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Total Lesion Glycolysis Levels as Predictive Indicators in Patients With Metastatic and Recurrent Breast Cancer Undergoing Endocrine Therapy With or Without CDK4/6 Inhibitor
- Source :
- Anticancer Research. 42:4813-4824
- Publication Year :
- 2022
- Publisher :
- Anticancer Research USA Inc., 2022.
-
Abstract
- Endocrine therapy (ET) with or without CDK4/6 inhibitors is the primary treatment choice for patients with estrogen receptor (ER)-positive and HER2-negative subtype of metastatic breast cancer (MBC). We examined the metabolic parameters identified usingWe included 136 patients with MBC treated with ET alone (n=107) or combined with CDK4/6 inhibitor (n=29) and examined using FDG-PET before treatment began. The highest maximum value of the standard uptake value (SUVmax), whole-body metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were calculated.Progression-free survival (PFS) was significantly longer in patients with low levels of MTV, TLG, and SUVmax than those with higher levels (median PFS 49.5 vs. 20.7 months, p=0.001 for MTV, 49.5 vs. 20.7 months, p=0.0016 for TLG, 37.0 vs. 20.7 months, p=0.012 for SUVmax). Multivariable analysis revealed that TLG (hazard ratio=6.383, 95% confidence interval=1.167-34.913, p=0.033) was independently and significantly associated with PFS. The relationship between TLG levels and PFS was significant in patients treated with ET with (p=0.0054) and without (p=0.0188) CDK4/6 inhibitor.TLG at baseline was a significant predictor for sensitivity to ET alone or combined with CDK4/6 inhibitor. These data may be useful to identify patients that would benefit from ET.
- Subjects :
- Cancer Research
Cyclin-Dependent Kinase 4
Breast Neoplasms
Cyclin-Dependent Kinase 6
General Medicine
Prognosis
Tumor Burden
Receptors, Estrogen
Oncology
Fluorodeoxyglucose F18
Positron Emission Tomography Computed Tomography
Humans
Female
Neoplasm Recurrence, Local
Radiopharmaceuticals
Glycolysis
Protein Kinase Inhibitors
Retrospective Studies
Subjects
Details
- ISSN :
- 17917530 and 02507005
- Volume :
- 42
- Database :
- OpenAIRE
- Journal :
- Anticancer Research
- Accession number :
- edsair.doi.dedup.....fa51cee0fac1924d9fc81927d0c05f28
- Full Text :
- https://doi.org/10.21873/anticanres.15986