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Impact of access to novel therapies on the initial management of castrate‐resistant prostate cancer: an Australian multicentre study

机译:新疗法对抗阉割前列腺癌初步管理的影响:澳大利亚多期面研究

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Abstract Background The impact of regulatory approvals of new therapies for castration‐resistant prostate cancer (CRPC) in Australia is unclear. Aims To determine if changes in novel therapy access in Australia affected how clinicians initially managed men with newly diagnosed CRPC. Methods Data from patients diagnosed with CRPC from 2013 to 2016 across three Australian hospitals were retrospectively collected. Baseline clinicopathological factors and initial management decision at the time of CRPC development (early treatment (ET) vs deferred treatment (DT)) were recorded. Categorical variables between cohorts were compared by Chi‐squared analysis. Cox regression analysis was performed to assess the impact of CRPC diagnosis year on time to commencing life‐prolonging systemic treatment (TTT). Results Our study identified 137 CRPC patients, with 126 (92%) patients receiving life‐prolonging systemic treatment. The median age was 73 years. The initial management decision was DT in 71 (52%) patients and ET in 66 (48%) patients. There was a significant shift from DT to ET during the study period (2013–2014: DT 61% vs ET 33%; 2015–2016: DT 39% vs ET 67%; P = 0.004), with a rise in novel androgen receptor signalling inhibitor use and simultaneous reduction in first‐generation antiandrogen use at CRPC development. Each successive CRPC diagnosis year was associated with shorter TTT on univariate analysis (HR: 1.5, 95% CI: 1.3–1.7, P 0.001). Conclusion Over time, clinicians are favouring earlier introduction of life‐prolonging systemic treatment at the development of CRPC. This trend is largely driven by substantial uptake of novel androgen receptor signalling inhibitors as the preferred initial treatment for CRPC patients.
机译:摘要背景澳大利亚抵抗前列腺癌(CRPC)的新疗法对抵抗前列腺癌(CRPC)的影响尚不清楚。旨在确定澳大利亚新型治疗途径的变化影响了临床医生如何用新诊断的CRPC初步管理男性。方法回顾性收集2013年至2016年患有CRPC的患者的数据。 CRPC开发时基线临床病理因素和初始管理决策(早期治疗(ET)vs延期治疗(DT))。 Chi平方分析比较了群组之间的分类变量。进行COX回归分析,以评估CRPC诊断年度对开始寿命的全身治疗(TTT)的影响。结果我们的研究确定了137名CRPC患者,126例(92%)患者接受延长的全身治疗。中位年龄为73岁。初始管理决策是在71名(52%)患者中的DT和66名(48%)患者。在研究期间(2013-2014:DT 61%VS ET 33%有重大转变; 2015-2016:DT 39%VS ET 67%; P = 0.004),具有新的雄激素受体升高CRPC发育中的发信号抑制剂使用和同时降低第一代抗抗原使用。每次连续的CRPC诊断年与单变量分析的较短TTT有关(HR:1.5,95%CI:1.3-1.7,P <0.001)。结论随着时间的推移,临床医生早期引入CRPC发育过程中的生命延长的全身治疗。这种趋势在很大程度上是由于基本上摄取新的雄激素受体信号传导抑制剂作为CRPC患者的优选初始治疗。

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