Abstract

In spite of aggressive multi-modality treatments, patients diagnosed with anaplastic astrocytoma and glioblastoma continue to display poor median survival. The success of our current conventional and targeted chemotherapies are largely hindered by systemic- and neurotoxicity, as well as poor central nervous system (CNS) penetration. Interstitial drug administration via convection-enhanced delivery (CED) is an alternative that potentially overcomes systemic toxicities and CNS delivery issues by directly bypassing the blood–brain barrier (BBB). This novel approach not only allows for directed administration, but also allows for newer, tumor-selective agents, which would normally be excluded from the CNS due to molecular size alone. To date, randomized trials of CED therapy have yet to definitely show survival advantage as compared with today's standard of care, however, early studies appear to have been limited by “first generation” delivery techniques. Taking into consideration lessons learned from early trials along with decades of research, newer CED technologies and therapeutic agents are emerging, which are reviewed herein.

Highlights

  • In spite of aggressive multi‐modality treatments, patients diagnosed with glioblastoma (GBM, WHO Grade IV glioma) have median survival rates of only 14.6 months,[59] and 11.1–58.6 months if they have an anaplastic astrocytoma (WHO Grade III glioma).[13]

  • Neurotoxicity, and poor central nervous system (CNS) penetration secondary to passive and active blood– brain barrier (BBB) mechanisms limit the efficacious delivery of chemotherapeutics to gliomas

  • Convection‐enhanced delivery (CED) methods may offer many of the same benefits as intracavitary delivery, including reduced risk of systemic toxicity

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Summary

Introduction

In spite of aggressive multi‐modality treatments, patients diagnosed with glioblastoma (GBM, WHO Grade IV glioma) have median survival rates of only 14.6 months,[59] and 11.1–58.6 months if they have an anaplastic astrocytoma (WHO Grade III glioma).[13].

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Conclusion

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