Structures gynecologic cancer evaluation with staging, treatment planning, and surveillance. Use when managing gynecologic cancers, staging ovarian/uterine malignancies, or planning treatment.
Structures gynecologic cancer evaluation with FIGO staging, multidisciplinary treatment planning, and surveillance protocols for endometrial, ovarian, cervical, and vulvar malignancies.
Gynecologic cancers — endometrial, ovarian, cervical, vulvar, and vaginal — collectively account for over 115,000 new cases and 34,000 deaths annually in the United States. Endometrial cancer is the most common gynecologic malignancy (incidence rising with the obesity epidemic), while ovarian cancer has the highest mortality due to late-stage diagnosis. FIGO staging is the international standard for all gynecologic malignancies and was updated for endometrial cancer in 2023 and cervical cancer in 2018.
Accurate staging determines treatment (surgery, chemotherapy, radiation, or combination), eligibility for clinical trials, and prognosis. Molecular classification (particularly for endometrial cancer — POLE, MSI-H, CN-low, CN-high/p53-abnormal) is now integrated into treatment planning. This skill ensures that evaluation, staging, and treatment planning follow NCCN and SGO/FIGO guidelines.
| Stage | Description |
|---|---|
| IA | Tumor limited to endometrium or < 50% myometrial invasion |
| IB | ≥ 50% myometrial invasion |
| IC | Invasion of cervical stroma (formerly stage II) |
| II | Tumor beyond uterus to ovaries, fallopian tubes, broad ligament, or vagina |
| IIIA | Tumor invading uterine serosa or adnexa |
| IIIB | Vaginal or parametrial involvement |
| IIIC1 | Pelvic lymph node metastasis |
| IIIC2 | Para-aortic lymph node metastasis |
| IVA | Invasion of bladder or bowel mucosa |
| IVB | Distant metastasis |
| Subtype | Prognosis | Treatment Implications |
|---|---|---|
| POLE ultramutated | Excellent (even if high-grade histology) | May de-escalate adjuvant therapy |
| MSI-high / MMR-deficient | Intermediate-favorable | Checkpoint immunotherapy (pembrolizumab) if advanced; Lynch syndrome screening |
| Copy-number low (CN-L) | Intermediate | Standard stage-based adjuvant therapy |
| Copy-number high (CN-H) / p53-abnormal | Poor | Aggressive adjuvant therapy (chemo + radiation); clinical trials |
| Stage | Description |
|---|---|
| I | Limited to ovaries/fallopian tubes |
| IA | One ovary, capsule intact, no surface involvement, negative washings |
| IB | Both ovaries, capsule intact |
| IC | Capsule rupture, surface involvement, or positive washings |
| II | Pelvic extension |
| III | Peritoneal metastasis beyond pelvis and/or retroperitoneal nodes |
| IIIC | Peritoneal metastasis > 2 cm and/or retroperitoneal nodes |
| IV | Distant metastasis (liver parenchymal, extra-abdominal) |
| Stage | Description |
|---|---|
| IA1 | Stromal invasion ≤ 3 mm depth |
| IA2 | Stromal invasion > 3 mm and ≤ 5 mm depth |
| IB1 | Clinically visible ≤ 2 cm |
| IB2 | Clinically visible > 2 cm and ≤ 4 cm |
| IB3 | Clinically visible > 4 cm |
| IIA | Upper 2/3 vagina, no parametrial invasion |
| IIB | Parametrial invasion |
| IIIA | Lower 1/3 vagina |
| IIIB | Pelvic sidewall / hydronephrosis |
| IIIC1 | Pelvic lymph node metastasis |
| IIIC2 | Para-aortic lymph node metastasis |
| IVA | Bladder or rectal mucosal invasion |
| IVB | Distant metastasis |
| Cancer Type | Surveillance Schedule | Key Assessments |
|---|---|---|
| Endometrial | Q3–6 months × 2 years, then Q6–12 months × 3 years | Symptom review, pelvic exam, vaginal cuff cytology (if risk factors), imaging only if symptomatic |
| Ovarian | Q2–4 months × 2 years, then Q3–6 months × 3 years | CA-125, exam, CT if rising markers or symptoms |
| Cervical | Q3–4 months × 2 years, then Q6 months × 3 years | Pap smear (if treated with surgery), pelvic exam, imaging if indicated |
| Vulvar | Q6 months × 2 years, then annually | Vulvar exam, biopsy any suspicious lesions |