CPC ovary Flashcards

1
Q

epidemiology of ovarian cancer

A

600 cases p/a scotland
400 deaths p/a

5YS all stages 40-45%
most present with advanced disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

how common is ovarian cancer

A

rare <30y/o

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

who are the high risk families for ovarian cancer

A

5-10% of all cases
early onset presentation

HNPCC/Lynch type II familial cancer syndrome
BRCA1
BRCA2

incessant ovulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what can be protective for ovarian cancer

A

OCP
breast feeding
numerous pregnancies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

origins of ovarian cancer

A

most cases originate from the fimbrial end of fallopian tube
some derive from pre-existing benign ovarian cysts (often low grade cancers)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

ovarian cancer origins and pathogenesis - molecular alterations

A
P53
BRCA1 and 2
ARID1A
PIK3CA
PTEN
BRAF
KRAS
NRAS
ERBB2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

pathogenesis of ovarian cancer

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what mutation causes an aggressive ovarian cancer

A

p53 mutations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

role of pathology in ovarian cancer

A

type of tumour (epithelial, stromal, sex cord; benign, borderline, malignant), tumour grade and stage determines treatment and prognosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what type of tumour is this

how common

A

commonest epithelial tumour type

serous cystadenoma

benign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

describe the appearance of serous cystademonas

A

unilocular cyst

thin wall

flat epithelial lining

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what tumour type is shown here

A

borderline serous tumour

tree like area on left

atypical epithelium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

describe the features of borderline serous tumours

A

develop from benign cysts and mutate and proliferate

tree like papillary excrescences - overgrowth of epithelial lining of a cyst

can develop areas of invasive disease

concerning but not as aggressive as high grade carcinomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is shown here

which is high grade and which is low grade

A

serous carcinoma

low - top
high - bottom

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

features of high grade carcinomas

A

often serous carcinomas

more solid tumours
involvement of omentum - present at high stage disease

nuclearpleomorphism and prominent nucleoli

invasion into stroma

high mitotic rate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

in what grade carcinomas are psammoma bodies seen

A

low grade carcinomas

they are calcifications

17
Q

ovarian cancer symptoms

A

vague
indigestion, early satiety, poor appetite
altered bowel habit/pain
bloating, discomfort, weight gain
pelvic mass - asymptomatic, pressure symptoms

be aware of these symptoms presenting for the first time, esp if 50-60y/o

18
Q

ovarian cancer diagnosis

A
surgical/pathological
USS abdo and pelvis
CT scan - chest, abdo, pelvis - extent of disease
CA125
surgery - gold standard
19
Q

what is CA 125

A

glyco-protein antigen

tumour marker

non-specific

20
Q

what malignancies is CA125 associated with

A

ovary
colon/pancreas
breast

also lung

e.g. anything that causes disease in peritoneal cavity

21
Q

what benign conditions is CA125 associated with

A

menstruation, endometriosis, PID

liver disease, recent surgery, effusions

22
Q

how is CA125 used in the diagnosis of ovarian cancer

A

80% of women w/ ovarian ca have raised CA125

50% of women w/ stage 1 disease

used in detecting and monitoring epithelial ovarian tumours

23
Q

ovarian cancer RMI

A

used in all women who present with ovarian masses

RMI = U x M x CA125

risk of malignancy index
U = US features
M = menopausal status (pre = 1, post = 3)
CA125 level

RMI >200 - suggestive of ovarian malignancy

24
Q

US features for RMI

A
1 point for 1 feature, 3 points for >1: 
multi-locular
solid areas
bilateral 
ascites
intra-abdominal
25
Q

stage 1 ovarian cancer

A

limited to ovaries w/ capsule intact/cytology

26
Q

stage 2 ovarian cancer

A

one or both ovaries w/ pelvic extension

27
Q

stage 3 ovarian cancer

A

one or both ovaries with peritoneal implants outside pelvis or +ve nodes

28
Q

stage 4 ovarian cancer

A

distant mets or complications

29
Q

ovarian cancer treatment

A

surgical
chemotherapy - adjuvant, neoadjuvant

gold standard = surgery followed by chemo

30
Q

laparotomy for ovarian cancer

A

obtain tissue diagnosis
stage disease
disease clearance
debulk disease - if not possible to remove all visible disease

31
Q

chemotherapy for ovarian cancer

A
1st line: platinum + taxane (Taxol)
post-op: within 8wks of surgery
complete/partial response
cure unlikely - esp stage 3
avg response 2yrs (i.e. relapse in stage 3 disease following remission)
32
Q

cure rates for ovarian cancer

A

1 - 85%
2 - 47%
3 - 15%
4 - 10%

33
Q

management of recurring disease

A
chemotherapy 
palliation for symptomatic recurrence
platinum if >6mths since last recurrence
?surgery if 1st recurrence and able to remove all disease
tamoxifen - if unable to manage chemo
34
Q

normal CA125

A

up to 35

35
Q

ovarian cancer screening

A

population screening not proven
high risk women (cancer gene mutation carriers, ≥2 relatives) - little positive evidence

pelvic exam, USS ovaries, CA 125

difficult to detect women in precancerous stage

no prognostic/survival benefit

36
Q

what can be offered to high risk women to prevent ovarian cancer

A

prophylactic laparoscopic bilateral salpinogoophorectomy

removal of tubes and ovaries following completion of families

residual risk of 1y peritoneal cancer

potential for risk reducing early salpingectomy and delayed oophorectomy

37
Q

why is ovarian cancer screeening not recommended

A

limited sensitivity and specificity

FIGO stages of cancer detected rather than pre-cancerous change