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Second primary cancers after radiation for prostate cancer: a review of data from planning studies

A review of planning studies was undertaken to evaluate estimated risks of radiation induced second primary cancers (RISPC) associated with different prostate radiotherapy techniques for localised prostate cancer. A total of 83 publications were identified which employed a variety of methods to esti...

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Autores principales: Murray, Louise, Henry, Ann, Hoskin, Peter, Siebert, Frank-Andre, Venselaar, Jack
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724744/
https://www.ncbi.nlm.nih.gov/pubmed/23835163
http://dx.doi.org/10.1186/1748-717X-8-172
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author Murray, Louise
Henry, Ann
Hoskin, Peter
Siebert, Frank-Andre
Venselaar, Jack
author_facet Murray, Louise
Henry, Ann
Hoskin, Peter
Siebert, Frank-Andre
Venselaar, Jack
author_sort Murray, Louise
collection PubMed
description A review of planning studies was undertaken to evaluate estimated risks of radiation induced second primary cancers (RISPC) associated with different prostate radiotherapy techniques for localised prostate cancer. A total of 83 publications were identified which employed a variety of methods to estimate RISPC risk. Of these, the 16 planning studies which specifically addressed absolute or relative second cancer risk using dose–response models were selected for inclusion within this review. There are uncertainties and limitations related to all the different methods for estimating RISPC risk. Whether or not dose models include the effects of the primary radiation beam, as well as out-of-field regions, influences estimated risks. Regarding the impact of IMRT compared to 3D-CRT, at equivalent energies, several studies suggest an increase in risk related to increased leakage contributing to out-of-field RISPC risk, although in absolute terms this increase in risk may be very small. IMRT also results in increased low dose normal tissue irradiation, but the extent to which this has been estimated to contribute to RISPC risk is variable, and may also be very small. IMRT is often delivered using 6MV photons while conventional radiotherapy often requires higher energies to achieve adequate tissue penetration, and so comparisons between IMRT and older techniques should not be restricted to equivalent energies. Proton and brachytherapy planning studies suggest very low RISPC risks associated with these techniques. Until there is sufficient clinical evidence regarding RISPC risks associated with modern irradiation techniques, the data produced from planning studies is relevant when considering which patients to irradiate, and which technique to employ.
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spelling pubmed-37247442013-07-27 Second primary cancers after radiation for prostate cancer: a review of data from planning studies Murray, Louise Henry, Ann Hoskin, Peter Siebert, Frank-Andre Venselaar, Jack Radiat Oncol Review A review of planning studies was undertaken to evaluate estimated risks of radiation induced second primary cancers (RISPC) associated with different prostate radiotherapy techniques for localised prostate cancer. A total of 83 publications were identified which employed a variety of methods to estimate RISPC risk. Of these, the 16 planning studies which specifically addressed absolute or relative second cancer risk using dose–response models were selected for inclusion within this review. There are uncertainties and limitations related to all the different methods for estimating RISPC risk. Whether or not dose models include the effects of the primary radiation beam, as well as out-of-field regions, influences estimated risks. Regarding the impact of IMRT compared to 3D-CRT, at equivalent energies, several studies suggest an increase in risk related to increased leakage contributing to out-of-field RISPC risk, although in absolute terms this increase in risk may be very small. IMRT also results in increased low dose normal tissue irradiation, but the extent to which this has been estimated to contribute to RISPC risk is variable, and may also be very small. IMRT is often delivered using 6MV photons while conventional radiotherapy often requires higher energies to achieve adequate tissue penetration, and so comparisons between IMRT and older techniques should not be restricted to equivalent energies. Proton and brachytherapy planning studies suggest very low RISPC risks associated with these techniques. Until there is sufficient clinical evidence regarding RISPC risks associated with modern irradiation techniques, the data produced from planning studies is relevant when considering which patients to irradiate, and which technique to employ. BioMed Central 2013-07-08 /pmc/articles/PMC3724744/ /pubmed/23835163 http://dx.doi.org/10.1186/1748-717X-8-172 Text en Copyright © 2013 Murray et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Murray, Louise
Henry, Ann
Hoskin, Peter
Siebert, Frank-Andre
Venselaar, Jack
Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title_full Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title_fullStr Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title_full_unstemmed Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title_short Second primary cancers after radiation for prostate cancer: a review of data from planning studies
title_sort second primary cancers after radiation for prostate cancer: a review of data from planning studies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724744/
https://www.ncbi.nlm.nih.gov/pubmed/23835163
http://dx.doi.org/10.1186/1748-717X-8-172
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