Abstract

Dramatic advances in the molecular analysis of diffuse intrinsic pontine glioma have occurred over the last decade and resulted in the identification of potential therapeutic targets. In spite of these advances, no significant improvement in the outcome has been achieved and median survival remains approximately 10 months. An understanding of the approaches that have been taken to date, why they failed, and how that information can lead the field forward is critical if we are to change the status quo. In this review, we will discuss the clinical trial landscape in North America with an overview of historical approaches that failed and what might account for this failure. We will then provide a discussion of how our understanding of the genotype of this disease has led to the development of a number of trials targeting the mutations and epigenome of diffuse intrinsic pontine gliomas and the issues related to these trials. Similarly, the introduction of methodologies to address penetration across the blood–brain barrier will be considered in the context of both targeted approaches, epigenetic modification, and immune surveillance of these tumors. The comprehensive analysis of these data, generated through cooperative groups, collaborative clinical trials, and pilot studies in North America will be the focus of the IVth Memorial Alicia Pueyo international symposium in Barcelona on March 12th, 2018 and will be compared and contrasted with a similar comprehensive analysis of the European data with the goal of bringing all of these data together to develop a uniform platform on which new rational trials can be based.

Highlights

  • Integration of Biology Into the Treatment of Diffuse Intrinsic PontineDramatic advances in the molecular analysis of diffuse intrinsic pontine glioma have occurred over the last decade and resulted in the identification of potential therapeutic targets

  • Diffuse-intrinsic pontine gliomas (DIPG) are the most common brainstem tumors in children and remain the deadliest cancer diagnosis in this population

  • The proteins which package DNA into chromatin, have been found in approximately 80% of DIPG [28, 29]. This consistent finding led to a revision in the WHO classification of CNS tumors—diffuse midline glioma, H3K27M-mutant [30]—for tumors once referred to as DIPG. This change has important implications as new clinical trials increasingly focus on the 80% of DIPG with histone mutations

Read more

Summary

Integration of Biology Into the Treatment of Diffuse Intrinsic Pontine

Dramatic advances in the molecular analysis of diffuse intrinsic pontine glioma have occurred over the last decade and resulted in the identification of potential therapeutic targets. In spite of these advances, no significant improvement in the outcome has been achieved and median survival remains approximately 10 months. We will discuss the clinical trial landscape in North America with an overview of historical approaches that failed and what might account for this failure. We will provide a discussion of how our understanding of the genotype of this disease has led to the development of a number of trials targeting the mutations and epigenome of diffuse intrinsic pontine gliomas and the issues related to these trials.

INTRODUCTION
CLINICAL PRESENTATION AND DIAGNOSIS
STANDARD TREATMENT OF DIPG
RADIATION SENSITIZER CLINICAL TRAILS
CHEMOTHERAPY CLINICAL TRIALS
BIOLOGIC ADVANCES
University of Texas MD Anderson Cancer Center
New York University and University of Texas MD Anderson Cancer Center
Refractory or progressive DIPG trials
Hospital Infantil de Mexico Federico Gomez
SURGICAL THERAPEUTIC APPROACHES
CURRENT STRATEGIES
Findings
CONCLUSION
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.