Martin Köbel1, Eshetu G Atenafu2, Peter F Rambau3, Sarah E Ferguson4, Gregg S Nelson5, T C Ho6, Tony Panzarella2, Jessica N McAlpine7, C Blake Gilks8, Blaise A Clarke9, Marcus Q Bernardini4. 1. Department of Pathology and Laboratory Medicine, University of Calgary, Canada. Electronic address: martin.koebel@cls.ab.ca. 2. Biostatistics Department, Princess Margaret Cancer Centre, Canada; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Canada. 3. Department of Pathology and Laboratory Medicine, University of Calgary, Canada. 4. Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Toronto, Canada. 5. Division of Gynecologic Oncology, University of Calgary, Canada. 6. Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Canada. 7. Division of Gynecologic Oncology, University of British Columbia, Canada. 8. Division of Anatomic Pathology, University of British Columbia, Canada. 9. Department of Pathology and Laboratory Medicine, University of Toronto, Canada.
Abstract
OBJECTIVE: To assess the association of hormone receptor expression with outcome in high-grade endometrial carcinomas. METHODS: This study included three sites participating in the Canadian High Risk Endometrial Cancer (CHREC) consortium. Sections from tissue microarrays containing cases with a diagnosis of endometrioid grade 3 (EC3) and endometrial serous carcinoma (ESC) were assessed for estrogen (ER) and progesterone receptor (PR) expression by immunohistochemistry. Expression was considered present if >1% of tumor cell nuclei were labeled. Associations with overall survival were assessed. RESULTS: ER expression was present in 168/216 (78%) of EC3 and 124/192 (65%) of ESC. PR expression was present in 148/212 (70%) of EC3 and 83/196 (42%) of ESC. PR expression was significantly associated with favorable overall survival in EC3 and ESC (log rank, p=0.018 and p=0.0024) but ER expression was not. PR expression was significantly associated with favorable overall survival in EC3 independent of age, stage, center and lymph-vascular invasion (hazard ratio=0.457, 95% CI 0.257-0.811, p=0.0075) as well as in stage I and II ESC (hazard ratio=0.266, 95% CI 0.094-0.750, p=0.0123). CONCLUSION: Our data provide support for the assessment of the PR expression status in EC3 and ESC. Future work will be required to determine how PR expression may be incorporated into management of patients with EC3 and ESC.
OBJECTIVE: To assess the association of hormone receptor expression with outcome in high-grade endometrial carcinomas. METHODS: This study included three sites participating in the Canadian High Risk Endometrial Cancer (CHREC) consortium. Sections from tissue microarrays containing cases with a diagnosis of endometrioid grade 3 (EC3) and endometrial serous carcinoma (ESC) were assessed for estrogen (ER) and progesterone receptor (PR) expression by immunohistochemistry. Expression was considered present if >1% of tumor cell nuclei were labeled. Associations with overall survival were assessed. RESULTS: ER expression was present in 168/216 (78%) of EC3 and 124/192 (65%) of ESC. PR expression was present in 148/212 (70%) of EC3 and 83/196 (42%) of ESC. PR expression was significantly associated with favorable overall survival in EC3 and ESC (log rank, p=0.018 and p=0.0024) but ER expression was not. PR expression was significantly associated with favorable overall survival in EC3 independent of age, stage, center and lymph-vascular invasion (hazard ratio=0.457, 95% CI 0.257-0.811, p=0.0075) as well as in stage I and II ESC (hazard ratio=0.266, 95% CI 0.094-0.750, p=0.0123). CONCLUSION: Our data provide support for the assessment of the PR expression status in EC3 and ESC. Future work will be required to determine how PR expression may be incorporated into management of patients with EC3 and ESC.
Authors: Peter Rambau; Linda E Kelemen; Helen Steed; May Lynn Quan; Prafull Ghatage; Martin Köbel Journal: Int J Mol Sci Date: 2017-02-27 Impact factor: 5.923
Authors: Anthony N Karnezis; Samuel Leung; Jamie Magrill; Melissa K McConechy; Winnie Yang; Christine Chow; Martin Kobel; Cheng-Han Lee; David G Huntsman; Aline Talhouk; Friederich Kommoss; C Blake Gilks; Jessica N McAlpine Journal: J Pathol Clin Res Date: 2017-10-14