CS 1 treatment Flashcards

1
Q
sperm banking
viral screen
how many samples
abstience
max storage
payment
max age storage
A
fertility clinic
screen HIV, hep B and C
T, LH, FSH
3 samples with 2-3 days abstinence prior
sample forzen
maximum storage 10 years
up to 55 years old
1st year NHS pays then £200 per year
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2
Q

% azoospermic before orchidectomy

% abnormal sperm counts

A

10-24% azoospermic

50% abnormal sperm counts

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3
Q

when does sperms return after chemo

A

after 4 years post chemo

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4
Q

complications prosthesis

A

almost all discomfort swelling bruising
1/2 to 1/10 higher different size, feel stitch
1/6 dissastifaction result
up to 1/250 bleeding, infection, pain, chronic, leakage, unknown long term risk silicone

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5
Q

risk of tumour in CL biopsy
risk of GCNIS
general GCNIS risk pop

A

GCNIS 9%
risk tumour 2.5%
background GCNIS
general risk 0.8%

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6
Q

progression GCNIS to cancer

A

50% five years 70% 7 years

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7
Q

risk GCNIS with Harland criteria

A

under 30 and 12mls or less 18-34% incidence

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8
Q

type of CL biopsy

A

2 site biopsy recommended Dieckmann Eur Urol 2007

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9
Q

radiotherapy for GCNIS

A

20Gy in 2Gy fractions

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10
Q

risk relapse seminoma with rete testis and 4cm

A

32% vs 6% relapse

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11
Q

chemo for seminoma

A

carboplatin x 1 or DXT for higher risk relapse

4cm rete testis

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12
Q

Stage 2 or 3 seminoma

A

3 x BEP

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13
Q

Residual mass after seminoma treatment

A

> 3cm FDG PET at least 2 months after chemo

<3cm follow up imaging serum markers

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14
Q

NSGCT stage 1

A

with LVI BEP x 1 (RPLND)

no LVI surveillance

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15
Q

NSGCT pure teratoma

A

RPLND

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16
Q

NSGCT stage 2 A/B marker negative and positive

A

BEP x 3

M-ve RPLND - if positive BEP x 2

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17
Q

NSGCT porpotion with subclinical mets

A

50% subclinical mets

92% present first 2 years

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18
Q

Stage 2C NSGCT good and poor prognosis

A

good prognosis BEP x 3

intermediate or poor prognosis BEP x 4

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19
Q

residual mass NSGCT after chemo

necrosis vs viable tumour

A

if >1cm RPLND
10% viable tumour, 50% teratoma. 40% necrosis

if <1cm uncertain follow up with imaging and tumour markers

20
Q

action of cisplatin

side effects

A

inhibits DNA synthesis
neuro
oto
nephro

21
Q

bleomycin mode action

A

anti tumour antibiotics
cases DNA stand break
pulmonary fibrosis

22
Q

etoposide action

side effect

A

topoisomerase 2 inhibitor
induces cell arrest
causes myelosuppression and hair loss

23
Q

RPLND template

A

RIGHT
right renal vein to lateral border aorta
right ureter
right bifurcation common iliac

LEFT
left renal vein
left ureter
medial border aorta
left common iliac bifurcation
24
Q

side effects RPLND
morbidity
mortality

A

morbidity 10%
mortality 0.5-1%

1/2 to 1/10
weak absent ejcaultion
lymphocele
infection incision site bulging, pain
ileus

1 in 10
need removal of organ

1 in 10 to 1 in 50
bleeding
further treatment
injury other structures
entry to lung cavity drain
25
``` Primary RPLND who for , who many be suitable how many will cure how many operated unessecarily how many develop mets need salvage chemo ```
for stage 1 NSGCT, those unwilling to do surveillance or primary chemo cure 90% of CS 1 without need chemo and provides accurate staging 70% operated unescearily as only 30% will relapse and in 10% after RPLND will still develop systemic mets requiring salvage chemo
26
who can have TSS | rate associated GCNIS
tumour less than 30% of volume of testicle synchronous bilateral metachronous bilateral solitary testis with normal preop T levels rate of associated GNCIS 82%
27
radical orchidectomy consent
almost all swelling bruising scrotum 10-50% high position feel stitch 20% not happy look prosthesis ``` 2-10% not cancer not cured need c/l biopsy need remove implant fertility cosmetic result ``` <1% bleeding infection pain <0.04% leakage implant anesthetic risk
28
complications prosthesis
extrusion 5% migration 5% chronic pain 1%
29
paper testicular prosthesis
Ramani 904 men rate infection same
30
indications organ sparing 4
solitary testicle with normal testosterone levels with tumour contra lateral TC tumour <30% of testicle volume strong suspcicion benign tumour
31
maximun storage sperm
10 years or age 55 in NHS
32
cost sperm banking after 1st year
£200 | covered in 1st year
33
azoospermic if banking not done before orchidectomy
4-10% will be azoospermic if sperm banking not done before orchidectomy
34
surveillance protocol stage 1 seminoma
year 1-3 6 monthly ct and 6 monthly clinnic assessment no cxr then once in year 4-5 then tailored
35
surveillance protocol stage 1 NSGCt
3 montly doctor visit year 1-2, then 6 montly year 3 | 6 monthly ct and cxr
36
how many later relapses of seminoa after 4 years
20%
37
how many NSGCT have sub clinic mets
30% so will relapse on surveillance
38
what are adverse features of NSGCT
embryonal compinent | lack yolk sac component
39
salvage chemo in NSGCT response rate
very good >99% so surveillance is option
40
what proportion relapse year 1 NSGCT
80% | of which 1/3 will have normal tumour markers
41
how is BEP given
3 weeks | 2 weeks of chemo with 1 week rest
42
RPLND role in NSGCT | what happens if LN on RPLND
if unwilling chemo or surveillance if LN then have 2 cycles BEP if stage II NSGCT Some patients may wish to consider primary RPLND although they need to be aware of the potential additional requirement of adjuvant chemotherapy if nodes contain active disease, as well as the 10% risk of systemic relapse requiring subsequent chemotherapy treatment (BEP X 3).
43
RPLND role in NSGCT | what happens if LN on RPLND
if unwilling chemo or surveillance if LN then have 2 cycles BEP if stage II NSGCT Some patients may wish to consider primary RPLND although they need to be aware of the potential additional requirement of adjuvant chemotherapy if nodes contain active disease, as well as the 10% risk of systemic relapse requiring subsequent chemotherapy treatment (BEP X 3).
44
relapse rate after ajuvant bep in stage 1 nsgct
less than 3% | Adjuvant chemotherapy with BEP is superior to adjuvant RPLND in terms of the risk of relapse
45
sperm quality papers
Rives 2012 semen quality Peterson JCO 1999 50% drop in semen parameters post orchidectomy 10% will become azoospermic post orchidectomy 10% will be azoospermic before orchidectomy
46
risk relapse after chemo for stage I seminoma
In non-randomised prospective series five-year relapse rates with adjuvant carboplatin are 2% in patients without risk factors and 9% in patients with one or two risk factors single cycle carboplatin (MRC trial showed lowest toxicity and equal low relapse of2% comparing carbo vs RT 30Gy vs RT 20Gy
47
pros and cons adjuvant radio vs chemo in stage 1
Adjuvant chemotherapy with one course carboplatin AUC 7 is not inferior to adjuvant radiotherapy when pathological risk-factors are taken into account. Relapse rates with both adjuvant treatments are around 5%. Adjuvant radiotherapy is associated with an increased risk of developing secondary non-germ cell malignancies