TY - JOUR
T1 - Hippocampal sparing radiotherapy for pediatric medulloblastoma
T2 - Impact of treatment margins and treatment technique
AU - Brodin, N. Patrik
AU - Munck Af Rosenschöld, Per
AU - Blomstrand, Malin
AU - Kiil-Berthlesen, Anne
AU - Hollensen, Christian
AU - Vogelius, Ivan R.
AU - Lannering, Birgitta
AU - Bentzen, Søren M.
AU - Björk-Eriksson, Thomas
PY - 2014/4
Y1 - 2014/4
N2 - Background. We investigated how varying the treatment margin and applying hippocampal sparing and proton therapy impact the risk of neurocognitive impairment in pediatric medulloblastoma patients compared with current standard 3D conformal radiotherapy. Methods. We included 17 pediatric medulloblastoma patients to represent the variability in tumor location relative to the hippocampal region. Treatment plans were generated using 3D conformal radiotherapy, hippocampal sparing intensity-modulated radiotherapy, and spot-scanned proton therapy, using 3 different treatment margins for the conformal tumor boost. Neurocognitive impairment risk was estimated based on dose-response models from pediatric CNS malignancy survivors and compared among different margins and treatment techniques. Results. Mean hippocampal dose and corresponding risk of cognitive impairment were decreased with decreasing treatment margins (P <. 05). The largest risk reduction, however, was seen when applying hippocampal sparing proton therapy - the estimated risk of impaired task efficiency (95% confidence interval) was 92% (66%-98%), 81% (51%-95%), and 50% (30%-70%) for 3D conformal radiotherapy, intensity-modulated radiotherapy, and proton therapy, respectively, for the smallest boost margin and 98% (78%-100%), 90% (60%-98%), and 70% (39%-90%) if boosting the whole posterior fossa. Also, the distance between the closest point of the planning target volume and the center of the hippocampus can be used to predict mean hippocampal dose for a given treatment technique. Conclusions. We estimate a considerable clinical benefit of hippocampal sparing radiotherapy. In choosing treatment margins, the tradeoff between margin size and risk of neurocognitive impairment quantified here should be considered.
AB - Background. We investigated how varying the treatment margin and applying hippocampal sparing and proton therapy impact the risk of neurocognitive impairment in pediatric medulloblastoma patients compared with current standard 3D conformal radiotherapy. Methods. We included 17 pediatric medulloblastoma patients to represent the variability in tumor location relative to the hippocampal region. Treatment plans were generated using 3D conformal radiotherapy, hippocampal sparing intensity-modulated radiotherapy, and spot-scanned proton therapy, using 3 different treatment margins for the conformal tumor boost. Neurocognitive impairment risk was estimated based on dose-response models from pediatric CNS malignancy survivors and compared among different margins and treatment techniques. Results. Mean hippocampal dose and corresponding risk of cognitive impairment were decreased with decreasing treatment margins (P <. 05). The largest risk reduction, however, was seen when applying hippocampal sparing proton therapy - the estimated risk of impaired task efficiency (95% confidence interval) was 92% (66%-98%), 81% (51%-95%), and 50% (30%-70%) for 3D conformal radiotherapy, intensity-modulated radiotherapy, and proton therapy, respectively, for the smallest boost margin and 98% (78%-100%), 90% (60%-98%), and 70% (39%-90%) if boosting the whole posterior fossa. Also, the distance between the closest point of the planning target volume and the center of the hippocampus can be used to predict mean hippocampal dose for a given treatment technique. Conclusions. We estimate a considerable clinical benefit of hippocampal sparing radiotherapy. In choosing treatment margins, the tradeoff between margin size and risk of neurocognitive impairment quantified here should be considered.
KW - Cognitive risk estimation
KW - Hippocampal sparing
KW - Medulloblastoma
KW - Tumor bed boost
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U2 - 10.1093/neuonc/not225
DO - 10.1093/neuonc/not225
M3 - Article
C2 - 24327585
AN - SCOPUS:84896998133
SN - 1522-8517
VL - 16
SP - 594
EP - 602
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 4
ER -