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首页> 外文期刊>Journal of Clinical Oncology >Adjuvant Androgen Deprivation for High-Risk Prostate Cancer After Radical Prostatectomy: SWOG S9921 Study.
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Adjuvant Androgen Deprivation for High-Risk Prostate Cancer After Radical Prostatectomy: SWOG S9921 Study.

机译:前列腺癌根治术后高危前列腺癌的辅助雄激素剥夺:SWOG S9921研究。

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摘要

PURPOSE Men with high-risk features (extraprostatic extension or high Gleason grade) face a high risk of prostate cancer recurrence after radical prostatectomy. Clinical trials of adjuvant systemic therapy for such patients have been limited. PATIENTS AND METHODS The SWOG (Southwest Oncology Group) S9921 study randomly assigned 983 men with high-risk features at prostatectomy to receive adjuvant therapy with androgen deprivation (ADT) alone or in combination with mitoxantrone chemotherapy. ADT consisted of goserelin and bicalutamide for 2 years. Results Although the final primary treatment comparison results are not ready for publication, this article reports results in the ADT-alone control arm with a median follow-up of 4.4 years. For these 481 men, the estimated 5-year biochemical failure-free survival is 92.5% (95% CI, 90 to 95), and 5-year overall survival is 95.9% (95% CI, 93.9 to 97.9). CONCLUSION The results of this trial, taken in context, make a compelling argument for counseling all high-risk patients with prostate cancer about adjuvant ADT. This article discusses the challenges in the design and implementation of clinical trials to take the next step forward in adjuvant therapy for prostate cancer because of the excellent survival achieved with currently available therapies and highlights the need for better molecular markers to personalize care.
机译:目的具有高风险特征(前列腺延长或格里森评分高)的男性在前列腺癌根治术后面临前列腺癌复发的高风险。对于这类患者的辅助全身治疗的临床试验是有限的。患者和方法SWOG(西南肿瘤学组)S9921研究随机分配了983位前列腺癌高危男性,接受单独的雄激素剥夺(ADT)或米托蒽醌化疗联合辅助治疗。 ADT由戈舍瑞林和比卡鲁胺组成,历时2年。结果尽管最终的主要治疗比较结果尚未准备好发表,但本文报道了仅ADT对照组的结果,中位随访时间为4.4年。对于这481名男性,估计的5年生化无失败生存率为92.5%(95%CI,90至95),而5年总生存率为95.9%(95%CI,93.9至97.9)。结论本研究的结果是在上下文中提出的,对于为所有高危前列腺癌患者提供佐剂ADT咨询服务具有说服力。本文讨论了设计和实施临床试验所面临的挑战,以使前列腺癌的辅助治疗迈出新的一步,因为目前可获得的疗法可实现出色的生存率,并强调了需要更好的分子标记物来个性化护理的需求。

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