Vulnerability of white matter to insult during childhood: evidence from patients treated for medulloblastoma

Author:

Moxon-Emre Iska123,Bouffet Eric4,Taylor Michael D.56,Laperriere Normand78,Sharpe Michael B.78,Laughlin Suzanne9,Bartels Ute4,Scantlebury Nadia1,Law Nicole12,Malkin David3410,Skocic Jovanka1,Richard Logan12,Mabbott Donald J.12

Affiliation:

1. Program in Neuroscience and Mental Health and

2. Departments of Psychology,

3. Pediatric Oncology Group of Ontario, Toronto; and

4. Divisions of Hematology/Oncology,

5. Neurosurgery, and

6. Neurosurgery,

7. Radiation Oncology, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada

8. Radiation Oncology, and

9. Diagnostic Imaging, Hospital for Sick Children, Toronto;

10. Paediatrics, University of Toronto;

Abstract

OBJECTIVE Craniospinal irradiation damages the white matter in children treated for medulloblastoma, but the treatment-intensity effects are unclear. In a cross-sectional retrospective study, the effects of treatment with the least intensive radiation protocol versus protocols that delivered more radiation to the brain, in addition to the effects of continuous radiation dose, on white matter architecture were evaluated. METHODS Diffusion tensor imaging was used to assess fractional anisotropy, mean diffusivity, radial diffusivity, and axial diffusivity. First, regional white matter analyses and tract-based spatial statistics were conducted in 34 medulloblastoma patients and 38 healthy controls. Patients were stratified according to those treated with 1) the least intensive radiation protocol, specifically reduced-dose craniospinal irradiation plus a boost to the tumor bed only (n = 17), or 2) any other dose and boost combination that delivered more radiation to the brain, which was also termed the “all-other-treatments” group (n = 17), and comprised patients treated with standard-dose craniospinal irradiation plus a posterior fossa boost, standard-dose craniospinal irradiation plus a tumor bed boost, or reduced-dose craniospinal irradiation plus a posterior fossa boost. Second, voxel-wise dose-distribution analyses were conducted on a separate cohort of medulloblastoma patients (n = 15). RESULTS The all-other-treatments group, but not the reduced-dose craniospinal irradiation plus tumor bed group, had lower fractional anisotropy and higher radial diffusivity than controls in all brain regions (all p < 0.05). The reduced-dose craniospinal irradiation plus tumor bed boost group had higher fractional anisotropy (p = 0.05) and lower radial diffusivity (p = 0.04) in the temporal region, and higher fractional anisotropy in the frontal region (p = 0.04), than the all-other-treatments group. Linear mixed-effects modeling revealed that the dose and age at diagnosis together 1) better predicted fractional anisotropy in the temporal region than models with either alone (p < 0.005), but 2) did not better predict fractional anisotropy in comparison with dose alone in the occipital region (p > 0.05). CONCLUSIONS Together, the results show that white matter damage has a clear association with increasing radiation dose, and that treatment with reduced-dose craniospinal irradiation plus tumor bed boost appears to preserve white matter in some brain regions.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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