Ovarian cancer Flashcards
Epidemiology
Leading cause of death from gynecologic malignancies
Pathophysiology
“Incessant ovulation”
Women’s risk of developing ovarian cancer is related to her number of ovulatory cycles due to disruption and repair of epithelial line of ovaries
Genetic mutations/Hereditory
BRCA1
BRCA2
TP53
HNPCC (Lynch II syndrome)
Risk factors
Age
Family history: increases with two or more 1st degree relatives
Early menarche (<12 yo) or late menopause (>55 yo)
Nulliparity
IVF
Prevention
Multiple pregnancies
OC (> 50% after 5 years of use)
Prophylactic oophorectomy
Presentation
Most patients with Stage 1 and II disease are asymptomatic
Signs/Symptoms
Bloating, fatigue, abdominal pain, vaginal bleeding, pelvic pain, back pain, urinary incontinence, pain with intercourse, weight loss, nausea
In advanced disease symptoms could include:
ascites, pleural effusion, constipation, small bowel obstruction, N/V
If a women experiences the symptoms above for more than 12 days out of the month for 2 consecutive months, she should seek medical attention by her gynecologist
History of disease
Disease is extensive before it is detected
60-70% of patients present with advanced disease
Initial treatment approach
Goal is cure
Standard + adjuvant chemotherapy is standard approach first line
+/- neoadjuvant chemo
Homologous Recombination Deficiency
50% high-grade serous ovarian carcinomas are homologous recombination deficient
Includes germ line and somatic BRCA pathogenic pathways
Screening
There is no effective screening tool
Women at low risk: annual physical and pelvic
Women at high risk (FH, BRCA1/2): Pelvic exam, transvaginal ultrasound, and CA-125 every 6 to 12 months starting at age 25-35)
Surgery
“Debulking” surgery
Outcomes:
Optimally debulked: < 1 cm of disease
Sub-optimally debulked: > 1 cm of disease remaining
Stage IA or IB
Observation and follow up every 3 months
All other stages
Debulking surgery followed by adjuvant chemo
Paclitaxel over 3 hours + Carboplatin every 21 days x 6 cycles
Carboplatin dosing
Carboplatin dose=AUC x (GFR +25)
AUC is usually 5-7.5
Type I Hypersensitivity
Initial contact with agent
Anaphylaxis, itching, rash, chest tightness
PACLITAXEL
Type IV Hypersensitivity
With repeated exposure to agent
Erythema, induration
Drug allergic reaction
symptoms persist after stopping infusion
Infusion related reactions
symptoms resolve quickly after stopping infusion
Paclitaxel standard pre medications
Dexamethasone
Diphenhydramine
Famotidine
PARP inhibitors
Olaparib
Niraparib
Rucaparib
Monitor: CBC baseline then monthly
Renal function
SE: ANEMIA
Platinum sensitive
If the pt relapses > 6 months following completion of their initial platinum containing regimen
May be treated with the initial chemo again
Paclitaxel + carboplatin
Platinum resistant
If the patient relapses < 6 months after receiving platinum containing regimen
salvage regimen is chosen
Treatment if platinum sensitive
Treatment if platinum resistant
liposomal doxorubicin