Article
MiRNA-181d expression significantly affects treatment responses to carmustine wafer implantation in glioblastoma patients
Das Ansprechverhalten auf eine Carmustin-Wafer Therapie wird signifikant von der miRNA-181d beeinflusst
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Published: | May 8, 2019 |
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Objective: Standard therapeutic protocols for glioblastoma, the most aggressive type of brain cancer, include surgery followed by chemoradiotherapy. Additionally, carmustine-eluting wafers can be implanted locally into the resection cavity. This study evaluated micro RNA (miRNA)-181d as a prognostic marker of responses to carmustine wafer implantation.
Methods: Eighty glioblastoma patients (40/group) were included in a matched pair analysis. One group (carmustine wafer group) received concomitant chemoradiotherapy with carmustine wafer implantation (Stupp protocol). The second group (control group) received only concomitant chemoradiotherapy. All tumor specimens were subjected to evaluations of miRNA-181d expression. Results were correlated with further individual clinical data. A TCGA (The cancer genome atlas) dataset of 149 patients was used as an independent cohort to validate the results.
Results: Patients in the carmustine wafer group with low miRNA-181d expression had significantly longer overall (hazard ratio [HR], 35.03, [95% CI: 3.50–350.23], p=0.002) and progression-free survival (HR, 20.23, [95% confidence interval (CI): 2.19–186.86], p=0.008) than patients of the same group with a high miRNA-181d expression. These correlations were not observed in the control group. The non-significance in the control group was confirmed in the independent TCGA dataset. The carmustine wafer group patients with low miRNA-181d expression also had a significantly longer progression-free (p=0.049) and overall survival (p=0.034), compared with control group patients. Gross total resection correlated significantly with longer overall survival (p=0.023).
Conclusion: MiRNA-181d expression significantly affects treatment responses to carmustine wafer implantation.