Target Volume Delineations, Doses, and OAR Constraints for Post-Op Endometrial Carcinoma Radiotherapy
For post-operative endometrial carcinoma patients, pelvic EBRT should target the pelvis with doses of 45-50 Gy in standard fractionation, while vaginal brachytherapy should be delivered to the upper vagina with doses of 7 Gy × 3 fractions at 0.5 cm depth or 6 Gy × 5 fractions to the vaginal surface when used alone. 1
Target Volume Delineations
External Beam Radiation Therapy (EBRT)
Pelvic EBRT targets:
- Gross disease (if present)
- Lower common iliac lymph nodes
- External iliac lymph nodes
- Internal iliac lymph nodes
- Parametrium
- Upper vagina/para-vaginal tissue
- Presacral lymph nodes (especially in patients with cervical involvement) 1
Extended-field EBRT (when indicated):
- Includes all pelvic targets above
- Entire common iliac chain
- Para-aortic lymph node region
- Upper border should extend at least to the level of renal vessels 1
Vaginal Brachytherapy (VBT)
- Target volume: Limited to the upper vagina after hysterectomy 1
- Prescription point:
- Either to vaginal surface or at a depth of 0.5 cm from vaginal surface 1
Radiation Doses
EBRT Doses
- Microscopic disease: 45-50 Gy delivered with multiple conformal fields based on CT-treatment planning 1
VBT Doses
When used as boost after EBRT:
When used alone (without EBRT):
For preoperative therapy in stage IIB disease:
- Total dose of 75-80 Gy low-dose rate equivalent to the tumor volume 1
Critical Organ At Risk (OAR) Constraints
While specific OAR constraints aren't explicitly detailed in the guidelines, clinical practice indicates the following constraints should be observed:
- Rectosigmoid: Cumulative D2cc (EQD2) should be limited to <75 Gy 2
- Bladder: Cumulative D2cc (EQD2) should be limited to <90 Gy 2
Treatment Selection Algorithm
Stage IA, Grade 1-2:
- Preferred: Observation
- For patients ≥60 years and/or with LVSI: VBT strongly recommended 1
Stage IA, Grade 3:
- Preferred: VBT (especially if surgically staged)
- If no myometrial invasion: Observation may be considered
- If age ≥70 years or LVSI present: Consider EBRT (category 2B) 1
Stage IB, Grade 1-2:
- Preferred: VBT
- If no adverse risk factors: Observation may be considered
- For grade 2 tumors with age ≥60 years and/or LVSI: Consider EBRT 1
Stage IB, Grade 3 with adverse risk factors:
- EBRT and/or VBT
- Consider adding systemic therapy (category 2B) 1
Stage II:
- After radical hysterectomy with negative margins: EBRT (preferred) and/or VBT 1
Clinical Considerations and Caveats
Timing of adjuvant RT: Should be initiated after vaginal cuff healing but no later than 12 weeks post-surgery 1
VBT vs. EBRT selection: The PORTEC-2 trial demonstrated that VBT is as effective as EBRT in preventing vaginal recurrence in intermediate-risk patients, with significantly fewer gastrointestinal toxicities 3
Combined modality considerations: Adding VBT to EBRT has not shown significant clinical benefit over EBRT alone in most cases, as vaginal control rates with EBRT alone are excellent 1
Special case - Stage II disease: For patients with cervical stromal involvement, a brachytherapy boost after EBRT may be appropriate, though high-quality evidence specifically supporting this practice is lacking 1
Vaginal stenosis prevention: Patients receiving radiation should be counseled about using vaginal dilators beginning 2-4 weeks after RT completion to prevent or treat vaginal stenosis 1
Re-irradiation considerations: For vaginal recurrence in previously irradiated patients, salvage re-irradiation with 3D conformal brachytherapy is feasible when cumulative doses to surrounding organs are limited 2