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An Alternative Pipeline for Glioblastoma Therapeutics: A Systematic Review of Drug Repurposing in Glioblastoma
Seán B Lyne1, Bakhtiar Yamini1
1Department of Neurological Surgery, University of Chicago Medicine and Biological Sciences, Chicago, IL 60637, USA.
Abstract:
The treatment of glioblastoma (GBM) remains a significant challenge, with outcome for most pa-tients remaining poor. Although novel therapies have been developed, several obstacles restrict the incentive of drug developers to continue these efforts including the exorbitant cost, high failure rate and relatively small patient population. Repositioning drugs that have well-characterized mechanistic and safety profiles is an attractive alternative for drug development in GBM. In ad-dition, the relative ease with which repurposed agents can be transitioned to the clinic further supports their potential for examination in patients. Here, a systematic analysis of the literature and clinical trials provides a comprehensive review of primary articles and unpublished trials that use repurposed drugs for the treatment of GBM. The findings demonstrate that numerous drug classes that have a range of initial indications have efficacy against preclinical GBM models and that certain agents have shown significant potential for clinical benefit. With examination in randomized, placebo-controlled trials and the targeting of particular GBM subgroups, it is pos-sible that repurposing can be a cost-effective approach to identify agents for use in multimodal anti-GBM strategies.
Insights
Drug repurposing offers a promising, cost-effective strategy for glioblastoma (GBM) treatment. This approach leverages existing drugs to overcome challenges in developing novel therapies for this challenging brain cancer.
Area of Science:
- Neuro-oncology
- Pharmacology
- Drug Discovery
Background:
- Glioblastoma (GBM) treatment remains a significant clinical challenge with poor patient outcomes.
- Developing novel therapies for GBM is hindered by high costs, failure rates, and small patient populations.
Purpose of the Study:
- To systematically review the literature and clinical trials on repurposed drugs for glioblastoma treatment.
- To assess the potential of drug repurposing as a viable strategy for GBM therapy development.
Main Methods:
- Comprehensive literature search of primary articles and unpublished clinical trials.
- Systematic analysis of efficacy data for repurposed agents in preclinical GBM models and clinical settings.
Main Results:
- Numerous drug classes with diverse initial indications show efficacy against preclinical GBM models.
- Certain repurposed agents demonstrate significant potential for clinical benefit in GBM patients.
Conclusions:
- Drug repurposing presents an attractive, cost-effective alternative for GBM drug development.
- Further investigation in randomized trials, targeting specific GBM subgroups, can optimize repurposed agents for multimodal GBM strategies.
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