CA‐125 change after chemotherapy in prediction of treatment outcome among advanced mucinous and clear cell epithelial ovarian cancers |
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Authors: | Chunqiao Tian MS Maurie Markman MD Richard Zaino MD Robert F. Ozols MD William P. McGuire MD Franco M. Muggia MD Peter G. Rose MD David Spriggs MD Deborah K. Armstrong MD |
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Affiliation: | 1. Gynecologic Oncology Group Statistical and Data Center, Roswell Park Cancer Institute, Buffalo, New York;2. Department of Gynecologic Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas;3. Fax: (713) 563‐9586;4. M. S. Hershey Medical Center, Pennsylvania State University, Hershey, Pennsylvania;5. Fox Chase Cancer Center, Philadelphia, Pennsylvania;6. Harry and Jeanette Weinberg Cancer Institute, Franklin Square Hospital Center, Baltimore, Maryland;7. Kaplan Cancer Center, New York University Medical Center, New York, New York;8. Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Cleveland Clinic Foundation, Cleveland, Ohio;9. Memorial Sloan‐Kettering Cancer Center, New York, New York;10. Johns Hopkins Kimmel Cancer Center, Baltimore, Maryland |
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Abstract: |
BACKGROUND: There are limited data regarding unique clinical or laboratory features associated with advanced clear cell (CC) and mucinous (MU) epithelial ovarian cancers (EOC), particularly the relationship between CA‐125 antigen levels and prognosis. METHODS: A retrospective review of 7 previously reported Gynecologic Oncology Group phase 3 trials in patients with stage III/IV EOC was conducted. A variety of clinical parameters were examined, including the impact of baseline and changes in the CA‐125 level after treatment of CC and MU EOC on progression‐free (PFS) and overall survival (OS). RESULTS: Clinical outcomes among patients with advanced CC and MU EOC were significantly worse when compared with other cell types (median PFS, 9.7 vs 7.0 vs 16.7 months, respectively, P < .001; median OS, 19.4 vs 11.3 vs 40.5 months, respectively, P < .001). Suboptimal debulking was associated with significantly decreased PFS and OS among both. Although baseline CA‐125 values were lower in CC (median, 154 μ/mL) and MU (100 μ/mL), compared with other cell types (275 μ/mL), this level did not appear to influence outcome among these 2 specific subtypes of EOC. However, an elevated level of CA‐125 at the end of chemotherapy was significantly associated with decreased PFS and OS (P < .01 for all). CONCLUSIONS: Surgical debulking status is the most important variable at prechemotherapy predictive of prognosis among advanced CC and MU EOC patients. Changes in the CA‐125 levels at the end treatment as compared with baseline can serve as valid indicators of PFS and OS, and likely the degree of inherent chemosensitivity. Cancer 2009. © 2009 American Cancer Society. |
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Keywords: | CA‐125 clear cell cancer mucinous cell cancer ovarian cancer |
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