Ovarian Cancer for USMLE Step 1

Ovarian Cancer for the USMLE Step 1 Exam
Ovarian Cancer
  • Epidemiology:
    • Ovarian cancer has a high mortality rate among gynecologic cancers due to its tendency for late-stage presentation.
    • Risk Factors:
    • Increased age, especially postmenopausal women (50–70 years).
    • Family history of ovarian or breast cancer.
    • BRCA1/BRCA2 mutations and Lynch syndrome, both of which significantly elevate risk.
    • Increased lifetime ovulation (nulliparity, early menarche, late menopause).
    • Protective Factors:
    • Oral contraceptives, pregnancy, and breastfeeding, which reduce ovulatory cycles.
Types of Ovarian Cancer
  • Epithelial Tumors:
    • Account for approximately 90% of ovarian cancers and are classified by cell type:
    • Serous Carcinomas: Most common and often high-grade.
    • Mucinous Carcinomas: Less common; may grow large.
    • Endometrioid and Clear Cell Carcinomas: Frequently associated with endometriosis.
    • Low-Grade vs. High-Grade Serous Tumors: High-grade serous carcinomas are more aggressive, presenting at later stages.
  • Germ Cell Tumors:
    • Originate from germ cells, primarily affect younger women, and have a good prognosis when treated.
    • Types include dysgerminomas, yolk sac tumors, and immature teratomas.
  • Sex Cord-Stromal Tumors:
    • Arise from ovarian stromal tissue, producing hormones that can cause symptoms like abnormal uterine bleeding.
    • Granulosa Cell Tumors: Produce estrogen, which can lead to symptoms like endometrial hyperplasia.
    • Sertoli-Leydig Cell Tumors: Produce androgens, which may cause virilization.
Clinical Presentation
  • Symptoms:
    • Often asymptomatic in early stages; common symptoms in advanced stages include:
    • Abdominal bloating or distension.
    • Pelvic or abdominal pain.
    • Early satiety.
    • Urinary urgency or frequency.
    • Advanced Disease: May present with ascites, bowel obstruction, or pleural effusion.
  • Physical Exam:
    • Findings may include a palpable abdominal or pelvic mass, ascites, or pleural effusion (if metastasis has occurred).
Diagnosis
  • Imaging:
    • Pelvic Ultrasound: First-line imaging for adnexal masses, with malignant features including solid areas, thick septations, papillary projections, and ascites.
    • CT Scan of the Abdomen and Pelvis: Used for staging and assessing metastatic disease.
  • Laboratory Tests:
    • CA-125: A tumor marker often elevated in epithelial ovarian cancer, though it lacks specificity.
    • Other Tumor Markers:
    • AFP, hCG, and LDH: Used to evaluate germ cell tumors.
    • Inhibin: Elevated in granulosa cell tumors.
  • Histopathology:
    • Required for definitive diagnosis, usually obtained through surgical exploration or biopsy.
Staging
  • FIGO Staging:
    • Stage I: Confined to the ovaries.
    • Stage II: Involves the pelvis.
    • Stage III: Spread to abdominal organs or lymph nodes.
    • Stage IV: Distant metastasis (e.g., pleural effusion, liver parenchyma).
Treatment
  • Surgical Treatment:
    • Debulking Surgery: Main treatment in advanced stages, involving removal of the ovaries, fallopian tubes, uterus, omentum, and affected tissues.
    • Fertility-Sparing Surgery: Considered in young patients with early-stage disease.
  • Chemotherapy:
    • Platinum-Based Chemotherapy: Standard treatment for epithelial tumors, typically carboplatin and paclitaxel.
    • Germ Cell Tumors: Respond well to BEP regimen (bleomycin, etoposide, and cisplatin).
  • Targeted Therapy:
    • PARP Inhibitors: Effective in BRCA-mutated ovarian cancers, inhibiting DNA repair in cancer cells.
    • Anti-Angiogenic Therapy: Bevacizumab (anti-VEGF) can be used in advanced cases to inhibit tumor blood supply.
Key Points
  • Ovarian Cancer is often asymptomatic until advanced stages; epithelial tumors are the most common type.
  • Risk Factors include age, family history, BRCA mutations, and high lifetime ovulatory cycles, while protective factors include oral contraceptive use and pregnancy.
  • Diagnosis relies on ultrasound and CA-125 marker, with definitive diagnosis by histopathology.
  • Staging follows the FIGO system, with prognosis worsening at later stages.
  • Treatment involves debulking surgery and chemotherapy, while targeted therapies like PARP inhibitors and anti-angiogenics (bevacizumab) are used in specific cases.

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