Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000064
A. Shukla
{"title":"EDITORIAL COMMENT for: The Minimal Utility of Analyzing Ureteropelvic Junction Tissue at the Time of Pyeloplasty, Has Been Accepted for Publication in JU Open Plus","authors":"A. Shukla","doi":"10.1097/ju9.0000000000000064","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000064","url":null,"abstract":"","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"56 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139305346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000068
Jesse Persily, Katie S. Murray
Female exclusion from clinical trials has been a topic of debate and discussion for well over 30 years, with an ever-growing body of literature to support ongoing disparities related to female patient enrollment, along with concerns about downstream effects on treatment efficacy and health outcomes in this patient population.1-3 Awareness of this disparity is the first step in correction. In this edition of JU Open Plus, Miyagi et al4 took a multipronged approach to assess gender representation in major urologic clinical trials, focusing on advanced bladder cancer (BC). To assess the scope of the problem, the team reviewed all trials included as evidence in the National Comprehensive Cancer Network BC guidelines on systemic therapies and found a lower percentage of female participants (20%) than would be expected based on the proportion of female patients with BC in the Surveillance, Epidemiology, and End Results database (26.9%, P < .001). There was also lower female representation in later-stage trials and randomized controlled trials. They then looked at the National Cancer Database (NCDB) to assess how these findings translated to actual patient care and found a significant difference between the proportion of male and female patients who received systemic and immunotherapy for advanced BC (42.6% vs 46% and 1.9% vs 2.8%, respectively, both P < .001). We commend the group for tackling this important and timely topic. The advanced BC management landscape has begun to shift from an almost exclusively chemotherapy-focused treatment paradigm to one that includes immunotherapy, targeted therapy, and antibody-drug conjugate-based therapies.5 A proper understanding of the state of clinical trial recruitment will allow for proactive strategy development to ensure recruitment of under-represented groups, thus ensuring adequate access to these emerging therapies. This is even more important in BC clinical trials. The Bacillus Calmette-Guerin shortage in non–muscle-invasive disease and platinum ineligibility in advanced BC each result in a larger cohort of patients who could potentially benefit from early clinical trial enrollment.6 By outlining the details of the gender disparity in one disease cohort, the authors lay the groundwork for working toward gender equality in trial recruitment. We offer some additional thoughts to build upon their analysis and discussion. Although we agree that factors influencing patient decision to participate in clinical trials should be assessed, we feel that the gender discrepancy likely extends beyond individual patient choice. The consistent and persistent finding of gender, racial, and ethnic disparities in clinical trial enrollment suggests the need for a systematic correction.7 This may come in the form of explicit differential recruitment of female participants and racial minorities with a goal of over-representation to combat historic under-representation. More dramatic adjustments to predetermined secondary or ev
30多年来,女性被排除在临床试验之外一直是争论和讨论的话题,越来越多的文献支持与女性患者入组相关的持续差异,以及对该患者群体治疗疗效和健康结果的下游影响的担忧。意识到这种差异是改正的第一步。在本期的《JU Open Plus》中,Miyagi等人4采用了多管齐下的方法来评估主要泌尿外科临床试验中的性别代表性,重点是晚期膀胱癌(BC)。为了评估问题的范围,研究小组回顾了国家综合癌症网络BC系统治疗指南中作为证据的所有试验,发现女性参与者的比例(20%)低于基于监测、流行病学和最终结果数据库中女性BC患者比例(26.9%,P < 0.001)的预期。在后期试验和随机对照试验中,女性的代表性也较低。然后,他们查看了国家癌症数据库(NCDB),以评估这些发现如何转化为实际的患者护理,并发现接受系统性和免疫治疗晚期BC的男性和女性患者比例之间存在显著差异(分别为42.6%对46%和1.9%对2.8%,P < 0.001)。我们赞扬工作组处理这一重要和及时的问题。先进的BC管理格局已经开始从几乎完全以化疗为中心的治疗范式转变为包括免疫治疗,靶向治疗和基于抗体-药物偶联治疗的治疗对临床试验招募状况的正确理解将有助于制定积极的战略,以确保招募代表性不足的群体,从而确保充分获得这些新兴疗法。这在BC临床试验中更为重要。在非肌肉侵袭性疾病中卡介苗芽孢杆菌的短缺和晚期BC中铂的不适合性都导致更大的患者队列可能从早期临床试验中获益通过概述一个疾病队列中性别差异的细节,作者为在试验招募中实现性别平等奠定了基础。在他们的分析和讨论的基础上,我们提供了一些额外的想法。虽然我们同意应该评估影响患者参与临床试验决定的因素,但我们认为性别差异可能超出了患者个人选择的范围。在临床试验入组中,性别、种族和民族差异的一致和持续的发现表明需要进行系统的纠正这可能会以明确的区别招募女性参与者和少数民族的形式出现,目的是增加代表性,以解决历史上代表性不足的问题。由于研究表明,在过去的20年里,这些人群的入学人数甚至没有上升的趋势,因此可能还需要对预定的中学甚至小学终点进行更大幅度的调整随着新药物在二线、三线和四线的应用,以及基于既往治疗暴露的不同纳入和排除标准,这些考虑将变得越来越重要。尽管绝对差异很小,但女性患者接受全身治疗的可能性较低这一发现既令人惊讶又意义重大。虽然缺乏数据,但考虑到各种假设及其含义将是减轻这种差异的关键,如果真的存在的话。在这方面缺失的关键数据包括这种差异是否反映了未能提供标准治疗化疗或不适合化疗。如果有更多的女性患者不符合条件,那么必须进行进一步的工作来了解为什么会出现这种情况。这一发现可能反映了先前的研究表明,女性BC患者的诊断延迟,并且可能更频繁地出现晚期疾病Marinaro等人在2021年发表的ndb分析提供了相互矛盾的结果。该小组没有发现显著的性别相关治疗差异,但确实发现女性90天死亡率较高,总体存活率较低。综上所述,显然必须开展更多的工作,也许可以使用更多样化的数据来源,以更好地评估这一潜在趋势。本研究仅关注BC的全身治疗范围是合适的,但仍有需要进一步研究的领域。关于临床试验招募的差异,我们所知甚少,因为它涉及到晚期BC的膀胱定向治疗。
{"title":"Underenrolled and Undertreated Advanced Bladder Cancer in Women: It is Time to Improve","authors":"Jesse Persily, Katie S. Murray","doi":"10.1097/ju9.0000000000000068","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000068","url":null,"abstract":"Female exclusion from clinical trials has been a topic of debate and discussion for well over 30 years, with an ever-growing body of literature to support ongoing disparities related to female patient enrollment, along with concerns about downstream effects on treatment efficacy and health outcomes in this patient population.1-3 Awareness of this disparity is the first step in correction. In this edition of JU Open Plus, Miyagi et al4 took a multipronged approach to assess gender representation in major urologic clinical trials, focusing on advanced bladder cancer (BC). To assess the scope of the problem, the team reviewed all trials included as evidence in the National Comprehensive Cancer Network BC guidelines on systemic therapies and found a lower percentage of female participants (20%) than would be expected based on the proportion of female patients with BC in the Surveillance, Epidemiology, and End Results database (26.9%, P < .001). There was also lower female representation in later-stage trials and randomized controlled trials. They then looked at the National Cancer Database (NCDB) to assess how these findings translated to actual patient care and found a significant difference between the proportion of male and female patients who received systemic and immunotherapy for advanced BC (42.6% vs 46% and 1.9% vs 2.8%, respectively, both P < .001). We commend the group for tackling this important and timely topic. The advanced BC management landscape has begun to shift from an almost exclusively chemotherapy-focused treatment paradigm to one that includes immunotherapy, targeted therapy, and antibody-drug conjugate-based therapies.5 A proper understanding of the state of clinical trial recruitment will allow for proactive strategy development to ensure recruitment of under-represented groups, thus ensuring adequate access to these emerging therapies. This is even more important in BC clinical trials. The Bacillus Calmette-Guerin shortage in non–muscle-invasive disease and platinum ineligibility in advanced BC each result in a larger cohort of patients who could potentially benefit from early clinical trial enrollment.6 By outlining the details of the gender disparity in one disease cohort, the authors lay the groundwork for working toward gender equality in trial recruitment. We offer some additional thoughts to build upon their analysis and discussion. Although we agree that factors influencing patient decision to participate in clinical trials should be assessed, we feel that the gender discrepancy likely extends beyond individual patient choice. The consistent and persistent finding of gender, racial, and ethnic disparities in clinical trial enrollment suggests the need for a systematic correction.7 This may come in the form of explicit differential recruitment of female participants and racial minorities with a goal of over-representation to combat historic under-representation. More dramatic adjustments to predetermined secondary or ev","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"4 2","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135614932","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000069
Kevin Krughoff, Jordan Foreman, Thomas Dvergsten, Andrew C. Peterson
Purpose: For patients undergoing urethroplasty with buccal mucosa grafting, the impact of oral care pathways on infection and pain control remains unstudied. We hypothesize that the elimination of dietary restrictions and mouthwash regimens from the oral care pathway would not alter the rate of donor site complications. Materials and Methods: One hundred urethroplasty cases using buccal mucosa were retrospectively reviewed for donor site and perineal wound complications. No preoperative or intraoperative antibiotic oral cleanses were used in any case. Records were categorized by use of postoperative dietary restrictions and mouthwash regimens. Graft harvest size, preexisting oral issues, baseline comorbidities, dental assessments, perioperative antibiotics, and postoperative pain control regimens were accounted for. Results: Forty patients were included in the oral care pathway and 60 in the nonoral care pathway. Baseline demographics, dental assessment, and graft harvest details were similar between groups. There were no cases of graft site infection, with a median follow-up of 226 days. All graft site issues resolved in 3 to 4 weeks or less. Perineal wound infections for oral care pathway 2 (5%), and no oral care pathway 4 (6.7%), P = .6. Urinary tract infections for oral care pathway 7 (17.5%), and no oral care pathway 2 (3.3%), P = .027. Conclusions: Postoperative oral complications remain low without the use of oral cleanses, dietary restrictions, or mouthwash regimens. Routine use of donor site care pathways is likely unnecessary in this patient population.
{"title":"Postoperative Oral Care Pathways Are Not Required at the Time of Buccal Mucosa Harvest","authors":"Kevin Krughoff, Jordan Foreman, Thomas Dvergsten, Andrew C. Peterson","doi":"10.1097/ju9.0000000000000069","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000069","url":null,"abstract":"Purpose: For patients undergoing urethroplasty with buccal mucosa grafting, the impact of oral care pathways on infection and pain control remains unstudied. We hypothesize that the elimination of dietary restrictions and mouthwash regimens from the oral care pathway would not alter the rate of donor site complications. Materials and Methods: One hundred urethroplasty cases using buccal mucosa were retrospectively reviewed for donor site and perineal wound complications. No preoperative or intraoperative antibiotic oral cleanses were used in any case. Records were categorized by use of postoperative dietary restrictions and mouthwash regimens. Graft harvest size, preexisting oral issues, baseline comorbidities, dental assessments, perioperative antibiotics, and postoperative pain control regimens were accounted for. Results: Forty patients were included in the oral care pathway and 60 in the nonoral care pathway. Baseline demographics, dental assessment, and graft harvest details were similar between groups. There were no cases of graft site infection, with a median follow-up of 226 days. All graft site issues resolved in 3 to 4 weeks or less. Perineal wound infections for oral care pathway 2 (5%), and no oral care pathway 4 (6.7%), P = .6. Urinary tract infections for oral care pathway 7 (17.5%), and no oral care pathway 2 (3.3%), P = .027. Conclusions: Postoperative oral complications remain low without the use of oral cleanses, dietary restrictions, or mouthwash regimens. Routine use of donor site care pathways is likely unnecessary in this patient population.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"36 11","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136102249","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000073
Nellowe C. Candelario, Ilana Kafer, Simon P. Kim, Elizabeth R. Kessler
Introduction: Renal cell carcinoma (RCC) has a predisposition to vascular invasion that manifest as an inferior vena cava tumor thrombus (IVC TT). Radical nephrectomy with an IVC thrombectomy is associated with high morbidity. We present our single-center experience on the neoadjuvant use of the combination of anti-vascular endothelial growth factor (VEGF) tyrosine kinase inhibitors (TKI) and immune check point inhibitor (IO) for patients with RCC with IVC TT. Patient and Methods: Five patients with RCC and associated IVC TT received a neoadjuvant combination anti-VEGF TKI and IO. The IVC TT reduction was evaluated. The extent of tumor thrombus was defined based on the Mayo Classification, and TT volume was measured by the largest anteroposterior diameter. The safety of therapy, perioperative outcome, and number of patients who were able to undergo definitive surgery are described. Results: Two (40%) had a reduction in IVC TT based on the Mayo Classification. Tumor thrombus volume reduction was seen in all patients (100%). Four of 5 patients (80%) were able to have surgery. Conclusion: The neoadjuvant combination of an anti-VEGF TKI and IO is effective in reducing the extent of IVC TT. Prospective research is needed to characterize the safety, and long-term outcomes of this approach.
{"title":"Combination of an Anti-Vascular Endothelial Growth Factor Tyrosine Kinase Inhibitor and Immunotherapy as a Neoadjuvant Approach in Renal Cell Carcinoma With Associated Inferior Vena Cava Tumor Thrombus: A Single-Center Experience and Review of Literature","authors":"Nellowe C. Candelario, Ilana Kafer, Simon P. Kim, Elizabeth R. Kessler","doi":"10.1097/ju9.0000000000000073","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000073","url":null,"abstract":"Introduction: Renal cell carcinoma (RCC) has a predisposition to vascular invasion that manifest as an inferior vena cava tumor thrombus (IVC TT). Radical nephrectomy with an IVC thrombectomy is associated with high morbidity. We present our single-center experience on the neoadjuvant use of the combination of anti-vascular endothelial growth factor (VEGF) tyrosine kinase inhibitors (TKI) and immune check point inhibitor (IO) for patients with RCC with IVC TT. Patient and Methods: Five patients with RCC and associated IVC TT received a neoadjuvant combination anti-VEGF TKI and IO. The IVC TT reduction was evaluated. The extent of tumor thrombus was defined based on the Mayo Classification, and TT volume was measured by the largest anteroposterior diameter. The safety of therapy, perioperative outcome, and number of patients who were able to undergo definitive surgery are described. Results: Two (40%) had a reduction in IVC TT based on the Mayo Classification. Tumor thrombus volume reduction was seen in all patients (100%). Four of 5 patients (80%) were able to have surgery. Conclusion: The neoadjuvant combination of an anti-VEGF TKI and IO is effective in reducing the extent of IVC TT. Prospective research is needed to characterize the safety, and long-term outcomes of this approach.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"33 7","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136102257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000060
Brian Stork, Ehab Eltahawy
{"href":"Single Video Player","role":"media-player-id","content-type":"play-in-place","position":"float","orientation":"portrait","label":"","caption":"","object-id":[{"pub-id-type":"doi","id":""},{"pub-id-type":"other","content-type":"media-stream-id","id":"1_1g0jdjaq"},{"pub-id-type":"other","content-type":"media-source","id":"Kaltura"}]} Introduction A penile ring, or cock ring, is a mechanical device used by men to help maintain an erection. Penile rings are commercially available in a wide variety of different materials, shapes, and sizes. Once a man obtains an erection, the ring is positioned at the base of the penis. As such, it is important for men to choose a ring that is adjustable and fits comfortably. Penile rings work by occluding venous outflow from the penis.1 Rings should be removed as soon as possible after sexual activity to avoid ischemic damage to the corpora cavernosa.2 Rings left in place for extended periods of time cause progressive penile swelling, edema, and, ultimately, entrapment. Entrapped rings made of stretchable materials can often be slide over the penis or cut and removed. Rings made from metal, however, can be very challenging to remove. As a result, urologists are often called on to help manage these challenging cases. Methods A 72-year-old man with a medical history significant for hypertension developed increasing difficulty obtaining and maintaining an erection. His symptoms were refractory to phosphodiesterase-5 inhibitors. Prior to attempted intercourse, patient placed a 0.7-cm thick, stainless steel ring at the base of his penis. The patient had previously never tried penile occlusive therapy. He did not use any form of intracavernosal injection therapy in conjunction with the ring. After intercourse, he was unable to remove the ring. He presented to the emergency room 12 hours later with penile pain and swelling (Figure 1).Figure 1.: Penile entrapment with metal ring.The emergency room staff made multiple attempts to relieve the phimosis and remove the ring including lubrication and sliding, manual compression of the circumcised penis, wrapping the penis with gauze, and aspiration. An unsuccessful attempt was also made to cut the ring with a standard emergency room ring cutter. The patient went on to develop urinary retention, and a Foley catheter was placed. Options for management were discussed, and after obtaining informed consent, the patient was taken to the operating room. A general anesthetic was administered, and the Foley catheter was removed. The penis was prepped, and a cystoscopy drape was placed over the patient. The cystoscopy drape made it possible to contain and drain irrigation used during the procedure. A surgical time out was performed. Both corpora were then aspirated with 18 gauge needles. A total of 10 cc of dark blood was drained. The penis was then wrapped with gauze and manual compression was applied for 20 minutes in an attempt to reduce soft-tissue edema. After these maneuvers,
{"title":"Cutting of Entrapped Metal Penile Ring With Diamond Cutting Disk","authors":"Brian Stork, Ehab Eltahawy","doi":"10.1097/ju9.0000000000000060","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000060","url":null,"abstract":"{\"href\":\"Single Video Player\",\"role\":\"media-player-id\",\"content-type\":\"play-in-place\",\"position\":\"float\",\"orientation\":\"portrait\",\"label\":\"\",\"caption\":\"\",\"object-id\":[{\"pub-id-type\":\"doi\",\"id\":\"\"},{\"pub-id-type\":\"other\",\"content-type\":\"media-stream-id\",\"id\":\"1_1g0jdjaq\"},{\"pub-id-type\":\"other\",\"content-type\":\"media-source\",\"id\":\"Kaltura\"}]} Introduction A penile ring, or cock ring, is a mechanical device used by men to help maintain an erection. Penile rings are commercially available in a wide variety of different materials, shapes, and sizes. Once a man obtains an erection, the ring is positioned at the base of the penis. As such, it is important for men to choose a ring that is adjustable and fits comfortably. Penile rings work by occluding venous outflow from the penis.1 Rings should be removed as soon as possible after sexual activity to avoid ischemic damage to the corpora cavernosa.2 Rings left in place for extended periods of time cause progressive penile swelling, edema, and, ultimately, entrapment. Entrapped rings made of stretchable materials can often be slide over the penis or cut and removed. Rings made from metal, however, can be very challenging to remove. As a result, urologists are often called on to help manage these challenging cases. Methods A 72-year-old man with a medical history significant for hypertension developed increasing difficulty obtaining and maintaining an erection. His symptoms were refractory to phosphodiesterase-5 inhibitors. Prior to attempted intercourse, patient placed a 0.7-cm thick, stainless steel ring at the base of his penis. The patient had previously never tried penile occlusive therapy. He did not use any form of intracavernosal injection therapy in conjunction with the ring. After intercourse, he was unable to remove the ring. He presented to the emergency room 12 hours later with penile pain and swelling (Figure 1).Figure 1.: Penile entrapment with metal ring.The emergency room staff made multiple attempts to relieve the phimosis and remove the ring including lubrication and sliding, manual compression of the circumcised penis, wrapping the penis with gauze, and aspiration. An unsuccessful attempt was also made to cut the ring with a standard emergency room ring cutter. The patient went on to develop urinary retention, and a Foley catheter was placed. Options for management were discussed, and after obtaining informed consent, the patient was taken to the operating room. A general anesthetic was administered, and the Foley catheter was removed. The penis was prepped, and a cystoscopy drape was placed over the patient. The cystoscopy drape made it possible to contain and drain irrigation used during the procedure. A surgical time out was performed. Both corpora were then aspirated with 18 gauge needles. A total of 10 cc of dark blood was drained. The penis was then wrapped with gauze and manual compression was applied for 20 minutes in an attempt to reduce soft-tissue edema. After these maneuvers,","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135410329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000074
Pedro Rodrigues Beal, Tiago Aparecido Silva, Vitor Bonadia Buonfiglio, Luciana Saboya Brito Dal Col, Renato Meirelles Mariano Da Costa Junior, Luiz Henrique Correa Portari FIlho, Marcus Vinicius Sadi
Abstract Cryptorchidism remains as one of the most significant risk factors for the development of testicular cancer (TC). The occurrence of TC in undescended testes can represent challenges to both diagnosis and management because the clinical presentation can delay a definitive diagnosis, and surgical management of intra-abdominal masses can be difficult. We present a case of an adult male with bilateral cryptorchidism diagnosed with a large intra-abdominal TC which was subjected to surgical resection.
{"title":"Large Intra-abdominal Testicular Neoplasm Involving the Bladder and Ureter in an Adult Male with Bilateral Cryptorchidism","authors":"Pedro Rodrigues Beal, Tiago Aparecido Silva, Vitor Bonadia Buonfiglio, Luciana Saboya Brito Dal Col, Renato Meirelles Mariano Da Costa Junior, Luiz Henrique Correa Portari FIlho, Marcus Vinicius Sadi","doi":"10.1097/ju9.0000000000000074","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000074","url":null,"abstract":"Abstract Cryptorchidism remains as one of the most significant risk factors for the development of testicular cancer (TC). The occurrence of TC in undescended testes can represent challenges to both diagnosis and management because the clinical presentation can delay a definitive diagnosis, and surgical management of intra-abdominal masses can be difficult. We present a case of an adult male with bilateral cryptorchidism diagnosed with a large intra-abdominal TC which was subjected to surgical resection.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"13 2","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135613966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000052
Hiroko Miyagi, Shahab Bozorgmehri, Nikhil V. Batra, Jonathan A. Chatzkel, Brian Hemendra Ramnaraign, Kathryn Hitchcock, Robert A. Zlotecki, Wayne Brisbane, Paul L. Crispen, Padraic O'Malley
Objectives: The objectives of this study was (1) to examine the representation of women in clinical trials for systemic therapy in muscle-invasive (MIBC) or metastatic bladder cancer (BC) and (2) to determine the association between sex and systemic therapy in the treatment of MIBC or metastatic BC. Methods: A review of bladder cancer systemic therapy clinical trials cited by the National Comprehensive Cancer Network guidelines was performed. Proportions of women were compared with the corresponding proportions in the US population with bladder cancer between 1975 and 2018, based on the Surveillance, Epidemiology, and End Results database. We also used the National Cancer Database (NCDB) to identify 55,951 patients with American Joint Committee on Cancer clinical stage II, III, and IV bladder cancer between 2004 and 2015. We determined the predictors of systemic therapy for bladder cancer treatment using a multivariable logistic regression model. Results: 26.9% of the US bladder cancer population were women; however, only 17.7% of participants in US clinical trials and 19.9% of participants in all clinical trials were female, indicating an absolute difference of 9.2% (95% confidence interval [CI]: 6.2%-12.1%; P < .001) and 7.0% (95% CI: 6.1%-7.9%; P < .001), respectively. Multivariable analysis of the NCDB showed that women had decreased odds of receiving systemic therapy compared with male patients with MIBC or metastatic BC (odds ratio: 0.93, 95% CI: 0.89-0.96; P < .001). Conclusion: Women are underrepresented in MIBC and/or metastatic BC systemic therapy clinical trials. In addition, women are less likely than men to receive systemic therapy for the treatment of MIBC or metastatic BC. Further research is needed to investigate the reasons for gender disparities in treatment of MIBC or metastatic BC as well as the participation in clinical trials.
{"title":"Gender Disparities in the Clinical Trials and Real-World Utilization of Systemic Therapy in the Management of Urothelial Carcinoma","authors":"Hiroko Miyagi, Shahab Bozorgmehri, Nikhil V. Batra, Jonathan A. Chatzkel, Brian Hemendra Ramnaraign, Kathryn Hitchcock, Robert A. Zlotecki, Wayne Brisbane, Paul L. Crispen, Padraic O'Malley","doi":"10.1097/ju9.0000000000000052","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000052","url":null,"abstract":"Objectives: The objectives of this study was (1) to examine the representation of women in clinical trials for systemic therapy in muscle-invasive (MIBC) or metastatic bladder cancer (BC) and (2) to determine the association between sex and systemic therapy in the treatment of MIBC or metastatic BC. Methods: A review of bladder cancer systemic therapy clinical trials cited by the National Comprehensive Cancer Network guidelines was performed. Proportions of women were compared with the corresponding proportions in the US population with bladder cancer between 1975 and 2018, based on the Surveillance, Epidemiology, and End Results database. We also used the National Cancer Database (NCDB) to identify 55,951 patients with American Joint Committee on Cancer clinical stage II, III, and IV bladder cancer between 2004 and 2015. We determined the predictors of systemic therapy for bladder cancer treatment using a multivariable logistic regression model. Results: 26.9% of the US bladder cancer population were women; however, only 17.7% of participants in US clinical trials and 19.9% of participants in all clinical trials were female, indicating an absolute difference of 9.2% (95% confidence interval [CI]: 6.2%-12.1%; P < .001) and 7.0% (95% CI: 6.1%-7.9%; P < .001), respectively. Multivariable analysis of the NCDB showed that women had decreased odds of receiving systemic therapy compared with male patients with MIBC or metastatic BC (odds ratio: 0.93, 95% CI: 0.89-0.96; P < .001). Conclusion: Women are underrepresented in MIBC and/or metastatic BC systemic therapy clinical trials. In addition, women are less likely than men to receive systemic therapy for the treatment of MIBC or metastatic BC. Further research is needed to investigate the reasons for gender disparities in treatment of MIBC or metastatic BC as well as the participation in clinical trials.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"36 10","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136102250","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000076
Susan M. MacDonald
{"title":"Editorial Comment in Response to: Postoperative Oral Care Pathways are Not Required at the Time of Buccal Mucosa Harvest","authors":"Susan M. MacDonald","doi":"10.1097/ju9.0000000000000076","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000076","url":null,"abstract":"","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"70 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139295183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000070
Amy Zheng, Austin K. Bramwell, Jennifer A. Kane, Jonathan T. Pham, Susan M. MacDonald
Purpose: We determined the prevalence of pelvic floor dysfunction (PFD) as an etiology for chronic orchialgia in a single tertiary care practice and characterized the presenting symptoms of chronic orchialgia patients with PFD. Materials and Methods: An IRB-approved retrospective review was performed for patients diagnosed with chronic orchialgia from 2016 to 2021 using CPT codes N50.82 (scrotal pain), N50.819 (testicle pain), and G89.29 (chronic pain in testicle). Patients with acute orchialgia (<3 months) were excluded. PFD was diagnosed on a 360-degree digital rectal examination when increased tone or pain to palpation of the levator ani muscle group was noted. Suspected etiology of the orchialgia and accompanying urinary, bowel, or sexual symptoms were recorded. Unpaired t -tests were used to determine significant associations while accounting for differences in sample size. Results: Of 136 patients with chronic orchialgia, the most common etiologies were classified as idiopathic (37.7%); prior surgery (32.1%); varicocele, hydrocele, or spermatocele (28.3%); PFD (17.6%); and postinfection (11.3%). Chronic orchialgia patients with PFD (n = 24) were significantly more likely to present with accompanying urinary ( P < .01), bowel ( P < .01), and sexual dysfunction ( P = .04) symptoms. Orchialgia patients with PFD were more likely to report symptoms of functional obstruction, particularly urinary hesitancy ( P < .01), constipation ( P < .01), and painful ejaculation ( P < .01), compared with patients without PFD. Conclusions: PFD was determined to be the etiology in 1 in 6 patients with chronic orchialgia. All patients presenting with chronic orchialgia and obstructive symptoms warrant a 360-degree rectal examination as part of their initial evaluation. IRB Protocol Number: 10677.
{"title":"Pelvic Floor Dysfunction: A Common Cause of Chronic Orchialgia","authors":"Amy Zheng, Austin K. Bramwell, Jennifer A. Kane, Jonathan T. Pham, Susan M. MacDonald","doi":"10.1097/ju9.0000000000000070","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000070","url":null,"abstract":"Purpose: We determined the prevalence of pelvic floor dysfunction (PFD) as an etiology for chronic orchialgia in a single tertiary care practice and characterized the presenting symptoms of chronic orchialgia patients with PFD. Materials and Methods: An IRB-approved retrospective review was performed for patients diagnosed with chronic orchialgia from 2016 to 2021 using CPT codes N50.82 (scrotal pain), N50.819 (testicle pain), and G89.29 (chronic pain in testicle). Patients with acute orchialgia (<3 months) were excluded. PFD was diagnosed on a 360-degree digital rectal examination when increased tone or pain to palpation of the levator ani muscle group was noted. Suspected etiology of the orchialgia and accompanying urinary, bowel, or sexual symptoms were recorded. Unpaired t -tests were used to determine significant associations while accounting for differences in sample size. Results: Of 136 patients with chronic orchialgia, the most common etiologies were classified as idiopathic (37.7%); prior surgery (32.1%); varicocele, hydrocele, or spermatocele (28.3%); PFD (17.6%); and postinfection (11.3%). Chronic orchialgia patients with PFD (n = 24) were significantly more likely to present with accompanying urinary ( P < .01), bowel ( P < .01), and sexual dysfunction ( P = .04) symptoms. Orchialgia patients with PFD were more likely to report symptoms of functional obstruction, particularly urinary hesitancy ( P < .01), constipation ( P < .01), and painful ejaculation ( P < .01), compared with patients without PFD. Conclusions: PFD was determined to be the etiology in 1 in 6 patients with chronic orchialgia. All patients presenting with chronic orchialgia and obstructive symptoms warrant a 360-degree rectal examination as part of their initial evaluation. IRB Protocol Number: 10677.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"58 6","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135614941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-01DOI: 10.1097/ju9.0000000000000071
Ernest Kaufmann, Peter C. Black, James W. F. Catto, H. Djaladat, S. Ghodoussipour, Jill M. Hamilton-Reeves, Bente Thoft Jensen, W. Kassouf, S. V. Lauridsen, S. P. Lerner, Carlos Llorente, Katherine Loftus, Ilaria Lucca, Alberto Martini, Mark A. Preston, S. P. Psutka, J. Sfakianos, Jay Shah, M. S. Wettstein, Stephen B. Williams, S. Daneshmand, C. Fankhauser
Follow-up after urinary diversion aims to detect functional complications to prevent harm and improve quality of life. We conducted a literature search and reviewed guidelines and institutional follow-up protocols. We included 14 studies providing data of 3282 patients. Functional complications can be seen in up to 90% of all patients within 15 years after urinary diversion and mainly include impairment of urinary or sexual function as well as renal/metabolic disturbances, but only limited evidence supporting any functional follow-up recommendation was identified. Current guideline recommendation should be rephrased to ensure routine implementation of functional follow-up investigation. Future research is required to assess whether, which, and how follow-up protocols after cystectomy affect functional results to inform optimal surveillance procedures after treatment. In this review of recommended follow-up protocols after cystectomy, we observed different recommendations and discuss future research areas.
{"title":"Functional Follow-Up After Cystectomy and Urinary Diversion: A Narrative Review","authors":"Ernest Kaufmann, Peter C. Black, James W. F. Catto, H. Djaladat, S. Ghodoussipour, Jill M. Hamilton-Reeves, Bente Thoft Jensen, W. Kassouf, S. V. Lauridsen, S. P. Lerner, Carlos Llorente, Katherine Loftus, Ilaria Lucca, Alberto Martini, Mark A. Preston, S. P. Psutka, J. Sfakianos, Jay Shah, M. S. Wettstein, Stephen B. Williams, S. Daneshmand, C. Fankhauser","doi":"10.1097/ju9.0000000000000071","DOIUrl":"https://doi.org/10.1097/ju9.0000000000000071","url":null,"abstract":"Follow-up after urinary diversion aims to detect functional complications to prevent harm and improve quality of life. We conducted a literature search and reviewed guidelines and institutional follow-up protocols. We included 14 studies providing data of 3282 patients. Functional complications can be seen in up to 90% of all patients within 15 years after urinary diversion and mainly include impairment of urinary or sexual function as well as renal/metabolic disturbances, but only limited evidence supporting any functional follow-up recommendation was identified. Current guideline recommendation should be rephrased to ensure routine implementation of functional follow-up investigation. Future research is required to assess whether, which, and how follow-up protocols after cystectomy affect functional results to inform optimal surveillance procedures after treatment. In this review of recommended follow-up protocols after cystectomy, we observed different recommendations and discuss future research areas.","PeriodicalId":74033,"journal":{"name":"JU open plus","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139292831","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}