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The Clinical Application of Tumor Treating Fields Therapy in Glioblastoma
Published on: April 16, 2019
Temozolomide for high grade glioma
Michael G Hart1, Robert Grant, Ruth Garside
1Clinical Neurosciences, Bramwell Dott Building, Western General Hospital, Crewe Road, Edinburgh, Midlothian, UK, EH4 2XU. m.g.hart@doctors.net.uk
The Cochrane Database of Systematic Reviews
|October 10, 2008
Summary
Temozolomide improves survival and delays progression in high-grade glioma (HGG) primary therapy without impacting quality of life. For recurrent HGG, it delays progression but not overall survival, with low early adverse events.
Area of Science:
- Neuro-oncology
- Clinical trials
- Pharmacotherapy
Background:
- High-grade glioma (HGG) is an aggressive brain tumor.
- Standard treatment includes surgery and radiotherapy.
- Temozolomide is an oral chemotherapy agent with brain penetration and low adverse effects.
Purpose of the Study:
- To evaluate the efficacy of temozolomide compared to conventional therapy for HGG.
- To assess temozolomide's benefit in both primary and recurrent disease settings.
Main Methods:
- Systematic review of randomized controlled trials (RCTs).
- Searched multiple databases including Cochrane, Medline, and EMBASE.
- Included patients of all ages with pathologically diagnosed HGG.
Main Results:
- In primary Glioblastoma Multiforme (GBM), temozolomide significantly increased survival (HR 0.84) and time to progression (HR 0.52) without negatively impacting quality of life.
- Early adverse events were low, with 5-14% Grade 3/4 hematological toxicity.
- In recurrent GBM, temozolomide improved time to progression (HR 0.68) but not overall survival, with low severe adverse events.
Conclusions:
- Temozolomide is effective in primary GBM for prolonging survival and delaying progression with minimal impact on quality of life and low early adverse events.
- Late adverse event data for temozolomide is currently unknown.
- Temozolomide improves time to progression in recurrent GBM but not overall survival.
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