Evidence map›Paper›PMID 41836595›Full record

ArticleCancer management and research2026

Ki-67 and Platelet-to-Lymphocyte Ratio (PLR) as Predictors of Progression-Free Survival in Metastatic Breast Cancer Receiving CDK4/6 Inhibitors: Clinical Implications.

Savas Gokcek, Mehmet Uzun, Ilkay Tugba Unek

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Article in Cancer management and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Savas GokcekDepartment of Medical Oncology, Necip Fazıl City Hospital, Kahramanmaraş, Turkey.ORCID 0000-0001-5928-0447
Mehmet UzunUniversity of Health Sciences Izmir Tepecik Training and Research Hospital, Department of Medical Oncology, Izmir, Turkey.ORCID 0000-0002-8596-4233
Ilkay Tugba UnekDepartment of Medical Oncology, Dokuz Eylul University, Izmir, Turkey.ORCID 0000-0002-9124-6123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: We aimed to investigate the prognostic power of Platelet-to-Lymphocyte Ratio (PLR) and Ki-67 index in predicting progression-free survival (PFS) in patients with metastatic HR+/HER2- breast cancer treated with CDK4/6 inhibitors. Materials and Methods: In this retrospective study, 121 patients who received CDK4/6 inhibitors (palbociclib, ribociclib) at the Department of Medical Oncology, Dokuz Eylul University, between January 2015 and January 2025, were analyzed. PLR was calculated using baseline complete blood count parameters. The optimal cut-off value of 168.37 was determined using ROC analysis, and patients were stratified into low and high PLR groups. Survival analyses were performed using the Kaplan-Meier method and Cox regression. Results: A lower progression rate was observed in the high PLR group (p=0.01), although PLR was not identified as an independent prognostic factor for PFS in multivariate analysis. Patients with lung metastases showed a higher proportion of low PLR (p=0.04).Although PLR was associated with PFS in univariate analysis, it did not retain independent prognostic significance in multivariate analysis.Conversely, Ki-67 was significantly associated with shorter PFS in both univariate (p<0.001) and multivariate analyses (p=0.007). Conclusion: While PLR did not independently predict survival outcomes, it may provide complementary information regarding metastatic distribution and disease behavior. Ki-67 remains a strong and independent prognostic marker for PFS in metastatic HR+/HER2- breast cancer. Our findings indicate that Ki-67 is the strongest and most consistent independent prognostic marker in this patient population.

Indexed as

CDK4/6 inhibitorsKi-67metastatic breast cancerplatelet-to-lymphocyte ratioprogression-free survival

Identifiers

PMID41836595
PMCPMC12984046

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