Full Guidelines
Reproduced from the official EAU 2025 publication.
Recommendations
Recommendations for bladder cancer classification
| Recommendation | Strength rating |
|---|---|
| Use the 2017 TNM (Tumour, Node, Metastasis Classification) system for classification of the depth of tumour invasion (staging). | Strong |
| Provide T1 sub-stage if the lamina propria is adequately sampled using either micrometric (T1e and T1m) or histo- anatomic (T1a and T1b) principles. | Weak |
| Use both the 1973 and 2004/2022 World Health Organization (WHO) grading classification systems, or a hybrid system. | Weak |
| Do not use the term 'superficial bladder cancer'. | Strong |
Recommendations for the primary assessment of NMIBC
| Recommendation | Strength rating |
|---|---|
| Take a patient history, focusing on urinary tract symptoms and haematuria. | Strong |
| Use renal and bladder ultrasound and/ or computed tomography-intravenous urography (CT-IVU) during the initial work- up in patients with haematuria. | Strong |
| Once a bladder tumour has been detected, perform a CT urography in selected cases (e.g., tumours located in the trigone, multiple- or high-risk tumours). | Strong |
| If an MRI is performed for local staging of bladder cancer it should be done before TURB. | Strong |
| Perform cystoscopy in patients with symptoms suggestive of bladder cancer or during surveillance. It cannot be replaced by cytology or by any other non-invasive test. | Strong |
| Use a flexible cystoscope, if available, in both men and women. In men apply irrigation ‘bag squeeze’ to decrease procedural pain when passing the proximal urethra. | Strong |
| Describe all macroscopic features of the tumour (site, size, number, and appearance) and mucosal abnormalities during cystoscopy. Use a bladder diagram. | Strong |
| Use voided urine cytology as an adjunct to cystoscopy to detect high-grade tumour. | Strong |
| Perform cytology on at least 25 mL fresh urine or urine with adequate fixation. First morning urine is not suitable because of the frequent presence of cytolysis. | Strong |
| Use the Paris System 2nd Edn., for cytology reporting. | Strong |
Recommendations for transurethral resection of the bladder (TURB), biopsies and pathology report
| Recommendation | Strength rating |
|---|---|
| Perform a TURB followed by pathology investigation of the obtained specimen(s) as a diagnostic procedure and initial treatment step in patients suspected of having bladder cancer. | Strong |
| Perform TURB systematically in individual steps: • bimanual palpation under anaesthesia before starting the procedure and at the end; • insertion of the resectoscope, under visual control with inspection of the whole urethra; • inspection of the whole urothelial lining of the bladder; • biopsy from the prostatic urethra (if indicated); • cold-cup bladder biopsies (if indicated); • resection of the tumour; • recording of findings in the surgery report/record including visual impression of grade/stage; • precise description of the specimen(s) for pathology evaluation. | Strong |
| Performance of individual steps | |
| Perform en-bloc resection or resection in fractions (exophytic part of the tumour, the underlying bladder wall and the edges of the resection area). | Strong |
| Avoid cauterisation as much as possible during TURB to avoid tissue deterioration. | Strong |
| Take biopsies from abnormal-looking urothelium. | Strong |
| Take multiple biopsies (mapping biopsies from the trigone, bladder dome, right, left, anterior and posterior bladder wall) or perform fluorescence-guided (PDD) biopsies, in case of normal looking urothelium and positive urine cytology. | Strong |
| Take a sample of the prostatic urethra if there is positive urine cytology without evidence of tumour in the bladder, or if abnormalities of the prostatic urethra are visible. | Strong |
| Take a sample biopsy of the prostatic urethra in cases of bladder neck tumour, suspicion of bladder CIS and/or T1 disease. If a sample was not taken during the initial procedure, it should be performed at the time of second resection, if the latter is needed. | Weak |
| Use methods to improve tumour visualisation (fluorescence cystoscopy, narrow-band imaging) during TURB, if available. | Weak |
| Refer the specimens from different biopsies and resection fractions to the pathologist in separately labelled containers. Submit the tumour base separately especially in large and multifocal tumours or when en-bloc resection is not feasible. | Weak |
| The TURB record must describe tumour location, appearance, size and multifocality, all steps of the procedure, extent, macroscopic completeness of resection as well as any complications. | Strong |
| In patients with positive cytology, but negative cystoscopy, exclude an upper tract urothelial carcinoma, CIS in the bladder (by mapping biopsies or PDD- guided biopsies) and tumour in the prostatic urethra (by prostatic urethra biopsy). | Strong |
| Perform a second TURB in the following situations: • after incomplete initial TURB, or in case of doubt about completeness of a TURB; • if there is no detrusor muscle in the specimen after initial resection, with the exception of Ta LG/G1 tumours and primary CIS; • in T1 tumours. | Strong |
| If indicated, perform a second TURB within two to six weeks after the initial resection. This second TURB should include resection of the primary tumour site. | Weak |
| Record the pathology results of the second TURB as it reflects the quality of the initial resection. | Weak |
| Inform the pathologist of prior treatments (intravesical therapy, radiotherapy, etc.). | Strong |
| The pathological report should specify tumour location, tumour grade and stage, lymphovascular invasion, subtypes of urothelial carcinoma, presence of CIS and detrusor muscle. | Strong |
Recommendations for stratification of non-muscle invasive bladder cancer
| Recommendation | Strength rating |
|---|---|
| Stratify patients into four risk groups to predict progression groups according to Table 2. A patient’s risk group can be determined by using the 2021 EAU risk group calculator available at www.nmibc.net. | Strong |
| For information about the risk of disease progression in a patient with primary TaT1 tumours not treated with bacillus Calmette-Guerin (BCG), use the data from Table 3. | Strong |
| Use the 2006 EORTC scoring model to predict the risk of tumour recurrence in individual patients not treated with BCG. | Strong |
| Use the 2016 EORTC scoring model or the CUETO risk scoring model to predict the risk of tumour recurrence in individual patients treated with BCG intravesical immunotherapy (the 2016 EORTC model is calculated for one to three year of maintenance, the CUETO model for five to six months). | Strong |
General recommendations for adjuvant therapy in TaT1 tumours and for therapy of carcinoma in situ (CIS)
| Recommendation | Strength rating |
|---|---|
| Counsel smokers to stop smoking. | Strong |
| The type of further therapy after transurethral resection of the bladder (TURB) should be based on the risk groups shown in Table 2. For determination of a patient’s risk group use the 2021 EAU risk group calculator available at www.nmibc.net. | Strong |
| In patients with tumours presumed to be at low risk and in those with small papillary recurrences (presumably Ta LG/ G1) detected more than one year after previous TURB, offer one immediate single chemotherapy instillation. | Strong |
| Offer post-operative saline or water continuous irrigation of the bladder to patients who cannot receive a single instillation of chemotherapy. | Strong |
| Patients with small recurrent low grade Ta tumours can be effectively and safely offered office fulguration. | Strong |
| Offer active surveillance and/or chemoablation to selected patients with presumed low-grade tumours as an alternative to endoscopic ablation. | Weak |
| In patients with high-risk tumours, full-dose intravesical bacillus Calmette-Guérin (BCG) for one to three years (induction plus three- weekly instillations at 3, 6, 12, 18, 24, 30 and 36 months), is indicated. The additional beneficial effect of the second and third years of maintenance should be weighed against its added costs, side effects and access to BCG. Immediate radical cystectomy (RC) may also be discussed with the patient. | Strong |
| Discuss immediate RC in patients with very high-risk tumours. Intravesical full-dose BCG instillations for one to three years remains an option for selected patients, particularly those who decline or are unfit for RC. | Strong |
| Offer transurethral resection of the prostate, followed by intravesical instillation of BCG to patients with Carcinoma in situ (CIS) in the epithelial lining of the prostatic urethra if a bladder sparing strategy is considered. | Weak |
| Cautiously offer quinolones to treat BCG- related side effects*. | Weak |
| The definition of ‘BCG unresponsive’ should be respected as it most precisely defines the patients who are unlikely to respond to further BCG instillations. | Strong |
| Offer a RC to patients with BCG unresponsive tumours. | Strong |
| Offer patients with BCG unresponsive tumours, who are not candidates for RC due to comorbidities, preservation strategies (intravesical chemotherapy, chemotherapy and microwave-induced hyperthermia, electromotive administration of chemotherapy, intravesical- or systemic immunotherapy; preferably within clinical trials). | Weak |
| Discuss high-risk and very high-risk patients within a multidisciplinary board, when possible. | Weak |
| Recommendations – technical aspects for treatment | |
| Intravesical chemotherapy | |
| If given, administer a single immediate instillation of chemotherapy within 24 hours after TURB. | Weak |
| Omit a single immediate instillation of chemotherapy in any case of overt or suspected bladder perforation or bleeding requiring bladder irrigation. | Strong |
| The optimal schedule and duration of further intravesical chemotherapy instillation is not defined; however, it should not exceed one year. | Weak |
| If intravesical chemotherapy is given, use the drug at its optimal pH and maintain the concentration of the drug by reducing fluid intake before and during instillation. | Strong |
| The length of individual instillation should be a minimum of one, and up to two hours. | Weak |
| BCG intravesical immunotherapy | |
| Absolute contraindications of BCG intravesical instillation are: • during the first two weeks after TURB; • in patients with visible haematuria; • after traumatic catheterisation; • in patients with symptomatic urinary tract infection. | Strong |
Recommendations for the treatment of TaT1 tumours and carcinoma in situ according to risk stratification
| Recommendation | Strength rating |
|---|---|
| EAU risk group: Low | |
| Offer one immediate instillation of intravesical chemotherapy after transurethral resection of the bladder (TURB). | Strong |
| EAU Risk Group: Intermediate | |
| In general, chemotherapy (the optimal schedule is unknown) is a reasonable first-line option in the majority of patients. One-year full-dose BCG treatment (induction plus three-weekly instillations at 3, 6 and 12 months), is an alternative option. The final choice should reflect the individual patient’s risk of recurrence and progression as well as the efficacy and side effects of each treatment modality. Offer one immediate chemotherapy instillation to patients with small papillary recurrences detected more than one year after previous TURB. | Strong |
| EAU risk group: High | |
| Offer intravesical full-dose BCG instillations for one to three years but discuss immediate radical cystectomy (RC). | Strong |
| EAU risk group: Very High | |
| Offer RC or intravesical full-dose bacillus Calmette-Guérin (BCG) instillations for one to three years, particularly to those who decline or are unfit for RC. | Strong |
Recommendations for follow-up of patients after transurethral resection of the bladder for NMIBC
| Recommendation | Strength rating |
|---|---|
| Base follow-up of TaT1 tumours and carcinoma in situ (CIS) on regular cystoscopy. | Strong |
| Patients with low-risk Ta tumours should undergo cystoscopy at three months. If negative, subsequent cystoscopy is advised nine months later, and then yearly for five years. | Weak |
| Patients with intermediate-risk Ta low- grade tumours should undergo cystoscopy at three months. If negative, subsequent cystoscopy can be repeated every six months for two years, and then annually for ten years. The subgroup of intermediate- risk that are high-grade should be followed up as high-risk. | Weak |
| Patients with high-risk and those with very high-risk tumours treated conservatively should undergo cystoscopy and urinary cytology at three months. If negative, subsequent cystoscopy and cytology should be repeated every three months for a period of two years, and every six months thereafter until five years, and then annually lifelong. | Weak |
| Take regular and long-term upper tract imaging (computed tomography urography) for high-risk and very high-risk tumours. | Weak |
| Perform endoscopy under anaesthesia and bladder biopsies when office cystoscopy shows suspicious findings or if urinary cytology is positive. | Strong |
| During follow-up in patients with positive cytology and no visible tumour in the bladder, mapping biopsies or PDD-guided biopsies (if equipment is available) and investigation of extravesical locations (CT urography, prostatic urethra biopsy) are recommended. | Strong |
Classification & Evidence Tables
| T - Primary Tumour |
|---|
| TX Primary tumour cannot be assessed |
| T0 No evidence of primary tumour |
| Ta Non-invasive papillary carcinoma |
| Tis Carcinoma in situ: ’flat tumour’ |
| T1 Tumour invades subepithelial connective tissue |
| T2 Tumour invades muscle |
| T2a Tumour invades superficial muscle (inner half) |
| T2b Tumour invades deep muscle (outer half) |
| T3 Tumour invades perivesical tissue |
| T3a Microscopically |
| T3b Macroscopically (extravesical mass) |
| T4 Tumour invades any of the following: prostate stroma, seminal vesicles, uterus, vagina, pelvic wall, abdominal wall |
| T4a Tumour invades prostate stroma, seminal vesicles, uterus or vagina |
| T4b Tumour invades pelvic wall or abdominal wall |
| N – Regional Lymph Nodes |
| NX Regional lymph nodes cannot be assessed |
| N0 No regional lymph node metastasis |
| N1 Metastasis in a single lymph node in the true pelvis (hypogastric, obturator, external iliac, or presacral) |
| N2 Metastasis in multiple regional lymph nodes in the true pelvis (hypogastric, obturator, external iliac, or presacral) |
|---|
| N3 Metastasis in common iliac lymph node(s) |
| M - Distant Metastasis |
| M0 No distant metastasis |
| M1a Non-regional lymph nodes |
| M1b Other distant metastases |
| Risk Group | Description |
|---|---|
| Low Risk | • A primary, single, TaT1 LG/G1 tumour < 3 cm in diameter without CIS in a patient ≤ 70 years • A primary Ta LG/G1 tumour without CIS with at most ONE of the additional clinical risk factors |
| Intermediate Risk | • P atients without CIS who are not included in either the low-, high-, or very high-risk groups |
|---|---|
| High Risk | • A ll T1 HG/G3 without CIS, EXCEPT those included in the very high-risk group • A ll CIS patients, EXCEPT those included in the very high-risk group |
| Stage, grade with additional clinical risk factors: • T a LG/G2 or T1G1, no CIS with all 3 risk factors • T a HG/G3 or T1 LG, no CIS with at least 2 risk factors • T1G2 no CIS with at least 1 risk factor | |
| Very High Risk | Stage, grade with additional clinical risk factors: • T a HG/G3 and CIS with all 3 risk factors • T 1 G2 and CIS with at least 2 risk factors • T 1 HG/G3 and CIS with at least 1 risk factor • T1 HG/G3 no CIS with all 3 risk factors |
| Risk group | Probability of Progression and 95% Confidence Interval (CI) | ||
|---|---|---|---|
| 1 Year | 5 Years | 10 Years | |
| New Risk Groups with WHO 2004/2016 | |||
| Low | 0.06% (CI: 0.01%−0.43%) | 0.93% (CI: 0.49%−1.7%) | 3.7% (CI: 2.3%−5.9%) |
| Intermediate | 1.0% (CI: 0.50%−2.0%) | 4.9% (CI: 3.4%−7.0%) | 8.5% (CI: 5.6%−13%) |
| High | 3.5% (CI: 2.4%−5.2%) | 9.6% (CI: 7.4%−12%) | 14% (CI: 11%−18%) |
| Very High | 16% (CI: 10%−26%) | 40% (CI: 29%−54%) | 53% (CI: 36%−73%) |
| New Risk Groups with WHO 1973 | |||
| Low | 0.12% (CI: 0.02%−0.82%) | 0.57% (CI: 0.21%−1.5%) | 3.0% (CI: 1.5%−6.3%) |
| Intermediate | 0.65% (CI: 0.36%−1.2%) | 3.6% (CI: 2.7%−4.9%) | 7.4% (CI: 5.5%−10%) |
| High | 3.8% (CI: 2.6%−5.7%) | 11% (CI: 8.1%−14%) | 14% (CI: 10%−19%) |
| Very High | 20% (CI: 12%−32%) | 44% (CI: 30%−61%) | 59% (CI: 39%−79%) |
| Whenever a MIBC is detected during follow-up. |
|---|
| BCG-refractory tumour |
| 1. If T1 HG/G3 tumour is present at three months. |
| 2. If Ta HG/G3 tumour is present after three months and/ or at 6 months, after either re-induction or first course of maintenance. |
| 3. If CIS (without concomitant papillary tumour) is present at three months and persists at six months after either re-induction or first course of maintenance. If patients with CIS present at three months, an additional BCG course can achieve a complete response in > 50% of cases. |
| 4. If HG tumour appears during BCG maintenance therapy*. |
| BCG-relapsing tumour |
| Recurrence of HG/G3) tumour after completion of BCG maintenance, despite an initial response. |
| BCG unresponsive tumour |
|---|
| BCG-unresponsive tumours include all BCG refractory tumours and those who develop T1/Ta HG recurrence within six months of completion of adequate BCG exposure** or develop CIS within twelve months of completion of adequate BCG exposure. |
| BCG-exposed tumour |
| 1. If Ta HG/G3 or CIS is present at three months evaluation after induction BCG only. |
| 2. Delayed relapse after adequate or inadequate BCG. |
| BCG intolerance |
| Severe side effects that prevent further BCG instillation before completing treatment. |
| Category | Treatment options |
|---|---|
| BCG-unresponsive | 1. Radical cystectomy (RC). 2. E nrolment in clinical trials assessing new treatment strategies. 3. O ther bladder-preserving strategies in patients ineligible for or refusing RC. |
| BCG-relapsing: TaT1 HG recurrence > 6 months or CIS > 12 months since last BCG exposure | 1. Radical cystectomy or repeat BCG course according to a patient’s individual situation. 2. Enrolment in clinical trials assessing new treatment strategies. 3. Other bladder-preserving strategies. |
| BCG exposed | 1. R epeat BCG course or RC according to a patient’s individual situation. 2. E nrolment in clinical trials assessing new treatment strategies. |
| LG recurrence after BCG for primary intermediate-risk tumour | 1. R epeat BCG or intravesical chemotherapy. 2. E nrolment in clinical trials assessing new treatment strategies. |