Uterine-Conserving Treatment Options for Atypical Endometrial Hyperplasia and Early Endometrial Cancer

Naomi N. Adjei & Shannon N. Westin et al. · 2024-10-03

This review aims to synthesize available literature on uterine-conserving treatment options for atypical endometrial hyperplasia and grade 1 endometrial carcinoma while highlighting remaining unanswered questions. The need for uterine-conserving treatment options for atypical endometrial hyperplasia and grade 1 endometrial carcinoma is growing with the increasing number of cases in younger patients or those who cannot undergo surgery. We reviewed the oncological and reproductive outcomes associated with endocrine therapies used for atypical endometrial hyperplasia and grade 1 endometrial carcinoma. The rising prevalence of delayed childbearing, obesity, and diabetes in reproductive-age individuals and of medical comorbidities associated with high surgical risk continues to amplify the demand for uterine-conserving therapies. Appropriate patient selection for such therapies is imperative to maximize likelihood of treatment response. The ideal candidates are patients with atypical endometrial hyperplasia or early-stage, low-grade endometrial cancer with no evidence of myometrial invasion or extrauterine disease. The most accepted conservative therapeutic approach is hormonal therapy with close surveillance, with or without eventual hysterectomy following childbearing or failure of treatment. Further prospective and randomized trials are needed to address optimal patient and treatment selection, as well as the use of molecular profiling for treatment individualization and prognostication.
Authors
Naomi N. Adjei, Mikayla Borthwick Bowen, Roni Nitecki Wilke, Melinda S. Yates, Shannon N. Westin
Funding

NCI NIH HHS

T32 CA101642

NCI NIH HHS

P30 CA016672

UTHealth Innovation for Cancer Prevention Research Training Program Pre-doctoral Fellowship

Cancer Prevention and Research Institute of Texas grant RP210042

NIH HHS

NIH T32 CA101642 grant

MD Anderson Cancer Center Support Grant

NIH/NCI P30 CA016672

NCI NIH HHS

P50 CA098258

National Institutes of Health Specialized Programs of Excellence in Uterine Cancer

5P50CA098258

National Institutes of Health

NIH T32 CA101642 grant

GOG Foundation Scholar Investigator Award