Dose compliance of estramustine phosphate in neoadjuvant chemohormonal therapy combined with degarelix acetate predicts the biochemical recurrence in patients with very high‐risk prostate cancer who underwent robot‐assisted radical prostatectomy

IF 1.8 3区 医学 Q3 UROLOGY & NEPHROLOGY
Takanari Kambe, Toshinari Yamasaki, Akihiro Yamamoto, Akihiko Nagoshi, Tasuku Fujiwara, Yuta Mine, Hiroki Hagimoto, Atsushi Igarashi, Hidetoshi Kokubun, Shiori Murata, Naoki Akagi, Yuto Hattori, Yohei Abe, Naofumi Tsutsumi, Noboru Shibasaki, Mutsushi Kawakita
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Abstract

ObjectivesThe objective of this study is to evaluate the safety and efficacy of neoadjuvant degarelix acetate and low‐dose estramustine phosphate for high−/very high‐risk prostate cancer.MethodsOverall, 187 patients diagnosed with National Comprehensive Cancer Network high−/very high‐risk cTanyN0M0 localized prostate cancer who consented to undergo robot‐assisted radical prostatectomy after receiving neoadjuvant chemohormonal therapy for 6 months were prospectively enrolled between December 2017 and March 2023. Adverse events, perioperative and histopathological outcomes, and biochemical recurrence‐free survival rates were examined. Survival analysis compared the estramustine phosphate completion and reduction groups.ResultsThirty‐six patients discontinued neoadjuvant therapy in <5 months owing to adverse events (n = 34) or other reasons (n = 2). Eleven were excluded for being in the postoperative castration range. Of the 140 patients who underwent surgery, 124 continued with two tablets of estramustine phosphate and 16 with one tablet. Overall, 82 patients were very high‐risk. Histopathological outcomes were significantly worse in the very high‐risk group than those in the high‐risk group. Very high‐risk status and estramustine phosphate reduction were significant factors in biochemical recurrence in multivariate analysis. The biochemical recurrence‐free survival rate in very high‐risk patients was significantly lower in the estramustine phosphate dose reduction group than in the completion group but not significant in high‐risk patients. Major adverse events were anemia (n = 174), elevated transaminase levels (n = 68), and deep vein thrombosis (n = 24). Severe adverse events included acute coronary syndrome (n = 4) and pulmonary embolism (n = 3).ConclusionsDose compliance with estramustine phosphate predicted biochemical recurrence in patients with very high‐risk prostate cancer undergoing robot‐assisted radical prostatectomy with neoadjuvant chemohormonal therapy.
在接受机器人辅助前列腺癌根治术的极高危前列腺癌患者中,新辅助化疗激素疗法结合醋酸地加瑞克的磷酸雌莫司汀剂量依从性可预测生化复发情况
方法在2017年12月至2023年3月期间,前瞻性入组了187名确诊为国家综合癌症网络高危/极高危cTanyN0M0局部前列腺癌的患者,这些患者在接受6个月的新辅助化疗激素治疗后同意接受机器人辅助前列腺癌根治术。对不良事件、围手术期和组织病理学结果以及无生化复发生存率进行了研究。生存分析比较了磷酸雌莫司汀完成组和减少组。结果36名患者由于不良事件(34人)或其他原因(2人)在<5个月内停止了新辅助治疗。11名患者因处于术后阉割范围而被排除在外。在接受手术的 140 名患者中,124 人继续服用两片磷酸雌莫司汀,16 人服用一片。总的来说,82 名患者属于高危人群。极高风险组的组织病理学结果明显差于高风险组。在多变量分析中,极高风险状态和磷酸雌莫司汀减量是影响生化复发的重要因素。雌莫司汀磷酸减量组极高危患者的无生化复发生存率明显低于完成组,但在高危患者中无明显差异。主要不良反应包括贫血(174 例)、转氨酶水平升高(68 例)和深静脉血栓(24 例)。结论在接受机器人辅助前列腺癌根治术和新辅助化疗的极高危前列腺癌患者中,磷酸雌莫司汀的剂量依从性可预测生化复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Urology
International Journal of Urology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
11.50%
发文量
340
审稿时长
3 months
期刊介绍: International Journal of Urology is the official English language journal of the Japanese Urological Association, publishing articles of scientific excellence in urology. Submissions of papers from all countries are considered for publication. All manuscripts are subject to peer review and are judged on the basis of their contribution of original data and ideas or interpretation.
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