The Recent Updates in Primary CNS Tumors

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Molecular Cancer Biology".

Deadline for manuscript submissions: closed (29 February 2024) | Viewed by 1002

Special Issue Editor


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Guest Editor
Department of Neurology, Division of Neuro-Oncology, Mount Sinai Hospital, New York, NY 10029, USA
Interests: brain tumor; glioblastoma

Special Issue Information

Dear Colleagues,

There have been some notable advances in the field of neuro-oncology in recent years. The diagnosis of primary CNS tumors has shifted from the traditional histology- and morphology-based diagnosis as per the diagnostic criteria in the 2016 WHO Classification to more molecular-based diagnosis in the 2021 WHO Classification. With advancing technology and techniques in neuroimaging studies, more defined surgical resection can be achieved by utilizing the fluorescence-guided 5-Aminolevulinic acid (5-ALA). In addition, for tumors that were previously considered as nonresectable or tumors for which no additional radiation therapy can be rendered, minimally invasive Laser Interstitial Thermal Therapy (LITT) could be a viable option, and both modalities could be potential treatment armamentaria in selected cases for malignant brain tumors. Tumor-Treating Fields (TTF) with low-intensity intermediate frequency clinical trials for newly diagnosed and recurrent malignant gliomas have shown to improve some survival benefits. There have also been significant advances in molecular targeted therapies based on the next-generation sequencing profile of each specific tumor. As more drugs are being developed for each specific target of the up- and downstream regulation pathways, more viable treatment options could be available with potential improvement in the tumor response and survival. Rare CNS tumors and skull-based tumors also appear to have some unique makers such as BRAF in craniopharyngiomas and SMO and FAK in meningiomas, which have shown some excellent responses to their respective targeted therapies. Immunotherapies with and without checkpoint inhibitors and vaccine therapies such as the recent DCVax trial for newly diagnosed glioblastomas have shown some encouraging results and are being actively investigated.

Dr. Lyndon Kim
Guest Editor

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Keywords

  • primary brain tumors
  • glioblastoma
  • malignant gliomas
  • 5-ALA
  • LITT
  • craniopharyngioma
  • meningioma
  • skull-based tumors
  • molecular targeted therapy
  • immunotherapy
  • vaccine therapy

Published Papers (1 paper)

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16 pages, 1162 KiB  
Systematic Review
Safety and Efficacy of Laser Interstitial Thermal Therapy as Upfront Therapy in Primary Glioblastoma and IDH-Mutant Astrocytoma: A Meta-Analysis
by Aryan Pandey, Anubhav Chandla, Mahlet Mekonnen, Gabrielle E. A. Hovis, Zoe E. Teton, Kunal S. Patel, Richard G. Everson, Madhuri Wadehra and Isaac Yang
Cancers 2024, 16(11), 2131; https://doi.org/10.3390/cancers16112131 - 3 Jun 2024
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Abstract
Although primary studies have reported the safety and efficacy of LITT as a primary treatment in glioma, they are limited by sample sizes and institutional variation in stereotactic parameters such as temperature and laser power. The current literature has yet to provide pooled [...] Read more.
Although primary studies have reported the safety and efficacy of LITT as a primary treatment in glioma, they are limited by sample sizes and institutional variation in stereotactic parameters such as temperature and laser power. The current literature has yet to provide pooled statistics on outcomes solely for primary brain tumors according to the 2021 WHO Classification of Tumors of the Central Nervous System (WHO CNS5). In the present study, we identify recent articles on primary CNS neoplasms treated with LITT without prior intervention, focusing on relationships with molecular profile, PFS, and OS. This meta-analysis includes the extraction of data from primary sources across four databases using the Covidence systematic review manager. The pooled data suggest LITT may be a safe primary management option with tumor ablation rates of 94.8% and 84.6% in IDH-wildtype glioblastoma multiforme (GBM) and IDH-mutant astrocytoma, respectively. For IDH-wildtype GBM, the pooled PFS and OS were 5.0 and 9.0 months, respectively. Similar to rates reported in the prior literature, the neurologic and non-neurologic complication rates for IDH-wildtype GBM were 10.3% and 4.8%, respectively. The neurologic and non-neurologic complication rates were somewhat higher in the IDH-mutant astrocytoma cohort at 33% and 8.3%, likely due to a smaller cohort size. Full article
(This article belongs to the Special Issue The Recent Updates in Primary CNS Tumors)
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