Pitt Shield

Updates for newly diagnosed and recurrent glioblastoma: a review of recent clinical trials.

Authors: Fukushima CM, de Groot J

Glioblastoma (GBM) is the most common and devastating primary malignant brain tumor. We summarize recent advances in radiotherapy, immunotherapy, and targeted therapy approaches for the treatment of newly diagnosed and recurrent glioblastoma. We also introduce ongoing clinical trials. Recent clinical trials have explored multiple novel strategies to treat GBM including the use of oncoviruses, chimeric antigen receptor (CAR) T cell therapy, vaccines, radiotherapy, and novel drug delivery techniques to improves drug penetrance across the blood brain barrier. Approaches to improve drug delivery to brain tumors have the potential to expand treatment options of existing therapies that otherwise have poor brain tumor penetrance. Immunotherapy has been of keen interest in both newly diagnosed and recurrent glioblastoma. Vaccines SurVaxM and DCVax-L have shown initial promise in phase II and III trials, respectively. CAR T cell therapy trials are in their early phases but hold promise in both newly diagnosed and recurrent glioblastoma. Although progress to improve outcomes for GBM patients has been modest, multiple novel strategies utilizing combination therapies, focused ultrasound to improve drug delivery, and novel immunotherapies are underway.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To summarize recent advances and ongoing clinical trials in radiotherapy, immunotherapy, and targeted therapies for newly diagnosed and recurrent glioblastoma.
Animal model / Human subject Homo sapiens (human patients); strain: N/A; age: not specified; sex: not specified
Disease model Glioblastoma
MRI or image guidance method Not specified in the provided text.
Targeted brain region(s) Blood-Brain Barrier
Cargo name and characteristics SurVaxM — synthetic peptide vaccine targeting the tumor-associated antigen survivin (peptide/protein vaccine); DCVax-L — autologous dendritic cell vaccine loaded with patient tumor lysate (cell-based immunotherapy/dendritic cell vaccine); CAR T cell therapy — patient T cells genetically engineered to express chimeric antigen receptors against GBM antigens (cell therapy/genetically modified cellular product); Oncolytic/onco-viruses — replication-competent viral vectors engineered to selectively infect and lyse tumor cells (viral vector/oncolytic virus).
Route of administration Not specified in the text; the paper mentions vaccines, CAR T cells, oncoviruses and the use of focused ultrasound and other novel drug delivery techniques to improve blood–brain barrier penetrance but does not state specific administration routes.

Outcomes and Safety

Summary of Outcomes Novel therapies—vaccines (SurVaxM, DCVax-L), CAR T cells, oncolytic viruses, focused ultrasound–enhanced drug delivery, and radiotherapy modifications—show early promise for newly diagnosed and recurrent glioblastoma, but overall clinical benefit to date has been modest.
Duration of biological effect not reported
Safety-related matter No safety issues or adverse effects are mentioned in the provided text.

Brain Region

Ultrasound Parameters

Ultrasound instrument Not specified in text
FUS Frequency Not reported
FUS Intensity Not reported
FUS Pressure Not specified
FUS Mode unspecified
Pulse duration Not reported in the provided text
Duration of a single FUS session Not specified in the provided text
Focal Characteristics Not specified
Treatment frequency multiple sessions

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