithmic scale, with hazard ratios per doubling; an external cut-off (46.27) served for Kaplan-Meier illustration only. GPS was calculated in its original form. As both contain albumin, each entered a separate multivariable Cox model with identical covariates. Endpoints were overall survival (OS) and progression-free survival (PFS). Results: Over a median follow-up of 50.0 months, 72 deaths and 110 progression events occurred. LAR was independently associated with OS (adjusted HR 2.87 per doubling, 95% CI 1.78-4.62, p < 0.001) and PFS (2.21, 1.45-3.35, p < 0.001). GPS was independently associated with OS (1.72, 1.05-2.82, p = 0.032) but not PFS (1.32, 0.88-1.98, p = 0.187). LAR-based models had lower Akaike information criterion values (ΔAIC 12.3 and 10.9), but concordance did not differ significantly between the indices (ΔC ≈ 0.04, p > 0.20). Conclusions: Baseline LAR, an inexpensive routine index, was associated with both endpoints, whereas GPS was associated with overall survival alone. Discrimination was modest for both indices (C-index ≤ 0.61) and did not differ significantly between them. External validation is required.
SN  - 1198-0052
SN  - 1718-7729
ER  -