高危和极高危前列腺癌的联合治疗:新辅助治疗的结果

A. V. Troyanov, V. Biryukov, I. V. Zaborsky, V. S. Chaykov, I. Dementev, E. O. Shchukina, O. Karyakin
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引用次数: 0

摘要

研究目的:无远处转移的高风险和极高风险前列腺癌新辅助化疗激素治疗的安全性和短期有效性评估患者和方法。对33例无远处转移的高风险和极高风险前列腺癌患者进行激素联合放化疗治疗。检查资料(MRI、MSCT)发现9例转移至区域淋巴结,24例未发现转移。所有患者均接受化疗激素联合治疗,每3周静脉注射75 mg/m2的多西他赛4个疗程作为第一阶段治疗。在进行根治性放射治疗(联合或远程)之前,与GnRH激动剂或拮抗剂的雄激素剥夺治疗联合使用。所有患者均接受了新辅助激素治疗:16例患者使用GnRH拮抗剂(Degarelix), 17例使用GnRH激动剂(Gozerelin/Leuprorelin/Triptorelin)。评估了所提出的治疗方案的毒性及其对前列腺特异性抗原(PSA)水平、前列腺体积和排尿质量的影响。治疗方案在降低PSA方面非常有效(新辅助治疗后中位水平从最初的77,67 ng/ml降至1,45 ng/ml),所有受试者均反应良好,未观察到无反应。治疗后前列腺中位体积由44 cm3降至25 cm3,保证了进一步根治放疗的有效性和安全性。初步尿潴留的所有受试者均恢复了泌尿功能。新辅助化疗治疗在PSA水平、前列腺体积减少和功能改善方面非常有效,这保证了其中一种类型的进一步根治性放射治疗。毒性是可以接受的,在大多数情况下,不良事件没有超过II级,在任何情况下都没有导致治疗中断,而生活质量仍然足够高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined treatment of high and very high risk prostate cancer: results of neoadjuvant treatment
Purpose of the study. Assessment of safety and short‑term effectiveness of high and very high‑risk prostate cancer neoadjuvant chemo‑ hormonal treatment without distant metastases.Patients and methods. Combined hormone chemo‑ radiation treatment of 33 patients with prostate cancer of high and very high risk of progression without distant metastases was performed. Metastases to regional lymph nodes were found in 9 patients according to the examination data (MRI, MSCT), no metastases were detected in 24 patients. All patients underwent combined chemohormonal therapy in the amount of 4 courses of docetaxel intravenously at a dose of 75 mg/m2 every 3 weeks as the first stage of treatment. in combination with androgen deprivation therapy with agonists or antagonists of GnRH before performing radical radiation therapy (combined or remote). All patients underwent neoadjuvant hormone therapy: 16 patients – with the use of GnRH antagonists (Degarelix), 17 – with the use of GnRH agonists (Gozerelin/Leuprorelin/Triptorelin). The toxicity of the presented treatment regimen and its immediate effectiveness – the effect on the level of prostate‑s pecific antigen (PSA), prostate volume, and the quality of urination – were evaluated.Results. Treatment regimen was highly effective concerning PSA decrease (from initial median level 79,67 ng/ml to 1,45 ng/ml after neoadjuvant treatment), all subjects responded well, no non‑responders observed. Median prostate volume decreased from 44 cm3 to 25 cm3 after treatment, which guaranteed availability and safety of further radical radiation treatment. Urinary function was restored in all subject with initial urinary retention.Conclusion. Neoadjuvant chemo‑h ormonal treatment was highly effective in PSA level, prostate volume decrease and functional results improvement which secured further radical radiation treatment in one of its types. Toxicity was acceptable, adverse events did not exceed grade II in most cases and did not lead to treatment discontinuation in any cases, while quality of life remained high enough.
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