Minimizing side effects for pediatric patients treated with craniospinal irradiation

Publikation: Bog/antologi/afhandling/rapportPh.d.-afhandlingForskning

Standard

Minimizing side effects for pediatric patients treated with craniospinal irradiation. / Gram, Daniel Adam Peter.

Niels Bohr Institute, Faculty of Science, University of Copenhagen, 2020. 150 s.

Publikation: Bog/antologi/afhandling/rapportPh.d.-afhandlingForskning

Harvard

Gram, DAP 2020, Minimizing side effects for pediatric patients treated with craniospinal irradiation. Niels Bohr Institute, Faculty of Science, University of Copenhagen.

APA

Gram, D. A. P. (2020). Minimizing side effects for pediatric patients treated with craniospinal irradiation. Niels Bohr Institute, Faculty of Science, University of Copenhagen.

Vancouver

Gram DAP. Minimizing side effects for pediatric patients treated with craniospinal irradiation. Niels Bohr Institute, Faculty of Science, University of Copenhagen, 2020. 150 s.

Author

Gram, Daniel Adam Peter. / Minimizing side effects for pediatric patients treated with craniospinal irradiation. Niels Bohr Institute, Faculty of Science, University of Copenhagen, 2020. 150 s.

Bibtex

@phdthesis{b9199afaf2ed4873a4b9713fa1fdcaa9,
title = "Minimizing side effects for pediatric patients treated with craniospinal irradiation",
abstract = "Second only to leukemia, primary tumors in the central nervous system (CNS) are the most commonly occurring malignancies in children, with medulloblastoma being the most prevalent. The standard-of-care for medulloblastoma consists of a combination of surgery, chemotherapy and craniospinal irradiation (CSI) and isusually administered to children above 3-5 years of age. Pediatric CNS tumors, although rare, have a devastating impact on patients and their families both due to the disease and the severe treatment related side effects. Most long-term survivors of malignant pediatric CNS tumors treated with CSI have significant late effects, such as perturbed growth, hearing or vision loss, cardiovascular events, lung toxicity and neurocognitive impairment, and patients irradiated at a younger age tend to have worse outcomes. Since the frequency and severity of late side effects generally increase with time, they are especially debilitating for pediatric cancer survivors as they mature into adulthood.The purpose of this PhD project was to investigate different possibilities of reducing side effects to organsat-risk (OARs) for pediatric patients with CNS malignancies treated with CSI. We investigated setup errors and uncertainties to evaluate margins and robustness perturbations needed for CSI treatments. These results were used to create realistic hippocampal-sparing proton therapy treatment plans aimed at reducing neurocognitive impairment. The results from that study demonstrated that it is possible to reduce the risk of neurocognitiveimpairment with only a minimal impact on target coverage and without reducing the estimated tumor control. We further investigated the effects of linear energy transfer (LET) and how it impacts the radiobiologically weighted dose distribution generally and how these results affect the sparing of the hippocampi specifically. We found that areas of where the proton beam stops can be highly affected depending on the tissue specific parameters assigned to the tumor and OARs. This field of study needs further investigation before biologicallyweighted doses can be used clinically, especially in the setting of hippocampal-sparing (HS) CSI. We also created mathematical models for predicting OAR doses from spinal irradiation treatments delivered in the era before 3D treatment planning and volumetric dose reporting. The aim of this was to be able to link OAR doses with longterm follow-up data for an increased understanding of dose-response relationships in cohorts of pediatric cancer survivors, which could further reduce the side effects to this patient group.The work conducted and results presented in this thesis show that there are actionable opportunities for minimizing side effects of pediatric patients with CNS malignancies treated with CSI.",
author = "Gram, {Daniel Adam Peter}",
year = "2020",
language = "English",
publisher = "Niels Bohr Institute, Faculty of Science, University of Copenhagen",

}

RIS

TY - BOOK

T1 - Minimizing side effects for pediatric patients treated with craniospinal irradiation

AU - Gram, Daniel Adam Peter

PY - 2020

Y1 - 2020

N2 - Second only to leukemia, primary tumors in the central nervous system (CNS) are the most commonly occurring malignancies in children, with medulloblastoma being the most prevalent. The standard-of-care for medulloblastoma consists of a combination of surgery, chemotherapy and craniospinal irradiation (CSI) and isusually administered to children above 3-5 years of age. Pediatric CNS tumors, although rare, have a devastating impact on patients and their families both due to the disease and the severe treatment related side effects. Most long-term survivors of malignant pediatric CNS tumors treated with CSI have significant late effects, such as perturbed growth, hearing or vision loss, cardiovascular events, lung toxicity and neurocognitive impairment, and patients irradiated at a younger age tend to have worse outcomes. Since the frequency and severity of late side effects generally increase with time, they are especially debilitating for pediatric cancer survivors as they mature into adulthood.The purpose of this PhD project was to investigate different possibilities of reducing side effects to organsat-risk (OARs) for pediatric patients with CNS malignancies treated with CSI. We investigated setup errors and uncertainties to evaluate margins and robustness perturbations needed for CSI treatments. These results were used to create realistic hippocampal-sparing proton therapy treatment plans aimed at reducing neurocognitive impairment. The results from that study demonstrated that it is possible to reduce the risk of neurocognitiveimpairment with only a minimal impact on target coverage and without reducing the estimated tumor control. We further investigated the effects of linear energy transfer (LET) and how it impacts the radiobiologically weighted dose distribution generally and how these results affect the sparing of the hippocampi specifically. We found that areas of where the proton beam stops can be highly affected depending on the tissue specific parameters assigned to the tumor and OARs. This field of study needs further investigation before biologicallyweighted doses can be used clinically, especially in the setting of hippocampal-sparing (HS) CSI. We also created mathematical models for predicting OAR doses from spinal irradiation treatments delivered in the era before 3D treatment planning and volumetric dose reporting. The aim of this was to be able to link OAR doses with longterm follow-up data for an increased understanding of dose-response relationships in cohorts of pediatric cancer survivors, which could further reduce the side effects to this patient group.The work conducted and results presented in this thesis show that there are actionable opportunities for minimizing side effects of pediatric patients with CNS malignancies treated with CSI.

AB - Second only to leukemia, primary tumors in the central nervous system (CNS) are the most commonly occurring malignancies in children, with medulloblastoma being the most prevalent. The standard-of-care for medulloblastoma consists of a combination of surgery, chemotherapy and craniospinal irradiation (CSI) and isusually administered to children above 3-5 years of age. Pediatric CNS tumors, although rare, have a devastating impact on patients and their families both due to the disease and the severe treatment related side effects. Most long-term survivors of malignant pediatric CNS tumors treated with CSI have significant late effects, such as perturbed growth, hearing or vision loss, cardiovascular events, lung toxicity and neurocognitive impairment, and patients irradiated at a younger age tend to have worse outcomes. Since the frequency and severity of late side effects generally increase with time, they are especially debilitating for pediatric cancer survivors as they mature into adulthood.The purpose of this PhD project was to investigate different possibilities of reducing side effects to organsat-risk (OARs) for pediatric patients with CNS malignancies treated with CSI. We investigated setup errors and uncertainties to evaluate margins and robustness perturbations needed for CSI treatments. These results were used to create realistic hippocampal-sparing proton therapy treatment plans aimed at reducing neurocognitive impairment. The results from that study demonstrated that it is possible to reduce the risk of neurocognitiveimpairment with only a minimal impact on target coverage and without reducing the estimated tumor control. We further investigated the effects of linear energy transfer (LET) and how it impacts the radiobiologically weighted dose distribution generally and how these results affect the sparing of the hippocampi specifically. We found that areas of where the proton beam stops can be highly affected depending on the tissue specific parameters assigned to the tumor and OARs. This field of study needs further investigation before biologicallyweighted doses can be used clinically, especially in the setting of hippocampal-sparing (HS) CSI. We also created mathematical models for predicting OAR doses from spinal irradiation treatments delivered in the era before 3D treatment planning and volumetric dose reporting. The aim of this was to be able to link OAR doses with longterm follow-up data for an increased understanding of dose-response relationships in cohorts of pediatric cancer survivors, which could further reduce the side effects to this patient group.The work conducted and results presented in this thesis show that there are actionable opportunities for minimizing side effects of pediatric patients with CNS malignancies treated with CSI.

M3 - Ph.D. thesis

BT - Minimizing side effects for pediatric patients treated with craniospinal irradiation

PB - Niels Bohr Institute, Faculty of Science, University of Copenhagen

ER -

ID: 252770803