PATH-30. Exosomes as a source of plasma CTDNA to identify point mutations in pediatric glioma patients
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Neuro Oncology
Abstract
PURPOSE: By reducing dose to normal brain tissue, proton radio therapy (PRT) may lessen neurocognitive risk traditionally associated with
photon radiotherapy (XRT). We examined change in neurocognitive scores
over time in pediatric medulloblastoma patients treated with PRT versus
XRT. METHODS: Neurocognitive scores from 79 patients (37 PRT, 42
XRT) were examined. Patients were treated between 2007–2018 on the
same treatment protocols that differed only by craniospinal modality (PRT
versus XRT). Change in scores over time since diagnosis were compared
between groups. RESULTS: Groups were similar on most demographic/
clinical variables: sex (67.1% male), age at diagnosis (mean 8.6 years), CSI
dose (median 23.4 Gy), length of follow-up (mean 4.3 years), and parental
education (mean 14.3 years). Boost dose (p<0.001) and margin (p=0.001)
differed between groups. Adjusting for covariates, the PRT group exhibited
superior outcomes in global IQ, perceptual reasoning, and working memory
versus the XRT group (all p<0.05). The XRT group exhibited significant de cline in global IQ, working memory, and processing speed (all p<0.05). The
PRT group exhibited stable scores in all domains except processing speed
(p=0.003). Posterior fossa syndrome imparted risk independent of mo dality. CONCLUSION: This is the first study comparing neurocognitive tra jectories between pediatric patients treated for medulloblastoma with PRT
versus XRT on comparable, contemporary protocols. PRT was associated
with more favorable neurocognitive outcomes in most domains compared to
XRT, although processing speed emerged as vulnerable in both groups. This
is the strongest evidence to date of an intellectual sparing advantage with
PRT in the treatment of pediatric medulloblastoma.
Description
p. 430–431.
Citation
NOBRE, Liana Figueiredo et al. PATH-30. Exosomes as a source of plasma CTDNA to identify point mutations in pediatric glioma patients. Neuro Oncology, v. 22, supl 3, p. 430–431, dec. 2020.