首页> 外文期刊>Japanese journal of clinical oncology. >Effect of delayed maximal androgen blockade therapy for patients with advanced prostate cancer who fail to respond to initial androgen deprivation monotherapy.
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Effect of delayed maximal androgen blockade therapy for patients with advanced prostate cancer who fail to respond to initial androgen deprivation monotherapy.

机译:延迟最大雄激素阻断治疗对晚期男性前列腺癌剥夺性单药治疗无效的晚期前列腺癌患者的疗效。

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OBJECTIVES: We analyzed the efficacy of additional antiandrogens as second- and third-line treatments after the failure of initial androgen deprivation monotherapy. METHODS: This retrospective study included 53 patients with advanced prostate cancer initially treated with androgen deprivation monotherapy alone. An antiandrogen was added to androgen deprivation monotherapy as the second-line treatment after the failure of the initial androgen deprivation monotherapy. Another antiandrogen, estrogen or steroid was given as the third-line treatment after the second-line treatment failed. RESULTS: The initial androgen deprivation monotherapy was effective in all 53 patients for a median of 9.6 months. Thirty-three (62.3%) patients showed a prostate-specific antigen response to the second-line treatment for a median of 10.7 months. Of the 46 patients who received the third-line treatment, 16 (34.8%) showed a prostate-specific antigen response for a median of 6.0 months. Patients who responded to the second-line treatment had a significantly higher cancer-specific survival rate than those without a response. In multivariate analysis, a nadir prostate-specific antigen of 4.0 ng/ml or greater during androgen deprivation monotherapy and prostate-specific antigen doubling time of less than 10 months after androgen deprivation monotherapy failure were independent risk factors for prostate cancer death after androgen deprivation monotherapy failure, with hazards ratios of 5.59 and 8.00, respectively. The 5-year cancer-specific survival rates were 100%, 65.0% and 15.5% in patients with 0, 1 and 2 risk factors, respectively (P = 0.047). CONCLUSIONS: In this study, the second- and third-line treatments were effective for patients with advanced prostate cancer. Nadir prostate-specific antigen during androgen deprivation monotherapy and prostate-specific antigen doubling time just after the failure of androgen deprivation monotherapy are factors that can predict the prognosis.
机译:目的:我们分析了最初的雄激素剥夺单药治疗失败后,其他抗雄激素作为二线和三线治疗的疗效。方法:这项回顾性研究包括53例最初仅接受雄激素剥夺单药治疗的晚期前列腺癌患者。最初的雄激素剥夺单药治疗失败后,将抗雄激素作为雄激素剥夺单药治疗的二线治疗。在第二线治疗失败后,另一种抗雄激素,雌激素或类固醇作为第三线治疗被给予。结果:最初的雄激素剥夺单一疗法对所有53例患者有效,中位数为9.6个月。 33名患者(62.3%)对二线治疗表现出前列腺特异性抗原反应,中位值为10.7个月。在接受三线治疗的46例患者中,有16例(34.8%)的前列腺特异性抗原反应持续了6.0个月。对二线治疗有反应的患者比无反应的患者具有更高的癌症特异性生存率。在多变量分析中,雄激素剥夺单药治疗期间最低谷蛋白前列腺特异性抗原为4.0 ng / ml或更高,雄激素剥夺单药治疗失败后不到10个月的前列腺特异性抗原加倍时间是雄激素剥夺单药治疗后前列腺癌死亡的独立危险因素。故障,危险比分别为5.59和8.00。具有0、1和2个危险因素的患者的5年癌症特异性生存率分别为100%,65.0%和15.5%(P = 0.047)。结论:在这项研究中,二线和三线治疗对晚期前列腺癌患者有效。雄激素剥夺单药治疗期间的最低点前列腺特异性抗原和雄激素剥夺单药治疗失败后的前列腺特异性抗原加倍时间是可以预测预后的因素。

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