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abstract
Objectives
ACOG
guidelines for the evaluation of women with a pelvic mass employ a
combination of physical exam, imaging, and CA125 to guide physicians in
the triage of women to gynecologic oncologists. We studied the use of
ROMA with clinical assessment for cancer risk assessment in women with a
pelvic mass.
Methods
This was a
prospective, multicenter trial evaluating women with a pelvic mass who
had an initial clinical risk assessment (ICRA) performed by a
generalist. ROMA scores were calculated and sensitivity, specificity,
PPV and NPV were determined for ICRA and ICRA + ROMA.
Results
A
total of 461 women were entered into the study. There were 375 benign
tumors, 48 EOC, 18 LMP tumors and 20 non-ovarian malignancies. For
detection of ovarian cancer alone, ICRA had a sensitivity of 85.4%, a
specificity of 84.3%, and a NPV of 97.8%. Adding ROMA to ICRA produced a
significant improvement of 8.4% in sensitivity, achieving a sensitivity
of 93.8% with a specificity of 67.2% and a NPV of 98.8%. Examination of
all malignancies (ovarian & non-ovarian) provided a sensitivity of
89.7% for ROMA + ICRA in comparison to 77.9% for ICRA alone, a
significant increase in sensitivity of 11.8%. The NPV also significantly
increased from 95.5% to 97.3%. Overall, ROMA detected 13 additional
malignancies missed by ICRA.
Conclusions
Adjunctive
use of ROMA with clinical assessment improves the stratification of
women with a pelvic mass into low and high risk groups for ovarian
cancer. The combination is particularly effective in ruling out
malignant disease.
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