2. Tumours of the urinary system - urothelial and renal cancer Flashcards

(45 cards)

1
Q

what areas are affected by urothelial cancers

A
bladder
upper tract (ie ureter, renal pelvis, collecting system)
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2
Q

define what urothelial tumours are

A

malignant tumours of the lining transitional cell epithelium (urothelium)

can occur at any point from renal calyces to tip of the urethra

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3
Q

what is the most common site of urothelial cancers

A

bladder - make up 90% cases

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4
Q

what are the different types of bladder cancer

A

transitional cell carcinoma (TCC) - most common

squamous cell carcinoma

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5
Q

what are three risk factors for TC

A

smoking (accounts for 40% of cases)

aromatic amines

non-hereditary genetic abnormalities (e.g. TSG incl. p53 and Rb)

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6
Q

what are five risk factors for squamous cell carcinoma

A

Schistosomiasis (S. haematobium only)

chronic cystitis (e.g. recurrent UTI, long term catheter, bladder stone)

cyclophosphamide therapy

pelvic radiotherapy

Adenocarcinoma
-Urachal

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7
Q

what are the most common presenting features of bladder cancer

A

**painless visible haematuria
(BUT haematuria can be frank or microscopic )

others

  • recurrent UTI
  • storage bladder symptoms (dysuria, frequency, nocturia, urgency +/- urge)
  • pain
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8
Q

what investigations should be done to investigate the haematuria

A

urine culture
- majority of painful haematuria = UTI

cystourethoscopy
- commonest neoplastic cause is TCC bladder

Upper tract imagine

  • CT urogram (IVU)
  • US scan

urine cytology
- limited use in dipstick haematuria

BP

U&E’s

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9
Q

what is the risk of malignancy in >50yrs with FRANK haematuria

A

25-35%

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10
Q

what investigations should be done if there is FRANK haematuria

A

Flexible cystourethroscopy within 2 weeks

Ct urogram & USS

Urine Cytology may also be useful (but not very sensitive nor specific)

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11
Q

what is the risk of malignancy in >50yrs with DIPSTIX or MICROSCOPIC haematuria

A

5-10%

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12
Q

what investigations should be done if there is DIPSTIX or MICROSCOPIC haematuria

A

Flexible cystourethroscopy within 4-6 weeks

IVU & USS

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13
Q

why are IVU and USS used together

A

IVU alone will miss a proportion of renal cell tumours (especially if <3cm)

USS alone will miss a proportion of urothelial tumours of the upper tracts

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14
Q

How are bladder cancers diagnosed

A

cystoscopy and endoscopic resection (TURBT)

EUA to assess bladder mass/thickening before and after TURBT

TURBT = transurethral resection of bladder cancer

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15
Q

what investigations can help stage bladder cancer

A

cross sectional imagine (CT, MRI)

bone scan if symptomatic

CTU for upper tract TCC

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16
Q

how are bladder tumours classified

A

grade of tumour
stage of tumour

combined to describe TCC eg G1pTa

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17
Q

what are the grades (G) of TCC

A

G1 = Well diff. - commonly non-invasive

G2 = Mod. diff. - often non-invasive

G3 = Poorly diff. - often invasive

Carcinoma in situ (CIS) – non-muscle invasive but VERY aggressive (hence treated differently)

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18
Q

what are the stagings of TCC

A

TNM classification

T-stage

  • non-muscle invasive (or ‘superficial’)
  • muscle invasive

from Tis, Ta, T1, T2a, T2b, T3a, T3b, T4a, T4b - getting more invasive as number and letter go up

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19
Q

what determines treatment of bladder cancer

A

site
clinical stage
histological grade of tumour
patient age and co-morbidities

20
Q

how would you treat low grade non-muscle invasive tumours (i.e. Ta or T1)

A

endoscopic resection followed by single intravesical chemo (mitomycin) within 24hrs

prolonged endoscopic follow up

prolonged course of intravesical chemo for repeated recurrences

21
Q

how would you treat a high grade non-muscle invasive or CIS tumour

A

very aggressively

endoscopic resection alone not sufficient

intravesical BCG therapy - maintenance course weekly for 3 weeks repeated 6 monthly over 3 years

patients refractory to BCG - need radical surgery

22
Q

how would you treat muscle invasive bladder tumours (i.e. T2-T3)

A

neoadjuvant chemo fr local and systemic control followed by either:

  • radical radiotherapy
  • radical surgery
23
Q

what determines prognosis form bladder cancer

A
stage
grade
size
multifocality
presence of concurrent CIS
recurrence at 3 months
24
Q

what is the % 5 year survival for non-invasive, low grade bladder tumour

25
what is the % 5 year survival for invasive, high grade bladder tumour
50%
26
what are the main symptoms for Upper tract urothelial cancer (UTUC)
Frank haematuria Unilateral ureteric obstruction Flank or loin pain Symptoms of nodal or metastatic disease - Bone pain - Hypercalcaemia - Lung - Brain
27
what diagnostic investigations are used to diagnose UTUC
CT- IVU or IVU - shows filling defects in renal pelvis urine cytology ureteroscopy and biopsy
28
where is the most common site of UTUC
renal pelvis or collecting system
29
what is the most common treatment for UTUC
nephro-ureterectomy due to high risk of recurrence if treated endoscopically or my segmental resection
30
what treatment would be used if a patient could not undergo nephron-ureterectomy
nephron-sparring endoscopica treatements - ureteroscopic laser ablation also need regular surveillance
31
why is surveillance cystoscopy needed in UTUC
in all cases there is a high risk of synchronous and metachronous bladder TCC (40% over 10 years)
32
what are the benign renal tumours called
oncocytoma | angiomyolipoma
33
what are the malignant renal tumours called
renal adenocarcinoma hypernephroma grawits tumour
34
where do most malignant renal tumours arise
from the proximal tubule
35
what are the 4 histological subtypes of malignant renal tumours
clear cell (85%) papillary (10%) chromophobe (4%) Bellini type ductal carcinoma (1%)
36
what are risk factors for renal adenocarcinoma
Family history (autosomal dominant e.g. vHL, familial clear cell RCC, hereditary papillary RCC; can be bilateral and/or multifocal) Smoking Anti-hypertensive medication Obesity End-stage renal failure Acquired renal cystic disease
37
how does adenocarcinoma present
asymptotically - 50% classic triad - 10% - flank pain, mass, haematuria paraneoplastic syndrome - 30% - anorexia, cachexia and pyrexia - hypertension, hypercalcaemia and abnormal LFTs - anaemia, polycythaemia and raised ESR metastatic disease - 30% - bone, brain, lungs, liver
38
what are the stages of renal cancer
T1 - tumour <7cm confined within renal capsule T2 - tumour >7cm confined within capsule T3 - Local extension outside capsule - T3a - Into adrenal or peri-renal fat - T3b - Into renal vein or IVC below diaphragm - T3c - Tumour thrombus in IVC extends above diaphragm T4 - Tumour invades beyond Gerota’s fascia
39
how does renal adenocarcinoma spread
- direct spread (invasion) through renal capsule - venous invasion to renal vein and vena cava - haematogenous spread to lungs and bone/lymphatic spread to paracaval nodes
40
what are mandatory investigations for renal adenocarcinoma
CT scan of abdomen and chest - provides radiological diagnosis and complete TNM staging - assesses contralateral kidney Bloods - U&Es, FBC
41
what are optional investigations for renal adenocarcinoma
IVU shows calyceal distortion and soft tissue mass Ultrasound differentiates tumour from cyst DMSA or MAG-3 renogram to assess split renal function if doubts about contralateral kidney
42
what is the treatment for adenocarcinoma
surgical i.e. radical nephrectomy standard for T1 tumours = laparoscopic radical nephrectomy (curative if
43
how can patients with metastatic disease who have symptoms from primary tumour be treated
palliative cytoreductive nephrectomy still beneficial can prolong median survival by 6 months
44
how are adenocarcinoma metastases treated
1. multitargeted receptro tyrosine kinase inhibitors - sunitinib, sorafenib, panzopanib,temsirolimus 2. immunotherapy - Interferon alpha - Interleukin-2 response rate with either 20% at most
45
what are the prognosis' for different stage adenocarcinoma
T1 – 95% 5-year survival T2 – 90% 5-year survival T3 – 60% 5-year survival T4 – 20% 5-year survival N1 or N2 – 20% 5-year survival M1 – Median survival 12-18 months