| Bladder cancer |
| Classification and external resources |
Histopathology of urothelial carcinoma of the urinary bladder. Transurethral biopsy. H&E stain.
|
| ICD-10 |
C67, C67.9 |
| ICD-9 |
188 |
| OMIM |
109800 |
| DiseasesDB |
1427 |
| MedlinePlus |
000486 |
| eMedicine |
radio/711 med/2344 med/3022 |
| MeSH |
D001749 |
Bladder cancer is any of several types of malignancy arising from the epithelial lining (i.e., the urothelium) of the urinary bladder. Rarely the bladder is involved by non-epithelial cancers, such as lymphoma or sarcoma, but these are not ordinarily included in the colloquial term "bladder cancer." It is a disease in which abnormal cells multiply without control in the bladder.[1] The bladder is a hollow, muscular organ that stores urine; it is located in the pelvis. The most common type of bladder cancer recapitulates the normal histology of the urothelium and is known as transitional cell carcinoma or more properly urothelial cell carcinoma. It is estimated that there are 383,000 cases of bladder cancer worldwide.[2]
Contents
- 1 Signs and symptoms
- 2 Causes
- 3 Prevention
- 4 Diagnosis
- 4.1 Pathological classification
- 4.2 Staging
- 5 Screening
- 6 Treatment
- 7 Epidemiology
- 8 References
- 9 External links
Signs and symptoms
Location of bladder cancer
Bladder cancer characteristically causes blood (redness) in the urine. This blood in the urine may be visible to the naked eye (gross/macroscopic hematuria) or detectable only by microscope (microscopic hematuria). Hematuria is the most common symptom in bladder cancer.
Other possible symptoms include pain during urination, frequent urination, or feeling the need to urinate without being able to do so. These signs and symptoms are not specific to bladder cancer, and are also caused by non-cancerous conditions, including prostate infections, over-active bladder and cystitis. There are many other causes of haematuria, such as bladder or ureteric stones, infection, kidney disease, kidney cancers and vascular malformations.
Causes
Tobacco smoking is the main known contributor to urinary bladder cancer; in most populations, smoking is associated with over half of bladder cancer cases in men and one-third of cases among women.[3] There is a linear relationship between smoking and risk, and quitting smoking reduces the risk.[4] Passive smoking has not been proven to be involved.[5]
In a 10-year study involving almost 48,000 men, researchers found that men who drank 1.5 liters of water per day had a significantly reduced incidence of bladder cancer when compared with men who drank less than 240mL (around 1 cup) per day. The authors proposed that bladder cancer might partly be caused by the bladder directly contacting carcinogens that are excreted in urine, although this has not yet been confirmed in other studies.[6]
Thirty percent of bladder tumors probably result from occupational exposure in the workplace to carcinogens such as benzidine. 2-Naphthylamine, which is found in cigarette smoke, has also been shown to increase bladder cancer risk. Occupations at risk are bus drivers, rubber workers, motor mechanics, leather (including shoe) workers, blacksmiths, machine setters, and mechanics.[7] Hairdressers are thought to be at risk as well because of their frequent exposure to permanent hair dyes.
It has been suggested that mutations at HRAS, KRAS2, RB1, and FGFR3 may be associated in some cases.[8]
Prevention
A 2008 study commissioned by the World Health Organisation concluded that "specific fruit and vegetables may act to reduce the risk of bladder cancer."[6] Fruit and yellow-orange vegetables, particularly carrots and those containing selenium,[9] are probably associated with a moderately reduced risk of bladder cancer. Citrus fruits and cruciferous vegetables were also identified as having a possibly protective effect. However an analysis of 47,909 men in the Health Professionals Follow-Up Study showed little correlation between cancer reduction and high consumption of fruits and vegetables overall, or yellow or green leafy vegetables specifically, compared to the statistically significant reduction among those men who consumed large amounts of cruciferous vegetables.
Several studies have suggested the bladder is one of the most responsive organs to induction of detoxification enzymes by extract. This was evident in human bladder cancer cells in vitro and in animal models in vivo. Sulforaphane and broccoli sprout extract were also observed to induce apoptosis and cell cycle arrest in human bladder cancer cells in vitro, an anti-cancer effect attributed to the sulforaphane potential in the sprouts.[10][11][12][13]
Diagnosis
Bladder tumor in FDG PET due to the high physiological FDG-concentration in the bladder, furosemide was supplied together with 200 MBq FDG. The uptake cranial to the lesion is a physiological uptake in the colon.
Many patients with a history, signs, and symptoms suspicious for bladder cancer are referred to a urologist or other physician trained in cystoscopy, a procedure in which a flexible tube bearing a camera and various instruments is introduced into the bladder through the urethra. Suspicious lesions may be biopsied and sent for pathologic analysis.[citation needed]
The gold standard for diagnosing bladder cancer is biopsy obtained during cystoscopy. Sometimes it is an incidental finding during cystoscopy.[14] Urine cytology can be obtained in voided urine or at the time of the cystoscopy ("bladder washing"). Cytology is not very sensitive (a negative result cannot reliably exclude bladder cancer).[15] There are newer non-invasive urine bound markers available as aids in the diagnosis of bladder cancer, including human complement factor H-related protein, high-molecular-weight carcinoembryonic antigen, and nuclear matrix protein 22 (NMP22).[16] NMP22 is also available as a prescription home test. Other non-invasive urine based tests include the CertNDx Bladder Cancer Assay, which combines FGFR3 mutation detection with protein and DNA methylation markers to detect cancers across stage and grade, UroVysion, and Cxbladder.
The diagnosing of bladder cancer can also be done with a Hexvix/Cysview guided fluorescence cystoscopy (blue light cystoscopy, Photodynamic diagnosis), as an adjunct to conventional white-light cystoscopy. This procedure improves the detection of bladder cancer and reduces the rate of early tumor recurrence, compared with white light cystoscopy alone. Cysview cystoscopy detects more cancer and reduce recurrency. Cysview is marketed in Europe under the brand name Hexvix [17][18][19][20]
However, visual detection in any form listed above, is not sufficient for establishing pathological classification, cell type or the stage of the present tumor. A so-called cold cup biopsy during an ordinary cystoscopy (rigid or flexible) will not be sufficient for pathological staging either. Hence, a visual detection needs to be followed by transurethral surgery. The procedure is called transurethral resection (TUR). Further, bimanual examination should be carried out before and after the TUR to assess whether there is a palpable mass or if the tumour is fixed ("tethered") to the pelvic wall. The pathological classification obtained by the TUR-procedure, is of fundamental importance for making the appropriate choice of ensuing treatment and/or follow-up routines.[21]
Pathological classification
90% of bladder cancers are transitional cell carcinoma. The other 10% are squamous cell carcinoma, adenocarcinoma, sarcoma, small cell carcinoma, and secondary deposits from cancers elsewhere in the body.[citation needed]
Carcinoma in situ (CIS) invariably consists of cytologically high grade tumour cells.[citation needed]
Staging
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
- 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)
- T4a Tumour invades prostate, uterus or vagina
- T4b Tumour invades pelvic wall or abdominal wall
N (Lymph nodes)
- NX Regional lymph nodes cannot be assessed
- N0 No regional lymph node metastasis
- N1 Metastasis in a single lymph node 2 cm or less in greatest dimension
- N2 Metastasis in a single lymph node more than 2 cm but not more than 5 cm in greatest dimension,or multiple lymph nodes, none more than 5 cm in greatest dimension
- N3 Metastasis in a lymph node more than 5 cm in greatest dimension
M (Distant metastasis)
- MX Distant metastasis cannot be assessed
- M0 No distant metastasis
- M1 Distant metastasis.
[22]
Screening
As of 2010 there is insufficient evidence to determine if screening for bladder cancer in people without symptoms is effective or not.[23]
Devices are being tested (one involved a preliminary, small study of 98 samples of urine, all from men- 24 who had cancer, and 74 with bladder-related problems but no cancer yet) in which the heating of urine samples causes chemicals in the urine to release certain gases, and are detected by the device, presumably because of irregularities in the chemicals and gases. The researchers became interested in such a method after hearing that dogs could be trained to detect cancer-related odors.[24]
Treatment
Flow chart of the Bladder Cancer Treatment Guide
Attenuated strain of M. bovis used in the treatment of bladder cancer
The treatment of bladder cancer depends on how deep the tumor invades into the bladder wall. Superficial tumors (those not entering the muscle layer) can be "shaved off" using an electrocautery device attached to a cystoscope, which in that case is called a resectoscope. The procedure is called transurethral resection—TUR—and serves primarily for pathological staging. In case of non-muscle invasive bladder cancer the TUR is in itself the treatment, but in case of muscle invasive cancer, the procedure is insufficient for final treatment.[21]
Immunotherapy by intravesicular delivery of Bacillus Calmette–Guérin is also used to treat and prevent the recurrence of superficial tumors.[25] Bacillus Calmette–Guérin is a vaccine against tuberculosis that is prepared from attenuated (weakened) live bovine tuberculosis bacillus, Mycobacterium bovis, that has lost its virulence in humans. BCG immunotherapy is effective in up to 2/3 of the cases at this stage, and in randomized trials has been shown to be superior to standard chemotherapy.[26] The mechanism by which BCG prevents recurrence is unknown, but the presence of bacteria in the bladder may trigger a localized immune reaction which clears residual cancer cells.[27]
Instillations of chemotherapy, such as valrubicin (Valstar) into the bladder, can also be used to treat BCG-refractory CIS disease when cystectomy is not an option.[28] The drug Urocidin is currently in Phase III of trials for this procedure.[29]
Patients whose tumors recurred after treatment with BCG are more difficult to treat.[30] Many physicians recommend cystectomy for these patients. This recommendation is in accordance with the official guidelines of the European Association of Urologists (EAU)[31] and the American Urological Association (AUA)[32] However, many patients refuse to undergo this life changing operation, and prefer to try novel conservative treatment options before opting to this last radical resort. Device assisted chemotherapy is one such group of novel technologies used to treat superficial bladder cancer.[33] These technologies use different mechanisms to facilitate the absorption and action of a chemotherapy drug instilled directly into the bladder. Another technology uses an electrical current to enhance drug absorption.[34] Another technology, thermotherapy, uses radio-frequency energy to directly heat the bladder wall, which together with chemotherapy shows a synergistic effect, enhancing each other's capacity to kill tumor cells. This technology was studied by different investigators.[35][36][37][38]
Untreated, superficial tumors may gradually begin to infiltrate the muscular wall of the bladder. Tumors that infiltrate the bladder require more radical surgery where part or all of the bladder is removed (a cystectomy) and the urinary stream is diverted into an isolated bowel loop (called an ileal conduit or Urostomy). In some cases, skilled surgeons can create a substitute bladder (a neobladder) from a segment of intestinal tissue, but this largely depends upon patient preference, age of patient, renal function, and the site of the disease.
A combination of radiation and chemotherapy can also be used to treat invasive disease. It has not yet been determined how the effectiveness of this form of treatment compares to that of radical ablative surgery.
Photodynamic diagnosis may improve surgical outcome on bladder cancer.[39]
For muscle invasive urothelial urinary bladder cancer there are a number of treatment options. Gold standard is radical cystectomy as mentioned. In males this usually includes also the removal of the prostate and in females; ovaries, uterus and parts of the vagina. In order to address the problem of micrometastatic disease which in itself has implications on longtime survival, new treatment options are dearly needed. Micrometastatic dissemination is often not treatable with only major surgery and the concept of neoadjuvant chemotherapy has evolved. In a number of meta-analyses of randomised prospective trials worldwide, the results have shown survival benefits between 5–8% with this therapy, in a follow up time of 5 years.[40][41][42][43] Thus patients first receive chemotherapy in 3 or 4 cycles, and first after that proceed to major surgery.
Epidemiology
Age-standardized death from bladder cancer per 100,000 inhabitants in 2004.[44]
no data
less than 1.5
1.5–3
3–4.5
4.5–6
6–7.5
7.5–9
9–10.5
10.5–12
12–13.5
13.5–15
15–16.5
more than 16.5
Globally, in 2010, bladder cancer resulted in 170,000 deaths up from 114,000 in 1990.[45]
In the United States, bladder cancer is the fourth most common type of cancer in men and the ninth most common cancer in women. More than 50,000 men and 16,000 women are diagnosed with bladder cancer each year. Smoking can only partially explain this higher incidence in men.[46] One other reason is that the androgen receptor, which is much more active in men than in women, plays a major part in the development of the cancer.[47]
References
- ^ Bladder cancer at Mount Sinai Hospital
- ^ "Bladder — Estimated incidence, all ages: both sexes". GLOBOCAN 2008: Estimated cancer Incidence, Mortality, Prevalence and Disability-adjusted life years (DALYs) Worldwide in 2008. International Agency for Research on Cancer (IARC), World Health Organization.
- ^ Zeegers MP; Tan, FE; Dorant, E; Van Den Brandt, PA (2000). "The impact of characteristics of cigarette smoking on urinary tract cancer risk: a meta-analysis of epidemiologic studies". Cancer 89 (3): 630–9. doi:10.1002/1097-0142(20000801)89:3<630::AID-CNCR19>3.0.CO;2-Q. PMID 10931463.
- ^ Boffetta P (2008). "Tobacco smoking and risk of bladder cancer". Scand J Urol Nephrol Suppl 42 (S218): 45–54. doi:10.1080/03008880802283664. PMID 18815916.
- ^ Zeegers MP; Goldbohm, RA; Van Den Brandt, PA (2002). "A prospective study on active and environmental tobacco smoking and bladder cancer risk". Cancer Causes Control 13 (1): 83–90. doi:10.1023/A:1013954932343. PMID 11899922.
- ^ a b Brinkman M, Zeegers MP (September 2008). "Nutrition, total fluid and bladder cancer". Scandinavian Journal of Urology and Nephrology. Supplementum 42 (218): 25–36. doi:10.1080/03008880802285073. PMID 18815914.
- ^ Reulen RC, Zeegers MP (September 2008). "A meta-analysis on the association between bladder cancer and occupation". Scandinavian journal of urology and nephrology. Supplementum 42 (218): 64–78. doi:10.1080/03008880802325192. PMID 18815919.
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 109800
- ^ Brinkman M, Zeegers MP (2006). "Use of selenium in chemoprevention of bladder cancer". Lancet Oncol 7 (9): 766–74. doi:10.1016/S1470-2045(06)70862-2. PMID 16945772.
- ^ Journal of the National Cancer Institute, 1999, 91(7):605–613.
- ^ J. Nutrition, 2004, 134:2004–2010.
- ^ Mol. Cancer Ther., 2006, 5(4):935–944
- ^ Cancer Research, 2008, 68(5):1593–1600.
- ^ Walid MS, Heaton RL (2008). "Can posthysterectomy cystoscopy be utilized as a screening test for bladder cancer?". German Medical Science 6: Doc13. PMC 2703254. PMID 19675739.
- ^ Lotan, Y.; Roehrborn, C. G. (2003). "Sensitivity and specificity of commonly available bladder tumor markers versus cytology: Results of a comprehensive literature review and meta-analyses". Urology 61 (1): 109–118; discussion 118. doi:10.1016/S0090-4295(02)02136-2. PMID 12559279. edit
- ^ Shariat et al.; Karam, JA; Lotan, Y; Karakiewizc, PI (2008). "Critical Evaluation of Urinary Markers for Bladder Cancer Detection and Monitoring". Reviews in Urology 10 (2): 120–135. PMC 2483317. PMID 18660854.
- ^ http://www.hexvix.com
- ^ "Photocure—Cysview Hexaminolevulinate (HCL)". Cysview.net. Retrieved 2013-01-10.
- ^ http://urotoday.com/bladder-cancer-1038/fluorescence-guided-transurethral-resection-of-bladder-tumours-reduces-bladder-tumour-recurrence-due-to-less-residual-tumour-tissue-in-t-at1-patients-a-randomized-two-centre-study-abstract.html Fluorescence-guided transurethral resection of bladder tumours reduces bladder tumour recurrence due to less residual tumour tissue in Ta/T1 patients
- ^ Hexvix guided fluorescence cystoscopy reduces recurrence in patients
- ^ a b "European Association of Urology (EAU)—Guidelines—Online Guidelines". Uroweb.org. Retrieved 2013-01-10.
- ^ Longe, Jacqueline L. (2005). Gale Encyclopedia Of Cancer: A Guide To Cancer And Its Treatments. Detroit: Thomson Gale. p. 137. ISBN 978-1-4144-0362-5.
- ^ Chou R, Dana T (October 2010). "Screening adults for bladder cancer: a review of the evidence for the U.S. preventive services task force". Ann. Intern. Med. 153 (7): 461–8. doi:10.1059/0003-4819-153-7-201010050-00009. PMID 20921545.
- ^ http://www.bbc.co.uk/news/health-23231195
- ^ Alexandroff AB, Jackson AM, O'Donnell MA, James K (May 1999). "BCG immunotherapy of bladder cancer: 20 years on". Lancet 353 (9165): 1689–94. doi:10.1016/S0140-6736(98)07422-4. PMID 10335805.
- ^ Lamm, Donald L.; Blumenstein, Brent A.; Crawford, E. David; Montie, James E.; Scardino, Peter; Grossman, H. Barton; Stanisic, Thomas H.; Smith Jr, Joseph A.; Sullivan, Jerry; Sarosdy, Michael F.; Crissman, John D.; Coltman, Charles A. (1991). "A Randomized Trial of Intravesical Doxorubicin and Immunotherapy with Bacille Calmette–Guérin for Transitional-Cell Carcinoma of the Bladder". New England Journal of Medicine 325 (17): 1205–9. doi:10.1056/NEJM199110243251703. PMC 1164610. PMID 1922207.
- ^ Bacillus Calmette-Guerin (BCG) for Bladder Cancer
- ^ Valstar Prescribing Information, available at
- ^ "Bioniche Earns $4M Milestone from Endo following Positive Phase III Urocidin Data". Nov 2010.
- ^ Witjes JA (May 2006). "Management of BCG failures in superficial bladder cancer: a review". European Urology 49 (5): 790–7. doi:10.1016/j.eururo.2006.01.017. PMID 16464532.
- ^ Babjuk W, Oosterlinck W, Sylvester R, et al. (2010). "Guidelines on TaT1 (Non-muscle invasive) Bladder Cancer". European Association of Urology.
- ^ Bladder Cancer Clinical Guideline Update Panel (2007). Bladder Cancer: Guideline for the Management of Nonmuscle Invasive Bladder Cancer: (Stages Ta,T1, and Tis): 2007 Update. American Urological Association. [page needed]
- ^ Witjes JA, Hendricksen K (January 2008). "Intravesical pharmacotherapy for non-muscle-invasive bladder cancer: a critical analysis of currently available drugs, treatment schedules, and long-term results". European Urology 53 (1): 45–52. doi:10.1016/j.eururo.2007.08.015. PMID 17719169.
- ^ Di Stasi SM, Riedl C (June 2009). "Updates in intravesical electromotive drug administration of mitomycin-C for non-muscle invasive bladder cancer". World Journal of Urology 27 (3): 325–30. doi:10.1007/s00345-009-0389-x. PMID 19234707.
- ^ Nativ O, Witjes JA, Hendricksen K, et al. (October 2009). "Combined thermo-chemotherapy for recurrent bladder cancer after bacillus Calmette-Guerin". The Journal of Urology 182 (4): 1313–7. doi:10.1016/j.juro.2009.06.017. PMID 19683278.
- ^ Colombo R, Da Pozzo LF, Salonia A, et al. (December 2003). "Multicentric study comparing intravesical chemotherapy alone and with local microwave hyperthermia for prophylaxis of recurrence of superficial transitional cell carcinoma". Journal of Clinical Oncology 21 (23): 4270–6. doi:10.1200/JCO.2003.01.089. PMID 14581436.
- ^ Alfred Witjes J, Hendricksen K, Gofrit O, Risi O, Nativ O (June 2009). "Intravesical hyperthermia and mitomycin-C for carcinoma in situ of the urinary bladder: experience of the European Synergo working party". World Journal of Urology 27 (3): 319–24. doi:10.1007/s00345-009-0384-2. PMC 2694311. PMID 19234857.
- ^ Halachmi S, Moskovitz B, Maffezzini M, et al. (April 2009). "Intravesical mitomycin C combined with hyperthermia for patients with T1G3 transitional cell carcinoma of the bladder". Urologic Oncology 29 (3): 259–264. doi:10.1016/j.urolonc.2009.02.012. PMID 19395285.
- ^ O'Brien T, Thomas K (November 2010). "Bladder cancer: Photodynamic diagnosis can improve surgical outcome". Nature Reviews Urology 7 (11): 598–9. doi:10.1038/nrurol.2010.183. PMID 21068759.
- ^ Advanced Bladder Cancer (ABC) Meta-analysis Collaboration (August 2005). "Neoadjuvant chemotherapy in invasive bladder cancer: update of a systematic review and meta-analysis of individual patient data advanced bladder cancer (ABC) meta-analysis collaboration". Eur. Urol. 48 (2): 202–5; discussion 205–6. doi:10.1016/j.eururo.2005.04.006. PMID 15939524.
- ^ Grossman HB, Natale RB, Tangen CM, et al. (August 2003). "Neoadjuvant chemotherapy plus cystectomy compared with cystectomy alone for locally advanced bladder cancer". N. Engl. J. Med. 349 (9): 859–66. doi:10.1056/NEJMoa022148. PMID 12944571.
- ^ Hall R. Updated results of a randomised controlled trial of neoadjuvant cisplatin (C), methotrexate (m) and vinblastin (V) chemotherapy for muscle-invasive bladder cancer. Proc Am Soc Clin Oncol 2002;21:178A, abstr 710.
- ^ Sherif A, Holmberg L, Rintala E, et al. (March 2004). "Neoadjuvant cisplatinum based combination chemotherapy in patients with invasive bladder cancer: a combined analysis of two Nordic studies". Eur. Urol. 45 (3): 297–303. doi:10.1016/j.eururo.2003.09.019. PMID 15036674.
- ^ "WHO Disease and injury country estimates". World Health Organization. 2009. Retrieved 11 Nov 2009.
- ^ Lozano, R (15 December 2012). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet 380 (9859): 2095–128. doi:10.1016/S0140-6736(12)61728-0. PMID 23245604.
- ^ Hemelt M, Zeegers MP (2000). "The effect of smoking on the male excess of bladder cancer: a meta-analysis and geographical analyses". Int J Cancer 124 (2): 412–9. doi:10.1002/ijc.23856. PMID 18792102.
- ^ "Scientists Find One Reason Why Bladder Cancer Hits More Men". University of Rochester Medical Center. 20 April 2007. Retrieved 20 April 2007.
External links
- UK Support Charity www.fightbladdercancer.co.uk
- Bladder cancer at DMOZ
- Clinically reviewed bladder cancer information for patients, from Cancer Research UK
- UK bladder cancer statistics from Cancer Research UK
- Cancer.Net: Bladder Cancer
- Blue-light cystoscopy for non-muscle invasive bladder cancer. For HCP
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Tumors: urogenital neoplasia: urinary organs (C64–C68/D30, 188–189/223)
|
|
| Abdominal |
| Kidney |
| Glandular and epithelial neoplasm: |
- Renal cell carcinoma
- Renal oncocytoma
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|
| Complex and mixed tumor: |
- Wilms' tumor
- Mesoblastic nephroma
- Clear-cell sarcoma of the kidney
- Angiomyolipoma
- Cystic nephroma
- Metanephric adenoma
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|
| by location: |
- Renal medullary carcinoma
- Juxtaglomerular cell tumor
- Renal medullary fibroma
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| Ureter |
|
|
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| Pelvic |
| Bladder |
- Transitional cell carcinoma
- Inverted papilloma
- Squamous-cell carcinoma
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|
| Urethra |
- Transitional cell carcinoma
- Squamous-cell carcinoma
- Adenocarcinoma
- Melanoma
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|
|
| Retroperitoneum |
- Malignant fibrous histiocytoma
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noco/acba/cong/tumr, sysi/epon, urte
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proc/itvp, drug (G4B), blte, urte
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