A contemporary analysis of the ability of preoperative serum CA-125 to predict primary cytoreductive outcome in patients with advanced ovarian, tubal and peritoneal carcinoma
Introduction
At the time of diagnosis, approximately 70% of women with ovarian cancer will have advanced-stage disease [1]. Currently, the standard management for advanced-stage epithelial ovarian cancer is attempted optimal surgical cytoreduction followed by platinum and taxane combination chemotherapy. Several studies have demonstrated that optimal primary cytoreduction improves survival in patients of ovarian cancer [2], [3], [4], [5], [6]. However, suboptimal cytoreduction confers no survival advantage and can increase morbidity as compared to delaying attempts at cytoreduction and treating with initial chemotherapy. Therefore, over the past two decades, significant research has focused on developing accurate and reliable preoperative models and strategies for predicting whether or not optimal cytoreduction can be accomplished. Computed tomography (CT) scans and preoperative CA-125 levels have been the two most studied preoperative modalities for predicting cytoreductive outcome.
In 2000, we reported that preoperative serum CA-125 may predict primary cytoreductive outcome in patients with stage III ovarian carcinoma [7]. Subsequent to that publication, however, we initiated a programmatic change in our primary surgical approach to advanced gynecologic malignancies using a more comprehensive debulking of upper abdominal disease [8]. The use of extensive upper abdominal procedures has led to a significantly increased rate of optimal primary cytoreduction, with improved progression-free and overall survival [8], [9].
The purpose of this study was to re-analyze the ability of preoperative CA-125 to predict primary cytoreductive outcome in patients with advanced ovarian, tubal, or primary peritoneal carcinoma since the incorporation of extensive upper abdominal procedures into our surgical armamentarium.
Section snippets
Methods
After obtaining approval from our Institutional Review Board, we retrospectively reviewed the records of all patients who underwent primary cytoreductive surgery at our institution for International Federation of Gynecology and Obstetrics (FIGO) stage III/IV ovarian, fallopian tube, or primary peritoneal carcinoma from January 1, 2001 to April 30, 2005. Some of these patients were previously enrolled in an ongoing prospective protocol evaluating the ability of preoperative serum CA-125 combined
Results
During the study period, a total of 277 patients who underwent attempted primary cytoreduction for advanced ovarian, fallopian tube, or peritoneal carcinoma were identified. The primary surgeon in all cases was an attending gynecologic oncologist. Patient characteristics are listed in Table 1. The median age of the study cohort was 62 years (range, 25–96). The majority of patients had primary ovarian carcinoma (84%), stage IIIC disease (78%), grade 3 tumors (84%), and of serous histology (87%).
Discussion
Since the seminal work of Griffiths in 1975, numerous retrospective studies have reported the benefits of tumor cytoreduction for advanced ovarian carcinoma [2], [3], [4], [5], [6], [9]. The appropriate cutoff level of residual disease that defines “optimal” cytoreduction remains an area of ongoing debate, with more recent studies including those of the Gynecologic Oncology Group (GOG) and our institution suggesting that no gross residual disease should be the goal of primary cytoreductive
Conflict of interest statement
YS has received research support from Plasma Surgical, served as a consultant for Covidien, and a speaker for Genzyme. All other authors have no conflicts of interest to declare.
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