Combining Clinical and Molecular Data to Predict the Benefits of Carmustine Wafers in Newly Diagnosed High-Grade Gliomas |
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Authors: | Tamara Ius Daniela Cesselli Miriam Isola Giovanni Toniato Giada Pauletto Giovanni Sciacca Sara Fabbro Enrico Pegolo Simona Rizzato Antonio Paolo Beltrami Carla di Loreto Miran Skrap |
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Affiliation: | 1.Neurosurgery Unit, Department of Neurosciences,Santa Maria della Misericordia University Hospital,Udine,Italy;2.Department of Medicine,University of Udine,Udine,Italy;3.Neurology Unit, Department of Neurosciences,Santa Maria della Misericordia University Hospital,Udine,Italy;4.Department of Oncology,Santa Maria della Misericordia University Hospital,Udine,Italy;5.Institute of Pathology,Santa Maria della Misericordia University Hospital,Udine,Italy |
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Abstract: |
Purpose of reviewThe purpose of this study was to retrospectively evaluate the use of carmustine wafers (CWs) in the management of high-grade gliomas (HGGs). The data from our monoinstitutional series was compared with studies reported in the literature. Special emphasis was placed on the evaluation of side effects and the analysis of extent of resection and molecular profile as risk factors.Recent findingsThe implantation of CWs into the resection cavity during HGG treatment to deliver localized chemotherapy, followed by the Stupp protocol, remains debated in a clinical setting, largely due to the lack of appropriate phase III studies. Given the high expense and poorly characterized side effects associated with CW treatment, identification of patients most likely to benefit from this therapy could be clinically relevant.SummaryCWs may represent an effective and safe first-line treatment for patients with HGG that exhibit complete tumor resection and harboring a methylated MGMT promoter. Our investigation showed a much larger group of patients exhibiting long-term survival (>?=?36 months), strongly supporting a potential survival benefit conferred via CW treatment. The pre-surgical definition of the MGMT promoter status could be of clinical use in identifying “good responders” to CW implantation. |
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