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Exploratory Analysis of CA125-MGL and –STn Glycoforms in the Differential Diagnostics of Pelvic Masses

Taija Heinosalo; Liina Salminen; Kim Pettersson; Anne Dørum; Kaisa Huhtinen; Seija Grènman; Anne Lone Rolfsen; Antti Perheentupa; Matti Poutanen; Nimrah Nadeem; Nils Bolstad; Sakari Hietanen; Urpo Lamminmäki; Johanna Hynninen; Kamlesh Gidwani; Teemu D Laajala; Olli Carpén

Exploratory Analysis of CA125-MGL and –STn Glycoforms in the Differential Diagnostics of Pelvic Masses

Taija Heinosalo
Liina Salminen
Kim Pettersson
Anne Dørum
Kaisa Huhtinen
Seija Grènman
Anne Lone Rolfsen
Antti Perheentupa
Matti Poutanen
Nimrah Nadeem
Nils Bolstad
Sakari Hietanen
Urpo Lamminmäki
Johanna Hynninen
Kamlesh Gidwani
Teemu D Laajala
Olli Carpén
Katso/Avaa
Accepted manuscript (10).pdf (478.0Kb)
Lataukset: 

Journal of Applied Laboratory Medicine
doi:10.1093/jalm/jfz012
URI
https://academic.oup.com/jalm/article/5/2/263/5743458
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042823093
Tiivistelmä
Background

The cancer antigen 125 (CA125) immunoassay (IA) does not distinguish epithelial ovarian cancer (EOC) from benign disease with the sensitivity needed in clinical practice. In recent studies, glycoforms of CA125 have shown potential as biomarkers in EOC. Here, we assessed the diagnostic abilities of two recently developed CA125 glycoform assays for patients with a pelvic mass. Detailed analysis was further conducted for postmenopausal patients with marginally elevated conventionally measured CA125 levels, as this subgroup presents a diagnostic challenge in the clinical setting.


Methods

Our study population contained 549 patients diagnosed with EOC, benign ovarian tumors, and endometriosis. Of these, 288 patients were postmenopausal, and 98 of them presented with marginally elevated serum levels of conventionally measured CA125 at diagnosis. Preoperative serum levels of conventionally measured CA125 and its glycoforms (CA125-MGL and CA125-STn) were determined.


Results

The CA125-STn assay identified EOC significantly better than the conventional CA125-IA in postmenopausal patients (85% vs. 74% sensitivity at a fixed specificity of 90%, P = 0.0009). Further, both glycoform assays had superior AUCs compared to the conventional CA125-IA in postmenopausal patients with marginally elevated CA125. Importantly, the glycoform assays reduced the false positive rate of the conventional CA125-IA.


Conclusions

The results indicate that the CA125 glycoform assays markedly improve the performance of the conventional CA125-IA in the differential diagnosis of pelvic masses. This result is especially valuable when CA125 is marginally elevated.

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