Study Objective
To investigate whether endometrial ablation carries an increased risk or delayed diagnosis of endometrial cancer compared to medical management for abnormal uterine bleeding.
Design
A multi-centered retrospective cohort study comparing rates of endometrial cancer in women who underwent treatment for abnormal uterine bleeding.
Design Classification
Canadian Task-Force Classification II-2
Setting
This study was conducted using data from The Health Improvement Network (THIN), a representative population-based cohort of patients in 495 outpatient General Practitioner practices in the UK.
Participants
Women >25 years of age with an abnormal uterine bleeding diagnosis between June 1994 and September 2010.
Interventions
Endometrial ablation, medical management, or both.
Measurements and Main Results
A total of 234,721 women met study inclusion and exclusion criteria, 4,776 of whom underwent endometrial ablation and the remaining 229,945 underwent medical management. Cox models compared endometrial cancer rates between ablation and medical management groups using hazard ratios (HRs). To investigate a possible diagnostic delay, the median time from bleeding diagnosis to endometrial cancer diagnosis among women who developed endometrial cancer was compared using the Mann-Whitney U test. All statistical tests were two-tailed with α=.05. Over a median observation time of 4.07 years (IQR, 1.88-7.17), three and 601 women developed endometrial cancer in the ablation and medical management groups, respectively (ablation HR, 0.45; 95% CI, 0.15-1.40; p=.17). Median time to diagnosis was 237 and 299 days (ablation IQR, 155-1350; medical management IQR, 144-1,133.5; p=.99) in the ablation and medical management groups, respectively. Adjusted and sensitivity analyses did not change the results.
Conclusions
No difference was seen in endometrial cancer rates, nor was there a delay in diagnosis when comparing endometrial ablation versus medical management. Further studies are needed to investigate the impact of prior ablation exposure on histology or cancer stage at presentation of endometrial cancer.