Home > Journals > Minerva Medica > Past Issues > Minerva Medica 2020 April;111(2) > Minerva Medica 2020 April;111(2):133-40

CURRENT ISSUE
 

JOURNAL TOOLS

Publishing options
eTOC
To subscribe
Submit an article
Recommend to your librarian
 

ARTICLE TOOLS

Publication history
Reprints
Permissions
Cite this article as
Share

 

ORIGINAL ARTICLE   

Minerva Medica 2020 April;111(2):133-40

DOI: 10.23736/S0026-4806.20.06474-5

Copyright © 2020 EDIZIONI MINERVA MEDICA

language: English

The generally low sensitivity of CA 125 for FIGO stage I ovarian cancer diagnosis increases for endometrioid histotype

Giovanni GRANDI 1 , Anna M. PERRONE 2, Angela TOSS 3, Amerigo VITAGLIANO 4, Stefano FRISO 2, Fabio FACCHINETTI 1, Laura CORTESI 3, Stefano CASCINU 3, Pierandrea DE IACO 2

1 Department of Medical and Surgical Sciences for Mother, Child and Adult, University Polyclinic of Modena, University of Modena and Reggio Emilia, Modena, Italy; 2 Unit of Gynecologic Oncology, S. Orsola-Malpighi Polyclinic,
University of Bologna, Bologna, Italy; 3 Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy; 4 Unit of Gynecology and Obstetrics, Department of Women and Children’s Health, University of Padua, Padua, Italy



BACKGROUND: The serum marker CA 125 is still the most widely used biomarker for ovarian cancer (OC) diagnosis in gynecological and oncological setting, but its predictive role in early-stage OC is still debated. The aim of this study was to explore the value of CA 125 in distinguishing between early-stage OC and borderline ovarian tumor (BOT) and to evaluate the accuracy of CA 125 in the detection of early stage OC.
METHODS: A retrospective cohort study was performed at the University Hospital of Bologna (Italy) on 1296 consecutive women suffering from OC or BOT (diagnosed at histology) between 1988-2017. Patients for whom CA 125 level was determined preoperatively were included. The positive cut-off level used was >35 U/mL.
RESULTS: Of 910 patients, 192 (21.1%) were diagnosed with BOT and 718 (78.9%) with OC. The sensitivity of CA 125 for stage I OC was 54.4 (95% CI: 45.3-63.3) (51.5 for IA, 54.6 for IB, 58.3 for IC), but it increased to 78.0 (95% CI: 63.7-88.0) for stage II. Interestingly, in stage I OC, CA 125 presented a significantly higher sensitivity for the endometrioid histotype [72.4 (95% CI: 52.5-86.5) vs. 49.0 (95% CI: 38.6-59.4), P=0.026]. The positive likelihood ratio of CA 125 for early-stage OC compared to BOT was 1.29 (95% CI: 1.06-1.58).
CONCLUSIONS: Despite its limited sensitivity for early-stage OCs, CA 125 still represents a useful serum marker to early differentiate between OCs and BOTs. Its sensitivity for stage I OC increases in endometrioid histotype.


KEY WORDS: Ovarian neoplasms; CA 125 antigen; Early diagnosis

top of page