Therapeutic Strategies for Gliomas Associated With Cancer Predisposition Syndromes

Author:

Lam Keng1ORCID,Kamiya-Matsuoka Carlos1,Slopis John M.1ORCID,McCutcheon Ian E.2,Majd Nazanin K.1ORCID

Affiliation:

1. Department of Neuro-Oncology, The University of Texas MD Anderson Cancer, Houston, TX

2. Department of Neurosurgery, The University of Texas MD Anderson Cancer, Houston, TX

Abstract

PURPOSE The purpose of this article was to provide an overview of syndromic gliomas. DESIGN The authors conducted a nonsystematic literature review. RESULTS Cancer predisposition syndromes (CPSs) are genetic conditions that increase one's risk for certain types of cancer compared with the general population. Syndromes that can predispose one to developing gliomas include neurofibromatosis, Li-Fraumeni syndrome, Lynch syndrome, and tuberous sclerosis complex. The standard treatment for sporadic glioma may involve resection, radiation therapy, and/or alkylating chemotherapy. However, DNA-damaging approaches, such as radiation and alkylating agents, may increase the risk of secondary malignancies and other complications in patients with CPSs. In some cases, depending on genetic aberrations, targeted therapies or immunotherapeutic approaches may be considered. Data on clinical characteristics, therapeutic strategies, and prognosis of syndromic gliomas remain limited. CONCLUSION In this review, we provide an overview of syndromic gliomas with a focus on management for patients with CPSs and the role of novel treatments that can be considered.

Publisher

American Society of Clinical Oncology (ASCO)

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