Clinical Efficacy of Immediate Radical Surgery for Locally Advanced Prostate Cancer
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摘要:
目的 探讨局部晚期前列腺癌确诊后即刻行腹腔镜前列腺癌根治术的临床疗效及安全性。 方法 回顾性分析2018年1月至2023年1月在云南省曲靖市第一人民医院确诊的63例符合纳入标准的局部晚期前列腺癌患者,所有患者均为超声引导下经会阴前列腺穿刺活检确诊,其中实验组37例,病理确诊后即刻接受腹腔镜前列腺癌根治术,术后辅助内分泌治疗;对照组26例,先接受3个月新辅助内分泌治疗,再行根治术,术后给予辅助内分泌治疗。观察两组患者在手术时间、术中出血量、住院时间、留置尿管时间、切缘阳性率、直肠损伤、淋巴结阳性率、尿瘘和淋巴漏发生率、PSA水平变化、术后尿控、生化复发及远处转移方面的差异。 结果 对照组接受新辅助内分泌治疗后,血清PSA、前列腺体积、临床分期明显降低;实验组切缘阳性率相比对照组显著升高,差异有统计学意义(P < 0.05);两组患者手术时间、术中出血量、住院时间、留置尿管时间、直肠损伤、淋巴结阳性率、尿瘘和淋巴漏发生率之间的差异无统计学意义(P > 0.05);随访18~36个月,两组患者术后1个月血清PSA水平、术后6个月完全尿控率、术后1年、2年生化复发及远处转移间的差异无统计学意义(P > 0.05)。 结论 局部晚期前列腺癌确诊后即刻行腹腔镜前列腺癌根治术是临床安全可行的治疗方案。新辅助内分泌治疗使局部晚期前列腺癌肿瘤分期降级、切缘阳性率降低,前列腺体积明显缩小,获得更大操作空间,不增加手术风险。 -
关键词:
- 前列腺癌 /
- 新辅助内分泌治疗 /
- 局部晚期前列腺癌 /
- 腹腔镜下前列腺癌根治术
Abstract:Objective To explore the clinical efficacy and safety of immediate laparoscopic radical prostatectomy immediately following the diagnosis of locally advanced prostate cancer. Methods A retrospective analysis was performed for 63 patients with locally advanced prostate cancer who met the inclusion criteria diagnosed in The 1st People's Hospital of Qujing City, Yunnan Province from January 2018 to January 2023. All patients were diagnosed via ultrasound-guided transperineal prostate biopsy. The experimental group consisted of 37 patients who underwent immediate laparoscopic radical prostatectomy after pathological diagnosis, followed by postoperative adjuvant hormone therapy. The control group included 26 patients who first received 3 months of neoadjuvant hormone therapy before undergoing radical surgery, followed by adjuvant hormone therapy postoperatively. The two groups were compared in terms of surgical duration, intraoperative blood loss, length of hospital stay, duration of catheterization, positive surgical margin rate, rectal injury, positive lymph node rate, incidence of urinary fistula and lymphatic leakage, changes in PSA level, postoperative urinary control, biochemical recurrence and distant metastasis. Results In the control group, serum PSA levels, prostate volume, and clinical staging significantly decreased after neoadjuvant hormon therapy. The positive surgical margin rate in the experimental group was significantly higher than that in the control group, with a statistically significant difference(P < 0.05). There were no statistically significant differences between the two groups in terms of surgical duration, intraoperative blood loss, length of hospital stay, duration of catheterization, rectal injury, positive lymph node rate, incidence of urinary fistula and lymphatic leakage (P > 0.05). Follow-up at 18 to 36 months revealed no statistically significant differences between the two groups in terms of serum PSA levels at one month post-surgery, complete urinary control rate at six months post-surgery, and biochemical recurrence and distant metastasis at one and two years post-surgery (P > 0.05). Conclusion Immediate laparoscopic radical prostatectomy following the diagnosis of locally advanced prostate cancer is a clinically safe and feasible treatment option. Noadjuvant hormone therapy reduces tumor staging, lowers the positive surgical margin rate, significantly decreases prostate volume, and provides greater operational space without increasing surgical risks. -
表 1 实验组与对照组患者临床资料[n(%)/$ \bar x \pm s $/ M(P25,P75)]
Table 1. Clinical data of patients in the experimental group and the control group[n(%)/$ \bar x \pm s $/ M(P25,P75)]
资料 对照组(n = 26) 实验组(n = 37) t/Z P 年龄(岁) 67.58 ± 3.29 67.22 ± 4.17 0.368 0.714 BMI(kg/m2) 22.79 ± 2.68 23.84 ± 2.72 −1.512 0.136 初诊血清PSA(ng/mL) 24.39(18.31,34.83) 19.57(15.60,29.49) −1.445 0.148 初诊前列腺体积(mL) 48.01 ± 8.84 46.49 ± 8.30 0.695 za0.489 术前Gleason评分 −0.287 0.774 6 3(11.53) 3(8.11) 7 14(53.85) 24(64.86) 8 7(26.92) 7(18.92) 9 2(7.69) 3(8.11) 10 0(0.00) 0(0.00) 临床TNM分期 −0.076 0.939 T3aN0M0 13(50.00) 18(48.65) T3aN1M0 1(3.85) 2(5.41) T3bN0M0 8(30.77) 13(35.12) T3bN1M0 3(11.54) 2(5.41) T4N0M0 1(3.85) 2(5.41) 表 2 对照组NHT治疗前后数据对比[n(%)/$ \bar x \pm s $/ M(P25,P75)]
Table 2. Comparison of data before and after NHT treatment in the control group[n(%)/$ \bar x \pm s $/ M(P25,P75)]
资料 NHT治疗前 NHT治疗后 Z/t P 前列腺体积(mL) 48.01 ± 8.84 40.33 ± 8.22 3.244 0.002* 血清PSA(ng/mL) 24.39(18.31,34.83) 0.445(0.085,0.820) −4.457 0.000* Gleason评分 6 3(11.53) 4(15.38) 7 14(53.85) 14(53.85) 8 7(26.92) 6(23.08) 9 2(7.69) 2(7.69) 10 0(0.00) 0(0.00) 临床TNM分期 T2cN0M0 0(0.00) 2(7.69) T3aN0M0 13(50.00) 14(53.85) T3aN1M0 1(3.85) 0(0.00) T3bN0M0 8(30.77) 8(30.77) T3bN1M0 3(11.54) 2(7.69) T4N0M0 1(3.85) 0(0.00) *P < 0.05。 表 3 围手术期情况对比[n(%)/ M(P25,P75)]
Table 3. Comparison of perioperative conditions[n(%)/ M(P25,P75)]
观察指标 对照组(n = 26) 实验组(n = 37) Z/χ2 P 手术时间(h) 3.2(2.3,4.0) 3.1(3.0,3.3) −0.035 0.972 术中出血量(mL) 175(100,225) 100(100,250) −0.146 0.884 住院时间(d) 10.5(8.0,12.0) 10.0(7.5,11.0) −0.928 0.353 留置尿管时间(d) 14.0(14.0,15.0) 14.0(13.0,14.5) −0.980 0.327 直肠损伤 1(3.80) 0(0.00) 1.446 0.413 切缘阳性 2(7.70) 11(29.70) 4.528 0.033* 淋巴结阳性 2(7.70) 5(13.50) 0.100 0.751 尿瘘 1(3.80) 1(2.70) 0.65 0.799 淋巴瘘 1(3.80) 2(5.40) 0.82 0.775 *P < 0.05。 表 4 术后随访情况对比[n(%)/ M(P25,P75)]
Table 4. Comparison of postoperative follow-up[n(%)/ M(P25,P75)]
观察指标 对照组(n = 26) 实验组(n = 37) Z/χ2 P 术后1个月 血清PSA(ng/mL) 0.012(0.006,0.068) 0.021(0.006,0.0625) −0.395 0.693 术后6个月 完全尿控率 20(76.90) 26(70.30) 0.343 0.558 生化复发 1年 2(7.70) 3(8.10) 0.004 0.952 2年 3(11.50) 6(16.20) 0.273 0.601 远处转移 2(7.70) 4(10.80) 1.72 0.678 -
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