Cancer antigen 125 is associated with disease status in uterine carcinosarcoma

Author:

Ross Malcolm Strachan1ORCID,Chandler Chelsea Kilpatrick2,Matsuo Koji3,Vargo John Austin4,Elishaev Esther5,Siripong Nalyn6,Berger Jessica Layne2,Kelley Joseph Leo2,Taylor Sarah Elizabeth2

Affiliation:

1. Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Magee-Womens Hospital, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

2. Department of Obstetrics and Gynecology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

3. Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, CA, USA

4. Division of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

5. Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

6. Clinical and Translational Science Institute, University of Pittsburgh, Pittsburgh, PA, USA

Abstract

Uterine carcinosarcoma is a rare and aggressive tumor with poor outcomes. Cancer antigen 125 is routinely used to track the disease course of ovarian cancer and has been suggested as a biomarker in other aggressive forms of uterine cancer. We sought to characterize cancer antigen 125 as a potential biomarker of disease status in uterine carcinosarcoma. Clinical and pathological data were abstracted for patients who had surgical staging for a pathologically confirmed uterine carcinosarcoma at our institution from January 2000 to March 2014. Non-parametric tests were used to compare changes in cancer antigen 125. Elevated cancer antigen 125 (>35 U/mL) as a predictor of survival was assessed via Kaplan–Meier curves. Among the 153 patients identified, 66 patients had at least one paired measure of cancer antigen 125 drawn preoperatively, post-treatment, or at the time of disease recurrence, and 19 patients had cancer antigen–125 levels at all three time points. Analysis of the 51 patients with both preoperative and post-treatment values found a significant drop in cancer antigen 125 ( p < 0.001). Among the 30 patients who had end-of-treatment and recurrence levels, a significant increase was noted ( p = 0.001). There was no significant difference in cancer antigen–125 levels preoperatively compared to at recurrence among the 23 patients with levels at both time-points ( p = 0.99). Elevated preoperative cancer antigen 125 was not associated with overall survival ( p = 0.12); elevated post-treatment cancer antigen 125 was associated with a worse overall survival ( p < 0.001). Based on this dataset, there seems to be utility in trending a cancer antigen–125 level in patients with uterine carcinosarcoma. A cancer antigen–125 level could predict recurrence and provide prognostic information regarding survival.

Funder

NIH Clinical Center

Publisher

SAGE Publications

Subject

Oncology,Histology

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