Long-Term Outcomes From a Prospective Trial of Stereotactic Body Radiotherapy for Low-Risk Prostate Cancer

Purpose Hypofractionated radiotherapy has an intrinsically different normal tissue and tumor radiobiology. The results of a prospective trial of stereotactic body radiotherapy (SBRT) for prostate cancer with long-term patient-reported toxicity and tumor control rates are presented. Methods and Mater...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2012-02, Vol.82 (2), p.877-882
Hauptverfasser: King, Christopher R., Ph.D., M.D, Brooks, James D., M.D, Gill, Harcharan, M.D, Presti, Joseph C., M.D
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container_title International journal of radiation oncology, biology, physics
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creator King, Christopher R., Ph.D., M.D
Brooks, James D., M.D
Gill, Harcharan, M.D
Presti, Joseph C., M.D
description Purpose Hypofractionated radiotherapy has an intrinsically different normal tissue and tumor radiobiology. The results of a prospective trial of stereotactic body radiotherapy (SBRT) for prostate cancer with long-term patient-reported toxicity and tumor control rates are presented. Methods and Materials From 2003 through 2009, 67 patients with clinically localized low-risk prostate cancer were enrolled. Treatment consisted of 36.25 Gy in 5 fractions using SBRT with the CyberKnife as the delivery technology. No patient received hormone therapy. Patient self-reported bladder and rectal toxicities were graded on the Radiation Therapy Oncology Group scale (RTOG). Results Median follow-up was 2.7 years. There were no grade 4 toxicities. Radiation Therapy Oncology Group Grade 3, 2, and 1 bladder toxicities were seen in 3% (2 patients), 5% (3 patients), and 23% (13 patients) respectively. Dysuria exacerbated by urologic instrumentation accounted for both patients with Grade 3 toxicity. Urinary incontinence, complete obstruction, or persistent hematuria was not observed. Rectal Grade 3, 2, and 1 toxicities were seen in 0, 2% (1 patient), and 12.5% (7 patients), respectively. Persistent rectal bleeding was not observed. Low-grade toxicities were substantially less frequent with QOD vs. QD dose regimen ( p = 0.001 for gastrointestinal and p = 0.007 for genitourinary). There were two prostate-specific antigen (PSA), biopsy-proven failures with negative metastatic workup. Median PSA at follow-up was 0.5 ± 0.72 ng/mL. The 4-year Kaplan-Meier PSA relapse-free survival was 94% (95% confidence interval, 85%–102%). Conclusion Significant late bladder and rectal toxicities from SBRT for prostate cancer are infrequent. PSA relapse-free survival compares favorably with other definitive treatments. The current evidence supports consideration of stereotactic body radiotherapy among the therapeutic options for localized prostate cancer.
doi_str_mv 10.1016/j.ijrobp.2010.11.054
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The results of a prospective trial of stereotactic body radiotherapy (SBRT) for prostate cancer with long-term patient-reported toxicity and tumor control rates are presented. Methods and Materials From 2003 through 2009, 67 patients with clinically localized low-risk prostate cancer were enrolled. Treatment consisted of 36.25 Gy in 5 fractions using SBRT with the CyberKnife as the delivery technology. No patient received hormone therapy. Patient self-reported bladder and rectal toxicities were graded on the Radiation Therapy Oncology Group scale (RTOG). Results Median follow-up was 2.7 years. There were no grade 4 toxicities. Radiation Therapy Oncology Group Grade 3, 2, and 1 bladder toxicities were seen in 3% (2 patients), 5% (3 patients), and 23% (13 patients) respectively. Dysuria exacerbated by urologic instrumentation accounted for both patients with Grade 3 toxicity. Urinary incontinence, complete obstruction, or persistent hematuria was not observed. Rectal Grade 3, 2, and 1 toxicities were seen in 0, 2% (1 patient), and 12.5% (7 patients), respectively. Persistent rectal bleeding was not observed. Low-grade toxicities were substantially less frequent with QOD vs. QD dose regimen ( p = 0.001 for gastrointestinal and p = 0.007 for genitourinary). There were two prostate-specific antigen (PSA), biopsy-proven failures with negative metastatic workup. Median PSA at follow-up was 0.5 ± 0.72 ng/mL. The 4-year Kaplan-Meier PSA relapse-free survival was 94% (95% confidence interval, 85%–102%). Conclusion Significant late bladder and rectal toxicities from SBRT for prostate cancer are infrequent. PSA relapse-free survival compares favorably with other definitive treatments. The current evidence supports consideration of stereotactic body radiotherapy among the therapeutic options for localized prostate cancer.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2010.11.054</identifier><identifier>PMID: 21300474</identifier><identifier>CODEN: IOBPD3</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; ANTIGENS ; Biological and medical sciences ; BIOPSY ; BLADDER ; Dose Fractionation ; FAILURES ; Gynecology. Andrology. Obstetrics ; HAZARDS ; Hematology, Oncology and Palliative Medicine ; HORMONES ; Humans ; Hypofractionation ; Male ; Male genital diseases ; Medical sciences ; METASTASES ; NEOPLASMS ; Nephrology. Urinary tract diseases ; PATIENTS ; Prospective Studies ; PROSTATE ; Prostate cancer ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - blood ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - surgery ; PSA ; RADIATION DOSES ; Radiation Injuries - complications ; Radiation Injuries - pathology ; RADIOBIOLOGY ; Radiology ; RADIOLOGY AND NUCLEAR MEDICINE ; Radiosurgery - adverse effects ; Radiosurgery - methods ; RADIOTHERAPY ; RECTUM ; Rectum - radiation effects ; Stereotactic body radiotherapy ; TOXICITY ; Treatment Outcome ; Tumors ; Tumors of the urinary system ; Urinary Bladder - radiation effects ; Urinary tract. Prostate gland ; Urination Disorders</subject><ispartof>International journal of radiation oncology, biology, physics, 2012-02, Vol.82 (2), p.877-882</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. 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The results of a prospective trial of stereotactic body radiotherapy (SBRT) for prostate cancer with long-term patient-reported toxicity and tumor control rates are presented. Methods and Materials From 2003 through 2009, 67 patients with clinically localized low-risk prostate cancer were enrolled. Treatment consisted of 36.25 Gy in 5 fractions using SBRT with the CyberKnife as the delivery technology. No patient received hormone therapy. Patient self-reported bladder and rectal toxicities were graded on the Radiation Therapy Oncology Group scale (RTOG). Results Median follow-up was 2.7 years. There were no grade 4 toxicities. Radiation Therapy Oncology Group Grade 3, 2, and 1 bladder toxicities were seen in 3% (2 patients), 5% (3 patients), and 23% (13 patients) respectively. Dysuria exacerbated by urologic instrumentation accounted for both patients with Grade 3 toxicity. Urinary incontinence, complete obstruction, or persistent hematuria was not observed. Rectal Grade 3, 2, and 1 toxicities were seen in 0, 2% (1 patient), and 12.5% (7 patients), respectively. Persistent rectal bleeding was not observed. Low-grade toxicities were substantially less frequent with QOD vs. QD dose regimen ( p = 0.001 for gastrointestinal and p = 0.007 for genitourinary). There were two prostate-specific antigen (PSA), biopsy-proven failures with negative metastatic workup. Median PSA at follow-up was 0.5 ± 0.72 ng/mL. The 4-year Kaplan-Meier PSA relapse-free survival was 94% (95% confidence interval, 85%–102%). Conclusion Significant late bladder and rectal toxicities from SBRT for prostate cancer are infrequent. PSA relapse-free survival compares favorably with other definitive treatments. The current evidence supports consideration of stereotactic body radiotherapy among the therapeutic options for localized prostate cancer.</description><subject>Aged</subject><subject>ANTIGENS</subject><subject>Biological and medical sciences</subject><subject>BIOPSY</subject><subject>BLADDER</subject><subject>Dose Fractionation</subject><subject>FAILURES</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>HAZARDS</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>HORMONES</subject><subject>Humans</subject><subject>Hypofractionation</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Medical sciences</subject><subject>METASTASES</subject><subject>NEOPLASMS</subject><subject>Nephrology. Urinary tract diseases</subject><subject>PATIENTS</subject><subject>Prospective Studies</subject><subject>PROSTATE</subject><subject>Prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - blood</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - surgery</subject><subject>PSA</subject><subject>RADIATION DOSES</subject><subject>Radiation Injuries - complications</subject><subject>Radiation Injuries - pathology</subject><subject>RADIOBIOLOGY</subject><subject>Radiology</subject><subject>RADIOLOGY AND NUCLEAR MEDICINE</subject><subject>Radiosurgery - adverse effects</subject><subject>Radiosurgery - methods</subject><subject>RADIOTHERAPY</subject><subject>RECTUM</subject><subject>Rectum - radiation effects</subject><subject>Stereotactic body radiotherapy</subject><subject>TOXICITY</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary Bladder - radiation effects</subject><subject>Urinary tract. Prostate gland</subject><subject>Urination Disorders</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks-L1DAUgIMo7uzqfyASEI8dX9KknV4EHVwVBlZ25-AtpMmLm-60KUlnZf77Te2q4MVTQvK9Xx-PkFcM1gxY9a5b-y6GdlxzmJ_YGqR4QlZsUzdFKeX3p2QFZQVFmeEzcp5SBwCM1eI5OeOsBBC1WJFuF4YfxR5jT6-Okwk9JnoZQ081_RZDGtFM_h7pPnp9oMHRmwkjhknnZ0M_Bnui19r6MN1i1OOJuhDpLvwsrn26-5Vg0hPSrR4MxhfkmdOHhC8fzwuyv_y0334pdlefv24_7AojBUyFhUpzo02ra2kaaVBXrmmtcZrxSgM4xznfWIeyanSTf83G1VboUgjZ8qa8IG-WtLm4V8n4Cc2tCcOQR1Gcg6xA8kyJhTK5yRTRqTH6XseTYqBmv6pTi181-1WMqew3h71ewsZj26P9E_RbaAbePgI6GX1wMY_u019OykaIimXu_cJhNnHvMc6dYtZkfZwbtcH_r5N_E5iDH3yueYcnTF04xiFbVkwlrkDdzLswrwKDfKtrVj4AX0Kwwg</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>King, Christopher R., Ph.D., M.D</creator><creator>Brooks, James D., M.D</creator><creator>Gill, Harcharan, M.D</creator><creator>Presti, Joseph C., M.D</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20120201</creationdate><title>Long-Term Outcomes From a Prospective Trial of Stereotactic Body Radiotherapy for Low-Risk Prostate Cancer</title><author>King, Christopher R., Ph.D., M.D ; Brooks, James D., M.D ; Gill, Harcharan, M.D ; Presti, Joseph C., M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-d06a2cacba75c95cea6f9bdcfa126a00ff2228dfe569a9ea6c8f7d4a3445b293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>ANTIGENS</topic><topic>Biological and medical sciences</topic><topic>BIOPSY</topic><topic>BLADDER</topic><topic>Dose Fractionation</topic><topic>FAILURES</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>HAZARDS</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>HORMONES</topic><topic>Humans</topic><topic>Hypofractionation</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Medical sciences</topic><topic>METASTASES</topic><topic>NEOPLASMS</topic><topic>Nephrology. Urinary tract diseases</topic><topic>PATIENTS</topic><topic>Prospective Studies</topic><topic>PROSTATE</topic><topic>Prostate cancer</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - blood</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - surgery</topic><topic>PSA</topic><topic>RADIATION DOSES</topic><topic>Radiation Injuries - complications</topic><topic>Radiation Injuries - pathology</topic><topic>RADIOBIOLOGY</topic><topic>Radiology</topic><topic>RADIOLOGY AND NUCLEAR MEDICINE</topic><topic>Radiosurgery - adverse effects</topic><topic>Radiosurgery - methods</topic><topic>RADIOTHERAPY</topic><topic>RECTUM</topic><topic>Rectum - radiation effects</topic><topic>Stereotactic body radiotherapy</topic><topic>TOXICITY</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary Bladder - radiation effects</topic><topic>Urinary tract. Prostate gland</topic><topic>Urination Disorders</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>King, Christopher R., Ph.D., M.D</creatorcontrib><creatorcontrib>Brooks, James D., M.D</creatorcontrib><creatorcontrib>Gill, Harcharan, M.D</creatorcontrib><creatorcontrib>Presti, Joseph C., M.D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>King, Christopher R., Ph.D., M.D</au><au>Brooks, James D., M.D</au><au>Gill, Harcharan, M.D</au><au>Presti, Joseph C., M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-Term Outcomes From a Prospective Trial of Stereotactic Body Radiotherapy for Low-Risk Prostate Cancer</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>82</volume><issue>2</issue><spage>877</spage><epage>882</epage><pages>877-882</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><coden>IOBPD3</coden><abstract>Purpose Hypofractionated radiotherapy has an intrinsically different normal tissue and tumor radiobiology. The results of a prospective trial of stereotactic body radiotherapy (SBRT) for prostate cancer with long-term patient-reported toxicity and tumor control rates are presented. Methods and Materials From 2003 through 2009, 67 patients with clinically localized low-risk prostate cancer were enrolled. Treatment consisted of 36.25 Gy in 5 fractions using SBRT with the CyberKnife as the delivery technology. No patient received hormone therapy. Patient self-reported bladder and rectal toxicities were graded on the Radiation Therapy Oncology Group scale (RTOG). Results Median follow-up was 2.7 years. There were no grade 4 toxicities. Radiation Therapy Oncology Group Grade 3, 2, and 1 bladder toxicities were seen in 3% (2 patients), 5% (3 patients), and 23% (13 patients) respectively. Dysuria exacerbated by urologic instrumentation accounted for both patients with Grade 3 toxicity. Urinary incontinence, complete obstruction, or persistent hematuria was not observed. Rectal Grade 3, 2, and 1 toxicities were seen in 0, 2% (1 patient), and 12.5% (7 patients), respectively. Persistent rectal bleeding was not observed. Low-grade toxicities were substantially less frequent with QOD vs. QD dose regimen ( p = 0.001 for gastrointestinal and p = 0.007 for genitourinary). There were two prostate-specific antigen (PSA), biopsy-proven failures with negative metastatic workup. Median PSA at follow-up was 0.5 ± 0.72 ng/mL. The 4-year Kaplan-Meier PSA relapse-free survival was 94% (95% confidence interval, 85%–102%). Conclusion Significant late bladder and rectal toxicities from SBRT for prostate cancer are infrequent. PSA relapse-free survival compares favorably with other definitive treatments. The current evidence supports consideration of stereotactic body radiotherapy among the therapeutic options for localized prostate cancer.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21300474</pmid><doi>10.1016/j.ijrobp.2010.11.054</doi><tpages>6</tpages></addata></record>
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subjects Aged
ANTIGENS
Biological and medical sciences
BIOPSY
BLADDER
Dose Fractionation
FAILURES
Gynecology. Andrology. Obstetrics
HAZARDS
Hematology, Oncology and Palliative Medicine
HORMONES
Humans
Hypofractionation
Male
Male genital diseases
Medical sciences
METASTASES
NEOPLASMS
Nephrology. Urinary tract diseases
PATIENTS
Prospective Studies
PROSTATE
Prostate cancer
Prostate-Specific Antigen - blood
Prostatic Neoplasms - blood
Prostatic Neoplasms - pathology
Prostatic Neoplasms - surgery
PSA
RADIATION DOSES
Radiation Injuries - complications
Radiation Injuries - pathology
RADIOBIOLOGY
Radiology
RADIOLOGY AND NUCLEAR MEDICINE
Radiosurgery - adverse effects
Radiosurgery - methods
RADIOTHERAPY
RECTUM
Rectum - radiation effects
Stereotactic body radiotherapy
TOXICITY
Treatment Outcome
Tumors
Tumors of the urinary system
Urinary Bladder - radiation effects
Urinary tract. Prostate gland
Urination Disorders
title Long-Term Outcomes From a Prospective Trial of Stereotactic Body Radiotherapy for Low-Risk Prostate Cancer
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