Larger tumor volume is associated with visual acuity loss and axonal degeneration in children with optic pathway gliomas secondary to neurofibromatosis type 1

Author:

Avery Robert A12ORCID,Mansoor Awais3,Liu Grant T1,Trimboli−Heidler Carmelina1,Ying Gui−Shuang2,Centrella Cameron R1,Eltoukhy Nadeen1,Packer Roger J3,Fisher Michael J12,Linguraru Marius George34

Affiliation:

1. Divisions of Ophthalmology and Neuro−Oncology, The Children’s Hospital of Philadelphia , Philadelphia, Pennsylvania , USA

2. Departments of Ophthalmology, Neurology and Pediatrics, The Perelman School of Medicine at the University of Pennsylvania , Philadelphia, Pennsylvania , USA

3. Center for Neuroscience and Behavior and Sheikh Zayed Institute for Pediatric Surgical Innovation, Children’s National Health System , Washington, District of Columbia , USA

4. Departments of Radiology and Pediatrics, School of Medicine and Health Sciences, George Washington University , Washington, District of Columbia , USA

Abstract

Abstract Background We investigated whether volumetric magnetic resonance imaging (MRI) measures of the anterior visual pathway (AVP) in optic pathway gliomas secondary to Neurofibromatosis type 1 (NF1−OPG) are associated with visual acuity (VA) loss and axonal loss, as measured using optical coherence tomography (OCT). Methods Children with NF1−OPGs enrolled in a prospective study of VA and OCT measures of the circumpapillary retinal nerve fiber layer (cpRNFL) thickness were eligible if they had undergone 3-Tesla MRI that included a T1-weighted volumetric sequence. The linear dimension and volume of the optic nerves, chiasm, and optic tracts were measured using our semi-automated algorithm. The combined volume of these components comprising the proximal AVP was used as a surrogate of total tumor burden. Regression models for VA and cpRNFL thickness were reported on a per-eye basis. Results Fifty−two study eyes (26 children, mean 7.1 years) met inclusion criteria, of which 40% (N = 21 eyes) had abnormal VA. In regression analysis, only total AVP volume demonstrated a significant relationship to axonal loss, such that for every 1 mL increase in AVP volume, cpRNFL declined by 5.4 microns (P = .01). Total AVP volume > 1.75 mL predicted both axonal loss and abnormal VA (positive predictive value of 83.3% and 70.8%, respectively; negative predictive value of 80.0% and 88.0%, respectively). Conclusions Volumetric measures of NF1-OPGs identified children with VA loss and axonal degeneration. Total tumor burden, as measured by AVP volume, had the strongest relationship with axonal injury. NF1-OPG volumetric measures may be helpful in making treatment decisions.

Funder

Department of Defense

National Institute of Health

Publisher

Oxford University Press (OUP)

Subject

Surgery,Oncology,Neurology (clinical)

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