What is the further management protocol for a patient with early-stage endometrial adenocarcinoma (Endometrial Cancer), FIGO (International Federation of Gynecology and Obstetrics) grade 1, who underwent Total Laparoscopic Hysterectomy (TLH) with Bilateral Salpingo-Oophorectomy (BSO) and Bilateral Pelvic Lymph Node Dissection, with a tumor size of 3.5x2x0.9 cm, less than half myometrial invasion, no Lymphovascular Invasion (LVI), and no lymph node metastasis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 10, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Further Management Protocol

No adjuvant therapy is required for this patient. 1, 2

Risk Stratification

This patient has low-risk, early-stage endometrial cancer based on the following pathologic features 1, 2:

  • Stage IA (FIGO 2009): Less than half myometrial invasion with tumor confined to uterus 1
  • Grade 1 endometrioid adenocarcinoma 1
  • No lymphovascular invasion (LVI) 1
  • Negative lymph nodes (0/9 nodes involved) 1
  • Adequate surgical staging completed: TLH with BSO and bilateral pelvic lymph node dissection 2, 3

According to ESMO guidelines, patients with stage IA/IB, grade 1 or 2, endometrioid histology are classified as low-risk and require no adjuvant therapy after complete surgical staging 1, 2.

Why No Adjuvant Therapy?

The tumor size of 3.5 cm, while noted as a risk factor when >2 cm, does not override the favorable combination of grade 1 histology, minimal myometrial invasion, absence of LVI, and negative nodes in determining overall low-risk status 1. The ESMO low-risk category specifically includes stage IA/IB grade 1-2 endometrioid tumors, and adjuvant radiotherapy has been shown to reduce locoregional recurrence but provides no overall survival benefit in this population 1.

Surveillance Protocol

Follow-up schedule 3:

  • Clinical examination every 3-6 months for the first 2 years
  • Every 6-12 months for years 3-5
  • Annual visits thereafter

Imaging is not routinely indicated for asymptomatic low-risk patients during surveillance 3. Order imaging only if symptoms develop (vaginal bleeding, pelvic pain, unexplained weight loss) or physical examination findings are concerning 3.

Critical Pitfalls to Avoid

Do not over-treat low-risk disease. Adjuvant pelvic radiotherapy in this population increases locoregional control but does not improve overall survival and adds unnecessary toxicity and cost 1. The intermediate-risk category requiring vaginal brachytherapy specifically includes patients ≥60 years with deeply invasive grade 1-2 tumors OR superficially invasive grade 3 tumors—neither applies here 1, 2.

Ensure complete pathologic review. Confirm that the final pathology definitively shows endometrioid histology (not serous, clear cell, or other high-risk subtypes) and that the grade is truly 1 (≤5% solid growth pattern) 1. Preoperative histology changes at final evaluation in up to 25% of cases 1.

Counsel the patient that her prognosis is excellent, with 5-year survival rates exceeding 90% for stage IA grade 1 disease 4, and that observation alone is the standard of care 1, 2.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Grade 1 Endometrial Cancer

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Approach to Endometrial Cancer

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Endometrial adenocarcinoma: a primer for the generalist.

Obstetrics and gynecology clinics of North America, 2001

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.