Wide Range of Clinical Outcomes in Patients with Gliomatosis Cerebri Growth Pattern: A Clinical, Radiographic, and Histopathologic Study

Author:

Ly K. Ina1,Oakley Derek H.2,Pine Alexander B.3,Frosch Matthew P.2,Chiou Sy Han4,Betensky Rebecca A.4,Pomerantz Stuart R.5,Hochberg Fred H.6,Batchelor Tracy T.1,Cahill Daniel P.7,Dietrich Jorg1

Affiliation:

1. Stephen E. and Catherine Pappas Center for Neuro-Oncology, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA

2. Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA

3. Department of Medicine, Yale New Haven Hospital, New Haven, Connecticut, USA

4. Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts, USA

5. Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA

6. Scintillon Institute, San Diego, California, USA

7. Department of Neurosurgery, Massachusetts General Hospital, Boston, Massachusetts, USA

Abstract

Abstract Background The 2016 World Health Organization Classification of Central Nervous System Tumors categorizes gliomatosis cerebri growth pattern (GC) as a subgroup of diffuse infiltrating gliomas, defined by extent of brain involvement on magnetic resonance imaging (MRI). Clinical and radiographic features in GC patients are highly heterogeneous; however, prognosis has historically been considered poor. Subjects, Materials, and Methods We performed a retrospective search for patients at our institution meeting radiographic criteria of primary, type I GC (defined as diffuse tumor infiltration without associated tumor mass and contrast enhancement on MRI) and analyzed their clinical, imaging, and histopathologic features. Results A total of 34 patients met radiographic criteria of primary, type I GC, and 33 had a confirmed histologic diagnosis of an infiltrating glial neoplasm. Age >47 years at diagnosis was associated with worse overall survival (OS) compared with age ≤47 years (hazard ratio [HR] 1.04, 95% confidence interval [CI] 1.01–1.07, p = .003). Patients with grade 2 tumors demonstrated a trend for improved OS compared with those with grade 3 tumors (HR 2.65, 95% CI 0.99–7.08, p = .051). Except for brainstem involvement, extent or location of radiographic involvement did not detectably affect clinical outcome. IDH mutation status identified a subgroup of GC patients with particularly long survival up to 25 years and was associated with longer time to progression (HR 4.81, 95% CI 0.99–23.47, p = .052). Conclusion Patients with primary, type I GC do not uniformly carry a poor prognosis, even in the presence of widespread radiographic involvement. Consistent with other reports, IDH mutation status may identify patients with improved clinical outcome. Molecular characterization, rather than MRI features, may be most valuable for prognostication and management of GC patients.

Funder

American Academy of Neurology

American Brain Tumor Association

Amy Gallagher Foundation

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference36 articles.

1. Gliomatosis cerebri;Nevin;Brain,1938

2. The 2007 WHO classification of tumours of the central nervous system;Louis;Acta Neuropathol,2007

3. WHO Classification of Tumours of the Central Nervous System;Louis,2016

4. Gliomatosis cerebri: A review of 22 cases;Vates;Neurosurgery,2003

5. Gliomatosis cerebri: Molecular pathology and clinical course;Herrlinger;Ann Neurol,2002

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