Ovarian Cancer Flashcards

1
Q

Incidence and survival of ovarian cancer

A
Increased incidence with increasing age (highest incidence in 75-79 years)
10% associated with inherited risk 
Mortality (5 years)
- Stage 1 = 85%
- Stage 4 = 10%
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2
Q

What are the four main pathologies of malignancy ovarian tumours

A

Epithelial ovarian cancer (90%)
Germ cell tumours -arise from oocytes
Ovarian stromal tumours - non germ cell/non epithelial components
Metastsis - a.k.a. Kurkenburg

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3
Q

What are the two types of epithelial ovarian cancer

A

High grade serious
- resembles the fallopian tube mucosa
- p53 mutations
Arise from ovarian surface epithelium and Mullerian inclusion cysts
- endometrioid, clear cell, mucinous and low grade serous

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4
Q

What is a borderline epithelial tumour

A

Low malignant potential because there is no stromal invasion
- however can get metastatic implants (invasive or non-invasive)
Generally a good prognosis
Seen in all ages, but generally the younger population

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5
Q

What are the ways in which ovarian cancer can spread

A

Direct extension
- transcoelomic
Exfoliation into the peritoneal cavity
Lymphatic invasion

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6
Q

Risk factors for ovarian cancer

A
Smoking
Low parity (one child is protective)
Oral contraceptives
Infertility
Tubal ligation 
Early menarche 
Late menopause 
- higher probability of spontaneous mutations with repetitive disruption and repair 
Genetics
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7
Q

Describe the genetic element of ovarian cancer

A
10% of cases
BRCA1 - chromosome 17q
- 30% lifetime risk
BRCA2 - chromosome 13q
- 27% lifetime risk
Lynch syndrome/HNPCC - mutation in Mismatch Repair Genes
- endometrial, ovarian and colon cancers 
Undiscovered genes
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8
Q

What features are suggestive of an ovarian cancer being as a result of a gene mutation

A
Male breast cancer
Early onset breast cancer <40 years
Ashkenazi Jewish ancestry
Bilateral breast cancer
Multiple genetically related family members with breast, colon, ovarian, stomach, upper renal tract, endometrial and small bowel cancer
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9
Q

What is the risk reducing surgery that can be used in those with genetic mutations

A

Prophylactic bilateral salpingo-oophorectomy
- remove ovary AND entire fallopian tube
Risk reduction of 96% of ovarian cancer and 53% of breast cases
2% have occult cancer at time of RRS
Risks associated with premature menopause

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10
Q

Clinical features of ovarian cancer

A
Vague and non-specific - often found at an advanced stage 
Altered bowel habit
Abdominal pain/bloating
Abdominal distension
- mass 
- ascites
Feeling full quickly
Difficulty eating 
Urinary/pelvic symptoms 
Bowel obstruction 
SOB - pleural effusion 
Nodules on PV exam
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11
Q

What investigations are required in?ovarian cancer

A

USS (TA or TV)
Ca125
- glycoprotein antigen
Caluculate RMI (risk of malignancy index)
CT
- determines initial treatment (surgery vs chemo)
- monitors response to treatment

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12
Q

What can elevate Ca125

A
Ovarian cancer
Pancreatic cancer
Breast cancer
Lung cancer
Colon cancer 
Menstruation 
Endometriosis
PID
Pleural and pericardial effusions 
Recent laparotomy
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13
Q

Describe the risk of malignancy index (RMI)

A

RMI = U x M x Ca125

U - ultrasound

  • multilocular, solid areas, ascites, intra-abdominal metastasis
  • score 0 = 0, 1 = 1 and 2/+ = 3

M - menopausal state

  • 1 = pre-menopause
  • 3 = post-menopause

Ca125 in units/m

RMI >200 carries a risk of malignancy
- CT and refer MDT/CNS

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14
Q

How are ovarian cancers managed

A

MDT
- guides investigations and makes decisions on management
Surgery
Chemotherapy

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15
Q

How are ovarian cancers diagnosed

A

Cytology - pleural/ascitic fluid
Biopsy
- percutaneous under US/CT guidance
- laparoscopic

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16
Q

What surgery is required for the management of ovarian cancer

A

Midline laparotomy
Total abdominal hysterectomy,
bilateral salpingo-oophorectomy,
omentectomy +/- appendicectomy/resection of peritoneal disease
Ultra-radical surgery involves splenectomy, bowel resection and peritoneal stripping
Fertility conserving surgery (9% risk of recurrence in contralateral ovary)
The aim is to leave no residual disease or optimal cytoreduction (<1cm)

17
Q

How is chemotherapy used in the management of ovarian cancer

A

Neoadjuvant
- advanced disease, not possible to resect
- poor performance status
Adjuvant (post-op) if
- completely resected or optimally cytoreduced
- MDT decision
1st line should include a platinum agent in combination or as a single agent
- carboplatin
- paclitaxel in combination
Intraperitoneal - post op if completely or optimally cytoreduced
Other chemo
- biologics (antiangiogenesis) VEGF inhibitor
- hormonal therapy
(tamoxifen/aromatase inhibitor)

18
Q

Describe the FIGO surgical staging for ovarian cancer

- Stage 1

A

1A: tumour on one ovary, capsule intact, no surface tumour and negative washings
1B: both ovaries
1C: ruptured capsule, surface tumour or positive washings limited to one or both ovaries

19
Q

Describe the FIGO surgical staging for ovarian cancer

- Stage 2

A

Limited to pelvis
2A: extension and/or implantation onto the uterus and/or fallopian tubes
2B: extension to other pelvic tissue

20
Q

Describe the FIGO surgical staging for ovarian cancer

- Stage 3

A

Limited to abdomen
3A: positive retroperitoneal lymph nodes and/or microscopic mets beyond the pelvis
3a1) positive retroperitoneal lymph nodes only
3a2) microscopic, extrapelvic peritoneal involvement +/- retroperitoneal lymph nodes
3B: macroscopic, extrapelvic peritoneal metastasis <2cm
3C: macroscopic, extrapelvic peritoneal metastasis >2cm

21
Q

Describe the FIGO surgical staging for ovarian cancer

- Stage 4

A

Distant mets
4A: pleural effusion with positive cytology
4B: hepatic/splenic parenchymal metastasis, metastasis to extra abdominal organs including inguinal lymph nodes