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Challenging dilemmas of low grade, non-invasive bladder cancer: a narrative review

ABSTRACT

Purpose:

To describe the current scientific knowledge and clinical experience in low-grade-non-muscle-invasive bladder cancer (LG-NMIBC) patients in challenging scenarios.

Materials and Methods:

Medline, Embase, Google Scholar, and Cochrane Central were searched until March 2021.

Results:

A total of 841 studies were identified, and abstracts were analyzed. Twenty-one relevant studies were then identified and reviewed. After all, information was gathered from 16 studies, the authors discussed the specific topics, and expert opinions were also included in the discussion. There have been some studies that can help us to have some insights on how to manage these patients. Very distinctive strategies have been reported in the literature, mainly anecdotally or in small randomized studies. Some of these treatments outlined in the present manuscript include repeated TURBTs, chemoablation, BCG immunoablation, partial cystectomy, radical cystectomy, radiotherapy, chemotherapy, and future perspectives. In the current manuscript, we have combined these strategies in a proposed algorithm.

Conclusion:

For those LG-NMIBC patients in challenging scenarios, we have found repeated TURBTs, chemoablation, BCG immunoablation, partial cystectomy, radical cystectomy, radiotherapy, and chemotherapy are attractive modalities to treat them effectively. Also, the current manuscript proposes an algorithm to overcome these challenges.

Keywords:
Urinary Bladder Neoplasms; Carcinoma; Transitional Cell; Review Literature as Topic

INTRODUCTION

Bladder cancer is the sixth most common cancer in the US and represents 4.6% of all new cancer diagnoses, equivalent to 80.470 new cases and 17.670 deaths in the US during 2019 (11[No Authors]. National Cancer Institute. Cancer Stat Facts: Bladder Cancer 2019. [Internet]. Available at. <https://seer.cancer.gov/statfacts/html/urinb.html>
<https://seer.cancer.gov/statfacts/html/...
). It also has significantly elevated expenses and perhaps the highest lifetime treatment costs per patient (22 Korkes F, Maluf F. Increasing costs from bladder cancer in the Brazilian Health System: the role of establishing public health policies. Int Braz J Urol. 2021; 47:443-7.).

In high-risk non-muscle-invasive bladder tumors (NMIBC), radical progression and metastasis are significant concerns. The standard treatment of these patients is TURBT and BCG installations. Nonetheless, a radical cystectomy is a good option (33 Babjuk M, BurgerM, MC Evaat, Mostafid AH, Palou J, van Rhijn BWG, et al. European Association of Urology Guidelines on Non-muscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ). EAU. 2019; 7 639-57.). On the other side, for muscle-invasive bladder cancer (MIBC), the last one is the standard intervention. However, nowadays, there is increasing evidence that trimodal therapy (complete TURBT, chemotherapy, and radiotherapy) might be an essential and acceptable intervention for selected cases (low-volume T2, absence of CIS, no hydronephrosis) (44 Hamad J, McCloskey H, Milowsky MI, Royce T, Smith A. Bladder preservation in muscle-invasive bladder cancer: a comprehensive review. Int Braz J Urol. 2020; 46:169-184.).

Non-muscle invasive bladder cancer (NMIBC) is commonly treated and cured through transurethral resection of the bladder tumor (TURBT). Low-grade, non-invasive tumors rarely metastasize, the high recurrence rates and progression risk are avoided through adjuvant measures and an extensive follow-up program (55 Flaig TW, Spiess PE, Agarwal N, Bangs R, Boorjian SA, Buyyounouski MK, et al. Bladder Cancer, Version 3.2020, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2020; 18:329-54.). Even though TURBT is a standard procedure mastered by most urologists, there are certain challenging situations. Sometimes the urologist faces a TURBT with an NMIBC located in an inaccessible position, a large prostate / urethral stricture precluding the resectoscope introduction or an extensive low-grade Ta lesion that cannot be endoscopically resected. Accordingly, large-volume, multifocal cancers can usually be managed with conservative techniques with a good prognosis (66 Gupta SK, Parr NJ. Outcome of very large superficial bladder tumours: a 10-year experience. Scand J Urol Nephrol. 2008; 42:243-8.).

We aimed to describe the current scientific knowledge and clinical experience LG-NMIBC patients challenging scenarios. An international panel of experts on bladder cancer treatment performed a review and identified alternatives in complex TURBT cases for LG NMIBC.

MATERIALS AND METHODS

We conducted this comprehensive review following Joanna Briggs Institute recommendations (77 Peters MD, Casey M, Tricco AC Pollock D, Munn Z, Alexander L et al. Updated methodological guidance for the conduct of scoping review. JBI Evid Synth. 2020;18:2119-26.).

Eligibility criteria: Studies including alternative interventions for patients over 18 years of age with a Ta NMIBC diagnosis and considered complex TURBT.

Information sources: We carried out the literature search in the MEDLINE (OVID), EMBASE, Google Scholar, and CENTRAL databases from inception to March 2021. We performed a structured search using terms and synonyms related to the condition of interest.

DATA COLLECTION

Two researchers identified each reference by title and abstract. Subsequently, we reviewed the full texts of relevant studies and applied pre-specified inclusion and exclusion criteria. Using a standardized form, the reviewers independently extracted the following information from each article.

Data synthesis: We showed each clinical trial result descriptively, trying to respond to the proposed objective.

RESULTS

Study selection

We identified 841documents from the search strategy. Finally, we included sixteen studies that were eligible for our review. (Figure-1)

Figure 1
Flowchart for study selection.

Characteristics of included studies

We found multiple design studies, including primary studies, reviews, and commentaries. They were all published in worldwide journals as the primary purpose of this study is to present the strategies, as a way to standardize alternative interventions in complex cases, we go ahead to present them.

Specific strategies

Strategies to access the tumor

Difficult-to-reach tumors

At times, urologists have to deal with challenging situations at the TURBT, such as large prostates, large-distended bladders, severe urethral strictures or stenosis, and often obese patients making access to the bladder tumor foci quite prohibitive (Table-1). Additionally, tumors located at the bladder dome and anterior bladder wall can pose additional difficulties. In these cases, conventional maneuvers as emptying the bladder, suprapubic pressure, or Trendelenburg position are not helpful tips.

Table 1
Frequent situations associated with LG-NMIBC challenges.

Correspondingly, the cystoscope or even the ureteroscope might be valuable tools to perform this procedure. It is possible to perform a cold-cup biopsy and Bugbee cauterization of some LG lesions through the cystoscope. Also, laser ablation or en-bloc resection with the resecoscope might be possible and accessible.

An extra-long resectoscope may be another tool to use in these challenging situations. If not readily available, the procedure can be postponed. Also, an old but exciting technique is a perineal urethrostomy, which can also be used as an access route in challenging cases (88 Papagiannopoulos D, Deane LA. Perineal urethrostomy: Still Essential in the Armamentarium for Transurethral Surgery. Rev Urol. 2017; 19:72-5., 99 Bissada NK, Redman JF, Welch LT. Transurethral resection of prostate via perineal urethrostomy. Prospective study. Urology. 1976; 7:70-2.).

Extensive tumors

In multiple LG-NMIBC tumors with almost no normal urothelium, the surgical resection might be difficult and dangerous. It is crucial to ensure a good visualization throughout the procedure, controlling significant hematuria, cauterizing bleeders throughout the resection, and evacuating clots with an Ellik or some other means of effective evacuation. For extensive tumors, incomplete resection may be unavoidable sometimes, and staged procedures are the safest approach. Even though there are no current formal recommendations for such cases, adjuvant treatment strategies, as mentioned below, can be of value.

Treatment strategies

Staged procedures

For extensive tumors, incomplete resection may be unavoidable sometimes, and staged procedures can be the safest approach (66 Gupta SK, Parr NJ. Outcome of very large superficial bladder tumours: a 10-year experience. Scand J Urol Nephrol. 2008; 42:243-8.). In such cases, we suggest a complete tumor resection in one area, providing meticulous hemostasis. A second procedure can be scheduled between two to four weeks to complete the procedure.

Also, for patients with a huge prostate or a huge median lobe that precludes access to a bladder tumor, benign prostatic hyperplasia can be initially treated, and the TURBT can be performed as a staged procedure.

Alternatively, if there is a high-volume prostate, it can be resected as a first-step procedure, and then a delayed TURBT in 6-8 weeks.

Chemoablation of NMIBC

A few studies describing chemoresection or chemoablation as an alternative to TURBT have been published during the last decade. Bono et al. (1010 Bono AV, Hall RR, Denis L, Lovisolo JA, Sylvester R. Chemoresection in Ta-T1 bladder cancer. Members of the EORTC Genito-Urinary Group. Eur Urol. 1996; 29:385-90.) evaluated mitomycin C (MMC) and epirubicin in two EORTC trials. They observed 57% and 67% complete response rates, respectively.

Similarly, in a prospective trial, Lindgren et al. (1111 Lindgren MS, Bue P, Azawi N, Blichert-Refsgaard L, Sundelin MO, Dyrskjøt L, et al. The DaBlaCa-13 Study: Short-term, Intensive Chemoresection Versus Standard Adjuvant Intravesical Instillations in Non-muscle-invasive Bladder Cancer-A Randomised Controlled Trial. Eur Urol. 2020; 78:856-62.) treated 120 patients with Ta-NMIBC (LG or HG), with intravesical MMC with 40mg/40mL/2 hours, three times a week for two weeks. They found 57% complete tumor response at four weeks. Interestingly, adverse events were less common after chemoablation than after TURBT plus MMC or BCG.

Colombo et al. (1212 Colombo R, Rocchini L, Suardi N, Benigni F, Colciago G, Bettiga A, et al. Neoadjuvant short-term intensive intravesical mitomycin C regimen compared with weekly schedule for low-grade recurrent non-muscle-invasive bladder cancer: preliminary results of a randomised phase 2 study. Eur Urol. 2012; 62:797-802. Erratum in: Eur Urol. 2019; 75:e81.) included 54 small-LG-Ta NMIBC patients. Patients received a weekly MMC instillation/6 weeks or three instillations/week for two weeks. They found a 70.4% complete response after 14 days. Contrarily, Mostafied et al. (1313 Mostafid H. Neoadjuvant Intravesical Therapy for Non-muscle-invasive Bladder Cancer: A New Approach for Old Agents? Eur Urol. 2020; 78:863-4.) evaluated 82 small LG-Ta-NMIBC patients. They only found 37% complete responses after four MMC instillations for one week.

It seems that a more intense (3x / week) and more extended period (two weeks) chemoablation with MMC might be more effective. Nonetheless, this is low-quality evidence, and we need high-quality clinical trials for decision-making. Other chemotherapies have not been tested in this setting.

Gemcitabine has also been studied in incomplete resection settings (1414 Serretta V, Galuffo A, Pavone C, Allegro R, Pavone-MacAluso M. Gemcitabine in intravesical treatment of Ta-T1 transitional cell carcinoma of bladder: Phase I-II study on marker lesions. Urology. 2005; 65:65-9.). A 6x / weekly gemcitabine reached a 23% complete response. An escalated dose of 2.000mg achieved a better complete response (33.3%). Another study found a similar 31% complete response in this setting (1515 Gårdmark T, Carringer M, Beckman E, Malmström PU; Members of the Intravesical Gemcitabine Study Group. Randomized phase II marker lesion study evaluating effect of scheduling on response to intravesical gemcitabine in recurrent Stage Ta urothelial cell carcinoma of the bladder. Urology. 2005; 66:527-30.).

BCG ablation

BCG is currently recommended as an adjuvant measure to reduce NMIBC recurrence after TURBT in high-risk patients. Nonetheless, it has been tested as a neoadjuvant treatment strategy in only one study (1616 Akaza H. BCG treatment of existing Ta, T1 tumours or carcinoma in situ of the bladder. Eur Urol. 1995; 27(Suppl 1):9-12.) (They also previously reported their outcomes with almost the same results (1717 Akaza H, Kameyama S, Kakizoe T, Kojima H, Koiso K, Aso Y, et al. [Ablative and prophylactic effects of BCG Tokyo 172 strain for intravesical treatment in patients with superficial bladder cancer and carcinoma in situ of the bladder. Bladder cancer BCG Study Group]. Nihon Hinyokika Gakkai Zasshi. 1992; 83:183-9.)). Akaza et al. applied 80mg weekly BCG for eight weeks in 125 Ta, T1, or CIS patients before TURBT. There was a complete response in 66.4% of the papillary tumors. For Cis, there was an 84% complete response (1616 Akaza H. BCG treatment of existing Ta, T1 tumours or carcinoma in situ of the bladder. Eur Urol. 1995; 27(Suppl 1):9-12.). It is noteworthy that this approach has been tested in a very controlled trial setting and needs more evidence to extrapolate its results. For larger tumors, persistent hematuria might delay treatment and require emergency treatments. It should therefore be considered very cautiously. To our knowledge, there are no other studies for this intervention.

Partial Cystectomy

Partial cystectomy (PC) is considered a treatment only for exceptional cases of urothelial bladder carcinoma. Even though there is no consensus regarding this intervention, the main indications are single tumors in diverticula or T2-small-single tumor with good bladder capacity in a favorable position and without extensive CIS.

One of the most extensive available series about this intervention in this setting is published by Capitanio et al. (1818 Capitanio U, Isbarn H, Shariat SF, Jeldres C, Zini L, Saad F, et al. Partial cystectomy does not undermine cancer control in appropriately selected patients with urothelial carcinoma of the bladder: a population-based matched analysist. Urology. 2009; 74:858-64.). They analyzed the SEER database and observed that 23.3% of all 1.753 PC were performed for Ta tumors. There was no recurrence nor other oncological outcomes report.

This situation is not widely mentioned in the literature and guidelines; however, there might be some room for PC in NMIBC. For instance, single large LG/Ta tumors, close to the bladder neck and not easily accessible by TURBT (Figures 2a and 2b).

Figure 2
Algorithm for challenging LG-NMIBC management.

Radiotherapy

Urothelial carcinoma is a radio-sensitive tumor. Radiotherapy may not be considered as monotherapy for treating MIBC. Instead, combined with chemotherapy and TURBT (Trimodal therapy) has essential effects in oncological outcomes of selected patients, even with fiducial markers as new tools for improving effectiveness (44 Hamad J, McCloskey H, Milowsky MI, Royce T, Smith A. Bladder preservation in muscle-invasive bladder cancer: a comprehensive review. Int Braz J Urol. 2020; 46:169-184., 1919 Shahbaz M, Ammar A, Wang Y, Farhaj Z, Qiao L, Niu J. Endoclips as novel fiducial markers in trimodality bladder-preserving therapy of muscle-invasive bladder carcinoma: feasibility and patient outcomes. Int Braz J Urol. 2021; 47:93-99.).

Rodel and Akcetin tried radiotherapy and radiochemotherapy in high-risk T1 bladder cancer. They found an 83-90% complete remission after TURBT. Also, overall survival of 75% at five years and 50% at ten years (2020 Rödel C, Dunst J, Grabenbauer GG, Kühn R, Papadopoulos T, Schrott KM, et al. Radiotherapy is an effective treatment for high-risk T1-bladder cancer. Strahlenther Onkol. 2001; 177:82-8., 2121 Akçetin Z, Todorov J, Tüzel E, Engehausen DG, Krause FS, Sauer R, et al. Radiochemotherapy after transurethral resection is an effective treatment method in T1G3 bladder cancer. Anticancer Res. 2005; 25 (3A):1623-8.).

Weiss et al. reported radiotherapy or chemoradiotherapy as an alternative for high-risk T1 bladder cancer (2222 Weiss C, Wolze C, Engehausen DG, Ott OJ, Krause FS, Schrott KM, et al. Radiochemotherapy after transurethral resection for high-risk T1 bladder cancer: an alternative to intravesical therapy or early cystectomy? J Clin Oncol. 2006; 24:2318-24.). They found 88% complete response, 30% progression at ten years, and disease-specific survival of 73% at ten years. However, there are no high-quality studies to confirm this data. We did not find any information for low-grade or large volume Ta tumors.

Neoadjuvant arterial chemotherapy

We found a single report of such treatment for an extensively large papillary NMIBC patient who was not amenable to endoscopic resection. This 50-year-old man underwent an arterial infusion of cisplatin (100mg/body) into the superior vesical artery twice, with a 5-week interval. A ten-time fold reduction in tumor volume was observed, and the low-grade-Ta tumor was rendered amenable to TURBT (2323 Kano H, Miwa S, Koshida K, Kawai K. Successful Treatment of a Large Superficial Bladder Cancer with Neoadjuvant Arterial Infusion Chemotherapy: A Case Report. Case Rep Oncol. 2018; 11:383-7.).

This use of single-agent intra-arterial chemotherapy seems to be an exciting strategy to be considered in low-grade large-volume NMIBC, where bladder preservation is intended.

Radical Cystectomy

Radical Cystectomy (RC) is currently considered the gold-standard treatment for patients with MIBC (2424 Witjes JA, Compérat E, Cowan NC, De Santis M, Gakis G, Lebrét T, et al. EAU Guidelines on Muscle-invasive and Metastatic Bladder Cancer: Summary of the 2020 Guidelines. Eur Urol. 2021;79:82-104. ). In NMIBC patients, RC is an option, mainly considered after BCG failure, especially for high-risk or very high-risk patients, unreachable T1 tumors, residual T1 tumors after resection, or high-grade tumors with CIS and lymphovascular invasion (33 Babjuk M, BurgerM, MC Evaat, Mostafid AH, Palou J, van Rhijn BWG, et al. European Association of Urology Guidelines on Non-muscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ). EAU. 2019; 7 639-57.). RC is not an option for intermediate-risk tumors.

EAU, NCCN, or AUA guidelines do not mention the specific treatment of a low-grade, extensive Ta tumor, not exposed to BCG treatment, and not amenable to endoscopic resection. The AUA guideline states that for a Ta low- or intermediate-risk patient, the clinician should not perform an RC until bladder-sparing modalities (staged TURBT, intravesical therapies) fail. We only found one reference (case series) supporting this statement for RC in such tumors (2525 Amling CL, Thrasher JB, Frazier HA, Dodge RK, Robertson JE, Paulson DF. Radical cystectomy for stages Ta, Tis and T1 transitional cell carcinoma of the bladder. J Urol. 1994; 151:31-5.).

Although a multifocal or very large LG NMIBC represents a rare situation, RC might be effective and considered in these cases where repeated endoscopic resections fail to succeed (Figure 2c, 2d and 2e).

DISCUSSION

Non-muscle invasive bladder cancer (NMIBC) is a disease that can commonly be cured through transurethral resection of the bladder tumor (TURBT). The high recurrence rates and progression risk are avoided through adjuvant measures and an extensive follow-up program (33 Babjuk M, BurgerM, MC Evaat, Mostafid AH, Palou J, van Rhijn BWG, et al. European Association of Urology Guidelines on Non-muscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ). EAU. 2019; 7 639-57.).

Although TURBT is a standard procedure mastered by most urologists, there are certain challenging situations to discuss. Sometimes urologists face an unreachable NMIBC, a high-volume prostate, or a urethral stricture that precludes the resectoscope introduction, or an extensive low-grade Ta tumor that cannot be endoscopically resected.

In this review, we have found some studies helping to have some insights on how to manage these patients, although those are low-quality evidence. Very distinctive strategies have been reported in the literature, mainly descriptive, anecdotally, or small randomized studies.

Some of these treatments outlined in the present manuscript include repeated TURBTs, chemoablation, BCG immunoablation, partial cystectomy, radical cystectomy, radiotherapy, and chemotherapy. In summary, we have combined these strategies into a proposed algorithm to be considered in this situation (Figure-3).

Figure 3
Computed Tomography (CT) scan of a patient who underwent a partial cystectomy for an anterior bladder neck LG-NMIBC (yellow arrow) could not be adequately resected endoscopically.

A) preoperative image. B) After 22 months of follow-up. Radical cystectomy was performed for an extensive LG Ta NMIBC. C) and D) CT scans demonstrating extensive LG-Ta lesion. E) surgical aspect of the bladder after radical cystectomy.


Another vital consideration for decision-making is prognostic factors and how to improve the outcomes with a more invasive procedure. Regarding the first one, we need to identify high-risk recurrence and progression patients with algorithms, artificial intelligence, or laboratory tools. To predict oncological outcomes and optimal, tailored therapeutic decision-making, we have found that a high neutrophil-to lymphocyte ratio (NLR) was already consistently associated with locally advanced disease. Also, it represents an independent prognostic factor of recurrence and progression in NMIBC patients (2626 Racioppi M, Di Gianfrancesco L, Ragonese M, Palermo G, Sacco E, Bassi PF. Can Neutrophil-to-Lymphocyte ratio predict the response to BCG in high-risk non muscle invasive bladder cancer? Int Braz J Urol. 2019; 45:315-24.). For the second issue, the Enhanced recovery after surgery (ERAS) program has been described as an alternative to reduce the perioperative morbidity and mortality in patients undergoing a radical cystectomy (2727 Moschini M, Stabile A, Mattei A, Montorsi F, Cathelineau X, Sanchez-Salas R. Enhanced recovery after surgery (ERAS) in radical cystectomy patients: from consensus to evidences. Int Braz J Urol. 2019; 45:655-7., 2828 Santoyo Vargas J, Castillo-Cobaleda DF, García-Perdomo HA. Aplicación del protocolo ERAS (Enhanced Recovery After Surgery) en cistectomía radical [Applying the ERAS (Enhanced Recovery After Surgery) protocol in radical cystectomy]. Arch Esp Urol. 2020; 73:600-10.). Therefore, we may counsel every urologist to follow these recommendations when deciding to perform an RC in these settings.

From a future perspective, the landscape of new drugs for the treatment of bladder cancer has widely improved in the last decade. The pathophysiology knowledge and genomic profile of such tumors have also been increasing rapidly (2929 Warrick JI, Knowles MA, Yves A, van der Kwast T, Grignon DJ, Kristiansen G, et al. Report From the International Society of Urological Pathology (ISUP) Consultation Conference On Molecular Pathology Of Urogenital Cancers. II. Molecular Pathology of Bladder Cancer: Progress and Challenges. Am J Surg Pathol. 2020; 44:e30-e46.). In such a context, we might have a near-future further option for these uncommon situations of challenging LG-Ta NMIBC. Immuno-oncology and targeted therapies have already been used for specific situations of NMIBC.

Some new drug trials evaluate oncolytic virus regimen, recombinant fusion proteins, immune modulation, cytotoxic therapies, and targeted small molecule kinase inhibitors. As research improves, we are likely to see an increase in the number of options for such patients.

CONCLUSIONS

For those patients with an unreachable LG-NMIBC, a high-volume prostate, an urethral stricture that precludes the resectoscope introduction, or an extensive low-grade Ta tumor, we have found that repeated TURBTs, chemoablation, BCG immunoablation, partial cystectomy, radical cystectomy, radiotherapy, and chemotherapy are attractive modalities to treat them effectively. Also, the current manuscript proposes an algorithm to overcome these challenges. We also consider that there is a wide gap to fill in with high-quality evidence.

REFERENCES

  • 1
    [No Authors]. National Cancer Institute. Cancer Stat Facts: Bladder Cancer 2019. [Internet]. Available at. <https://seer.cancer.gov/statfacts/html/urinb.html>
    » <https://seer.cancer.gov/statfacts/html/urinb.html
  • 2
    Korkes F, Maluf F. Increasing costs from bladder cancer in the Brazilian Health System: the role of establishing public health policies. Int Braz J Urol. 2021; 47:443-7.
  • 3
    Babjuk M, BurgerM, MC Evaat, Mostafid AH, Palou J, van Rhijn BWG, et al. European Association of Urology Guidelines on Non-muscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ). EAU. 2019; 7 639-57.
  • 4
    Hamad J, McCloskey H, Milowsky MI, Royce T, Smith A. Bladder preservation in muscle-invasive bladder cancer: a comprehensive review. Int Braz J Urol. 2020; 46:169-184.
  • 5
    Flaig TW, Spiess PE, Agarwal N, Bangs R, Boorjian SA, Buyyounouski MK, et al. Bladder Cancer, Version 3.2020, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2020; 18:329-54.
  • 6
    Gupta SK, Parr NJ. Outcome of very large superficial bladder tumours: a 10-year experience. Scand J Urol Nephrol. 2008; 42:243-8.
  • 7
    Peters MD, Casey M, Tricco AC Pollock D, Munn Z, Alexander L et al. Updated methodological guidance for the conduct of scoping review. JBI Evid Synth. 2020;18:2119-26.
  • 8
    Papagiannopoulos D, Deane LA. Perineal urethrostomy: Still Essential in the Armamentarium for Transurethral Surgery. Rev Urol. 2017; 19:72-5.
  • 9
    Bissada NK, Redman JF, Welch LT. Transurethral resection of prostate via perineal urethrostomy. Prospective study. Urology. 1976; 7:70-2.
  • 10
    Bono AV, Hall RR, Denis L, Lovisolo JA, Sylvester R. Chemoresection in Ta-T1 bladder cancer. Members of the EORTC Genito-Urinary Group. Eur Urol. 1996; 29:385-90.
  • 11
    Lindgren MS, Bue P, Azawi N, Blichert-Refsgaard L, Sundelin MO, Dyrskjøt L, et al. The DaBlaCa-13 Study: Short-term, Intensive Chemoresection Versus Standard Adjuvant Intravesical Instillations in Non-muscle-invasive Bladder Cancer-A Randomised Controlled Trial. Eur Urol. 2020; 78:856-62.
  • 12
    Colombo R, Rocchini L, Suardi N, Benigni F, Colciago G, Bettiga A, et al. Neoadjuvant short-term intensive intravesical mitomycin C regimen compared with weekly schedule for low-grade recurrent non-muscle-invasive bladder cancer: preliminary results of a randomised phase 2 study. Eur Urol. 2012; 62:797-802. Erratum in: Eur Urol. 2019; 75:e81.
  • 13
    Mostafid H. Neoadjuvant Intravesical Therapy for Non-muscle-invasive Bladder Cancer: A New Approach for Old Agents? Eur Urol. 2020; 78:863-4.
  • 14
    Serretta V, Galuffo A, Pavone C, Allegro R, Pavone-MacAluso M. Gemcitabine in intravesical treatment of Ta-T1 transitional cell carcinoma of bladder: Phase I-II study on marker lesions. Urology. 2005; 65:65-9.
  • 15
    Gårdmark T, Carringer M, Beckman E, Malmström PU; Members of the Intravesical Gemcitabine Study Group. Randomized phase II marker lesion study evaluating effect of scheduling on response to intravesical gemcitabine in recurrent Stage Ta urothelial cell carcinoma of the bladder. Urology. 2005; 66:527-30.
  • 16
    Akaza H. BCG treatment of existing Ta, T1 tumours or carcinoma in situ of the bladder. Eur Urol. 1995; 27(Suppl 1):9-12.
  • 17
    Akaza H, Kameyama S, Kakizoe T, Kojima H, Koiso K, Aso Y, et al. [Ablative and prophylactic effects of BCG Tokyo 172 strain for intravesical treatment in patients with superficial bladder cancer and carcinoma in situ of the bladder. Bladder cancer BCG Study Group]. Nihon Hinyokika Gakkai Zasshi. 1992; 83:183-9.
  • 18
    Capitanio U, Isbarn H, Shariat SF, Jeldres C, Zini L, Saad F, et al. Partial cystectomy does not undermine cancer control in appropriately selected patients with urothelial carcinoma of the bladder: a population-based matched analysist. Urology. 2009; 74:858-64.
  • 19
    Shahbaz M, Ammar A, Wang Y, Farhaj Z, Qiao L, Niu J. Endoclips as novel fiducial markers in trimodality bladder-preserving therapy of muscle-invasive bladder carcinoma: feasibility and patient outcomes. Int Braz J Urol. 2021; 47:93-99.
  • 20
    Rödel C, Dunst J, Grabenbauer GG, Kühn R, Papadopoulos T, Schrott KM, et al. Radiotherapy is an effective treatment for high-risk T1-bladder cancer. Strahlenther Onkol. 2001; 177:82-8.
  • 21
    Akçetin Z, Todorov J, Tüzel E, Engehausen DG, Krause FS, Sauer R, et al. Radiochemotherapy after transurethral resection is an effective treatment method in T1G3 bladder cancer. Anticancer Res. 2005; 25 (3A):1623-8.
  • 22
    Weiss C, Wolze C, Engehausen DG, Ott OJ, Krause FS, Schrott KM, et al. Radiochemotherapy after transurethral resection for high-risk T1 bladder cancer: an alternative to intravesical therapy or early cystectomy? J Clin Oncol. 2006; 24:2318-24.
  • 23
    Kano H, Miwa S, Koshida K, Kawai K. Successful Treatment of a Large Superficial Bladder Cancer with Neoadjuvant Arterial Infusion Chemotherapy: A Case Report. Case Rep Oncol. 2018; 11:383-7.
  • 24
    Witjes JA, Compérat E, Cowan NC, De Santis M, Gakis G, Lebrét T, et al. EAU Guidelines on Muscle-invasive and Metastatic Bladder Cancer: Summary of the 2020 Guidelines. Eur Urol. 2021;79:82-104. 
  • 25
    Amling CL, Thrasher JB, Frazier HA, Dodge RK, Robertson JE, Paulson DF. Radical cystectomy for stages Ta, Tis and T1 transitional cell carcinoma of the bladder. J Urol. 1994; 151:31-5.
  • 26
    Racioppi M, Di Gianfrancesco L, Ragonese M, Palermo G, Sacco E, Bassi PF. Can Neutrophil-to-Lymphocyte ratio predict the response to BCG in high-risk non muscle invasive bladder cancer? Int Braz J Urol. 2019; 45:315-24.
  • 27
    Moschini M, Stabile A, Mattei A, Montorsi F, Cathelineau X, Sanchez-Salas R. Enhanced recovery after surgery (ERAS) in radical cystectomy patients: from consensus to evidences. Int Braz J Urol. 2019; 45:655-7.
  • 28
    Santoyo Vargas J, Castillo-Cobaleda DF, García-Perdomo HA. Aplicación del protocolo ERAS (Enhanced Recovery After Surgery) en cistectomía radical [Applying the ERAS (Enhanced Recovery After Surgery) protocol in radical cystectomy]. Arch Esp Urol. 2020; 73:600-10.
  • 29
    Warrick JI, Knowles MA, Yves A, van der Kwast T, Grignon DJ, Kristiansen G, et al. Report From the International Society of Urological Pathology (ISUP) Consultation Conference On Molecular Pathology Of Urogenital Cancers. II. Molecular Pathology of Bladder Cancer: Progress and Challenges. Am J Surg Pathol. 2020; 44:e30-e46.

Publication Dates

  • Publication in this collection
    25 July 2022
  • Date of issue
    May-Jun 2022

History

  • Received
    24 Apr 2021
  • Accepted
    07 May 2021
  • Published
    20 June 2021
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