Potential skin morbidity reduction with intensity-modulated proton therapy for breast cancer with nodal involvement

Background: Different modern radiation therapy treatment solutions for breast cancer (BC) and regional nodal irradiation (RNI) have been proposed. In this study, we evaluate the potential reduction in radiation-induced skin morbidity obtained by intensity modulated proton therapy (IMPT) compared wit...

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Veröffentlicht in:Acta oncologica 2019-06, Vol.58 (6), p.934-942
Hauptverfasser: Fellin, Francesco, Iacco, Martina, D'Avino, Vittoria, Tommasino, Francesco, Farace, Paolo, Palma, Giuseppe, Conson, Manuel, Giacomelli, Irene, Zucchetti, Claudio, Falcinelli, Lorenzo, Amichetti, Maurizio, Aristei, Cynthia, Cella, Laura
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container_issue 6
container_start_page 934
container_title Acta oncologica
container_volume 58
creator Fellin, Francesco
Iacco, Martina
D'Avino, Vittoria
Tommasino, Francesco
Farace, Paolo
Palma, Giuseppe
Conson, Manuel
Giacomelli, Irene
Zucchetti, Claudio
Falcinelli, Lorenzo
Amichetti, Maurizio
Aristei, Cynthia
Cella, Laura
description Background: Different modern radiation therapy treatment solutions for breast cancer (BC) and regional nodal irradiation (RNI) have been proposed. In this study, we evaluate the potential reduction in radiation-induced skin morbidity obtained by intensity modulated proton therapy (IMPT) compared with intensity modulated photon therapy (IMXT) for left-side BC and RNI. Material and Methods: Using CT scans from 10 left-side BC patients, treatment plans were generated using IMXT and IMPT techniques. A dose of 50 Gy (or Gy [RBE] for IMPT) was prescribed to the target volume (involved breast, the internal mammary, supraclavicular, and infraclavicular nodes). Two single filed optimization IMPT (IMPT 1 and IMPT 2 ) plans were calculated without and with skin optimization. For each technique, skin dose-metrics were extracted and normal tissue complication probability (NTCP) models from the literature were employed to estimate the risk of radiation-induced skin morbidity. NTCPs for relevant organs-at-risk (OARs) were also considered for reference. The non-parametric Anova (Friedman matched-pairs signed-rank test) was used for comparative analyses. Results: IMPT improved target coverage and dose homogeneity even if the skin was included into optimization strategy (HI IMPT2 = 0.11 vs. HI IMXT = 0.22 and CI IMPT2 = 0.96 vs. CI IMXT = 0.82, p < .05). A significant relative skin risk reduction (RR = NTCP IMPT /NTCP IMXT ) was obtained with IMPT 2 including the skin in the optimization with a RR reduction ranging from 0.3 to 0.9 depending on the analyzed skin toxicity endpoint/model. Both IMPT plans attained significant OARs dose sparing compared with IMXT. As expected, the heart and lung doses were significantly reduced using IMPT. Accordingly, IMPT always provided lower NTCP values. Conclusions: IMPT guarantees optimal target coverage, OARs sparing, and simultaneously minimizes the risk of skin morbidity. The applied model-based approach supports the potential clinical relevance of IMPT for left-side BC and RNI and might be relevant for the setup of cost-effectiveness evaluation strategies based on NTCP predictions, as well as for establishing patient selection criteria.
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In this study, we evaluate the potential reduction in radiation-induced skin morbidity obtained by intensity modulated proton therapy (IMPT) compared with intensity modulated photon therapy (IMXT) for left-side BC and RNI. Material and Methods: Using CT scans from 10 left-side BC patients, treatment plans were generated using IMXT and IMPT techniques. A dose of 50 Gy (or Gy [RBE] for IMPT) was prescribed to the target volume (involved breast, the internal mammary, supraclavicular, and infraclavicular nodes). Two single filed optimization IMPT (IMPT 1 and IMPT 2 ) plans were calculated without and with skin optimization. For each technique, skin dose-metrics were extracted and normal tissue complication probability (NTCP) models from the literature were employed to estimate the risk of radiation-induced skin morbidity. NTCPs for relevant organs-at-risk (OARs) were also considered for reference. The non-parametric Anova (Friedman matched-pairs signed-rank test) was used for comparative analyses. Results: IMPT improved target coverage and dose homogeneity even if the skin was included into optimization strategy (HI IMPT2 = 0.11 vs. HI IMXT = 0.22 and CI IMPT2 = 0.96 vs. CI IMXT = 0.82, p &lt; .05). A significant relative skin risk reduction (RR = NTCP IMPT /NTCP IMXT ) was obtained with IMPT 2 including the skin in the optimization with a RR reduction ranging from 0.3 to 0.9 depending on the analyzed skin toxicity endpoint/model. Both IMPT plans attained significant OARs dose sparing compared with IMXT. As expected, the heart and lung doses were significantly reduced using IMPT. Accordingly, IMPT always provided lower NTCP values. Conclusions: IMPT guarantees optimal target coverage, OARs sparing, and simultaneously minimizes the risk of skin morbidity. 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In this study, we evaluate the potential reduction in radiation-induced skin morbidity obtained by intensity modulated proton therapy (IMPT) compared with intensity modulated photon therapy (IMXT) for left-side BC and RNI. Material and Methods: Using CT scans from 10 left-side BC patients, treatment plans were generated using IMXT and IMPT techniques. A dose of 50 Gy (or Gy [RBE] for IMPT) was prescribed to the target volume (involved breast, the internal mammary, supraclavicular, and infraclavicular nodes). Two single filed optimization IMPT (IMPT 1 and IMPT 2 ) plans were calculated without and with skin optimization. For each technique, skin dose-metrics were extracted and normal tissue complication probability (NTCP) models from the literature were employed to estimate the risk of radiation-induced skin morbidity. NTCPs for relevant organs-at-risk (OARs) were also considered for reference. The non-parametric Anova (Friedman matched-pairs signed-rank test) was used for comparative analyses. Results: IMPT improved target coverage and dose homogeneity even if the skin was included into optimization strategy (HI IMPT2 = 0.11 vs. HI IMXT = 0.22 and CI IMPT2 = 0.96 vs. CI IMXT = 0.82, p &lt; .05). A significant relative skin risk reduction (RR = NTCP IMPT /NTCP IMXT ) was obtained with IMPT 2 including the skin in the optimization with a RR reduction ranging from 0.3 to 0.9 depending on the analyzed skin toxicity endpoint/model. Both IMPT plans attained significant OARs dose sparing compared with IMXT. As expected, the heart and lung doses were significantly reduced using IMPT. Accordingly, IMPT always provided lower NTCP values. Conclusions: IMPT guarantees optimal target coverage, OARs sparing, and simultaneously minimizes the risk of skin morbidity. 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control</topic><topic>Survival Rate</topic><topic>Tomography, X-Ray Computed - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fellin, Francesco</creatorcontrib><creatorcontrib>Iacco, Martina</creatorcontrib><creatorcontrib>D'Avino, Vittoria</creatorcontrib><creatorcontrib>Tommasino, Francesco</creatorcontrib><creatorcontrib>Farace, Paolo</creatorcontrib><creatorcontrib>Palma, Giuseppe</creatorcontrib><creatorcontrib>Conson, Manuel</creatorcontrib><creatorcontrib>Giacomelli, Irene</creatorcontrib><creatorcontrib>Zucchetti, Claudio</creatorcontrib><creatorcontrib>Falcinelli, Lorenzo</creatorcontrib><creatorcontrib>Amichetti, Maurizio</creatorcontrib><creatorcontrib>Aristei, Cynthia</creatorcontrib><creatorcontrib>Cella, Laura</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Acta oncologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fellin, Francesco</au><au>Iacco, Martina</au><au>D'Avino, Vittoria</au><au>Tommasino, Francesco</au><au>Farace, Paolo</au><au>Palma, Giuseppe</au><au>Conson, Manuel</au><au>Giacomelli, Irene</au><au>Zucchetti, Claudio</au><au>Falcinelli, Lorenzo</au><au>Amichetti, Maurizio</au><au>Aristei, Cynthia</au><au>Cella, Laura</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential skin morbidity reduction with intensity-modulated proton therapy for breast cancer with nodal involvement</atitle><jtitle>Acta oncologica</jtitle><addtitle>Acta Oncol</addtitle><date>2019-06-03</date><risdate>2019</risdate><volume>58</volume><issue>6</issue><spage>934</spage><epage>942</epage><pages>934-942</pages><issn>0284-186X</issn><eissn>1651-226X</eissn><abstract>Background: Different modern radiation therapy treatment solutions for breast cancer (BC) and regional nodal irradiation (RNI) have been proposed. In this study, we evaluate the potential reduction in radiation-induced skin morbidity obtained by intensity modulated proton therapy (IMPT) compared with intensity modulated photon therapy (IMXT) for left-side BC and RNI. Material and Methods: Using CT scans from 10 left-side BC patients, treatment plans were generated using IMXT and IMPT techniques. A dose of 50 Gy (or Gy [RBE] for IMPT) was prescribed to the target volume (involved breast, the internal mammary, supraclavicular, and infraclavicular nodes). Two single filed optimization IMPT (IMPT 1 and IMPT 2 ) plans were calculated without and with skin optimization. For each technique, skin dose-metrics were extracted and normal tissue complication probability (NTCP) models from the literature were employed to estimate the risk of radiation-induced skin morbidity. NTCPs for relevant organs-at-risk (OARs) were also considered for reference. The non-parametric Anova (Friedman matched-pairs signed-rank test) was used for comparative analyses. Results: IMPT improved target coverage and dose homogeneity even if the skin was included into optimization strategy (HI IMPT2 = 0.11 vs. HI IMXT = 0.22 and CI IMPT2 = 0.96 vs. CI IMXT = 0.82, p &lt; .05). A significant relative skin risk reduction (RR = NTCP IMPT /NTCP IMXT ) was obtained with IMPT 2 including the skin in the optimization with a RR reduction ranging from 0.3 to 0.9 depending on the analyzed skin toxicity endpoint/model. Both IMPT plans attained significant OARs dose sparing compared with IMXT. As expected, the heart and lung doses were significantly reduced using IMPT. Accordingly, IMPT always provided lower NTCP values. Conclusions: IMPT guarantees optimal target coverage, OARs sparing, and simultaneously minimizes the risk of skin morbidity. The applied model-based approach supports the potential clinical relevance of IMPT for left-side BC and RNI and might be relevant for the setup of cost-effectiveness evaluation strategies based on NTCP predictions, as well as for establishing patient selection criteria.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>30938217</pmid><doi>10.1080/0284186X.2019.1591638</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0210-268X</orcidid><orcidid>https://orcid.org/0000-0003-0058-4029</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Taylor & Francis Journals Complete; Alma/SFX Local Collection
subjects Breast Neoplasms - pathology
Breast Neoplasms - radiotherapy
Female
Follow-Up Studies
Humans
Lymph Nodes - pathology
Lymph Nodes - radiation effects
Organs at Risk - radiation effects
Prognosis
Proton Therapy - adverse effects
Radiation Injuries - etiology
Radiation Injuries - mortality
Radiation Injuries - pathology
Radiotherapy Planning, Computer-Assisted - methods
Radiotherapy, Intensity-Modulated - adverse effects
Retrospective Studies
Risk Reduction Behavior
Skin Diseases - chemically induced
Skin Diseases - prevention & control
Survival Rate
Tomography, X-Ray Computed - methods
title Potential skin morbidity reduction with intensity-modulated proton therapy for breast cancer with nodal involvement
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