(P032) Current Management of Low-Grade Central Nervous System Glioma

Publication
Article
OncologyOncology Vol 29 No 4_Suppl_1
Volume 29
Issue 4_Suppl_1

Currently, low-grade glioma is commonly treated in the community setting by RT alone. A relatively high rate of local failure is noted (28%), and long-term survival appears to be shorter than might be expected. A number of patients are treated based on imaging alone without a detriment to survival. Low-grade glioma appears to be a more aggressive disease than usually considered, and efforts to improve the outcome would be served through clinical trials.

Ron R. Allison, MD, Dioval Reymond, Sharon Salenius, MPH, Andrej Hnatov, MD, Cynthia Ballenger, MD, Constantine Mantz, MD, Eduardo Fernandez, MD, PhD, Daniel Dosoretz, MD, Vershalee Shukla, MD, Timothy Shafman, MD, Steven Finkelstein, MD; 21st Century Oncology; The Brody School of Medicine, East Carolina University

BACKGROUND: Low-grade central nervous system (CNS) glioma is a rare diagnosis but is becoming more common as neuroimaging is now often undertaken for headache and other nonspecific neurologic signs and symptoms. Current management may include resection alone, radiation alone, or their combination, with chemotherapy as an adjunct. We reviewed the current management for this diagnosis based on a large cohort of freestanding and hospital-based cancer centers.

MATERIALS AND METHODS: An institutional review board (IRB)-approved chart review for all patients with low-grade primary CNS glioma who were treated at our facilities between 1989 and 2012 was undertaken. This search returned 25 patients (10 males, 15 females; mean age: 50.5 yr). Twenty patients were Caucasian. Presenting signs and symptoms were nonspecific CNS complaints: mainly generalized headache, vision changes, numbness, and weakness. Workup included magnetic resonance imaging (MRI) and/or computed tomography (CT). Biopsy reported low-gradeglioma, though imaging alone was used for diagnosis in some patients. Only two patients underwent gross total resection, and one patient underwent surgical debulking. All patients underwent external beam radiation therapy (RT), usually intensity-modulated RT (IMRT) or three-dimensional (3D) treatment with a mean dose of 48.6 Gy. Image guidance was employed in 24% of patients. Temodar was delivered to six patients (24%).

RESULTS: All patients have been followed for a mean of 9.3 months (range: 0.3–153.3 mo). Most patients were considered unresectable.RT was well tolerated, with most complications being grade I/II. One patient developed seizures as a late complication. All failures were local, occurring in 28% of patients. With regard to survival, eight patients are currently alive (32%). Statistical analysis showed no survival advantage for gender, age, performance status, biopsy, IMRT, radiation dose, chemotherapy, or surgery.

CONCLUSION: Currently, low-grade glioma is commonly treated in the community setting by RT alone. A relatively high rate of local failure is noted (28%), and long-term survival appears to be shorter than might be expected. A number of patients are treated based on imaging alone without a detriment to survival. Low-grade glioma appears to be a more aggressive disease than usually considered, and efforts to improve the outcome would be served through clinical trials.

Proceedings of the 97th Annual Meeting of the American Radium Society - americanradiumsociety.org

Articles in this issue

(P005) Ultrasensitive PSA Identifies Patients With Organ-Confined Prostate Cancer Requiring Postop Radiotherapy
(P001) Disparities in the Local Management of Breast Cancer in the United States According to Health Insurance Status
(P002) Predictors of CNS Disease in Metastatic Melanoma: Desmoplastic Subtype Associated With Higher Risk
(P003) Identification of Somatic Mutations Using Fine Needle Aspiration: Correlation With Clinical Outcomes in Patients With Locally Advanced Pancreatic Cancer
(P004) A Retrospective Study to Assess Disparities in the Utilization of Intensity-Modulated Radiotherapy (IMRT) and Proton Therapy (PT) in the Treatment of Prostate Cancer (PCa)
(S001) Tumor Control and Toxicity Outcomes for Head and Neck Cancer Patients Re-Treated With Intensity-Modulated Radiation Therapy (IMRT)-A Fifteen-Year Experience
(S003) Weekly IGRT Volumetric Response Analysis as a Predictive Tool for Locoregional Control in Head and Neck Cancer Radiotherapy 
(S004) Combination of Radiotherapy and Cetuximab for Aggressive, High-Risk Cutaneous Squamous Cell Cancer of the Head and Neck: A Propensity Score Analysis
(S005) Radiotherapy for Carcinoma of the Hypopharynx Over Five Decades: Experience at a Single Institution
(S002) Prognostic Value of Intraradiation Treatment FDG-PET Parameters in Locally Advanced Oropharyngeal Cancer
(P006) The Role of Sequential Imaging in Cervical Cancer Management
(P008) Pretreatment FDG Uptake of Nontarget Lung Tissue Correlates With Symptomatic Pneumonitis Following Stereotactic Ablative Radiotherapy (SABR)
(P009) Monte Carlo Dosimetry Evaluation of Lung Stereotactic Body Radiosurgery
(P010) Stereotactic Body Radiotherapy for Treatment of Adrenal Gland Metastasis: Toxicity, Outcomes, and Patterns of Failure
(P011) Stereotactic Radiosurgery and BRAF Inhibitor Therapy for Melanoma Brain Metastases Is Associated With Increased Risk for Radiation Necrosis
Recent Videos
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Although accuracy remains a focus in whole-body MRI testing in patients with Li-Fraumeni syndrome, comfortable testing experiences may ease anxiety.
Subsequent testing among patients in a prospective study may affirm the ability of cfDNA sequencing to detect cancers in those with Li-Fraumeni syndrome.
cfDNA sequencing may allow for more accessible, frequent, and sensitive testing compared with standard surveillance in Li-Fraumeni syndrome.
STX-478 showed efficacy in patients with advanced solid tumors regardless of whether they had kinase domain or helical PI3K mutations.
STX-478 may avoid adverse effects associated with prior PI3K inhibitors that lack selectivity for the mutated protein vs the wild-type protein.
Phase 1 data may show the possibility of rationally designing agents that can preferentially target PI3K mutations in solid tumors.
Funding a clinical trial to further assess liquid biopsy in patients with Li-Fraumeni syndrome may help with detecting cancers early across the board.
Michael J. Hall, MD, MS, FASCO, discusses the need to reduce barriers to care for those with Li-Fraumeni syndrome, including those who live in rural areas.
Related Content