首页> 外文期刊>Lancet Neurology >Predictive factors of long-term rectal toxicity following permanent iodine-125 prostate brachytherapy with or without supplemental external beam radiation therapy in 2216 patients
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Predictive factors of long-term rectal toxicity following permanent iodine-125 prostate brachytherapy with or without supplemental external beam radiation therapy in 2216 patients

机译:长期直肠毒性后长期直肠毒性在2216名患者中具有或不含补充外梁辐射治疗后的长期直肠毒性

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? 2018 American Brachytherapy Society ? 2018 American Brachytherapy Society Purpose: We analyzed factors associated with rectal toxicity after iodine-125 prostate brachytherapy (BT) with or without external beam radiation therapy (EBRT). Methods and Materials: In total, 2216 prostate cancer patients underwent iodine-125 BT with or without EBRT between 2003 and 2013. The median followup was 6.9 years. Cox proportional hazards modeling was used for univariate and multivariate analyses to assess clinical and dosimetric factors associated with rectal toxicity. Dosimetric parameters from 1 day after implantation (Day 1) and 1 month after implantation (Day 30) were included in the analyses. Results: The 7-year cumulative incidence of Grade 2 or higher rectal toxicity was 5.7% in all patients. The multivariate analysis revealed that antiplatelet or anticoagulant therapy, neoadjuvant androgen deprivation therapy, treatment modality, Day 1 rectal volume receiving 100% of the prescribed dose (RV 100 ), and the Day 30 minimal percent of the prescribed dose delivered to 30% of the rectum (RD 30 ) were associated with rectal toxicity. Day 1 RV 100 was a common predictor in both BT-alone and the BT + EBRT groups. The 5-year cumulative incidence of Grade 2 or higher rectal toxicity was 12.6%, 5.9%, and 1.7% for BT + 3-dimensional conformal radiation therapy, BT + intensity-modulated radiation therapy, and the BT-alone groups, respectively (p 0.001). Conclusions: Rectal dosimetric parameters in BT were associated with late rectal toxicity. Although the risk of rectal toxicity was higher when EBRT was combined with BT, with proper and achievable rectal dose constraints intensity-modulated radiation therapy yielded less toxicity than 3-dimensional conformal radiation therapy. Purpose: We analyzed factors associated with rectal toxicity after iodine-125 prostate brachytherapy (BT) with or without external beam radiation therapy (EBRT). Methods and Materials: In total, 2216 prostate cancer patients underwent iodine-125 BT with or without EBRT between 2003 and 2013. The median followup was 6.9 years. Cox proportional hazards modeling was used for univariate and multivariate analyses to assess clinical and dosimetric factors associated with rectal toxicity. Dosimetric parameters from 1 day after implantation (Day 1) and 1 month after implantation (Day 30) were included in the analyses. Results: The 7-year cumulative incidence of Grade 2 or higher rectal toxicity was 5.7% in all patients. The multivariate analysis revealed that antiplatelet or anticoagulant therapy, neoadjuvant androgen deprivation therapy, treatment modality, Day 1 rectal volume receiving 100% of the prescribed dose (RV 100 100 ), and the Day 30 minimal percent of the prescribed dose delivered to 30% of the rectum (RD 30 30 ) were associated with rectal toxicity. Day 1 RV 100 100 was a common predictor in both BT-alone and the BT + EBRT groups. The 5-year cumulative incidence of Grade 2 or higher rectal toxicity was 12.6%, 5.9%, and 1.7% for BT + 3-dimensional conformal radiation therapy, BT + intensity-modulated radiation therapy, and the BT-alone groups, respectively (p < 0.001). Conclusions: Rectal dosimetric parameters in BT were associated with late rectal toxicity. Although the risk of rectal toxicity was higher when EBRT was combined with BT, with proper and achievable rectal dose constraints intensity-modulated radiation therapy yielded less toxicity than 3-dimensional conformal radiation therapy.
机译:还2018年美国近距离治疗协会? 2018年美国近距表社会目的:在碘-125前列腺近六乳房放射治疗(BT)后分析与直肠毒性相关的因素,有或没有外部射线放射治疗(EBRT)。方法和材料:总共2216名前列腺癌患者在2003年至2013年间接受过碘-125英镑的碘-125英镑。中位后关注为6.9岁。 Cox比例危害建模用于单变量和多变量分析,以评估与直肠毒性相关的临床和剂量因子。从植入后1天(第1天)和植入(第30天)的1个月的剂量测定参数包括在分析中。结果:所有患者的2级或更高直肠毒性的7年累积发病率为5.7%。多变量分析显示,抗血小板或抗凝治疗,Neoadjuvant雄激素剥夺治疗,治疗方式,第1天直肠体积接受5%的规定剂量(RV 100),并将第30天的规定剂量百分比递送至30%直肠(RD 30)与直肠毒性有关。第1天RV 100是BT-Linse和BT + EBRT组中的常见预测因子。 2级或更高的直肠毒性的5年累积发病率为12.6%,5.9%和1.7%,分别为BT +强度调制的放射疗法和单独的BT单独组( P <0.001)。结论:BT中的直肠剂量分析与晚直肠毒性有关。虽然当EBRT与BT结合时直肠毒性的风险较高,但具有适当且可实现的直肠剂量约束,强度调制的放射治疗产生的毒性小于三维保形放射疗法。目的:我们分析了碘-125前列腺近六乳房近距离放射治疗(BT)的直肠毒性相关的因素,或没有外部光束放射治疗(EBRT)。方法和材料:总共2216名前列腺癌患者在2003年至2013年间接受过碘-125英镑的碘-125英镑。中位后关注为6.9岁。 Cox比例危害建模用于单变量和多变量分析,以评估与直肠毒性相关的临床和剂量因子。从植入后1天(第1天)和植入(第30天)的1个月的剂量测定参数包括在分析中。结果:所有患者的2级或更高直肠毒性的7年累积发病率为5.7%。多变量分析显示,抗血小板或抗凝血治疗,Neoadjuvant雄激素剥夺治疗,治疗方式,第1天直肠体积接受预定剂量(RV 100 100)的100%,并将第30天最小的规定剂量递送至30%直肠(RD 30 30)与直肠毒性有关。第1天RV 100 100是BT-InseL和BT + EBRT组中的常见预测因子。 2级或更高的直肠毒性的5年累积发病率为12.6%,5.9%和1.7%,分别为BT +强度调制的放射疗法和单独的BT单独组( p <0.001)。结论:BT中的直肠剂量分析与晚直肠毒性有关。虽然当EBRT与BT结合时直肠毒性的风险较高,但具有适当且可实现的直肠剂量约束,强度调制的放射治疗产生的毒性小于三维保形放射疗法。

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