Endometrial cancer detected with transvaginal ultrasound in postmenopausal women
Jacobs I. Lancet Oncol. 2010;doi:10.1016/S1470-2045(10)70268-0.
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Transvaginal ultrasound is an effective method of screening for endometrial cancer among postmenopausal women, according to data from the United Kingdom Collaborative Trial of Ovarian Cancer Screening. The sensitivity and specificity of the test was between 80% and 90%.
“In the general population, there has been limited enthusiasm to explore the usefulness of screening for endometrial cancer because patients have a good prognosis relative to other cancers,” the researchers wrote. “However, in view of the rising incidence of endometrial cancer, coupled with increasing life expectancy, there is now a need to revisit screening.”
Using data from the United Kingdom Collaborative Trial of Ovarian Cancer Screening (UKCTOCS), a prospective trial of ovarian cancer screening, researchers performed a nested case-control study of 48,230 postmenopausal women who underwent transvaginal ultrasound. At the time of the UKCTOCS, researchers recorded data on endometrial thickness and endometrial abnormalities and documented the diagnosis of endometrial cancer using national registries and a mailed questionnaire. The primary outcome measure was endometrial cancer and atypical endometrial hyperplasia, according to the researchers.
Within 1 year of transvaginal ultrasound, they also calculated performance characteristics of endometrial thickness and abnormalities for the detection of endometrial cancer. A logistic regression model was developed, and a screening strategy for women at higher risk was assessed. Median follow-up was 5.11 years.
Patients with hysterectomy (n=9,078) and those whose endometrial thickness was not measured (n=2,271) were excluded from the study; however, 157 of these women had an abnormality on transvaginal ultrasound and were included. The primary analysis included 136 women with endometrial cancer or atypical endometrial hyperplasia within 1 year of transvaginal ultrasound.
The optimum endometrial thickness cutoff for endometrial cancer or atypical endometrial hyperplasia was 5.15 mm; transvaginal ultrasound had 80.5% sensitivity (95% CI, 72.7-86.8) and 86.2% specificity (95% CI, 85.8-86.6). For a cutoff of at least 5 mm, sensitivity was 80.5% (95% CI, 72.7-86.8) and specificity was 85.7% (95% CI, 85.4-86.6); for women with a cutoff of at least 5 mm plus endometrial abnormalities, the sensitivity was 85.3% (95% CI, 78.2-90.8) and specificity was 80.4% (95% CI, 80-80.8). Sensitivity was 54.1% (95% CI, 45.3-62.8) and specificity was 97.2% (95% CI, 97.0-97.4) for a cutoff of at least 10 mm.
Ninety-six women had endometrial cancer or atypical endometrial hyperplasia with no symptoms of postmenopausal bleeding before diagnosis. Among these women, a cutoff of 5 mm had sensitivity of 77.1% (95% CI, 67.8-84.3) and specificity of 85.8% (95% CI, 85.7-85.9). According to the logistic regression model, 25% of patients were at high risk, and 39.5% of those with endometrial cancer or atypical endometrial hyperplasia were included in this high-risk group. A cutoff of 6.75 mm had 84.3% (95% CI, 71.4-93) sensitivity and 89.9% (95% CI, 89.3-90.5) specificity in this population.
“The rising incidence of endometrial cancer and the difficulty of doing a randomized controlled trial large enough to specify mortality as an endpoint suggest that the decision to introduce screening for all or a subgroup of asymptomatic women will rest on surrogate criteria such as the performance characteristics described in our report and future studies of acceptability, health economics and risk stratification,” the researchers wrote. “We do not advocate population screening for endometrial cancer until further data are available from these studies.”
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