Revisão Revisado por pares

Treatment of diffuse intrinsic brainstem gliomas: failed approaches and future strategies

2009; Volume: 3; Issue: 4 Linguagem: Inglês

10.3171/2008.11.peds08281

ISSN

1933-0715

Autores

James L. Frazier, James T. Lee, Ulrich W. Thomale, Joseph C. Noggle, Kenneth J. Cohen, George I. Jallo,

Tópico(s)

Meningioma and schwannoma management

Resumo

Diffuse intrinsic pontine gliomas constitute ~ 60-75% of tumors found within the pediatric brainstem. These malignant lesions present with rapidly progressive symptoms such as cranial nerve, long tract, or cerebellar dysfunctions. Magnetic resonance imaging is usually sufficient to establish the diagnosis and obviates the need for surgical biopsy in most cases. The prognosis of the disease is dismal, and the median survival is < 12 months. Resection is not a viable option. Standard therapy involves radiotherapy, which produces transient neurological improvement with a progression-free survival benefit, but provides no improvement in overall survival. Clinical trials have been conducted to assess the efficacy of chemotherapeutic and biological agents in the treatment of diffuse pontine gliomas. In this review, the authors discuss recent studies in which systemic therapy was administered prior to, concomitantly with, or after radiotherapy. For future perspective, the discussion includes a rationale for stereotactic biopsies as well as possible therapeutic options of local chemotherapy in these lesions.

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