The Brady Urological Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Urology, Loyola University Medical Center, Maywood, Illinois.
J Urol. 2021 Jun;205(6):1681-1688. doi: 10.1097/JU.0000000000001586. Epub 2021 Feb 3.
Erectile dysfunction significantly impacts quality of life for men undergoing radical prostatectomy for prostate cancer. Erythropoietin is a promising neurotrophic factor for neurogenic erectile dysfunction based on preclinical and retrospective data.
ERECT (NCT00737893) is a phase 2, double-blinded, randomized, placebo-controlled trial (July 2017-December 2019) evaluating the impact of perioperative erythropoietin on recovery of erectile function and other patient-reported, health-related quality of life outcomes after bilateral nerve-sparing radical prostatectomy (3, 6, 9, and 12 months). Erythropoietin (20,000 units) or saline placebo was injected subcutaneously the day before, day of, and day after surgery for 3 total doses.
Of 63 patients assessed for eligibility, 56 patients were randomized. Arms (29 erythropoietin, 27 placebo) were well balanced (89.3% robotic, median age 55.5 years). International Index of Erectile Function-Erectile Function Domain (IIEF-EF) scores increased from median 12.5 at 3 months to 24.5 at 12 months. Median 2-week serum hemoglobin was higher for the erythropoietin arm compared to placebo (14.7 vs 13.6, p=0.02). There was no statistically significant difference in IIEF-EF scores at 6 months comparing erythropoietin to placebo (p=0.50) or at other time points (mixed model regression coefficient: -1.7, 95% CI -6.1-2.7, p=0.45). Excellent nerve-sparing rating (10/10) was associated with improved IIEF-EF recovery (+5.2, p=0.022). Other patient-reported, health-related quality of life domains as well as oncologic outcome and complications were similar between arms during followup.
In the context of brief perioperative dosing, erythropoietin did not improve recovery of erectile function for men undergoing radical prostatectomy for prostate cancer compared to placebo. Further research to identify effective adjuncts to improve health-related quality of life for these men is needed.
勃起功能障碍会显著影响接受根治性前列腺切除术治疗前列腺癌的男性的生活质量。基于临床前和回顾性数据,促红细胞生成素是一种有前途的治疗神经原性勃起功能障碍的神经营养因子。
ERECT(NCT00737893)是一项 2 期、双盲、随机、安慰剂对照试验(2017 年 7 月至 2019 年 12 月),评估围手术期促红细胞生成素对双侧神经保留根治性前列腺切除术后(3、6、9 和 12 个月)勃起功能恢复和其他患者报告的健康相关生活质量结局的影响。促红细胞生成素(20000 单位)或生理盐水安慰剂在手术前一天、手术当天和手术后一天皮下注射,共 3 次剂量。
在 63 名符合入选标准的患者中,有 56 名患者被随机分配。两组(29 例促红细胞生成素,27 例安慰剂)平衡良好(89.3%机器人手术,中位年龄 55.5 岁)。国际勃起功能指数-勃起功能域(IIEF-EF)评分从 3 个月时的中位数 12.5 增加到 12 个月时的 24.5。与安慰剂相比,促红细胞生成素组的中位 2 周血清血红蛋白较高(14.7 对 13.6,p=0.02)。在 6 个月时,与安慰剂相比,促红细胞生成素对 IIEF-EF 评分没有统计学上的显著差异(p=0.50)或在其他时间点(混合模型回归系数:-1.7,95%置信区间-6.1-2.7,p=0.45)。优秀的神经保留评分(10/10)与 IIEF-EF 恢复增加(+5.2,p=0.022)相关。在随访期间,两组的其他患者报告的健康相关生活质量领域以及肿瘤学结果和并发症相似。
在短期围手术期用药的情况下,与安慰剂相比,促红细胞生成素并未改善接受根治性前列腺切除术治疗前列腺癌的男性勃起功能的恢复。需要进一步研究,以确定有效的辅助手段来改善这些男性的健康相关生活质量。