Radiotherapy contributing atlas for postoperative pelvic Radiotherapy in endometrial carcinoma and target guidelines

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Postoperative Pelvic Radiotherapy in Endometrial Carcinoma: Contouring Atlas & Target Volume Guidelines

1. Rationale and Foundational Atlases

The dominant reference framework is the RTOG/NRG Oncology Consensus Atlas, published in two versions:
  • Original atlas (2008): Small W Jr, Mell LK, Anderson P, et al. Int J Radiat Oncol Biol Phys 2008;71:428–34. [PMID: 18037584] — established CTV definitions using bony landmark references for IMRT in postoperative endometrial and cervical cancer.
  • Updated atlas (2021): Small W Jr, Bosch WR, Harkenrider MM, et al. NRG Oncology/RTOG Consensus Guidelines for Delineation of CTV for Intensity Modulated Pelvic Radiation Therapy in Postoperative Treatment of Endometrial and Cervical Cancer: An Update. Int J Radiat Oncol Biol Phys 2021;109:413–24. [PMID: 32905846] — removed all bony landmark references, added para-aortic and inferior obturator nodal regions, and produced a 95% agreement smoothed final contour atlas from 16 international experts.
The 2025 Chinese Anti-Cancer Association guideline (Holistic Integrative Oncology, 2025) and the 2025 ESGO/ESTRO/ESP guidelines have further updated these frameworks with molecular subtyping risk stratification.

2. Risk Stratification Driving RT Decisions

Before target delineation, patients are stratified by risk of recurrence. The principal routes of metastatic dissemination are:
RouteKey Predictors
Vaginal/contiguousGrade 3, lymphovascular space invasion (LVSI)
HematogenousDeep myometrial invasion (>50–66%)
LymphaticCervical stromal invasion, positive nodes (stage IIIC)
PeritonealStage IV; ≥2 of: cervical invasion, +cytology, +nodes, non-endometrioid histology
Patients with any one of these risk factors constitute ~35% of all endometrial cancer patients but account for 89% of hematogenous, lymphatic, and peritoneal relapses (Berek & Novak's Gynecology).

3. Treatment Volume Definitions (GTV / CTV / PTV)

GTV (Gross Tumor Volume)

  • Post-hysterectomy (standard postoperative setting): no GTV unless gross residual disease is present on imaging.
  • If residual disease exists: GTV = known extent of disease on CT/MRI/PET.

CTV (Clinical Target Volume)

The CTV encompasses regions of presumed microscopic dissemination. The 2021 NRG/RTOG atlas defines separate sub-CTVs that are contoured and then merged:

a. Vaginal Cuff CTV

  • The vaginal cuff and adjacent paravaginal soft tissue (3–5 mm lateral margin).
  • Upper 3 cm of vagina is the minimum treated length; in high-risk cases, the upper two-thirds of vagina.
  • Kappa agreement in 2021 atlas: moderate (κ = 0.47).

b. Obturator Nodal CTV

  • Nodes along the obturator vessels, medial to the external iliac vein and lateral to the bladder.
  • Most variable region in contouring — fair agreement only (κ = 0.21).
  • The updated 2021 atlas incorporated the inferior obturator nodal region (previously absent).

c. Internal Iliac Nodal CTV

  • Vessels and surrounding tissue from the internal iliac bifurcation to the level of the posterior superior iliac spine.
  • Includes presacral nodal chains anterolateral to S1–S2.
  • Kappa: moderate (κ = 0.52).

d. External Iliac Nodal CTV

  • Along the external iliac vessels, from the bifurcation of common iliac to the femoral ring.
  • Extends 7 mm around the vessels.
  • Kappa: moderate (κ = 0.60).

e. Presacral Nodal CTV

  • Region anterior to S1–S2, encompassing the median sacral vessels and presacral fat.
  • Only included when cervical involvement is present (stage II) or positive pelvic nodes.
  • Least agreement in 2021 atlas (κ = 0.36).

f. Common Iliac Nodal CTV

  • Vessels from aortic bifurcation (L4–L5) to common iliac bifurcation; 7 mm surrounding vessels.
  • Best agreement among all regions (κ = 0.64).
  • Included for: stage IIIC disease, cervical involvement, or high-risk features; often omitted for low-risk early-stage.

g. Para-Aortic Nodal CTV (new in 2021 atlas)

  • When extended-field RT is indicated (positive para-aortic nodes or very high-risk IIIC2).
  • Upper border: 1–2 cm above the level of the renal vessels (based on clinical situation).

PTV (Planning Target Volume)

  • PTV = CTV + setup margin, typically 7–10 mm (may reduce to 5 mm posteriorly near rectum with daily IGRT).
  • Organ motion is particularly relevant post-hysterectomy (bladder and bowel fill variability). The ITV (internal target volume) strategy incorporating bladder-filling states should be considered — some protocols treat the ITV as the CTV.

4. Standard Pelvic Field Boundaries

BorderLocation
SuperiorL4–L5 interspace (lower common iliacs)
InferiorInferior obturator foramen or 3 cm below vaginal apex (whichever is lower)
Lateral1–2 cm lateral to the pelvic brim (to include external iliacs)
AnteriorAnterior pubic symphysis
PosteriorS2–S3 junction (to cover presacral nodes if indicated)
For standard pelvic RT, the targets include: bilateral common iliac (distal), external iliac, internal iliac, obturator, parametria, and vaginal cuff/upper vagina.
For extended-field RT (EFRT): adds the entire common iliac chain and para-aortic region to the level of the renal vessels (L1–L2).

5. Dose Prescriptions

External Beam Radiotherapy (EBRT)

SettingDose
Microscopic disease (standard adjuvant)45–50 Gy in 25 fractions (1.8–2.0 Gy/fx)
Gross residual disease (boost)60–70 Gy total, using IMRT/VMAT boost
Involved nodes (stage IIIC) — simultaneous integrated boost (SIB)GTVnd: 55–65 Gy/25 fx (2.2–2.6 Gy/fx)
Para-aortic EFRT (microscopic)45–50 Gy
Unresectable nodal metastases (IMRT/VMAT)60–70 Gy/25–30 fx

Vaginal Brachytherapy (HDR) — Postoperative Alone

RegimenPrescription Point
7 Gy × 3 fx0.5 cm depth (most common)
6 Gy × 5 fxSurface
5.5 Gy × 4 fx0.5 cm depth
When combined with EBRT (45–50 Gy), brachytherapy boost is 4–6 Gy × 2–3 fx (total EQD₂ ≤75–80 Gy, α/β = 3 for late effects).
Timing: initiate no later than 12 weeks post-surgery; ideally 6–8 weeks after vaginal cuff healing.

6. Indications by Stage/Risk Group

Risk GroupRT Recommendation
Low-risk (Stage IA, grade 1–2, no LVSI)No adjuvant RT
Intermediate-risk (Stage IA G3 or IB G1–2, no LVSI, age <60)Observe or vaginal brachytherapy
High-intermediate-risk (IB G3 or any grade + LVSI, or age >60 + IB G2)Vaginal brachytherapy ± EBRT
High-risk early stage (Stage II, IB G3 LVSI+)Pelvic EBRT + vaginal brachytherapy
Stage IIIA–IIIBPelvic EBRT ± vaginal brachytherapy ± chemotherapy
Stage IIIC1 (pelvic nodes+)Pelvic EBRT + vaginal brachytherapy; consider concurrent/sequential chemo
Stage IIIC2 (PA nodes+)EFRT (pelvic + para-aortic) + vaginal brachytherapy + chemotherapy
The PORTEC-2 trial (46 Gy pelvic ERT vs. vaginal brachytherapy in high-intermediate-risk stage I) showed equivalent vaginal control (0.9% vs. 2%), but higher nonvaginal pelvic relapse with brachytherapy alone (3.6% vs. 0.7%), supporting continued use of EBRT in higher-risk patients.
PORTEC-3 and GOG258 established combined chemoradiotherapy (carboplatin/paclitaxel + EBRT) as standard for high-risk and advanced-stage endometrial cancer.

7. Technical Delivery and IMRT Considerations

  • Simulation: Supine with immobilization device, full bladder protocol (reduces small bowel dose), empty rectum.
  • Imaging: CT simulation with IV contrast; MRI fusion recommended for nodal delineation.
  • Technique: IMRT/VMAT is preferred over 3D-CRT for reduction of bowel, bladder, and bone marrow dose. RTOG 0418 validated IMRT technique for postoperative gynecological cancers.
  • IGRT: Daily cone-beam CT is recommended to account for interfractional organ motion (bladder, sigmoid, small bowel), especially in post-hysterectomy patients.
  • Bone marrow sparing: Use of whole-pelvic IMRT with bone marrow avoidance reduces hematologic toxicity (relevant with concurrent chemotherapy).

8. Organs at Risk (OARs) Constraints

OrganConstraint
RectumV45 <75%, V50 <50%
BladderV45 <35–50%
Small bowelV45 <195 cc (V15 <120–250 cc per RTOG 0418)
Femoral headsV30 <15%; max <50 Gy
Spinal cordMax <45 Gy
Kidney (each)Mean <18 Gy; V20 <32%

Key References

  1. Small W Jr et al. Consensus guidelines for delineation of CTV for IMRT in postoperative treatment of endometrial and cervical cancer. Int J Radiat Oncol Biol Phys 2008;71:428–34. [PMID: 18037584] — Original RTOG atlas.
  2. Small W Jr et al. NRG Oncology/RTOG Consensus Guidelines — an update. Int J Radiat Oncol Biol Phys 2021;109:413–24. [PMID: 32905846] — Current standard atlas, removes bony landmarks, adds para-aortic and inferior obturator regions.
  3. Nout RA et al. (PORTEC-2). Vaginal brachytherapy vs. pelvic ERT — establishes brachytherapy equivalence for vaginal control in high-intermediate risk. Lancet 2010.
  4. de Boer SM et al. (PORTEC-3). Chemoradiotherapy for high-risk endometrial cancer. Lancet Oncol 2018;19:295–309.
  5. China Anti-Cancer Association Brachytherapy Committee. Guidelines for radiation therapy for endometrial cancer (V 2025.1). Holistic Integrative Oncology 2025.
  6. ESGO/ESTRO/ESP 2025 guidelines — incorporate molecular subtyping (MMRd, POLE, p53abn, NSMP) into RT decision-making.
— Berek & Novak's Gynecology (10th ed.), Chapter 37
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