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Outcomes of high-dose intensity-modulated radiotherapy alone with 1 cm planning target volume posterior margin for localized prostate cancer
Clinically localized prostate cancer may be treated by different approaches of radiation therapy. The aim of this study was to report the results of disease control and toxicity in patients with clinically localized prostate cancer treated with high dose IMRT alone with 1 cm PTV posterior margin. Fr...
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Published in: | Radiation oncology (London, England) England), 2013-12, Vol.8 (1), p.285-285, Article 285 |
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creator | Gadia, Rafael Leite, Élton T Gabrielli, Flavia G Marta, Gustavo N Arruda, Fernando F Abreu, Carlos V Hanna, Samir A Haddad, Cecilia K Silva, João F Carvalho, Heloisa A Garicochea, Bernardo |
description | Clinically localized prostate cancer may be treated by different approaches of radiation therapy. The aim of this study was to report the results of disease control and toxicity in patients with clinically localized prostate cancer treated with high dose IMRT alone with 1 cm PTV posterior margin.
From September 2001 to April 2008, 140 patients with localized prostate cancer were treated with definitive IMRT (dose ≥ 74 Gy) without hormone therapy. Outcomes were measured from the conclusion of radiotherapy. Biochemical failure was defined as PSA nadir + 2.0 ng/dL. Toxicities were assessed using the NCI-CTCAE-version 3.0. Median follow-up was 58 months.
Biochemical failure occurred in 13.6% of patients. Actuarial 5-year biochemical control rates were 91.7%, 82.5% and 85.9% for low-, intermediate-, and high-risk patients, respectively. Stage T2 patients presented a risk of biochemical failure almost three times higher than stage T1 (RR = 2.91; 95% CI: 1.04; 8.17). Distant metastases occurred in 3 (2%) patients. Five-year metastasis-free and overall survivals were 96% and 97.5%, respectively. Late grade 3 genitourinary and gastrointestinal toxicity rates were, respectively, 1.6% and 3%.
High-dose IMRT alone with 1 cm posterior PTV margin was effective and safe for patients with localized prostate cancer. |
doi_str_mv | 10.1186/1748-717X-8-285 |
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From September 2001 to April 2008, 140 patients with localized prostate cancer were treated with definitive IMRT (dose ≥ 74 Gy) without hormone therapy. Outcomes were measured from the conclusion of radiotherapy. Biochemical failure was defined as PSA nadir + 2.0 ng/dL. Toxicities were assessed using the NCI-CTCAE-version 3.0. Median follow-up was 58 months.
Biochemical failure occurred in 13.6% of patients. Actuarial 5-year biochemical control rates were 91.7%, 82.5% and 85.9% for low-, intermediate-, and high-risk patients, respectively. Stage T2 patients presented a risk of biochemical failure almost three times higher than stage T1 (RR = 2.91; 95% CI: 1.04; 8.17). Distant metastases occurred in 3 (2%) patients. Five-year metastasis-free and overall survivals were 96% and 97.5%, respectively. Late grade 3 genitourinary and gastrointestinal toxicity rates were, respectively, 1.6% and 3%.
High-dose IMRT alone with 1 cm posterior PTV margin was effective and safe for patients with localized prostate cancer.</description><identifier>ISSN: 1748-717X</identifier><identifier>EISSN: 1748-717X</identifier><identifier>DOI: 10.1186/1748-717X-8-285</identifier><identifier>PMID: 24314072</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Aged ; Cancer ; Cancer therapies ; Care and treatment ; Confidence intervals ; Disease control ; Disease-Free Survival ; Endocrine therapy ; Follow-Up Studies ; Hospitalization ; Humans ; Male ; Metastasis ; Middle Aged ; Neoplasm Metastasis ; Oncology ; Oncology, Experimental ; Particle Accelerators ; Patient outcomes ; Prostate cancer ; Prostatic Neoplasms - radiotherapy ; Radiation therapy ; Radiotherapy ; Radiotherapy - methods ; Radiotherapy, Image-Guided - methods ; Radiotherapy, Intensity-Modulated - methods ; Retrospective Studies ; Risk ; Tomography, X-Ray Computed ; Treatment Outcome</subject><ispartof>Radiation oncology (London, England), 2013-12, Vol.8 (1), p.285-285, Article 285</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Gadia et al.; licensee BioMed Central Ltd. 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.</rights><rights>Copyright © 2013 Gadia et al.; licensee BioMed Central Ltd. 2013 Gadia et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4365-2e60290bd62a65a98b6f560f4f0f9787c55b4d8b88c674853a72485635e13d3e3</citedby><cites>FETCH-LOGICAL-c4365-2e60290bd62a65a98b6f560f4f0f9787c55b4d8b88c674853a72485635e13d3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996204/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1518732183?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24314072$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gadia, Rafael</creatorcontrib><creatorcontrib>Leite, Élton T</creatorcontrib><creatorcontrib>Gabrielli, Flavia G</creatorcontrib><creatorcontrib>Marta, Gustavo N</creatorcontrib><creatorcontrib>Arruda, Fernando F</creatorcontrib><creatorcontrib>Abreu, Carlos V</creatorcontrib><creatorcontrib>Hanna, Samir A</creatorcontrib><creatorcontrib>Haddad, Cecilia K</creatorcontrib><creatorcontrib>Silva, João F</creatorcontrib><creatorcontrib>Carvalho, Heloisa A</creatorcontrib><creatorcontrib>Garicochea, Bernardo</creatorcontrib><title>Outcomes of high-dose intensity-modulated radiotherapy alone with 1 cm planning target volume posterior margin for localized prostate cancer</title><title>Radiation oncology (London, England)</title><addtitle>Radiat Oncol</addtitle><description>Clinically localized prostate cancer may be treated by different approaches of radiation therapy. The aim of this study was to report the results of disease control and toxicity in patients with clinically localized prostate cancer treated with high dose IMRT alone with 1 cm PTV posterior margin.
From September 2001 to April 2008, 140 patients with localized prostate cancer were treated with definitive IMRT (dose ≥ 74 Gy) without hormone therapy. Outcomes were measured from the conclusion of radiotherapy. Biochemical failure was defined as PSA nadir + 2.0 ng/dL. Toxicities were assessed using the NCI-CTCAE-version 3.0. Median follow-up was 58 months.
Biochemical failure occurred in 13.6% of patients. Actuarial 5-year biochemical control rates were 91.7%, 82.5% and 85.9% for low-, intermediate-, and high-risk patients, respectively. Stage T2 patients presented a risk of biochemical failure almost three times higher than stage T1 (RR = 2.91; 95% CI: 1.04; 8.17). Distant metastases occurred in 3 (2%) patients. Five-year metastasis-free and overall survivals were 96% and 97.5%, respectively. Late grade 3 genitourinary and gastrointestinal toxicity rates were, respectively, 1.6% and 3%.
High-dose IMRT alone with 1 cm posterior PTV margin was effective and safe for patients with localized prostate cancer.</description><subject>Aged</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Confidence intervals</subject><subject>Disease control</subject><subject>Disease-Free Survival</subject><subject>Endocrine therapy</subject><subject>Follow-Up Studies</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Male</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Oncology</subject><subject>Oncology, Experimental</subject><subject>Particle Accelerators</subject><subject>Patient outcomes</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - radiotherapy</subject><subject>Radiation therapy</subject><subject>Radiotherapy</subject><subject>Radiotherapy - methods</subject><subject>Radiotherapy, Image-Guided - methods</subject><subject>Radiotherapy, Intensity-Modulated - 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radiotherapy</topic><topic>Radiation therapy</topic><topic>Radiotherapy</topic><topic>Radiotherapy - methods</topic><topic>Radiotherapy, Image-Guided - methods</topic><topic>Radiotherapy, Intensity-Modulated - methods</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Tomography, X-Ray Computed</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gadia, Rafael</creatorcontrib><creatorcontrib>Leite, Élton T</creatorcontrib><creatorcontrib>Gabrielli, Flavia G</creatorcontrib><creatorcontrib>Marta, Gustavo N</creatorcontrib><creatorcontrib>Arruda, Fernando F</creatorcontrib><creatorcontrib>Abreu, Carlos V</creatorcontrib><creatorcontrib>Hanna, Samir A</creatorcontrib><creatorcontrib>Haddad, Cecilia K</creatorcontrib><creatorcontrib>Silva, João F</creatorcontrib><creatorcontrib>Carvalho, Heloisa A</creatorcontrib><creatorcontrib>Garicochea, Bernardo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest - 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The aim of this study was to report the results of disease control and toxicity in patients with clinically localized prostate cancer treated with high dose IMRT alone with 1 cm PTV posterior margin.
From September 2001 to April 2008, 140 patients with localized prostate cancer were treated with definitive IMRT (dose ≥ 74 Gy) without hormone therapy. Outcomes were measured from the conclusion of radiotherapy. Biochemical failure was defined as PSA nadir + 2.0 ng/dL. Toxicities were assessed using the NCI-CTCAE-version 3.0. Median follow-up was 58 months.
Biochemical failure occurred in 13.6% of patients. Actuarial 5-year biochemical control rates were 91.7%, 82.5% and 85.9% for low-, intermediate-, and high-risk patients, respectively. Stage T2 patients presented a risk of biochemical failure almost three times higher than stage T1 (RR = 2.91; 95% CI: 1.04; 8.17). Distant metastases occurred in 3 (2%) patients. Five-year metastasis-free and overall survivals were 96% and 97.5%, respectively. Late grade 3 genitourinary and gastrointestinal toxicity rates were, respectively, 1.6% and 3%.
High-dose IMRT alone with 1 cm posterior PTV margin was effective and safe for patients with localized prostate cancer.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24314072</pmid><doi>10.1186/1748-717X-8-285</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Cancer Cancer therapies Care and treatment Confidence intervals Disease control Disease-Free Survival Endocrine therapy Follow-Up Studies Hospitalization Humans Male Metastasis Middle Aged Neoplasm Metastasis Oncology Oncology, Experimental Particle Accelerators Patient outcomes Prostate cancer Prostatic Neoplasms - radiotherapy Radiation therapy Radiotherapy Radiotherapy - methods Radiotherapy, Image-Guided - methods Radiotherapy, Intensity-Modulated - methods Retrospective Studies Risk Tomography, X-Ray Computed Treatment Outcome |
title | Outcomes of high-dose intensity-modulated radiotherapy alone with 1 cm planning target volume posterior margin for localized prostate cancer |
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