Ovarian Cancer Clinical Trial
Official title:
Regional Study Into the Performance and Cost-effectiveness of Simple Ultrasound-based Rules Compared to the Currently Used Risk of Malignancy Index in the Diagnosis of Ovarian Cancer
This study is performed to compare the diagnostic performance and cost-effectiveness of different diagnostic methods for differentiating benign from malignant adnexal (ovary or Fallopian tube) masses: the Risk of Malignancy Index (RMI) will be compared with a two-step triage test called "simple ultrasound-based rules" supplemented -if necessary- with either subjective assessment by an expert sonographer or Diffusion Weighted - Magnetic Resonance Imaging (DW-MRI). The investigators will test the hypothesis that this two-step triage test will have better diagnostic accuracy than the RMI and therefore will improve the management of women with adnexal masses.
Estimating whether an adnexal mass is malignant or not is essential in the preoperative
management of adnexal masses. Recognizing cancer means treatment is not delayed and
appropriate staging or debulking surgery can be carried out after referral to specialized
surgical centers. Vice versa, benign lesions may be managed conservatively or with minimal
invasive surgery in non-centre hospitals. This will limit morbidity and will avoid
unnecessary costs: laparoscopic surgery offers lower estimated blood loss, shorter hospital
stay, and fewer postoperative complications with an improved quality of life and faster
return to normal functioning.
There are several methods to distinguish benign from malignant adnexal masses. The commonly
used method in clinical practice is the Risk of Malignancy Index (RMI). The RMI is an easy
to use scoring system recommended by many national guidelines concerning the management of
ovarian masses, including the national guideline in the Netherlands. The RMI combines
ultrasound variables, menopausal status and serum CA125 into a score used to predict the
risk of ovarian cancer before surgery. However, the reported sensitivity and specificity of
RMI at a cut-off value of 200 are relatively low; 75-80% and 85-90%, respectively.
Another method called 'simple ultrasound-based rules' (simple rules), uses different
morphological ultrasound features of adnexal masses (without including menopausal status or
serum CA125 measurement). It includes five simple ultrasound-based rules to predict
malignancy (M-rules) and five rules to predict a benign tumor (B-rules). If both or none of
the M- and B-rules are met (20% of the patients) the test is inconclusive. Recent reports
show that simple rules might be superior to the RMI. In adnexal masses for which the simple
ultrasound rules yield an inconclusive result, subjective assessment of Gray-scale and color
Doppler ultrasound images by an experienced ultrasound examiner can be used as a second
stage test to achieve an optimal diagnostic performance. Subjective assessment by an expert
sonographer is superior to any scoring system or mathematical model when classifying adnexal
masses as benign or malignant. However, it is not feasible and efficient that every patient
would undergo an expert ultrasonography. Therefore, this method is better used as a second
stage test.
Another option is to use Diffusion Weighted - Magnetic Resonance Imaging (DW-MRI) as a
second stage test, when the simple rules yield an inconclusive result. The use of MRI - when
interpret by specialized radiologists- also seems to be superior to RMI in the preoperative
identification of adnexal masses.
The Risk of Malignancy Index (RMI) is the current standard in differentiating benign from
malignant adnexal masses. The simple ultrasound-based rules as a first stage triage test
followed by either subjective assessment by an experienced ultrasound examiner or DW-MRI in
case the simple rules are inconclusive, is the test of comparison. Both the RMI and the
simple rules will be performed in the regional hospitals and MUMC+ by general gynaecologists
during the same ultrasound scan. Only when the simple rules are inconclusive the patient
will be referred to the MUMC+ for a second stage test. From previous publications it can be
deducted that this will be in approximately 20% of patients. Approximately 80% of patients
will not need any additional second stage test.
The histology of the surgically removed adnexal masses is the clinical reference standard.
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