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Glioblastoma with Primitive Neuroectodermal Component Treated with Adjuvant Radiotherapy and Temozolomide: A Pooled
Rony Benson1, Supriya Mallick1, Suvendu Purkait2
1Department of Radiation Oncology, All India Institute of Medical Sciences, New Delhi, India.
Neurology India
|September 11, 2021
Summary
Glioblastoma with primitive neuroectodermal tumor (GBM-PNET) shows similar outcomes to conventional glioblastoma but has a higher risk of central nervous system dissemination. An individualized treatment approach is recommended for this rare entity.
Area of Science:
- Neuro-oncology
- Central Nervous System Tumors
- Cancer Histopathology
Background:
- Glioblastoma (GBM) is a highly aggressive brain tumor with poor prognosis.
- GBM with neuroectodermal differentiation (GBM-PNET) is a recently identified subtype.
- The neuroectodermal component may increase the risk of systemic spread.
Purpose of the Study:
- To analyze the treatment patterns and outcomes for GBM-PNET.
- To compare the clinical behavior of GBM-PNET with conventional GBM.
Main Methods:
- Retrospective analysis of four GBM-PNET cases treated at the institute.
- Literature review and pooled analysis of 23 additional GBM-PNET cases.
- Evaluation of treatment modalities including surgery, radiotherapy, and chemotherapy (temozolomide).
Main Results:
- Four GBM-PNET patients received surgery, radiotherapy, and temozolomide; one experienced local recurrence.
- Pooled analysis of 23 patients showed median progression-free survival of 10 months and overall survival of 25 months.
- Extent of surgery, radiation technique, and age did not significantly impact survival.
Conclusions:
- GBM-PNET is a rare entity with clinical behavior and outcomes comparable to conventional GBM.
- Patients with GBM-PNET face an elevated risk of cerebrospinal fluid (CSF) dissemination.
- An individualized treatment strategy is crucial for managing GBM-PNET.

