Four prognostic groups predict long-term survival from prostate cancer following radiotherapy alone on radiation therapy oncology group clinical trials

Purpose: Gleason score (GS), T stage, and pathologic lymph node status have been described as major independent predictors of death due to prostate cancer in men treated with external beam radiotherapy (XRT). In this analysis we combine these three factors to define prognostic subgroups that correla...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2000-06, Vol.47 (3), p.609-615
Hauptverfasser: Roach, Mack, Lu, Jiandong, Pilepich, Miljenko V., Asbell, Sucha O., Mohuidden, Mohammed, Terry, Roger, Grignon, David
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container_issue 3
container_start_page 609
container_title International journal of radiation oncology, biology, physics
container_volume 47
creator Roach, Mack
Lu, Jiandong
Pilepich, Miljenko V.
Asbell, Sucha O.
Mohuidden, Mohammed
Terry, Roger
Grignon, David
description Purpose: Gleason score (GS), T stage, and pathologic lymph node status have been described as major independent predictors of death due to prostate cancer in men treated with external beam radiotherapy (XRT). In this analysis we combine these three factors to define prognostic subgroups that correlate with disease-specific survival (DSS) death from prostate cancer. Methods and Materials: Men entered on one of four Radiation Therapy Oncology Group (RTOG) Phase III randomized trials between 1975 and 1992, for clinically localized prostate cancer (CAP) ( n = 1557), were selected for this analysis. Patients were included if: 1) they were evaluable, and eligible for the trial; 2) they received no hormonal therapy with their initial treatment; and 3) follow-up was available. For this study a DSS event was declared if: 1) death was certified as due to CAP; 2) death was due to complications of treatment; or 3) death was from unknown causes with active malignancy. The median follow-up for patients treated on early and late RTOG studies exceeded 11 and 6 years respectively. Subgroups were identified based on their pretreatment GS, T-stage, and lymph node such that patients with similar risk of dying from prostate cancer were combined. Results: By combining patients with similar DSS, four subgroups were identified. Risk Group 1 patients had a GS = 2–6, and T1–2Nx; Group 2: GS = 2–6, T3Nx; or GS = 2–6, N+, or GS = 7, T1–2Nx; Group 3: T3Nx, GS = 7; or N+, GS = 7, or T1–2Nx, GS = 8–10; and Group 4 patients were T3Nx, GS = 8–10, or N+, GS = 8–10. The 5-, 10-, and 15-year DSS was 96%, 86%, and 72%; 94%, 75%, and 61%; 83%, 62%, and 39%; and 64%, 34%, and 27% for Groups 1 through 4, respectively. Conclusions: Recognition of these four risk groups provides a basis for estimating the long-term DSS for men treated with XRT alone and should facilitate the design of future prospective randomized trials.
doi_str_mv 10.1016/S0360-3016(00)00578-2
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In this analysis we combine these three factors to define prognostic subgroups that correlate with disease-specific survival (DSS) death from prostate cancer. Methods and Materials: Men entered on one of four Radiation Therapy Oncology Group (RTOG) Phase III randomized trials between 1975 and 1992, for clinically localized prostate cancer (CAP) ( n = 1557), were selected for this analysis. Patients were included if: 1) they were evaluable, and eligible for the trial; 2) they received no hormonal therapy with their initial treatment; and 3) follow-up was available. For this study a DSS event was declared if: 1) death was certified as due to CAP; 2) death was due to complications of treatment; or 3) death was from unknown causes with active malignancy. The median follow-up for patients treated on early and late RTOG studies exceeded 11 and 6 years respectively. Subgroups were identified based on their pretreatment GS, T-stage, and lymph node such that patients with similar risk of dying from prostate cancer were combined. Results: By combining patients with similar DSS, four subgroups were identified. Risk Group 1 patients had a GS = 2–6, and T1–2Nx; Group 2: GS = 2–6, T3Nx; or GS = 2–6, N+, or GS = 7, T1–2Nx; Group 3: T3Nx, GS = 7; or N+, GS = 7, or T1–2Nx, GS = 8–10; and Group 4 patients were T3Nx, GS = 8–10, or N+, GS = 8–10. The 5-, 10-, and 15-year DSS was 96%, 86%, and 72%; 94%, 75%, and 61%; 83%, 62%, and 39%; and 64%, 34%, and 27% for Groups 1 through 4, respectively. Conclusions: Recognition of these four risk groups provides a basis for estimating the long-term DSS for men treated with XRT alone and should facilitate the design of future prospective randomized trials.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/S0360-3016(00)00578-2</identifier><identifier>PMID: 10837943</identifier><identifier>CODEN: IOBPD3</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; Biological and medical sciences ; Disease-Free Survival ; Diseases of the urinary system ; Humans ; Long-term survival ; Lymph Nodes - pathology ; Male ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Prognosis ; Prostate cancer ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - radiotherapy ; Radiotherapy ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Tumors of the urinary system ; Urinary tract. 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In this analysis we combine these three factors to define prognostic subgroups that correlate with disease-specific survival (DSS) death from prostate cancer. Methods and Materials: Men entered on one of four Radiation Therapy Oncology Group (RTOG) Phase III randomized trials between 1975 and 1992, for clinically localized prostate cancer (CAP) ( n = 1557), were selected for this analysis. Patients were included if: 1) they were evaluable, and eligible for the trial; 2) they received no hormonal therapy with their initial treatment; and 3) follow-up was available. For this study a DSS event was declared if: 1) death was certified as due to CAP; 2) death was due to complications of treatment; or 3) death was from unknown causes with active malignancy. The median follow-up for patients treated on early and late RTOG studies exceeded 11 and 6 years respectively. Subgroups were identified based on their pretreatment GS, T-stage, and lymph node such that patients with similar risk of dying from prostate cancer were combined. Results: By combining patients with similar DSS, four subgroups were identified. Risk Group 1 patients had a GS = 2–6, and T1–2Nx; Group 2: GS = 2–6, T3Nx; or GS = 2–6, N+, or GS = 7, T1–2Nx; Group 3: T3Nx, GS = 7; or N+, GS = 7, or T1–2Nx, GS = 8–10; and Group 4 patients were T3Nx, GS = 8–10, or N+, GS = 8–10. The 5-, 10-, and 15-year DSS was 96%, 86%, and 72%; 94%, 75%, and 61%; 83%, 62%, and 39%; and 64%, 34%, and 27% for Groups 1 through 4, respectively. Conclusions: Recognition of these four risk groups provides a basis for estimating the long-term DSS for men treated with XRT alone and should facilitate the design of future prospective randomized trials.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease-Free Survival</subject><subject>Diseases of the urinary system</subject><subject>Humans</subject><subject>Long-term survival</subject><subject>Lymph Nodes - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prognosis</subject><subject>Prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - radiotherapy</subject><subject>Radiotherapy</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. 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Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roach, Mack</creatorcontrib><creatorcontrib>Lu, Jiandong</creatorcontrib><creatorcontrib>Pilepich, Miljenko V.</creatorcontrib><creatorcontrib>Asbell, Sucha O.</creatorcontrib><creatorcontrib>Mohuidden, Mohammed</creatorcontrib><creatorcontrib>Terry, Roger</creatorcontrib><creatorcontrib>Grignon, David</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>MEDLINE - Academic</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roach, Mack</au><au>Lu, Jiandong</au><au>Pilepich, Miljenko V.</au><au>Asbell, Sucha O.</au><au>Mohuidden, Mohammed</au><au>Terry, Roger</au><au>Grignon, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Four prognostic groups predict long-term survival from prostate cancer following radiotherapy alone on radiation therapy oncology group clinical trials</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2000-06-01</date><risdate>2000</risdate><volume>47</volume><issue>3</issue><spage>609</spage><epage>615</epage><pages>609-615</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><coden>IOBPD3</coden><abstract>Purpose: Gleason score (GS), T stage, and pathologic lymph node status have been described as major independent predictors of death due to prostate cancer in men treated with external beam radiotherapy (XRT). In this analysis we combine these three factors to define prognostic subgroups that correlate with disease-specific survival (DSS) death from prostate cancer. Methods and Materials: Men entered on one of four Radiation Therapy Oncology Group (RTOG) Phase III randomized trials between 1975 and 1992, for clinically localized prostate cancer (CAP) ( n = 1557), were selected for this analysis. Patients were included if: 1) they were evaluable, and eligible for the trial; 2) they received no hormonal therapy with their initial treatment; and 3) follow-up was available. For this study a DSS event was declared if: 1) death was certified as due to CAP; 2) death was due to complications of treatment; or 3) death was from unknown causes with active malignancy. The median follow-up for patients treated on early and late RTOG studies exceeded 11 and 6 years respectively. Subgroups were identified based on their pretreatment GS, T-stage, and lymph node such that patients with similar risk of dying from prostate cancer were combined. Results: By combining patients with similar DSS, four subgroups were identified. Risk Group 1 patients had a GS = 2–6, and T1–2Nx; Group 2: GS = 2–6, T3Nx; or GS = 2–6, N+, or GS = 7, T1–2Nx; Group 3: T3Nx, GS = 7; or N+, GS = 7, or T1–2Nx, GS = 8–10; and Group 4 patients were T3Nx, GS = 8–10, or N+, GS = 8–10. The 5-, 10-, and 15-year DSS was 96%, 86%, and 72%; 94%, 75%, and 61%; 83%, 62%, and 39%; and 64%, 34%, and 27% for Groups 1 through 4, respectively. Conclusions: Recognition of these four risk groups provides a basis for estimating the long-term DSS for men treated with XRT alone and should facilitate the design of future prospective randomized trials.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10837943</pmid><doi>10.1016/S0360-3016(00)00578-2</doi><tpages>7</tpages></addata></record>
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subjects Aged
Biological and medical sciences
Disease-Free Survival
Diseases of the urinary system
Humans
Long-term survival
Lymph Nodes - pathology
Male
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Prognosis
Prostate cancer
Prostate-Specific Antigen - blood
Prostatic Neoplasms - mortality
Prostatic Neoplasms - pathology
Prostatic Neoplasms - radiotherapy
Radiotherapy
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Tumors of the urinary system
Urinary tract. Prostate gland
title Four prognostic groups predict long-term survival from prostate cancer following radiotherapy alone on radiation therapy oncology group clinical trials
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