Mechanism-Driven Evolution of Fertility-Sparing Treatment and Precision Management of Special Populations in Endometrial Cancer: A Review.
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CC-BY-4.0
Abstract
Endometrial cancer is increasingly diagnosed in patients who have not yet completed childbearing. For carefully selected patients with grade 1 endometrioid endometrial carcinoma confined to the endometrium, fertility-sparing treatment (FST) can preserve reproductive potential but requires rigorous histologic surveillance. In eligible patients, oral progestins and/or the levonorgestrel-releasing intrauterine system (LNG-IUS) remain the mainstay of fertility-sparing treatment, with hysteroscopic lesion resection incorporated in selected cases. Obesity, polycystic ovary syndrome, abnormalities in glucose metabolism, molecular subtype, and primary or acquired progestin resistance collectively contribute to heterogeneity in treatment response and the risk of recurrence. This narrative review critically integrates current guidelines, randomized controlled trials, prospective studies, retrospective cohorts, and early exploratory evidence to evaluate the biological rationale, clinical positioning, efficacy, safety, and maturity of evidence for progestin-based therapy, metabolic interventions, combined endocrine approaches, molecularly guided strategies, and exploratory immunotherapeutic approaches. We further propose an integrated clinical pathway encompassing candidate selection, molecular assessment, response evaluation, transition to pregnancy, retreatment after recurrence, and timely conversion to definitive surgery. Importantly, this review distinguishes guideline-supported approaches from adjunctive, investigational, and exploratory strategies. Major evidence gaps include inconsistent definitions of treatment response, limited prospective molecularly stratified data, uncertain reproductive safety of emerging systemic therapies, and insufficient long-term data on pregnancy outcomes and offspring.
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SciLite annotations
chemicals 85
androgen
progestin
levonorgestrel
glucose
progestin
progestin
progestin
glucose
progestin
progestin
progestin
levonorgestrel
metformin
progestin
estrogen
progesterone
progestin
progestin
estrogen
progestin
medroxyprogesterone
acetate
megestrol
acetate
progestin
progestin
progestin
progestin
levonorgestrel
progestin
levonorgestrel
progestin
progestin
progestin
progestin
glucose
estrogen
progestin
glucose
estrogen
levonorgestrel
progesterone
androgen
progestin
metformin
glucose
estrogen
estrogen
glucose
metformin
medroxyprogesterone
acetate
metformin
megestrol acetate
metformin
progestin
metformin
metformin
glucose
metformin
+25 more
organisms 4
noordeloos 2009062
human
human
human
Source provenance
- europepmc
- last seen: 2026-09-20T09:27:46.357103+00:00
- scilite
- last seen: 2026-09-20T10:02:19.494152+00:00
License: CC-BY-4.0
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Per Europe PMC
Per Europe PMC