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首页> 外文期刊>BJU international >Switch from abiraterone plus prednisone to abiraterone plus dexamethasone at asymptomatic PSA progression in patients with metastatic castration-resistant prostate cancer
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Switch from abiraterone plus prednisone to abiraterone plus dexamethasone at asymptomatic PSA progression in patients with metastatic castration-resistant prostate cancer

机译:从转移性阉割的前列腺癌患者的无症状PSA进展中从Abiraaterone加上泼尼松加上Abiraatorone加上地塞米松

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Objective To evaluate the effects of switching from prednisone (P) to dexamethasone (D) at asymptomatic prostate-specific antigen (PSA) progression in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with abiraterone acetate (AA). Materials and Methods Among 93 patients treated with AA between January 2013 and April 2016 in our institution, 48 consecutive asymptomatic patients with mCRPC, who experienced biochemical progression on treatment with AA+P 10 mg/day, were included. A corticosteroid switch to AA+D 0.5 mg/day at PSA increase was administered until radiological and/or clinical progression. The primary endpoint was progression-free-survival (PFS). A prognostic score based on independent prognostic factors was defined. Results The median time to PSA progression on AA+P was 8.94 months. The median PFS on AA+D and AA+corticosteroids (P then D) was 10.35 and 20.07 months, respectively. A total of 56.25% of patients showed a decrease or stabilization in PSA levels after the switch. In univariate analysis, three markers of switch efficiency were significantly associated with a longer PFS: long hormone-sensitivity duration (= 5 years; median PFS 16.62 vs 4.17 months, hazard ratio [HR] 0.30, 90% confidence interval [CI] 0.16-0.56); low PSA level at the time of switch (50 ng/mL; median PFS 15.21 vs 3.86 months, HR 0.33, 90% CI 0.18-0.60); and short time to PSA progression on AA+P (6 months; median PFS 28.02 vs 6.65 months, HR 0.41 (90% CI 0.21-0.81). In multivariate analysis, hormone sensitivity duration and PSA level were independent prognostic factors. Conclusion A steroid switch from P to D appears to be a safe and non-expensive way of obtaining long-term responses to AA in selected patients with mCRPC. A longer PFS has been observed in patients with previous long hormone sensitivity duration, and/or low PSA level and/or short time to PSA progression on AA+P.
机译:目的探讨从醋酸乙酸Abataterone(AA)处理的转移性阉割抗性前列腺癌(MCRPC)患者的无症状前列腺特异性抗原(PSA)进展中从泼尼松(P)到地塞米松(D)的影响。在2013年1月至2016年1月至2016年4月间治疗的93例患者中的材料和方法,包括含有AA + P 10 Mg /天的生物化学进展的48例MCRPC患者。在放射学和/或临床进展中施用至AA + D 0.5mg /天的皮质类固醇转换为AA + D.5mg /天。主要终点是无进展生存(PFS)。定义了基于独立预后因子的预后评分。结果AA + P对PSA进展的中位时间为8.94个月。 AA + D和AA +皮质类固醇(P然后D)的中值PFS分别为10.35和20.07个月。在开关后,共有56.25%的患者在PSA水平中表现出降低或稳定。在单变量分析中,三个开关效率的标记与较长的PFS显着相关:长激素敏感性持续时间(& = 5年;中位数PFS 16.62与4.17个月,危险比[HR] 0.30,90%置信区间[CI] 0.16-0.56);开关时的低PSA水平(<50 ng / ml;中位数PFS 15.21与3.86个月,HR 0.33,90%CI 0.18-0.60); + P上的PSA进展短时间(6个月;中位数PFS 28.02与6.65个月,HR 0.41(90%CI 0.21-0.81)。在多变量分析中,激素敏感性持续时间和PSA水平是独立的预后因素。结论来自P到D的类固醇开关似乎是在患有MCRPC的选定患者中获得长期反应的安全且不昂贵的方法。患者患者已经观察到更长的PFS患者,持续时间和/或低PSA水平和/或短时间为AA + P对PSA进展。

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