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Empowering Practitioners: Unveiling the Genetic Mysteries of Pediatric Glioblastoma

Empowering Practitioners: Unveiling the Genetic Mysteries of Pediatric Glioblastoma

Introduction

In the realm of pediatric oncology, high-grade gliomas represent a formidable challenge. Despite advances in medical science, the prognosis for children diagnosed with these aggressive brain tumors remains disheartening. A recent study titled Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma sheds light on the genetic intricacies of these tumors, offering insights that could transform therapeutic approaches. This blog aims to guide practitioners in leveraging these findings to enhance their clinical strategies.

Understanding the STAG2 Mutation

The study focuses on the STAG2 mutation, a genetic anomaly identified in a subset of glioblastomas. This mutation, affecting the cohesin complex, plays a pivotal role in tumor formation and resistance to standard therapies. Despite aggressive treatment regimens, including surgical resection, chemoradiation, and novel immunotherapies, the STAG2 mutation persisted, suggesting its critical role in tumorigenesis.

Implications for Clinical Practice

For practitioners, understanding the persistence of the STAG2 mutation is crucial. It highlights the need for personalized treatment plans that consider the genetic profile of each tumor. Here are some actionable steps practitioners can take:

Encouraging Further Research

While this study provides valuable insights, it also underscores the need for continued research. Practitioners are encouraged to delve deeper into the genetic landscape of glioblastomas. By participating in clinical trials and contributing to genetic databases, they can help build a more comprehensive understanding of these tumors, ultimately leading to more effective treatments.

Conclusion

The persistence of the STAG2 mutation in pediatric glioblastoma represents both a challenge and an opportunity. By embracing data-driven approaches and fostering a culture of research and collaboration, practitioners can play a pivotal role in transforming the landscape of pediatric oncology. For those interested in exploring the original research paper, please follow this link: Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma.


Citation: Hong, C. S., Vasquez, J. C., Kundishora, A. J., Elsamadicy, A. A., Beckta, J. M., Sule, A., Marks, A. M., Leelatian, N., Huttner, A., Bindra, R. S., DiLuna, M. L., Kahle, K. T., & Erson-Omay, E. Z. (2020). Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma. NPJ Genomic Medicine, Nature Publishing Group UK. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264170/?report=classic
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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