Correlation of tumor size with other prognostic factors in uterine serous carcinoma: A large multi-institutional study |
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Authors: | I. Winer H. Mahdi S. Bandyopadhyay A. Semaan K.K. Van de Vijver M.R. Nucci F. Abdul-Karim Y. Hussein F. Qureshi K. Hayek B. Alosh D. Schulz M. Cote A. Munkarah R. Morris E. Oliva R. Ali-Fehmi |
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Affiliation: | 1. Division of Gynecologic Oncology, Department of OB/GYN, Wayne State University and Karmanos Cancer Institute, Detroit, MI, USA;2. Department of OB/GYN, University of Washington Medical Center, Seattle, WA, USA;3. Department of Pathology, Wayne State University, Detroit, MI, USA;4. Department of Pathology, Brigham and Women''s Hospital, Harvard Medical School, Boston, MA, USA;5. Department of Anatomic Pathology, Cleveland Clinic Foundation, Cleveland, OH, USA;6. Department of Pathology, Henry Ford Health System, Detroit MI, USA;7. Department of Epidemiology, Karmanos Cancer Institute, Detroit, MI, USA;8. Division of Gynecologic Oncology, Department of OB/GYN, Henry Ford Health System, Detroit, MI, USA;9. Department of Pathology, Massachussetts General Hospital, Harvard Medical School, Boston, MA, USA |
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Abstract: | ObjectiveUterine serous carcinoma (USC) constitutes 10% of uterine cancers but ~ 40% of deaths. Tumor size is a known prognostic factor in other solid tumors. In endometriod cancers it is one element used to identify the need for complete staging, while its significance in USC is debated. Therefore tumor size was examined as an independent prognostic factor.MethodsClinical and pathologic variables were recorded for 236 institutional patients, and those patients in the SEER database with USC. Chi-square and Fisher exact t-tests were utilized and survival data generated via Kaplan–Meier method; multivariate analysis was performed via cox-regression.ResultsThe patients' mean age was 67.2 years (range 40–91). Survival ranged from 0 to 184 months (mean 42.8). We used a tumor size cut-off of 1 cm and noted significant associations with myometrial invasion (p < 0.0001), angiolymphatic invasion (p < 0.0001), peritoneal washings (p = 0.03), stage (p = 0.015) and positive lymph nodes (p = 0.05). Furthermore, recurrence was associated with larger tumors (p = 0.03). In multivariate analysis, extra-uterine disease was the only factor associated with both recurrence and survival. Review of the SEER database noted association of larger tumors with lymph node involvement and a significant survival advantage with tumors < 1 cm in both univariate and multivariate analysis.ConclusionsTreatment options for USC are often predicated on the surgical stage and therefore components of the staging are vitally important. The 1 cm tumor-size cut-off should be studied prospectively as a prognostic indicator of survival and recurrence in USC and considered for inclusion in USC staging. |
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