Evidence map›Paper›PMID 42213275›Full record

ArticleAnnals of nuclear medicine2026

The role of 18 F-FDG PET/CT SUVmax values in evaluating treatment response in hormone receptor-positive metastatic breast cancer patients receiving CDK4/6 inhibitor therapy.

Rahime Dilara Özbek, Aydın Aytekin, Enes Yerdes, Umut Elboga

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Article in Annals of nuclear medicine, 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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5 · Who and what money

Authors and funding

4 authors.

Rahime Dilara ÖzbekDepartment of Internal Medicine, Faculty of Medicine, Gaziantep University, Gaziantep, Türkiye, Turkey.
Aydın AytekinDivision of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, Gaziantep University, Gaziantep, Türkiye, Turkey.
Enes YerdesDepartment of Nuclear Medicine, Faculty of Medicine, Gaziantep University, Gaziantep, Türkiye, Turkey. e.yerdes@gmail.com.ORCID http://orcid.org/0000-0001-8990-2438
Umut ElbogaDepartment of Nuclear Medicine, Faculty of Medicine, Gaziantep University, Gaziantep, Türkiye, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMetastatic breast cancer is a disease with poor prognosis. For many years, it has been treated with endocrine therapy; however, due to the promising results of CDK 4/6 inhibitors, their combination with endocrine therapy has recently become an essential component of metastatic breast cancer treatment. Although no standardized approach exists for evaluating the response to CDK 4/6 inhibitors, assessment with 18 F-FDG PET/CT may be possible. In this study, we aimed to assess the treatment response using 18 F-FDG PET/CT SUVmax values in hormone receptor-positive metastatic breast cancer patients receiving CDK 4/6 inhibitors.

methodsOur study was designed as a single-center, retrospective analysis including 94 patients (93 females, 1 male). The mean age at diagnosis was 55 years. The most commonly used treatment combination was ribociclib + letrozole (45.7%). Neutropenia was the most frequent adverse event associated with CDK 4/6 inhibitors (35.5% of patients), followed by fatigue (25.8%) and nausea (19.4%).

resultsThe mean highest SUVmax value (primary tumor + metastases) before CDK4/6 inhibitor treatment was 11.20, which decreased to 7.32 after treatment initiation (p = 0.001). Patients with a marked absolute reduction in SUVmax (AUC: 0.769, p = 0.001, cut-off: 3.35) had longer progression-free survival (PFS) compared with those without a reduction (28.92 months vs. 14.47 months). The difference between pre- and post-treatment SUVmax values was significantly associated with both Clinical Benefit Rate (CBR) and Objective Response Rate (ORR) (p = 0.001).

conclusionEarly changes in 18 F-FDG PET/CT SUVmax values can serve as a valuable predictive marker for treatment response and survival in patients with metastatic breast cancer treated with CDK 4/6 inhibitors.

Indexed as

Breast NeoplasmsCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Fluorodeoxyglucose F18Positron Emission Tomography Computed TomographyProtein Kinase InhibitorsReceptors, EstrogenAdultAgedFemaleHumansMiddle AgedNeoplasm MetastasisRetrospective StudiesTreatment OutcomeCDK4 protein, humanCDK6 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Fluorodeoxyglucose F18Protein Kinase InhibitorsReceptors, EstrogenBreast cancerCDK 4/6 inhibitorsPET-CTSUVmax

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.