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Prognosis after radical prostatectomy in men older than 75 years: long-term results from a single tertiary center 75 岁以上男性前列腺癌根治术后的预后:一家三级医疗中心的长期研究结果
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2024-03-01 DOI: 10.1016/j.prnil.2023.09.004
Jaewon Lee , Jungkeun Song , Gyoohwan Jung , Sang Hun Song , Sung Kyu Hong

Background

Despite longer lifespans, guidelines for prostate cancer treatment recommend surgery for those with over 10 years of life expectancy, potentially leaving older patients undertreated. This study examines the outcomes of radical prostatectomy (RP) in a large cohort of men older than 75 years.

Materials and methods

We retrospectively analyzed 636 patients from a pool of 4,500 RP cases at a single tertiary institution from 2004 to 2022. Patients younger than 75 years or with incomplete records were excluded. Baseline clinical variables, including PSA and biopsy grade group (GG), as well as postoperative pathology and oncological outcomes, were assessed. Achievement of continence based on no pads and ≤1 pad at last follow-up were evaluated.

Results

Mean age and PSA were 76.4 years and 15.3 ng/ml, respectively. At biopsy, GG1 and 2 were found in 18.1% and 31.5%, respectively, with 28.5% harboring GG4-5 tumors. After RP, 41.5% had GG upgrade compared to biopsy results, with 46.5% with ≥pT3 tumors. In a mean follow-up of 41.5 months, 82.3% were able to attain total continence of 0 pads, and 89.5% used ≤1 pads at the last follow-up. Overall and cancer-specific mortality was observed in 4.3% and 0.9%, respectively, and biochemical recurrence (BCR) occurred in 20.3% after a median of 154 months. At multivariate analysis, age was not a significant factor for BCR, whereas preoperative PSA, biopsy GG, margin positivity, and lymph node invasion were significant.

Conclusion

RP is feasible in men older than 75 years with decent oncological outcome, with absolute age insignificant within this age group. Risk of undertreatment should be acknowledged, and definite treatment must be considered.

背景尽管人的寿命越来越长,但前列腺癌治疗指南仍建议预期寿命超过 10 年的患者接受手术治疗,这可能会导致老年患者得不到及时治疗。材料与方法我们回顾性分析了2004年至2022年一家三级医疗机构4500例前列腺癌根治术病例中的636例患者。排除了年龄小于 75 岁或记录不完整的患者。评估了基线临床变量,包括 PSA 和活检分级组(GG),以及术后病理学和肿瘤学结果。结果 平均年龄和 PSA 分别为 76.4 岁和 15.3 纳克/毫升。活检结果显示,18.1%和31.5%的肿瘤为GG1和GG2,28.5%的肿瘤为GG4-5。手术后,与活检结果相比,41.5%的患者GG升级,46.5%的患者肿瘤≥pT3。在平均41.5个月的随访中,82.3%的患者在最后一次随访时能够做到0个尿垫,89.5%的患者使用的尿垫少于1个。总体死亡率和癌症特异性死亡率分别为4.3%和0.9%,20.3%的患者在中位随访154个月后出现生化复发(BCR)。在多变量分析中,年龄不是导致 BCR 的重要因素,而术前 PSA、活检 GG、边缘阳性和淋巴结侵犯则是重要因素。应认识到治疗不足的风险,必须考虑明确的治疗。
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引用次数: 0
Infectious complications of transrectal prostate biopsy in patients receiving targeted antibiotic prophylaxis after urethral and rectal swab versus standard prophylaxis: A prospective comparative study 经尿道和直肠拭子后接受靶向抗生素预防的患者与标准预防的经直肠前列腺活检的感染并发症:一项前瞻性比较研究
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2024-03-01 DOI: 10.1016/j.prnil.2023.11.002
Sotirios Gatsos , Nikolaos Kalogeras , Georgios Dimakopoulos , Michael Samarinas , Anna Papakonstantinou , Efi Petinaki , Vassilios Tzortzis , Stavros Gravas

Background

To evaluate the role of targeted antibiotic prophylaxis (TAP) after rectal and urethral swab cultures compared to empiric antibiotic prophylaxis (EAP) for the prevention of infectious complications after transrectal ultrasound-guided prostate biopsy (TRUS-Bx).

Methods

We conducted a prospective comparative study on 141 patients who underwent TRUS-Bx and were allocated in two groups. The first group (n = 71) received EAP with ciprofloxacin and the second (n = 70) received TAP according to rectal and urethral cultures. Post-biopsy infectious complications rates were compared between the two groups. Fluoroquinolone resistance (FQ-R) in the urethral and rectal swabs was recorded. Baseline characteristics were analyzed to assess their relationship with infectious complications and antibiotic resistance.

Results

A total of 8 infectious complications were observed, 7 of them in the EAP group (9.85%) and 1 in the TAP group (1.4%). There was a statistically significant difference in febrile UTIs between the two groups (6 vs 0, P = 0.028). FQ-R rate was 4.3% and 12.9% for rectal and urethral samples, respectively. Recent antibiotic exposure was associated with higher post-biopsy infection rates for EAP group and FQ-R rates for TAP group.

Conclusion

Combination of rectal and urethral swab cultures for TAP was able to detect FQ-R bacteria carriers and was associated with fewer infectious complications compared to EAP.

目的:评价直肠和尿道拭子培养后靶向抗生素预防(TAP)与经验性抗生素预防(EAP)在预防经直肠超声引导前列腺活检(truss - bx)后感染并发症中的作用。方法我们对141例接受TRUS-Bx治疗的患者进行了前瞻性比较研究,并将其分为两组。第一组(n = 71)采用环丙沙星EAP,第二组(n = 70)根据直肠和尿道培养情况采用TAP。比较两组活检后感染并发症发生率。记录尿道和直肠拭子氟喹诺酮类药物耐药性(FQ-R)。分析基线特征以评估感染并发症和抗生素耐药性的关系。结果共观察到8例感染并发症,其中EAP组7例(9.85%),TAP组1例(1.4%)。两组患者发热性尿路感染发生率差异有统计学意义(6 vs 0, P = 0.028)。直肠和尿道标本的FQ-R率分别为4.3%和12.9%。近期抗生素暴露与EAP组较高的活检后感染率和TAP组较高的FQ-R率相关。结论与EAP相比,直肠和尿道联合拭子培养可检出FQ-R细菌携带者,感染并发症较少。
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引用次数: 0
Evaluation of the efficiency of transurethral enucleation with bipolar energy according to prostate volume for patients with benign prostate hyperplasia 根据前列腺体积评价经尿道双极能量切除对良性前列腺增生的疗效
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.08.001
Byeongdo Song , Sang Hun Song , Seong Jin Jeong

Background

This study evaluated the efficiency and safety of transurethral enucleation with bipolar energy (TUEB) using a spatula loop according to prostate volume.

Methods

We retrospectively evaluated 398 patients who underwent TUEB for benign prostatic hyperplasia at a single tertiary hospital between August 2018 and December 2022. The patients were divided into three groups according to estimated prostate volume (ePV): ≤40 mL (n = 67), 40–80 mL (n = 200), and ≥80 mL (n = 131). To compare the efficiency of TUEB, perioperative parameters including TUEB and enucleation efficiencies, were calculated as enucleated tissue weight per operation time and enucleated tissue weight per enucleation time, respectively. Preoperative and postoperative functional outcomes such as the International Prostate Symptom Score (IPSS), quality-of-life (QoL) score, maximum flow rate (Qmax), and post-void residual urine volume (PVR), were also compared.

Results

The IPSS total score, voiding sub-score, Qmax, and PVR improved after TUEB in all groups (all p < 0.05). The TUEB and enucleation efficiencies increased with increasing ePVs (all P < 0.001). When comparing the three prostate volume groups, there were no significant differences in functional outcomes within 12 months after TUEB (all-Bonferroni adjusted P > 0.017). A total of 57 patients experienced adverse events after TUEB, with no significant differences between the three groups (p = 0.507)

Conclusion

As prostate volume increases, the perioperative efficiency of TUEB is enhanced. Meanwhile, small prostates did not show significant differences in the improvement of functional outcomes and complications in comparison with larger prostates.

背景本研究根据前列腺体积评估了使用抹圈的经尿道双极能量去核术(TUEB)的效率和安全性。方法我们回顾性评估了2018年8月至2022年12月期间在一家三甲医院接受TUEB治疗良性前列腺增生的398例患者。根据估计前列腺体积(ePV)将患者分为三组:≤40 mL(n = 67)、40-80 mL(n = 200)和≥80 mL(n = 131)。为了比较 TUEB 的效率,围手术期参数(包括 TUEB 和去核效率)分别按每手术时间去核组织重量和每去核时间去核组织重量计算。此外,还比较了术前和术后的功能结果,如国际前列腺症状评分(IPSS)、生活质量(QoL)评分、最大尿流率(Qmax)和排尿后残余尿量(PVR)。随着 ePV 的增加,TUEB 和去核效率均有所提高(均为 P < 0.001)。比较三个前列腺体积组,TUEB术后12个月内的功能预后无显著差异(经邦弗罗尼调整的P值为0.017)。结论 随着前列腺体积的增加,TUEB 的围手术期效率会提高。同时,小前列腺与大前列腺相比,在改善功能预后和并发症方面没有明显差异。
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引用次数: 0
The feasibility of distance to the tumor of biopsy cores to estimate the extracapsular extension 用活组织切片核心到肿瘤的距离来估算囊外扩展的可行性
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.10.001
Chang Lim Hyun , Kyung Kgi Park

Background

To investigate the predictive capability of a new parameter, the distance between the fibromuscular capsule and the tumor as measured using a prostate biopsy core (referred to as “distance to the tumor” [DTT]), for the presence of extracapsular extension (ECE).

Materials and methods

We analyzed specimens obtained from 246 patients diagnosed with prostate cancer. All patients underwent prebiopsy, prostate magnetic resonance imaging (MRI), and subsequent prostatectomy. DTT measurements were obtained for each prostate biopsy core, and the minimum (min) DTT was extracted. We assessed the relationship between min DTT, MRI-estimated ECE, and pathological ECE, considering factors such as the PI-RADS score and tumor location.

Results

In this study of 246 patients, the mean age was 65.8 years, and the mean prostate-specific antigen (PSA) level was 18.9 ng/ml. Patients with suspicious lesions in the peripheral zone and pathological ECE displayed higher rates of positive digital rectal examination (DRE), elevated PSA levels, and shorter DTT values in the biopsy cores. DTT demonstrated an accurate estimation of the presence of ECE, similar to MRI findings. Min DTT exhibited higher accuracy for peripheral zone masses, with a cutoff value of 1.0 mm for min DTT predicting ECE (AUC: 0.84, sensitivity: 72.23%, specificity: 77.78%, P < 0.01). Of the 246 patients, 66 had no ECE on MRI; however, 18 of these patients displayed pathological ECE, with 14 having DTT values <1.0 mm.

Conclusions

Min DTT, positive DRE results, and a higher Gleason grade were significantly associated with ECE. DTT measurements of <1 mm can provide a more accurate prediction of ECE in the peripheral zone of the prostate than MRI-based assessments.

背景研究一个新参数--使用前列腺活检核心测量的纤维肌囊与肿瘤之间的距离(简称为 "到肿瘤的距离"[DTT])--对是否存在囊外扩展(ECE)的预测能力。所有患者均接受了前列腺活检、前列腺磁共振成像(MRI)和随后的前列腺切除术。我们对每个前列腺活检核心进行了 DTT 测量,并提取了最小(min)DTT。考虑到 PI-RADS 评分和肿瘤位置等因素,我们评估了最小 DTT、MRI 估计 ECE 和病理 ECE 之间的关系。外周可疑病变和病理 ECE 患者的数字直肠检查(DRE)阳性率较高,PSA 水平升高,活检核心的 DTT 值较短。DTT 能准确估计是否存在 ECE,与核磁共振成像结果类似。最小 DTT 对外周区肿块的准确性更高,最小 DTT 预测 ECE 的临界值为 1.0 mm(AUC:0.84,灵敏度:72.23%,特异性:77.78%,P < 0.01)。结论最小 DTT 值、DRE 阳性结果和较高的 Gleason 等级与 ECE 显著相关。与基于核磁共振成像的评估相比,1 毫米的 DTT 测量值能更准确地预测前列腺外周区的 ECE。
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引用次数: 0
Prostate-specific antigen doubling time predicts the efficacy of site-directed therapy for oligoprogressive castration-resistant prostate cancer 前列腺特异性抗原倍增时间可预测定点疗法对少进展期抗阉割前列腺癌的疗效
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.10.002
Taketo Kawai , Satoru Taguchi , Keina Nozaki , Naoki Kimura , Takahiro Oshina , Takuya Iwaki , Hotaka Matsui , Aya Niimi , Jun Kamei , Yoshiyuki Akiyama , Yuta Yamada , Yusuke Sato , Daisuke Yamada , Tomoyuki Kaneko , Subaru Sawayanagi , Hidetsugu Nakayama , Ryogo Minamimoto , Hideomi Yamashita , Hideyo Miyazaki , Tetsuya Fujimura , Haruki Kume

Background

In recent years, site-directed therapies (SDTs) targeting progressive lesions in patients with oligometastatic prostate cancer have attracted attention. However, whether they effectively treat oligoprogressive castration-resistant prostate cancer (CRPC) remains unclear. Here, we investigated the efficacy of SDT in patients with oligoprogressive CRPC and identified prognostic factors.

Methods

We reviewed 59 patients with oligoprogressive CRPC who underwent SDT targeting prostate or metastatic lesions between April 2014 and March 2022. We evaluated the associations between several pretreatment clinical variables and treatment procedures and a >50% prostate-specific antigen (PSA) response, progression-free survival (PFS), and time to next treatment (TTNT).

Results

A PSA response of >50% was observed in 66% of patients. The median PFS and TTNT were 8.3 months and 9.9 months, respectively. Patients with PSA doubling time ≥6 months showed a higher >50% PSA response rate (87% vs. 45%; P < 0.001), longer PFS (median, 15.0 vs. 5.0 months; P < 0.001), and longer TTNT (median, 16.3 vs. 5.9 months; P < 0.001) than patients with PSA doubling time <6 months. In multivariate analyses, a PSA doubling time of ≥6 months independently predicted a >50% PSA response, favorable PFS, and TTNT (P = 0.037, 0.025, and 0.017, respectively).

Conclusion

PSA doubling time of ≥6 months may be a key indicator of the favorable efficacy of SDT for oligoprogressive CRPC.

背景近年来,针对少转移性前列腺癌患者进展性病变的定点靶向疗法(SDTs)备受关注。然而,它们是否能有效治疗少转移进展性阉割耐药前列腺癌(CRPC)仍不清楚。在此,我们研究了SDT对少进展型CRPC患者的疗效,并确定了预后因素。方法我们回顾了2014年4月至2022年3月期间接受SDT治疗的59例少进展型CRPC患者,这些患者接受了针对前列腺或转移病灶的SDT治疗。我们评估了几个治疗前临床变量和治疗过程与>50%前列腺特异性抗原(PSA)反应、无进展生存期(PFS)和下次治疗时间(TTNT)之间的关系。结果66%的患者观察到>50%的PSA反应。中位无进展生存期(PFS)和下一次治疗时间(TTNT)分别为 8.3 个月和 9.9 个月。与PSA倍增时间为6个月的患者相比,PSA倍增时间≥6个月的患者PSA反应率为>50%(87% vs. 45%;P <0.001),PFS(中位数,15.0个月 vs. 5.0个月;P <0.001)和TTNT(中位数,16.3个月 vs. 5.9个月;P <0.001)更长。在多变量分析中,PSA倍增时间≥6个月可独立预测50%的PSA反应、良好的PFS和TTNT(P分别为0.037、0.025和0.017)。
{"title":"Prostate-specific antigen doubling time predicts the efficacy of site-directed therapy for oligoprogressive castration-resistant prostate cancer","authors":"Taketo Kawai ,&nbsp;Satoru Taguchi ,&nbsp;Keina Nozaki ,&nbsp;Naoki Kimura ,&nbsp;Takahiro Oshina ,&nbsp;Takuya Iwaki ,&nbsp;Hotaka Matsui ,&nbsp;Aya Niimi ,&nbsp;Jun Kamei ,&nbsp;Yoshiyuki Akiyama ,&nbsp;Yuta Yamada ,&nbsp;Yusuke Sato ,&nbsp;Daisuke Yamada ,&nbsp;Tomoyuki Kaneko ,&nbsp;Subaru Sawayanagi ,&nbsp;Hidetsugu Nakayama ,&nbsp;Ryogo Minamimoto ,&nbsp;Hideomi Yamashita ,&nbsp;Hideyo Miyazaki ,&nbsp;Tetsuya Fujimura ,&nbsp;Haruki Kume","doi":"10.1016/j.prnil.2023.10.002","DOIUrl":"10.1016/j.prnil.2023.10.002","url":null,"abstract":"<div><h3>Background</h3><p>In recent years, site-directed therapies (SDTs) targeting progressive lesions in patients with oligometastatic prostate cancer have attracted attention. However, whether they effectively treat oligoprogressive castration-resistant prostate cancer (CRPC) remains unclear. Here, we investigated the efficacy of SDT in patients with oligoprogressive CRPC and identified prognostic factors.</p></div><div><h3>Methods</h3><p>We reviewed 59 patients with oligoprogressive CRPC who underwent SDT targeting prostate or metastatic lesions between April 2014 and March 2022. We evaluated the associations between several pretreatment clinical variables and treatment procedures and a &gt;50% prostate-specific antigen (PSA) response, progression-free survival (PFS), and time to next treatment (TTNT).</p></div><div><h3>Results</h3><p>A PSA response of &gt;50% was observed in 66% of patients. The median PFS and TTNT were 8.3 months and 9.9 months, respectively. Patients with PSA doubling time ≥6 months showed a higher &gt;50% PSA response rate (87% vs. 45%; <em>P</em> &lt; 0.001), longer PFS (median, 15.0 vs. 5.0 months; <em>P</em> &lt; 0.001), and longer TTNT (median, 16.3 vs. 5.9 months; <em>P</em> &lt; 0.001) than patients with PSA doubling time &lt;6 months. In multivariate analyses, a PSA doubling time of ≥6 months independently predicted a &gt;50% PSA response, favorable PFS, and TTNT (<em>P</em> = 0.037, 0.025, and 0.017, respectively).</p></div><div><h3>Conclusion</h3><p>PSA doubling time of ≥6 months may be a key indicator of the favorable efficacy of SDT for oligoprogressive CRPC.</p></div>","PeriodicalId":20845,"journal":{"name":"Prostate International","volume":"11 4","pages":"Pages 239-246"},"PeriodicalIF":3.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2287888223000569/pdfft?md5=fc52a964e0d32452ba3d67a5945fb814&pid=1-s2.0-S2287888223000569-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136009400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cervi Parvum Cornu complex for men with lower urinary tract symptoms: a multicenter, randomized, double-blind, placebo-controlled trial 治疗男性下尿路症状的子宫颈抹片复合物:一项多中心、随机、双盲、安慰剂对照试验
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.09.002
Dongho Shin , Byung Il Yoon , Soomin Kim , JunJie Piao , Kyung-Hwa Jeon , Youngjoo Kwon , Sang-Hyuck Park , Young Tae Koo , Jin-Soo Kim , Dong Sup Lee , U-Syn Ha , Sae Woong Kim , Hoon Jang , Woong Jin Bae

Background

To evaluate the efficacy and safety of Cervi Parvum Cornu, Angelicae Gigantis Radix and Glycyrrhizae Radix complex (CAG) in men with moderate lower urinary tract symptoms (LUTS).

Materials and methods

From November 2020 to January 2022, participants with International Prostate Symptom Score (IPSS) of 12–19 in two centers were recruited and randomize into three groups: a CAG 500 mg/day group (CAG 500), a CAG 1000 mg/day group (CAG 1000), and a placebo group (PG). They were treated for 12 weeks. The primary endpoint was change of IPSS at the end of study from baseline. Secondary end points included change of prostate specific antigen (PSA), testosterone, dihydrotestosterone (DHT), maximum urinary flow rate (Q max), post-void residual volume (PVR), International Index of Erectile Function (IIEF), and drug safety.

Results

A total of 103 patients were able to finish the study according to the study protocol. Total IPSS and sub-scores (residual urine sensation, frequency, weak stream, hesistancy, nocturia, and quality of life) in CAG 500 and CAG 1000 were significantly improved at the 12th week compared to those of the PG. Changes of serum PSA, DHT, and testosterone levels at the 12th week from baseline did not show significant differences among the three groups. Q max and PVR changes did not show significant differences among the three groups either. Total IIEF and sub-scores (erectile function, orgasmic function, sexual desire, intercourse satisfaction) in CAG 1000 were significantly improved at 12th week compared to those in PG. No significant adverse events were found.

Conclusions

CAG is well tolerated in patients with moderate LUTS. Treatment with CAG for 12 weeks has a therapeutic effect on moderate LUTS.

背景评估中度下尿路症状(LUTS)男性服用鹿茸、当归、甘草复方制剂(CAG)的疗效和安全性。材料与方法2020年11月至2022年1月,在两个中心招募了国际前列腺症状评分(IPSS)为12-19分的参与者,并随机分为三组:CAG 500毫克/天组(CAG 500)、CAG 1000毫克/天组(CAG 1000)和安慰剂组(PG)。他们接受了为期 12 周的治疗。主要终点是研究结束时 IPSS 与基线相比的变化。次要终点包括前列腺特异性抗原(PSA)、睾酮、双氢睾酮(DHT)、最大尿流率(Q max)、排尿后残余尿量(PVR)、国际勃起功能指数(IIEF)和药物安全性的变化。与 PG 相比,CAG 500 和 CAG 1000 在第 12 周时的 IPSS 总分和子分(残余尿感、尿频、尿流细弱、排尿迟缓、夜尿和生活质量)均有显著改善。第 12 周时,血清 PSA、DHT 和睾酮水平与基线相比的变化在三组之间没有明显差异。Q max 和 PVR 的变化在三组之间也没有明显差异。第 12 周时,CAG 1000 的 IIEF 总分和子分(勃起功能、性高潮功能、性欲、性交满意度)与 PG 相比有明显改善。结论CAG对中度LUTS患者的耐受性良好。结论CAG对中度尿失禁患者的耐受性良好,CAG治疗12周对中度尿失禁有治疗效果。
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引用次数: 0
Safety and efficacy of tamsulosin 0.4 mg as an initial dose in 1,219 Korean patients with moderate to severe lower urinary tract symptoms: data from a phase IV study 坦索罗辛 0.4 毫克初始剂量对 1,219 名患有中度至重度下尿路症状的韩国患者的安全性和有效性:IV 期研究数据
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.09.003
Jun Ho Lee , Yeon Won Park , Moon-hwa Park , Tag Keun Yoo

Background

An initial dose of tamsulosin 0.2 mg is frequently prescribed for Asian men. We investigated the safety and efficacy of tamsulosin 0.4 mg as the initial dose in Korean men with moderate to severe lower urinary tract symptoms (LUTSs) in everyday clinical practice.

Materials and methods

A phase IV study was conducted in South Korea. Eligible patients were prescribed tamsulosin 0.4 mg for 6 months. We excluded patients with previous exposure to LUTS drugs and patients with an international prostate symptom score (IPSS) < 8.

Results

The mean total IPSS, storage subscore, voiding symptoms subscore, and quality of life significantly decreased from 18.0, 10.8, 7.2, and 3.8 to 12.8, 7.5, 5.3, and 2.6, respectively, after 6 months of treatment. The number of nocturia episodes significantly decreased from 3.0 to 2.2 in patients who reported at least 2 nocturia events at baseline. A mean reduction in the IPSS was quantitatively equivalent in all age groups. The mean reduction in the IPSS was greater in the IPSS ≥ 20 group than in the IPSS < 20 group (mean reduction in the total IPSS: −2.6 in the IPSS < 20 group; −9.4 in the IPSS ≥ 20 group). All treatment-emergent adverse events were mild. The most frequently recorded treatment-emergent adverse event was dizziness, which was reported in 22 patients (1.8%).

Conclusion

Treatment of LUTS with tamsulosin 0.4 mg as the initial dose for 6 months in Korean men was effective in improving LUTS and showed a favorable safety profile in a real-life setting.

背景亚洲男性常被处方初始剂量为0.2毫克的坦索罗辛。我们在日常临床实践中对患有中度至重度下尿路症状(LUTS)的韩国男性进行了坦索罗辛 0.4 毫克作为初始剂量的安全性和有效性研究。符合条件的患者接受了为期 6 个月的坦索罗辛 0.4 毫克处方治疗。结果治疗6个月后,平均IPSS总分、储尿子分数、排尿症状子分数和生活质量分别从18.0、10.8、7.2和3.8分显著下降至12.8、7.5、5.3和2.6分。在基线时报告至少有 2 次夜尿症的患者中,夜尿次数从 3.0 次显著降至 2.2 次。所有年龄组患者的 IPSS 平均降低幅度在数量上相当。IPSS ≥ 20 组的 IPSS 平均降低幅度大于 IPSS < 20 组(总 IPSS 平均降低幅度:IPSS ≥ 20 组-2.6):IPSS<20组为-2.6;IPSS≥20组为-9.4)。所有治疗引发的不良反应均为轻微。结论:以坦索罗辛 0.4 毫克作为初始剂量,对韩国男性 LUTS 进行为期 6 个月的治疗,能有效改善 LUTS,并在实际生活中显示出良好的安全性。
{"title":"Safety and efficacy of tamsulosin 0.4 mg as an initial dose in 1,219 Korean patients with moderate to severe lower urinary tract symptoms: data from a phase IV study","authors":"Jun Ho Lee ,&nbsp;Yeon Won Park ,&nbsp;Moon-hwa Park ,&nbsp;Tag Keun Yoo","doi":"10.1016/j.prnil.2023.09.003","DOIUrl":"10.1016/j.prnil.2023.09.003","url":null,"abstract":"<div><h3>Background</h3><p>An initial dose of tamsulosin 0.2 mg is frequently prescribed for Asian men. We investigated the safety and efficacy of tamsulosin 0.4 mg as the initial dose in Korean men with moderate to severe lower urinary tract symptoms (LUTSs) in everyday clinical practice.</p></div><div><h3>Materials and methods</h3><p>A phase IV study was conducted in South Korea. Eligible patients were prescribed tamsulosin 0.4 mg for 6 months. We excluded patients with previous exposure to LUTS drugs and patients with an international prostate symptom score (IPSS) &lt; 8.</p></div><div><h3>Results</h3><p>The mean total IPSS, storage subscore, voiding symptoms subscore, and quality of life significantly decreased from 18.0, 10.8, 7.2, and 3.8 to 12.8, 7.5, 5.3, and 2.6, respectively, after 6 months of treatment. The number of nocturia episodes significantly decreased from 3.0 to 2.2 in patients who reported at least 2 nocturia events at baseline. A mean reduction in the IPSS was quantitatively equivalent in all age groups. The mean reduction in the IPSS was greater in the IPSS ≥ 20 group than in the IPSS &lt; 20 group (mean reduction in the total IPSS: −2.6 in the IPSS &lt; 20 group; −9.4 in the IPSS ≥ 20 group). All treatment-emergent adverse events were mild. The most frequently recorded treatment-emergent adverse event was dizziness, which was reported in 22 patients (1.8%).</p></div><div><h3>Conclusion</h3><p>Treatment of LUTS with tamsulosin 0.4 mg as the initial dose for 6 months in Korean men was effective in improving LUTS and showed a favorable safety profile in a real-life setting.</p></div>","PeriodicalId":20845,"journal":{"name":"Prostate International","volume":"11 4","pages":"Pages 228-232"},"PeriodicalIF":3.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2287888223000533/pdfft?md5=a1b6756cd64d3f52e2070286e37ace11&pid=1-s2.0-S2287888223000533-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135389609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Detection of anterior prostate cancer using a magnetic resonance imaging-transrectal ultrasound fusion biopsy in cases with initial biopsy and history of systematic biopsies 磁共振成像经直肠超声融合活组织检查有系统活组织检查病史的前前列腺癌症
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.08.002
Masakazu Abe , Ryo Takata , Daiki Ikarashi , Kie Sekiguchi , Daichi Tamura , Shigekatsu Maekawa , Renpei Kato , Mitsugu Kanehira , Takashi Ujiie , Wataru Obara

Background

Prostate cancer in the anterior region may be missed on a transrectal systematic biopsy (SBx). Therefore, this study aimed to evaluate the performance of magnetic resonance imaging-transrectal ultrasound (MRI-TRUS) fusion targeted biopsy (TBx) in detecting anterior region cancer in patients with a history of SBxs.

Methods

Prostate biopsies were performed in 224 patients after multiparametric MRI, among whom 119 patients with prostate imaging reporting and data system (PI-RADS version 2) scores of 3 to 5 underwent MRI-TRUS fusion TBxs. Afterward, cancer detection rates (CDRs) and TBx-positive core regions were compared by categorizing patients into those with or without a history of SBxs.

Results

Total CDR was 68.8% (44/64 cases) in the initial biopsy group (Initial-Bx group) and 47.3% (26/55 cases) in the previous-negative-systematic biopsy group (Pre-Neg-SBx group) (P = 0.018). Interestingly, both TBx- and SBx-core positive cases were more common in the Initial-Bx group than in the Pre-Neg-SBx group (Initial-Bx group: 75% [33/44 cases] vs. Pre-Neg-SBx group: 42.3% [11/26 cases], P = 0.006). However, only TBx-core positive cases were more common in the Pre-Neg-SBx group than in the Initial-Bx group (Initial-Bx group: 11.4% [5/44 cases] vs. Pre-Neg-SBx group: 30.8% [8/26 cases], P = 0.043). In addition, the proportion of anterior lesions detected by TBx cores was higher in the Pre-Neg-SBx group than in the Initial-Bx group (Initial-Bx group: 26.3% [10/38 cases] vs. Pre-Neg-SBx group: 52.6% [10/19 cases], P = 0.049).

Conclusion

Using MRI-TRUS fusion TBx in the evaluation of previously negative SBx cases improved the detection rate of anterior lesions, which might have been missed in previous SBxs. Especially in patients with a history of SBxs mpMRI should be performed to screen for anterior lesions.

背景经直肠系统性活检(SBx)可能会漏检前区的前列腺癌。因此,本研究旨在评估磁共振成像-经直肠超声(MRI-TRUS)融合靶向活检(TBx)在检测有 SBx 病史的患者前区癌症方面的性能。方法对 224 名患者进行多参数磁共振成像后进行前列腺活检,其中 119 名前列腺成像报告和数据系统(PI-RADS 2 版)评分为 3 到 5 分的患者接受了磁共振成像-TRUS 融合 TBx。结果初次活检组(Initial-Bx 组)的总 CDR 为 68.8%(44/64 例),先前阴性系统活检组(Pre-Neg-SBx 组)的 CDR 为 47.3%(26/55 例)(P = 0.018)。有趣的是,TBx 和 SBx 核心阳性病例在 Initial-Bx 组比在阴性前-SBx 组更常见(Initial-Bx 组:75% [33/44 例] vs SBx-核心阳性病例):75%[33/44例] vs. 阴性前-SBx组:42.3%[11/26例],P = 0.006)。然而,只有 TBx 核心阳性病例在阴性前-SBx 组比初始-Bx 组更常见(初始-Bx 组:11.4% [5/44 例];阴性前-SBx 组:42.3% [11/26 例]):11.4%[5/44例] vs. 阴性前-SBx组:30.8% [8/26 例],P = 0.043)。此外,通过 TBx 核芯检测到前部病变的比例,阴性前-Bx 组高于初始-Bx 组(初始-Bx 组:26.3% [10/38 例] vs. 阴性前-Bx 组:52.6% [10/19 例]):结论在评估既往SBx阴性病例时使用MRI-TRUS融合TBx可提高既往SBx可能漏诊的前部病变的检出率。特别是对有 SBx 病史的患者,应进行 mpMRI 检查以筛查前部病变。
{"title":"Detection of anterior prostate cancer using a magnetic resonance imaging-transrectal ultrasound fusion biopsy in cases with initial biopsy and history of systematic biopsies","authors":"Masakazu Abe ,&nbsp;Ryo Takata ,&nbsp;Daiki Ikarashi ,&nbsp;Kie Sekiguchi ,&nbsp;Daichi Tamura ,&nbsp;Shigekatsu Maekawa ,&nbsp;Renpei Kato ,&nbsp;Mitsugu Kanehira ,&nbsp;Takashi Ujiie ,&nbsp;Wataru Obara","doi":"10.1016/j.prnil.2023.08.002","DOIUrl":"10.1016/j.prnil.2023.08.002","url":null,"abstract":"<div><h3>Background</h3><p>Prostate cancer in the anterior region may be missed on a transrectal systematic biopsy (SBx). Therefore, this study aimed to evaluate the performance of magnetic resonance imaging-transrectal ultrasound (MRI-TRUS) fusion targeted biopsy (TBx) in detecting anterior region cancer in patients with a history of SBxs.</p></div><div><h3>Methods</h3><p>Prostate biopsies were performed in 224 patients after multiparametric MRI, among whom 119 patients with prostate imaging reporting and data system (PI-RADS version 2) scores of 3 to 5 underwent MRI-TRUS fusion TBxs. Afterward, cancer detection rates (CDRs) and TBx-positive core regions were compared by categorizing patients into those with or without a history of SBxs.</p></div><div><h3>Results</h3><p>Total CDR was 68.8% (44/64 cases) in the initial biopsy group (Initial-Bx group) and 47.3% (26/55 cases) in the previous-negative-systematic biopsy group (Pre-Neg-SBx group) (<em>P</em> = 0.018). Interestingly, both TBx- and SBx-core positive cases were more common in the Initial-Bx group than in the Pre-Neg-SBx group (Initial-Bx group: 75% [33/44 cases] vs. Pre-Neg-SBx group: 42.3% [11/26 cases], <em>P</em> = 0.006). However, only TBx-core positive cases were more common in the Pre-Neg-SBx group than in the Initial-Bx group (Initial-Bx group: 11.4% [5/44 cases] vs. Pre-Neg-SBx group: 30.8% [8/26 cases], <em>P</em> = 0.043). In addition, the proportion of anterior lesions detected by TBx cores was higher in the Pre-Neg-SBx group than in the Initial-Bx group (Initial-Bx group: 26.3% [10/38 cases] vs. Pre-Neg-SBx group: 52.6% [10/19 cases], <em>P</em> = 0.049).</p></div><div><h3>Conclusion</h3><p>Using MRI-TRUS fusion TBx in the evaluation of previously negative SBx cases improved the detection rate of anterior lesions, which might have been missed in previous SBxs. Especially in patients with a history of SBxs mpMRI should be performed to screen for anterior lesions.</p></div>","PeriodicalId":20845,"journal":{"name":"Prostate International","volume":"11 4","pages":"Pages 212-217"},"PeriodicalIF":3.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2287888223000399/pdfft?md5=49af9f3de32857c6baf4678f9bb7a78e&pid=1-s2.0-S2287888223000399-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49153425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-port and multiport robot-assisted radical prostatectomy: A meta-analysis 单孔和多孔机器人辅助根治性前列腺切除术:荟萃分析
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.04.002
Tuan Thanh Nguyen , Ryan W. Dobbs , Huy Gia Vuong , Khoa Quy , Hanh Thi Tuyet Ngo , Anh Tuan Mai , Mai Tran Thi Tuyet , Minh Sam Thai , Ho Yee Tiong , Se Young Choi , Mohammed Shahait , David I. Lee

Objective

To compare the perioperative, oncological, and functional outcomes between single-port robot-assisted radical prostatectomy (SP-RARP) and multiport robot-assisted radical prostatectomy (MP-RARP) via a meta-analysis.

Methods

For relevant articles, three electronic databases, including PubMed, Scopus, and Web of Science, were searched from their inception until January 15, 2022. A meta-analysis has been reported in line with PRISMA 2020 and AMSTAR Guidelines. The risk ratio and weighted mean difference (MD) were applied for the comparison of dichotomous and continuous variables with 95% confidence intervals (CI).

Results

Of the 368 retrieved abstracts, 41 underwent full-text review, and seven studies were included in the final analysis, comprising a total cohort of 1,934 cases of RARP (355 SP-RARP cases and 1,579 MP-RARP cases). Compared to MP-RARP, the SP-RARP group had less postoperative pain score (MD = –0.7, 95% CI –1 to –0.4, P<0.001), morphine milligram equivalents usage (MD = –3.8, 95% CI –7.5 to –0.1, P=0.04), hospital stay (MD = –1, 95% CI –1.8 to –0.1, P=0.019), and urinary catheterization time (MD = –1.1, 95% CI –1.9 to –0.3, P=0.008). However, the SP-RARP group had a longer console time than the MP-RARP group (MD = 5.3, 95% CI 2.6 to 7.9, P<0.001).

Conclusions

Our study demonstrated that early results were mostly equivalent with the single-port approach. This technology may help to reduce the hospital stay and postoperative pain for patients undergoing radical prostatectomy compared to MP-RARP, without compromising the functional and early oncological outcomes.

目的通过荟萃分析比较单孔机器人辅助前列腺癌根治术(SP-RARP)和多孔机器人辅助前列腺癌根治术(MP-RARP)的围术期、肿瘤学和功能性结果。方法检索了PubMed、Scopus和Web of Science等三个电子数据库中从开始到2022年1月15日的相关文章。根据《PRISMA 2020》和《AMSTAR 指南》报告了一项荟萃分析。结果 在检索到的 368 篇摘要中,41 篇进行了全文审阅,最终分析纳入了 7 项研究,共包括 1,934 例 RARP(355 例 SP-RARP 和 1,579 例 MP-RARP)。与 MP-RARP 相比,SP-RARP 组的术后疼痛评分(MD = -0.7,95% CI -1 to -0.4,P<0.001)、吗啡毫克当量用量(MD = -3.8,95% CI -7.5 to -0.1,P=0.04)、住院时间(MD =-1,95% CI -1.8 to -0.1,P=0.019)和导尿时间(MD =-1.1,95% CI -1.9 to -0.3,P=0.008)。然而,SP-RARP 组的控制台时间长于 MP-RARP 组(MD = 5.3,95% CI 2.6 至 7.9,P<0.001)。与 MP-RARP 相比,该技术可能有助于减少前列腺癌根治术患者的住院时间和术后疼痛,同时不影响功能和早期肿瘤结果。
{"title":"Single-port and multiport robot-assisted radical prostatectomy: A meta-analysis","authors":"Tuan Thanh Nguyen ,&nbsp;Ryan W. Dobbs ,&nbsp;Huy Gia Vuong ,&nbsp;Khoa Quy ,&nbsp;Hanh Thi Tuyet Ngo ,&nbsp;Anh Tuan Mai ,&nbsp;Mai Tran Thi Tuyet ,&nbsp;Minh Sam Thai ,&nbsp;Ho Yee Tiong ,&nbsp;Se Young Choi ,&nbsp;Mohammed Shahait ,&nbsp;David I. Lee","doi":"10.1016/j.prnil.2023.04.002","DOIUrl":"10.1016/j.prnil.2023.04.002","url":null,"abstract":"<div><h3>Objective</h3><p>To compare the perioperative, oncological, and functional outcomes between single-port robot-assisted radical prostatectomy (SP-RARP) and multiport robot-assisted radical prostatectomy (MP-RARP) via a meta-analysis.</p></div><div><h3>Methods</h3><p>For relevant articles, three electronic databases, including PubMed, Scopus, and Web of Science, were searched from their inception until January 15, 2022. A meta-analysis has been reported in line with PRISMA 2020 and AMSTAR Guidelines. The risk ratio and weighted mean difference (MD) were applied for the comparison of dichotomous and continuous variables with 95% confidence intervals (CI).</p></div><div><h3>Results</h3><p>Of the 368 retrieved abstracts, 41 underwent full-text review, and seven studies were included in the final analysis, comprising a total cohort of 1,934 cases of RARP (355 SP-RARP cases and 1,579 MP-RARP cases). Compared to MP-RARP, the SP-RARP group had less postoperative pain score (MD = –0.7, 95% CI –1 to –0.4, <em>P</em>&lt;0.001), morphine milligram equivalents usage (MD = –3.8, 95% CI –7.5 to –0.1, <em>P</em>=0.04), hospital stay (MD = –1, 95% CI –1.8 to –0.1, <em>P</em>=0.019), and urinary catheterization time (MD = –1.1, 95% CI –1.9 to –0.3, <em>P</em>=0.008). However, the SP-RARP group had a longer console time than the MP-RARP group (MD = 5.3, 95% CI 2.6 to 7.9, <em>P</em>&lt;0.001).</p></div><div><h3>Conclusions</h3><p>Our study demonstrated that early results were mostly equivalent with the single-port approach. This technology may help to reduce the hospital stay and postoperative pain for patients undergoing radical prostatectomy compared to MP-RARP, without compromising the functional and early oncological outcomes.</p></div>","PeriodicalId":20845,"journal":{"name":"Prostate International","volume":"11 4","pages":"Pages 187-194"},"PeriodicalIF":3.0,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2287888223000181/pdfft?md5=637506a7442efdda055caf04e435b865&pid=1-s2.0-S2287888223000181-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42026495","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reviving intimacy: Penile rehabilitation strategies for men after prostate cancer treatment 恢复亲密关系:男性前列腺癌症治疗后的阴茎康复策略
IF 3 2区 医学 Q2 UROLOGY & NEPHROLOGY Pub Date : 2023-12-01 DOI: 10.1016/j.prnil.2023.06.001
James Stinson , Nelson Bennett

There have been considerable advances in the field of penile rehabilitation for upwards of 90% of men adversely affected by either short-term or long-term erectile dysfunction after definitive prostate cancer treatment. Despite the evolving landscape of treatment modalities for penile rehabilitation, there is a lack of consensus in the urologic community on the best therapies due to the level of evidence and efficacies of the current and emerging offerings. This review of current and next-generation interventions provides a practical approach to the myriad of data to make a better-informed decision based on the pathophysiology and highest-quality evidence available.

在前列腺癌明确治疗后出现短期或长期勃起功能障碍的男性中,多达 90% 的人在阴茎康复领域取得了长足的进步。尽管阴茎康复治疗模式不断发展,但由于现有和新兴疗法的证据和疗效水平不同,泌尿外科界对最佳疗法缺乏共识。这篇关于当前和下一代干预措施的综述提供了一种实用的方法来处理大量数据,以便根据病理生理学和现有的最高质量证据做出更明智的决定。
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引用次数: 0
期刊
Prostate International
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