Safety and Efficacy of Laser Interstitial Thermal Therapy as Upfront Therapy in Primary Glioblastoma and IDH-Mutant Astrocytoma: A Meta-Analysis

Author:

Pandey Aryan1,Chandla Anubhav1,Mekonnen Mahlet1ORCID,Hovis Gabrielle E. A.1,Teton Zoe E.12,Patel Kunal S.13,Everson Richard G.13456ORCID,Wadehra Madhuri37ORCID,Yang Isaac1234568ORCID

Affiliation:

1. Department of Neurosurgery, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA

2. Harbor-UCLA Medical Center, Torrance, CA 90502, USA

3. Jonsson Comprehensive Cancer Center, Los Angeles, CA 90095, USA

4. Department of Radiation Oncology, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA

5. The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA 90502, USA

6. Ronald Reagan UCLA Medical Center, Los Angeles, CA 90095, USA

7. Department of Pathology and Laboratory Medicine, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA

8. Department of Head and Neck Surgery, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA

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 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.

Publisher

MDPI AG

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