PURPOSE: We determined the risk of recurrence in men enrolled on a randomized trial for prostate cancer who were treated withradiation therapy (RT) alone or in conjunction with combined or less than combined androgen suppression therapy (AST). PATIENTS AND METHODS: Between 1995 and 2001, 206 men with localized but unfavorable-risk adenocarcinoma of the prostate were randomly assigned to receive RT or RT and AST, which was defined as 6 months of both a luteinizing hormone-releasing hormone agonist and an antiandrogen. A post-random assignment hypothesis that was generated by multivariable Cox regression analyses was used to evaluate whether the risk of prostate-specific antigen (PSA) recurrence was significantly associated with months of antiandrogen use; regression analysis adjusted for known prognostic factors, comorbidity score, and medications that can elevate liver function tests sufficiently to necessitate discontinuation of the antiandrogen. RESULTS: After a median follow-up of 8.2 years (interquartile range,7.0 to 9.5 years), 81 men sustained PSA recurrence. An increasing PSA level (P < .001); Gleason score of 8, 9, or 10 (P < .001); and clinical category T2 disease (P = .005) were significantly associated with an increased risk of recurrence. However, recurrence risk was significantly decreased (adjusted hazard ratio, 0.81; 95% CI, 0.72 to 0.92; P = .001) with each additional month of antiandrogen use after analysis was adjusted for these known prognostic factors. CONCLUSION:Men with localized but unfavorable-risk prostate cancer who were treated with RT and 6 months of planned combined AST appear to have an increased risk of recurrence when treated with less than as compared with 6 months of the antiandrogen.
RCT Entities:
PURPOSE: We determined the risk of recurrence in men enrolled on a randomized trial for prostate cancer who were treated with radiation therapy (RT) alone or in conjunction with combined or less than combined androgen suppression therapy (AST). PATIENTS AND METHODS: Between 1995 and 2001, 206 men with localized but unfavorable-risk adenocarcinoma of the prostate were randomly assigned to receive RT or RT and AST, which was defined as 6 months of both a luteinizing hormone-releasing hormone agonist and an antiandrogen. A post-random assignment hypothesis that was generated by multivariable Cox regression analyses was used to evaluate whether the risk of prostate-specific antigen (PSA) recurrence was significantly associated with months of antiandrogen use; regression analysis adjusted for known prognostic factors, comorbidity score, and medications that can elevate liver function tests sufficiently to necessitate discontinuation of the antiandrogen. RESULTS: After a median follow-up of 8.2 years (interquartile range,7.0 to 9.5 years), 81 men sustained PSA recurrence. An increasing PSA level (P < .001); Gleason score of 8, 9, or 10 (P < .001); and clinical category T2 disease (P = .005) were significantly associated with an increased risk of recurrence. However, recurrence risk was significantly decreased (adjusted hazard ratio, 0.81; 95% CI, 0.72 to 0.92; P = .001) with each additional month of antiandrogen use after analysis was adjusted for these known prognostic factors. CONCLUSION:Men with localized but unfavorable-risk prostate cancer who were treated with RT and 6 months of planned combined AST appear to have an increased risk of recurrence when treated with less than as compared with 6 months of the antiandrogen.
Authors: Xuehong Deng; Bennett D Elzey; Jean M Poulson; Wallace B Morrison; Song-Chu Ko; Noah M Hahn; Timothy L Ratliff; Chang-Deng Hu Journal: Am J Cancer Res Date: 2011-08-18 Impact factor: 6.166
Authors: N N Sanford; M-H Chen; M Loffredo; A Renshaw; P W Kantoff; A V D'Amico Journal: Prostate Cancer Prostatic Dis Date: 2016-11-08 Impact factor: 5.554
Authors: Anthony V D'Amico; Ming-Hui Chen; Juanita Crook; John G Armstrong; Shawn Malone; Allison Steigler; Mary Dunne; Philip W Kantoff; James W Denham Journal: J Clin Oncol Date: 2011-10-31 Impact factor: 44.544
Authors: D E Spratt; W C Jackson; A Abugharib; S A Tomlins; R T Dess; P D Soni; J Y Lee; S G Zhao; A I Cole; Z S Zumsteg; H Sandler; D Hamstra; J W Hearn; G Palapattu; R Mehra; T M Morgan; F Y Feng Journal: Prostate Cancer Prostatic Dis Date: 2016-05-24 Impact factor: 5.554