Impact of Dose to the Bladder Trigone on Long-Term Urinary Function After High-Dose Intensity Modulated Radiation Therapy for Localized Prostate Cancer

Purpose To determine the potential association between genitourinary (GU) toxicity and planning dose–volume parameters for GU pelvic structures after high-dose intensity modulated radiation therapy in localized prostate cancer patients. Methods and Materials A total of 268 patients who underwent int...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2014-02, Vol.88 (2), p.339-344
Hauptverfasser: Ghadjar, Pirus, MD, Zelefsky, Michael J., MD, Spratt, Daniel E., MD, Munck af Rosenschöld, Per, PhD, Oh, Jung Hun, PhD, Hunt, Margie, PhD, Kollmeier, Marisa, MD, Happersett, Laura, PhD, Yorke, Ellen, PhD, Deasy, Joseph O., PhD, Jackson, Andrew, PhD
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container_end_page 344
container_issue 2
container_start_page 339
container_title International journal of radiation oncology, biology, physics
container_volume 88
creator Ghadjar, Pirus, MD
Zelefsky, Michael J., MD
Spratt, Daniel E., MD
Munck af Rosenschöld, Per, PhD
Oh, Jung Hun, PhD
Hunt, Margie, PhD
Kollmeier, Marisa, MD
Happersett, Laura, PhD
Yorke, Ellen, PhD
Deasy, Joseph O., PhD
Jackson, Andrew, PhD
description Purpose To determine the potential association between genitourinary (GU) toxicity and planning dose–volume parameters for GU pelvic structures after high-dose intensity modulated radiation therapy in localized prostate cancer patients. Methods and Materials A total of 268 patients who underwent intensity modulated radiation therapy to a prescribed dose of 86.4 Gy in 48 fractions during June 2004-December 2008 were evaluated with the International Prostate Symptom Score (IPSS) questionnaire. Dose–volume histograms of the whole bladder, bladder wall, urethra, and bladder trigone were analyzed. The primary endpoint for GU toxicity was an IPSS sum increase ≥10 points over baseline. Univariate and multivariate analyses were done by the Kaplan-Meier method and Cox proportional hazard models, respectively. Results Median follow-up was 5 years (range, 3-7.7 years). Thirty-nine patients experienced an IPSS sum increase ≥10 during follow-up; 84% remained event free at 5 years. After univariate analysis, lower baseline IPSS sum ( P =.006), the V90 of the trigone ( P =.006), and the maximal dose to the trigone ( P =.003) were significantly associated with an IPSS sum increase ≥10. After multivariate analysis, lower baseline IPSS sum ( P =.009) and increased maximal dose to the trigone ( P =.005) remained significantly associated. Seventy-two patients had both a lower baseline IPSS sum and a higher maximal dose to the trigone and were defined as high risk, and 68 patients had both a higher baseline IPSS sum and a lower maximal dose to the trigone and were defined as low risk for development of an IPSS sum increase ≥10. Twenty-one of 72 high-risk patients (29%) and 5 of 68 low-risk patients (7%) experienced an IPSS sum increase ≥10 ( P =.001; odds ratio 5.19). Conclusions The application of hot spots to the bladder trigone was significantly associated with relevant changes in IPSS during follow-up. Reduction of radiation dose to the lower bladder and specifically the bladder trigone seems to be associated with a reduction in late GU toxicity.
doi_str_mv 10.1016/j.ijrobp.2013.10.042
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Methods and Materials A total of 268 patients who underwent intensity modulated radiation therapy to a prescribed dose of 86.4 Gy in 48 fractions during June 2004-December 2008 were evaluated with the International Prostate Symptom Score (IPSS) questionnaire. Dose–volume histograms of the whole bladder, bladder wall, urethra, and bladder trigone were analyzed. The primary endpoint for GU toxicity was an IPSS sum increase ≥10 points over baseline. Univariate and multivariate analyses were done by the Kaplan-Meier method and Cox proportional hazard models, respectively. Results Median follow-up was 5 years (range, 3-7.7 years). Thirty-nine patients experienced an IPSS sum increase ≥10 during follow-up; 84% remained event free at 5 years. After univariate analysis, lower baseline IPSS sum ( P =.006), the V90 of the trigone ( P =.006), and the maximal dose to the trigone ( P =.003) were significantly associated with an IPSS sum increase ≥10. After multivariate analysis, lower baseline IPSS sum ( P =.009) and increased maximal dose to the trigone ( P =.005) remained significantly associated. Seventy-two patients had both a lower baseline IPSS sum and a higher maximal dose to the trigone and were defined as high risk, and 68 patients had both a higher baseline IPSS sum and a lower maximal dose to the trigone and were defined as low risk for development of an IPSS sum increase ≥10. Twenty-one of 72 high-risk patients (29%) and 5 of 68 low-risk patients (7%) experienced an IPSS sum increase ≥10 ( P =.001; odds ratio 5.19). Conclusions The application of hot spots to the bladder trigone was significantly associated with relevant changes in IPSS during follow-up. Reduction of radiation dose to the lower bladder and specifically the bladder trigone seems to be associated with a reduction in late GU toxicity.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2013.10.042</identifier><identifier>PMID: 24411606</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Analysis of Variance ; BLADDER ; Follow-Up Studies ; Hematology, Oncology and Palliative Medicine ; Humans ; Male ; MULTIVARIATE ANALYSIS ; NEOPLASMS ; Organs at Risk - radiation effects ; PATIENTS ; PLANNING ; PROSTATE ; Prostatic Neoplasms - radiotherapy ; Radiation Dosage ; RADIATION DOSES ; Radiation Injuries - complications ; Radiology ; RADIOLOGY AND NUCLEAR MEDICINE ; RADIOTHERAPY ; Radiotherapy, Intensity-Modulated - adverse effects ; Radiotherapy, Intensity-Modulated - methods ; Rectum - radiation effects ; Surveys and Questionnaires ; TOXICITY ; Urethra - radiation effects ; Urinary Bladder - radiation effects ; Urogenital System - radiation effects</subject><ispartof>International journal of radiation oncology, biology, physics, 2014-02, Vol.88 (2), p.339-344</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. 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Methods and Materials A total of 268 patients who underwent intensity modulated radiation therapy to a prescribed dose of 86.4 Gy in 48 fractions during June 2004-December 2008 were evaluated with the International Prostate Symptom Score (IPSS) questionnaire. Dose–volume histograms of the whole bladder, bladder wall, urethra, and bladder trigone were analyzed. The primary endpoint for GU toxicity was an IPSS sum increase ≥10 points over baseline. Univariate and multivariate analyses were done by the Kaplan-Meier method and Cox proportional hazard models, respectively. Results Median follow-up was 5 years (range, 3-7.7 years). Thirty-nine patients experienced an IPSS sum increase ≥10 during follow-up; 84% remained event free at 5 years. After univariate analysis, lower baseline IPSS sum ( P =.006), the V90 of the trigone ( P =.006), and the maximal dose to the trigone ( P =.003) were significantly associated with an IPSS sum increase ≥10. After multivariate analysis, lower baseline IPSS sum ( P =.009) and increased maximal dose to the trigone ( P =.005) remained significantly associated. Seventy-two patients had both a lower baseline IPSS sum and a higher maximal dose to the trigone and were defined as high risk, and 68 patients had both a higher baseline IPSS sum and a lower maximal dose to the trigone and were defined as low risk for development of an IPSS sum increase ≥10. Twenty-one of 72 high-risk patients (29%) and 5 of 68 low-risk patients (7%) experienced an IPSS sum increase ≥10 ( P =.001; odds ratio 5.19). Conclusions The application of hot spots to the bladder trigone was significantly associated with relevant changes in IPSS during follow-up. 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Zelefsky, Michael J., MD ; Spratt, Daniel E., MD ; Munck af Rosenschöld, Per, PhD ; Oh, Jung Hun, PhD ; Hunt, Margie, PhD ; Kollmeier, Marisa, MD ; Happersett, Laura, PhD ; Yorke, Ellen, PhD ; Deasy, Joseph O., PhD ; Jackson, Andrew, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c696t-ef7e2b9ff1bdd584c2bedc6c229cee73ba89e147ab561da06ad95099de4df8633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Analysis of Variance</topic><topic>BLADDER</topic><topic>Follow-Up Studies</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Male</topic><topic>MULTIVARIATE ANALYSIS</topic><topic>NEOPLASMS</topic><topic>Organs at Risk - radiation effects</topic><topic>PATIENTS</topic><topic>PLANNING</topic><topic>PROSTATE</topic><topic>Prostatic Neoplasms - radiotherapy</topic><topic>Radiation Dosage</topic><topic>RADIATION DOSES</topic><topic>Radiation Injuries - complications</topic><topic>Radiology</topic><topic>RADIOLOGY AND NUCLEAR MEDICINE</topic><topic>RADIOTHERAPY</topic><topic>Radiotherapy, Intensity-Modulated - adverse effects</topic><topic>Radiotherapy, Intensity-Modulated - methods</topic><topic>Rectum - radiation effects</topic><topic>Surveys and Questionnaires</topic><topic>TOXICITY</topic><topic>Urethra - radiation effects</topic><topic>Urinary Bladder - radiation effects</topic><topic>Urogenital System - radiation effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghadjar, Pirus, MD</creatorcontrib><creatorcontrib>Zelefsky, Michael J., MD</creatorcontrib><creatorcontrib>Spratt, Daniel E., MD</creatorcontrib><creatorcontrib>Munck af Rosenschöld, Per, PhD</creatorcontrib><creatorcontrib>Oh, Jung Hun, PhD</creatorcontrib><creatorcontrib>Hunt, Margie, PhD</creatorcontrib><creatorcontrib>Kollmeier, Marisa, MD</creatorcontrib><creatorcontrib>Happersett, Laura, PhD</creatorcontrib><creatorcontrib>Yorke, Ellen, PhD</creatorcontrib><creatorcontrib>Deasy, Joseph O., PhD</creatorcontrib><creatorcontrib>Jackson, Andrew, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghadjar, Pirus, MD</au><au>Zelefsky, Michael J., MD</au><au>Spratt, Daniel E., MD</au><au>Munck af Rosenschöld, Per, PhD</au><au>Oh, Jung Hun, PhD</au><au>Hunt, Margie, PhD</au><au>Kollmeier, Marisa, MD</au><au>Happersett, Laura, PhD</au><au>Yorke, Ellen, PhD</au><au>Deasy, Joseph O., PhD</au><au>Jackson, Andrew, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Dose to the Bladder Trigone on Long-Term Urinary Function After High-Dose Intensity Modulated Radiation Therapy for Localized Prostate Cancer</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>88</volume><issue>2</issue><spage>339</spage><epage>344</epage><pages>339-344</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><abstract>Purpose To determine the potential association between genitourinary (GU) toxicity and planning dose–volume parameters for GU pelvic structures after high-dose intensity modulated radiation therapy in localized prostate cancer patients. Methods and Materials A total of 268 patients who underwent intensity modulated radiation therapy to a prescribed dose of 86.4 Gy in 48 fractions during June 2004-December 2008 were evaluated with the International Prostate Symptom Score (IPSS) questionnaire. Dose–volume histograms of the whole bladder, bladder wall, urethra, and bladder trigone were analyzed. The primary endpoint for GU toxicity was an IPSS sum increase ≥10 points over baseline. Univariate and multivariate analyses were done by the Kaplan-Meier method and Cox proportional hazard models, respectively. Results Median follow-up was 5 years (range, 3-7.7 years). Thirty-nine patients experienced an IPSS sum increase ≥10 during follow-up; 84% remained event free at 5 years. After univariate analysis, lower baseline IPSS sum ( P =.006), the V90 of the trigone ( P =.006), and the maximal dose to the trigone ( P =.003) were significantly associated with an IPSS sum increase ≥10. After multivariate analysis, lower baseline IPSS sum ( P =.009) and increased maximal dose to the trigone ( P =.005) remained significantly associated. Seventy-two patients had both a lower baseline IPSS sum and a higher maximal dose to the trigone and were defined as high risk, and 68 patients had both a higher baseline IPSS sum and a lower maximal dose to the trigone and were defined as low risk for development of an IPSS sum increase ≥10. Twenty-one of 72 high-risk patients (29%) and 5 of 68 low-risk patients (7%) experienced an IPSS sum increase ≥10 ( P =.001; odds ratio 5.19). Conclusions The application of hot spots to the bladder trigone was significantly associated with relevant changes in IPSS during follow-up. Reduction of radiation dose to the lower bladder and specifically the bladder trigone seems to be associated with a reduction in late GU toxicity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24411606</pmid><doi>10.1016/j.ijrobp.2013.10.042</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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ispartof International journal of radiation oncology, biology, physics, 2014-02, Vol.88 (2), p.339-344
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subjects Aged
Analysis of Variance
BLADDER
Follow-Up Studies
Hematology, Oncology and Palliative Medicine
Humans
Male
MULTIVARIATE ANALYSIS
NEOPLASMS
Organs at Risk - radiation effects
PATIENTS
PLANNING
PROSTATE
Prostatic Neoplasms - radiotherapy
Radiation Dosage
RADIATION DOSES
Radiation Injuries - complications
Radiology
RADIOLOGY AND NUCLEAR MEDICINE
RADIOTHERAPY
Radiotherapy, Intensity-Modulated - adverse effects
Radiotherapy, Intensity-Modulated - methods
Rectum - radiation effects
Surveys and Questionnaires
TOXICITY
Urethra - radiation effects
Urinary Bladder - radiation effects
Urogenital System - radiation effects
title Impact of Dose to the Bladder Trigone on Long-Term Urinary Function After High-Dose Intensity Modulated Radiation Therapy for Localized Prostate Cancer
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