2005
DOI: 10.1088/0031-9155/50/18/007
|View full text |Cite
|
Sign up to set email alerts
|

Simulation of organ-specific patient effective dose due to secondary neutrons in proton radiation treatment

Abstract: Cancer patients undergoing radiation treatment are exposed to high doses to the target (tumour), intermediate doses to adjacent tissues and low doses from scattered radiation to all parts of the body. In the case of proton therapy, secondary neutrons generated in the accelerator head and inside the patient reach many areas in the patient body. Due to the improved efficacy of management of cancer patients, the number of long term survivors post-radiation treatment is increasing substantially. This results in co… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

6
105
0
1

Year Published

2007
2007
2017
2017

Publication Types

Select...
6
4

Relationship

1
9

Authors

Journals

citations
Cited by 123 publications
(112 citation statements)
references
References 21 publications
6
105
0
1
Order By: Relevance
“…Thus, even the most conservative estimation of the relative biological effect (RBE=20) of neutron dose would still result in a neutron dose on the order of tens of milliSieverts per treatment Gray, and its inclusion in modeling risk estimates would not increase risk results for cardiac mortality or EAR for secondary lung or breast cancers. This conclusion is in agreement with similar studies 36 , 37 , 38 , 39 . This work represents a first estimation of risk due to different modalities as planned by commercially available TPS, which may be further refined in future work with Monte Carlo dose calculation to take RBE into account.…”
Section: Discussionsupporting
confidence: 92%
“…Thus, even the most conservative estimation of the relative biological effect (RBE=20) of neutron dose would still result in a neutron dose on the order of tens of milliSieverts per treatment Gray, and its inclusion in modeling risk estimates would not increase risk results for cardiac mortality or EAR for secondary lung or breast cancers. This conclusion is in agreement with similar studies 36 , 37 , 38 , 39 . This work represents a first estimation of risk due to different modalities as planned by commercially available TPS, which may be further refined in future work with Monte Carlo dose calculation to take RBE into account.…”
Section: Discussionsupporting
confidence: 92%
“…This result is similar to the effective dose from internal neutrons that was reported by for a prostate treatment (40%) and by Jiang et al (2005) for a lung treatment (36%).…”
Section: Discussionsupporting
confidence: 90%
“…Monte Carlo methods also turn out to be powerful in complex situations where measurements are difficult to achieve. They also have many other applications in proton therapy: verification of shielding design efficiency (Newhauser et al, 2002), assessment of secondary doses received by proton therapy patients (Agosteo et al, 1998;Jiang et al, 2005;Zacharatou Jarlskog and Paganetti 2008) and neutron fluence and ambient dose equivalent calculations (Zheng et al, 2008;Perez-Andujar et al, 2009). It should be noted that each Monte Carlo model must first be carefully validated with experimental data in order to verify the accuracy of results.…”
Section: Introductionmentioning
confidence: 99%