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Evaluation of HE4, CA125, risk of ovarian malignancy algorithm (ROMA) and risk of malignancy index (RMI) as diagnostic tools of epithelial ovarian cancer in patients with a pelvic mass
Authors:Mona Aarenstrup KarlsenNoreen Sandhu,Claus Hø  gdallIb Jarle Christensen,Lotte NedergaardLene Lundvall,Svend A. EngelholmAnette T. Pedersen,Dorthe HartwellMagnus Lydolph,Inga Alice Laursen,Estrid V.S. Hø  gdall
Affiliation:
  • a Department of Pathology, Molecular Unit, Herlev University Hospital, University of Copenhagen, Denmark
  • b Department of Clinical Biochemistry and Immunology, Statens Serum Institut, Copenhagen, Denmark
  • c Gynecologic Clinic, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
  • d Finsen Laboratory, Rigshospitalet, Copenhagen Biocenter, Copenhagen, Denmark
  • e Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
  • f Department of Radiation Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
  • Abstract:

    Objective

    Diagnostic factors are needed to improve the currently used serum CA125 and risk of malignancy index (RMI) in differentiating ovarian cancer (OC) from other pelvic masses, thereby achieving precise and fast referral to a tertiary center and correct selection for further diagnostics. The aim was to evaluate serum Human Epididymis protein 4 (HE4) and the risk of ovarian malignancy algorithm (ROMA) for these purposes.

    Methods

    Serum from 1218 patients in the prospective ongoing pelvic mass study was collected prior to diagnosis. The HE4 and CA125 data were registered and evaluated separately and combined in ROMA and compared to RMI.

    Results

    809 benign tumors, 79 borderline ovarian tumors, 252 OC (64 early and 188 late stage), 9 non-epithelial ovarian tumors and 69 non-ovarian cancers were evaluated. Differentiating between OC and benign disease the specificity was 62.2 (CA125), 63.2 (HE4), 76.5 (ROMA) and 81.5 (RMI) at a set sensitivity of 94.4 which corresponds to RMI = 200. The areas under the curve (AUC) were 0.854 (CA125), 0.864 (HE4), 0,897 (ROMA) and 0.905 (RMI) for benign vs. early stage OC. For premenopausal benign vs. OC AUC were 0.925 (CA125), 0.905 (HE4), 0.909 (ROMA) and 0.945 (RMI).

    Conclusion

    HE4 and ROMA helps differentiating OC from other pelvic masses, even in early stage OC. ROMA performs equally well as the ultrasound depending RMI and might be valuable as a first line biomarker for selecting high risk patients for referral to a tertiary center and further diagnostics. Further improvements of HE4 and ROMA in differentiating pelvic masses are still needed, especially regarding premenopausal women.
    Keywords:Ovarian cancer   HE4   ROMA   Tumor markers
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