- Open Access
Role of CA125 in predicting ovarian cancer survival - a review of the epidemiological literature
Journal of Ovarian Researchvolume 2, Article number: 13 (2009)
CA125 is the gold standard tumor marker in ovarian cancer. Serum level of CA125 is used to monitor response to chemotherapy, relapse, and disease progression in ovarian cancer patients. Thus, it is reasonable to investigate whether CA125 may have utility as a prognostic indicator as well in ovarian cancer. A large number of epidemiological studies have been carried out to this effect. This review summarizes all available epidemiological literature on the association between CA125 levels and survival in ovarian cancer. To place these studies in context, we provide some background information on CA125 and its role in ovarian cancer.
Ovarian cancer is the leading cause of mortality from gynecologic cancers in the United States (US), resulting in approximately 14,500 deaths annually . The overall lifetime risk of developing ovarian cancer for women in the US is 1.4% to 1.8%. This risk varies from 0.6% for women with no family history, at least three term pregnancies, and four or more years of oral contraceptive use, to 3.4% for nulliparous women with no oral contraceptive use. For women with a family history, the lifetime risk for ovarian cancer is estimated at 9.4% . The overall age-adjusted incidence rate for all ovarian cancer cases as reported by the Surveillance, Epidemiology, and End Results (SEER) Program of the National Cancer Institute is 16.23 cases per 100,000 women standardized to the 2000 US standard population . There is marked geographical variation in age standardized incidence and mortality rates of ovarian cancer, with the highest rates observed in Northern and Western Europe, notably Scandinavia, and in North America .
Ovarian cancer is often asymptomatic in its early stages and thus most patients have widespread disease at the time of diagnosis . Unfortunately, the majority of epithelial ovarian cancers remain clinically undetected until patients have developed late stage disease and only a mere 25% of cancers are detected as stage I disease . When diagnosed in Stage I, however, the cure rate can approach 90% with currently available cytoreductive surgery and combination chemotherapy . Ovarian cancer remains a disease that proves fatal to the majority of patients, but where chemotherapy has been established as a treatment that improves survival. A minority of patients attain long survival after such treatment . Despite the achievements of high response rates with surgery followed by chemotherapy [9–11], 75% of women ultimately die of complications associated with disease progression. Once stage III and IV ovarian cancer, which is defined by peritoneal and extra peritoneal metastatic spread, is diagnosed, the survival decreases from 95% at stage I to approximately 20-25% five-year survival despite appropriate treatment [12, 13]. Therefore, clinical outcome and possibly survival may be significantly improved by the identification of stage I disease without the need to change surgical or chemotherapeutic approaches . The development of an ovarian cancer-specific biomarker for the early detection of disease has the capacity to improve the dismal survival rate .
Tumor markers in ovarian cancer
The need for the development of reliable serum biomarkers for early detection and prognostication of ovarian cancer, which are both sensitive and specific, remains a long awaited priority. Investigators are aware of this need and the Early Detection Research Network (EDRN) established by the National Cancer Institute has proposed 'guidelines' for the development of screening biomarkers . In the management of ovarian cancer these biomarkers have been applied for monitoring response to treatment, for distinguishing malignant from benign pelvic masses, for estimating prognosis, for predicting response to individual drugs, and for detecting primary disease at an early stage . Several epitopes on the polymorphic epithelial mucin derived from the MUC1 gene have been identified as targets for a family of tumor markers which include CA549, CASA (cancer associated serum antigen), CA19-9, CA15-3, MCA, MOV-1 and TAG72. The cytokeratin proliferation markers TPS and CYFRA21-1 have also been explored in ovarian carcinoma . Amongst these markers the most extensively researched is CA125.
CA125 in ovarian cancer
The most widely used tumor marker in ovarian cancer, often considered the 'gold standard' is CA125 . It was first identified by Bast, Knapp, and colleagues  in 1981. CA125 is a high molecular weight glycoprotein which is raised in approximately 90% of patients with advanced epithelial ovarian cancer . CA125 is expressed by fetal amniotic and coelomic epithelium and in adult tissues derived from the coelomic (mesothelial cells of the pleura, pericardium, and peritoneum) and Mullerian (tubal, endometrial, and endocervical) epithelia. CA125 contains 2 major antigenic domains, namely, A and B, which bind the monoclonal antibodies OC125 and M11, respectively . Since its development, measurement of the serum level of the CA125 antigen has become a standard component of routine management of women with advanced ovarian cancer . CA125 levels of less than 35 U/mL are now accepted as normal [21, 24]. When stratified by disease stage, elevated levels were found in more than 90% of patients with advanced stage ovarian cancer but in only 50% of patients with stage I disease . In addition, elevated levels of CA125 are more strongly associated with serous, rather than mucinous tumors . Commonly accepted definitions of disease recurrence based on serum CA125 levels alone specify a doubling of this tumor marker level, either from the upper limit of normal (35 U/mL) in patients with normalization of this marker after primary treatment or from the nadir levels in patients with an elevated serum marker value that never normalizes after primary treatment [26, 27].
Numerous studies have confirmed the usefulness of CA125 levels in monitoring the progress of patients with epithelial ovarian cancer [18, 28–30]. Most reports indicate that a rise in CA125 levels precedes clinical detection by about 3 months . Unfortunately, a few prospective studies indicated the inadequate sensitivity of CA125 in the setting of ovarian cancer screening in asymptomatic populations [32–34]. Despite the well-characterized limitations in the interpretation of a solitary CA125 value, this biomarker is widely used to prospectively evaluate therapeutic efficacy and monitor disease status among ovarian cancer patients [35, 36]. CA125 antigen is a serum marker which has been sufficiently well validated to be of use in routine clinical care . Thus, it is reasonable to seek to determine whether CA125 may have utility as a prognostic indicator and could in the future be used to individualize treatment of patients with ovarian cancer . The goal of this review is to qualitatively summarize the scientific literature on serum CA125 and survival in ovarian cancer and to make recommendations for future research.
Search Strategy and Selection Criteria
We conducted MEDLINE searches to identify all the studies on the relationship between serum CA125 level and survival in ovarian cancer published between 1985 and 2009. We searched using the terms "survival/mortality/prognosis in ovarian cancer" in combination with the following terms: prechemotherapy serum CA125, postchemotherapy serum CA125, preoperative serum CA125, postoperative serum CA125, CA125 half-life, CA125 nadir level, time to reach nadir level, CA125 Area Under the Curve (AUC). We also searched the bibliographies of the selected papers to identify relevant articles that we might have missed during the primary MEDLINE search. To be included in the review, a study must have: been published in English, reported on data collected in humans with ovarian cancer, had CA125 as one of the predictor variables measured as follows (absolute value, half-life, nadir, time to reach nadir and AUC), had survival as one of the outcome measures (primary or secondary), and had any of the following study designs (case-control, cohort, cross-sectional, prospective, retrospective, case series, longitudinal, clinical trial, meta-analysis). There were no restrictions according to age, ethnicity, type or stage of ovarian cancer. All studies reviewed in this paper have been summarized in tables under separate headings and arranged chronologically by the year of publication.
Although we did not formally rate the quality of reports, we recorded and present information on variables that may reflect the quality of reporting. The variables included study design (retrospective or prospective), years of data collection, sample size, and inclusion of important prognostic factors in multivariate analyses.
Epidemiologic Studies on CA125 and Ovarian Cancer Survival
Prechemotherapy Absolute Serum CA125 and Ovarian Cancer Survival
Table 1 summarizes the epidemiologic studies on the association between absolute prechemotherapy CA125 levels and survival in ovarian cancer. A study assessed the relationship between survival and early changes in the serum level of the CA125 antigen in advanced ovarian cancer. While pretreatment CA125 values did not correlate with survival, the concentration of this tumor marker 8 weeks after initiation of therapy was a powerful independent prognostic factor. The median survival for patients (n = 51) with a CA125 < 35 U/ml, vs. patients (n = 50) with a CA125 > 35 U/ml, at this time point, were 26 months and 15 months, respectively. Further, women with serum CA125 values < 50% of their pre-treatment concentration at 8 weeks experienced a median survival of 21 months, compared to only 10 months for individuals with tumor marker levels > 50% of their baseline value . A multicentric study of CA125 kinetics under induction chemotherapy performed in 631 ovarian cancer patients found that prechemotherapy CA125, its half-life, nadir concentration and time to nadir all had a univariate prognostic value for disease free and overall survival . Another prospective study examined the value of pretherapeutic CA125 in 70 consecutive patients with recurrent ovarian cancer before the start of second-line chemotherapy. CA125 was not found to be significantly associated with survival by any of the cutoffs (35, 65, 132, and 339 U/mL) .
A retrospective multicentric study assessing the prognostic value of the serum CA125 assay in 225 patients with advanced epithelial ovarian cancer found that survival was significantly related to stage, residual disease, tumor grade, serum CA125 before the third cycle, and serum CA125 half-life. Cox proportional hazard model showed that residual disease, serum CA125 half-life, and tumor grade retained a significant value in predicting survival . Another study evaluated the prognostic value of serum CA125 levels both before chemotherapy and after each cycle of one or two courses in 48 patients with advanced ovarian adenocarcinoma. Patients with serum CA125 values below the normal value of 35 U/ml after two courses had a significantly longer median survival and longer disease-free survival than did those patients whose CA125 levels dropped to normal after the third or a later course of chemotherapy . In another study 55 patients with epithelial ovarian carcinoma treated with platinum-based chemotherapy were followed for a minimum period of 2 years. Of these 22 patients had a prechemotherapy serum CA125 level of less than 50 kU/l and 33 patients had a serum CA125 level of greater than or equal to 50 kU/l. The 5-year actuarial survival of the two groups were 75% and 10% respectively . A study evaluating the prognostic value of serum CA125 measurements in 54 patients with advanced ovarian adenocarcinoma found that the change in CA125 levels from before chemotherapy to 1 month later could be used to divide patients into different prognostic groups. The best discrimination was found by dividing the patients into those who showed a greater than sevenfold decrease in CA125 levels and those who showed a smaller change . Finally, a study conducted in 85 patients with epithelial ovarian cancer found that prechemotherapy CA125 level had no prognostic value if the patients were stratified for tumor size .
Of the eight studies reviewed under the relationship between prechemotherapy absolute serum CA125 levels and survival, four were prospective, one retrospective, one convenience sample, one consecutive case series type of study. Six studies [37, 38, 40–43] showed a highly significant relationship between prechemotherapy serum CA125 level changes and survival whereas one study  did not find such relationship. In one study, prechemotherapy CA125 was found to be strongly correlated with the probability of progression within 3 years but the data suggesting the relationship between prechemotherapy CA125 levels and survival was not provided . Consequently, the overall data reviewed on the relationship between prechemotherapy serum CA125 levels and survival in ovarian cancer suggests an inverse relationship between the two.
Postchemotherapy Absolute Serum CA125 and Ovarian Cancer Survival
Table 2 summarizes the epidemiologic studies on the association between absolute postchemotherapy CA125 levels and survival in ovarian cancer. A retrospective study evaluated the prognostic significance of the serum CA125 level after 6 cycles of systemic adjuvant chemotherapy. The median progression-free survival was 26, 14, and 10 months, and the median overall survival was 105, 42, and 37 months in group I (< 10 U/ml), group II (10-21 U/ml), and group III (> 21 U/ml) respectively . One study determined whether CA125 is an independent predictor of overall survival (OS) in patients with surgically defined disease status at the end of primary therapy prior to intraperitoneal (IP) consolidation chemotherapy. When considered as a continuous variable, CA125 was a predictor of OS. Using the median CA125 level as a cut-off, OS was increased in patients with CA125 ≤ 12 U/ml (median 5.8 years) compared with > 12 (3.7 years) .
A retrospective multicentric study was carried out to assess the prognostic value of the CA125 change after the first and the second courses of induction chemotherapy. CA125 change after the first course, residual tumor, CA 125 before the second course and patients' age were independent prognostic factors for OS . A study compared the predicted value of the blood levels variations of CA125 antigen and the imunohistochemical expression of CA125, with imagistic criteria regarding the survival estimation of female patients with relapsed ovarian carcinoma. In multivariate analysis only the variation of blood levels of CA125 and the free disease interval from the finalization of the first line chemotherapy were predictive of survival, while the other variables, including the RECIST criteria, had no impact on survival . Another prospective multicentric study evaluated the prognostic significance of CA125 and TPS levels above the discrimination value (25 kU/L and 100 U/L, respectively). Tumor marker levels in stage I and II were not correlated with survival. However, stage III and IV patients with elevated levels of CA125 or TPS after three chemotherapy courses had a worse 2-year OS (69% vs 26%, and 57% vs 20%, respectively) than patients with normal levels of the markers .
One study examined the prognostic value of early serum CA125 assay in 58 patients with advanced epithelial ovarian cancer. CA125 was a highly significant predictor of both progression free and overall survival after the first cycle and throughout primary chemotherapy. Patients in the upper quartile (CA125 > 450 U/ml) had a very poor median survival of 7 months while those in the lower quartile (CA125 < 55 U/ml) had a good median survival of 23 months. Those in the two interquartile groups, who had CA125 levels ranging from 58-221 U/ml and 228-434 U/ml, had relatively intermediate median survival times of 16 months and 15 months respectively . Another study found that patients with serum CA125 values below 35 U/ml after two chemotherapy courses were significantly more likely to achieve complete remission and had a significantly longer median survival. In multivariate analysis, serum CA125 levels after two courses were the most important independent prognostic factor .
Out of the eight studies reviewed in this section, three were retrospective, three prospective and one consecutive case series. Of these, seven studies [41, 45–50] demonstrated that postchemotherapy serum CA125 level is a good prognostic indicator for survival. These studies suggest that patients with serum CA125 values within the normal range after chemotherapy had a significantly longer overall and disease-free survival than did those patients whose CA125 levels remained high after chemotherapy. In one of the studies CA125 below 25 kU/l after 3 chemotherapy courses was not significantly correlated with overall survival in stage I and II patients, although it was, in the subgroup of patients with stage III and IV disease . Overall, there is a large body of evidence to suggest that postchemotherapy CA125 level is a good predictor of overall and progression free survival in ovarian cancer.
Absolute Serum CA125 during Chemotherapy and Ovarian Cancer Survival
Table 3 summarizes the epidemiologic studies on the association between absolute CA125 levels during chemotherapy and survival in ovarian cancer. A retrospective study assessed the prognostic value of prechemotherapy serum CA125 level, CA125 kinetics, and CA125 half-life in advanced ovarian cancer during induction cisplatin polychemotherapy. The prechemotherapy CA125 level had no prognostic value for survival. However, the median survival time of patients with CA125 levels below the upper normal limit of normality after two courses of CT was 101 months compared to a median survival of 21 months in patients without CA125 normalization . Another retrospective multicentric study assessed the prognostic value of the serum CA125 assay in 225 patients with advanced epithelial ovarian cancer. Multiple logistic regression showed that residual disease, serum CA 125 half-life, serum CA 125 before the third cycle, and serum CA 125 before the first cycle retained a significant value in predicting second-look findings. Survival was significantly related to stage, residual disease, tumor grade, serum CA125 before the third cycle, and serum CA125 half-life . Another study investigated the serum CA125 regression after cytoreductive surgery and during the first three courses of chemotherapy in 60 ovarian cancer patients. Within stage III-IV patients, a significant positive correlation was seen between survival and (a) stage III, (b) residual tumor ≤ 1 cm, (c) CA125 normalisation after three courses and (d) CA125 half-life ≤ 20 days. The median survival times of patients with and without a CA 125 normalization after three courses were 27 and 14 months respectively .
All three studies reviewed above were retrospective. Collectively, the findings from these studies coupled with those reported in tables 1 and 2 provide further evidence supporting the prognostic role of CA125 throughout the entire spectrum of chemotherapy treatment in ovarian cancer.
Preoperative Absolute Serum CA125 and Ovarian Cancer Survival
Table 4 summarizes the epidemiologic studies on the association between absolute preoperative CA125 levels and survival in ovarian cancer. A retrospective study of 75 patients with epithelial ovarian carcinoma found that the preoperative CA125 levels did not correlate significantly with stage, tumor grade or survival. Reduced survival was noted with increasing age at the time of surgery and bulk of the residual disease postoperatively . Another study evaluating preoperative CA125 as a prognostic factor in stage I epithelial ovarian cancer found that patients with preoperative serum CA125 levels < 65 U/mL had a significantly longer survival compared to stage I EOC patients with preoperative serum CA125 ≥ 65 U/mL . Another study assessing the association of preoperative CA125 levels with outcome found that after adjusting for covariates, there was a significant association between CA125 levels and disease-specific survival. As preoperative CA125 levels increased, the risk of death increased except at the highest values of CA125 .
One study determined the importance of the rate of decline of CA125 relative to conventional prognosticators of ovarian cancer survival and found that upon univariate analysis, slope of the CA125 exponential regression curve, number of cycles to normal CA125 levels, residual disease, and platinum treatment intensity were the most important predictors of survival . Another study evaluated the relationship between the degree of elevation of preoperative CA125 and length of survival in ovarian cancer. Decreased length of survival was found to be related to the degree of elevation of CA125 prior to initial exploratory laparotomy. The mean initial CA125 for patients surviving five years or more (15 patients) was 899 U/mL, with an SD of +/- 1,880 U/mL, while the CA125 for patients surviving less than five years (67 patients) was 1,978 U/mL, with an SD of +/- 1,852 U/mL .
A study evaluating the prognostic importance of preoperative CA125 in patients with stage I epithelial ovarian cancer found that in univariate analysis, overall survival decreased significantly in patients positive for CA125 (≥ 65 U/mL). Multivariate analysis identified preoperative CA125 as the most powerful prognostic factor for survival, the risk of dying of disease being 6.4 times higher in CA125-positive patients . In a study the prognostic significance of the serum CA125 level was evaluated in 687 patients with invasive epithelial ovarian malignancies. Using Cox multivariate analysis, the preoperative serum CA125 level showed no independent prognostic significance, whereas the postoperative level did . In a study serum CA125 levels determined before surgery and 3 months after surgery were evaluated as independent prognostic factors for survival. CA125 gave no additional information with regard to the relationship of survival prognosis to histologic grade and to the diameter of residual tumor mass .
A study evaluated whether the pre- and postoperative determination of CA 125 improves the prognostic information at the time of primary operation. There was a significantly longer survival for patients with preoperative values below 65/U/ml than for patients with levels above 65 U/ml. Elevated postoperative values also resulted in poor prognosis. The study found a survival of 5% after 5 years in this group vs. 42% for patients with normal postoperative values. The best prognosis was found in patients with pre- and postoperative values lower than 65 U/ml . In a prospective study of 52 patients with ovarian malignancy followed up for 3-18 months the clinical significance of pre-operative serum CA125 as a tumor marker was assessed. Data showed that 41 patients with epithelial ovarian cancer, the level of CA125 correlated well with tumor load as indicated by FIGO stage. However, no correlation was found between CA125 concentration and histopathological grade, also CA125 level didn't appear of any prognostic value .
Out of the eleven studies reviewed under the relationship between preoperative absolute serum CA125 levels and survival six studies were retrospective, two prospective and one convenience sample. Out of the six retrospective studies, four found a significant correlation between preoperative serum CA125 levels and survival. One study found CA125 as the strongest independent prognostic factor for survival. The two prospective studies did not find any significant correlation between preoperative serum CA125 level and survival. Finally, the convenience sample based study also recorded a significant correlation between preoperative serum CA125 levels and survival in ovarian cancer. The overall review of the literature in this section suggests a strong prognostic role of preoperative serum CA125 levels in ovarian cancer.
Postoperative Absolute Serum CA125 and Ovarian Cancer Survival
Table 5 summarizes the epidemiologic studies on the association between absolute postoperative CA125 levels and survival in ovarian cancer. A study found that postoperative CA125 correlated to FIGO stage, tumor grade and overall survival . Another retrospective analysis of 85 patients with elevated serum CA125 after surgery for ovarian cancer showed that the absolute CA125 serum levels were a poor guide to prognosis . A study found that in patients without residual disease after primary surgery, histologic type, postoperative CA125 level with 35 U/mL as the cutoff value, and tumor grade were independent prognostic factors for survival. For those with residual tumor after primary surgery, histologic type, postoperative treatment, size of residual disease, and postoperative serum CA125 level with 65 U/mL as a cutoff were independent prognostic factors . In another study evaluating 132 patients, postoperative CA125 was found the strongest independent prognostic factor for survival, as compared with histologic grade, FIGO stage, and diameter of residual tumor mass . A study evaluated whether the pre- and postoperative determination of CA 125 improves the prognostic information at the time of primary operation. Elevated postoperative values resulted in poor prognosis. The study found a survival of 5% after 5 years in this group vs. 42% for patients with normal postoperative values. The best prognosis was found in patients with pre- and postoperative values lower than 65 U/ml .
Out of the five studies reviewed under the relationship between postoperative absolute serum CA125 levels and survival, two were retrospective, two prospective and one convenience sample. Four studies [53, 59–61] found postoperative serum CA125 levels as a strong independent prognostic factor for survival in ovarian cancer. Whereas, only one study found postoperative serum CA15 having no significant prognostic value .
Serum CA125 Half-life and Ovarian Cancer Survival
Table 6 summarizes the epidemiologic studies on the association between serum CA125 half-life and survival in ovarian cancer. In one study nadir concentration, residual tumor volume and number of chemotherapy courses were found to be independent prognostic factors for DFS and OS. The CA125 group classification was found to be an independent prognostic factor only for DFS . In another study, CA125 half-life, nadir CA125 and time to nadir were studied. Median (range) for CA125 kinetics were: 263 kU/l (5-52000 kU/l) before 1st course, 15.8 days (4.5-417.9 days) for CA125 half-life, 16 kU/l (3-2610 kU/l) for nadir and 85 days (0-361 days) for time to nadir. In Cox models, CA125 half-life, residual tumor, nadir concentration and stage were the most powerful prognostic factors for DFS and OS .
In a retrospective study the 25%, 50%, and 75% quartiles of serum CA125 half-life during early chemotherapy were 10, 14, and 20 days, respectively. Taking the value corresponding to the 50% quintile (i.e., 14 days) as cutoff limit, serum CA125 half-life was an independent prognostic factor for the chance of achieving a complete response to treatment as well as for progression-free survival and overall survival . Another retrospective study found that the median survival times of patients with CA125 half-life < 20 days and > 20 days were 101+ and 18 months, respectively. In Cox analysis, independent prognostic variables for survival included therapeutic response, Karnofsky index, residual disease, tumor grade, CA125 half-life, and CA125 kinetics . Another study showed that residual disease, serum CA125 half-life, and tumor grade retained a significant value in predicting survival in 225 patients with advanced epithelial ovarian cancer .
In another study, stage, residual disease, minimum CA 125, and CA 125 t1/2 individually were predictive of persistent disease or recurrence within 3 years of diagnosis with sensitivities of 97, 70, 34, and 49%, respectively, and specificities of 33, 83, 100, and 83%, respectively . Another retrospective study found a significant positive correlation between survival and (a) stage III, (b) residual tumor ≤ 1 cm, (c) CA125 normalisation after three courses and (d) CA125 half-life ≤ 20 days. A CA125 half-life < or = 20 days vs > 20 days provides an independent prognostic factor for survival in stage III-IV patients early in the course of therapy .
A study found that patients with a serum CA125 half-life shorter than 16 days during induction chemotherapy had an estimated survival of 68% as compared with 18% in 49 patients with a CA125 half-life of more than 16 days . In another study, CA125 half-life of less than 20 days was associated with prolonged overall survival. In those patients who eventually were found to be disease-free at surgical surveillance procedures, normalization of serum CA125 levels to less than 35 U/ml within 65 days of primary operation also suggested an improved survival . A study found that CA125 half-life of less than 20 days, 20-40 days and greater than 40 days appeared to identify patients with a good, intermediate or poor prognosis, the two year actuarial survival being 76%, 48% and 0% respectively. The change of achieving a complete remission was 15% and 67% respectively for patients with a serum CA125 half-life of greater than 20 or less than 20 days . In another study, patients with a half-life of 20 days and more had a 3.2 times higher progression rate and a significantly shorter median time to progression of only 11 months, as compared to 43 months for patients with a half-life of less than 20 days .
Out of the twelve studies reviewed under the relationship between serum CA125 half life and survival in women with ovarian cancer, eight studies were retrospective, one prospective and three consecutive case series. Eleven studies showed that serum CA125 half life was an independent prognostic indicator for survival.
Nadir Serum CA125 and Ovarian Cancer Survival
Table 7 summarizes the epidemiologic studies on the association between nadir serum CA125 levels and survival in ovarian cancer. In one study, nadir concentration, residual tumor volume and number of chemotherapy courses were found to be independent prognostic factors for DFS and OS . In another study nadir CA125 concentration and time to nadir were studied. Median (range) for CA125 kinetics were: 16 kU/l (3-2610 kU/l) for nadir and 85 days (0-361 days) for time to nadir. In Cox models, CA125 half-life, residual tumor, nadir concentration and stage were the most powerful prognostic factors for DFS and OS . More recently, Crawford and Peace examined differences in nadir CA125 levels within the normal range as a prognostic factor for both overall and progression-free survival. Using arbitrarily defined groups of < 10 U/ml, 11-20 U/ml, and 21-30 U/ml, they demonstrated a statistically significant increase in overall survival only between patients with CA125 < 10 U/ml (median survival 2436 days) and those with CA125 > 11-20 U/ml or 21-30 (median survival 537 days for both groups). In a multivariate analysis, nadir remained highly significant . In another study, in 223 patients with epithelial ovarian carcinoma the CA125 trend was the most significant variable followed by the FIGO stage. The initial CA125 level and nadir CA125 level, although significant when considered alone, were not significant independent variables .
All four studies reviewed under the relationship between nadir CA125 levels and survival were retrospective. All studies found that nadir concentration was an independent prognostic factor for disease free survival and overall survival. Notably, one of these studies  reported that the initial CA125 level and nadir CA125 level were found significant when considered alone but were not significant as independent variables.
Time to Reach CA125 Nadir and Ovarian Cancer Survival
Table 8 summarizes the epidemiologic studies on the association between time to reach CA125 nadir and survival in ovarian cancer.
In one study, nadir CA125 concentration and time to nadir were studied. In Cox models, CA125 half-life, residual tumor, nadir concentration and stage were the most powerful prognostic factors for DFS and OS. This study concluded that among well-established prognostic factors in ovarian cancers, CA125 half-life and nadir concentration bear a strong and independent prognostic value . Another study evaluated the incorporation of CA125 normalization times into a prognostic model based on pretreatment variables in patients with ovarian carcinoma to determine if they could render second-look laparotomy (SLL) redundant. The time to normalization of CA125 serum levels (analyzed either as a continuous or as a two-category variable) had an independent prognostic role when included in the model. Patients with good prognostic pretreatment variables, and those with intermediate prognosis at the beginning of therapy who showed a quick normalization of CA125, had an 80% 5-year survival, compared with 16% 5-year survival in the remaining patients .
CA125 Area under the Curve (AUC) and Ovarian Cancer Survival
A study evaluated the usefulness of CA125 normalized in time area under the curve (CA125 AUC) to signalise epithelial ovarian cancer relapse. Data from 111 patients were submitted to two different approaches based on CA125 AUC increase values to predict patient relapse. In Criterion A the best accuracy was achieved with a factor (F) of 1.25 (increment of 25% from the previous status), while in Criterion B the best accuracies were achieved with cut-offs of 25, 50, 75 and 100 IU/mL. The mean lead time to relapse achieved with Criterion A was 181 days, while with Criterion B they were, respectively, 131, 111, 63 and 11 days. Based on the results of this study it was concluded that conjugation and sequential application of both criteria in patient relapse detection should be highly advisable . Another study investigated the usefulness of the CA125 area under the curve (AUC) as a new kinetic parameter for predicting overall survival. Patients with a complete response to primary chemotherapy had a mean CA125 AUC of 48.8, while patients with a partial response had a mean of 251.7 IU/ml*days, and patients with no response or disease progression had a mean of 316.5 IU/ml*days. The best CA125 AUC performance is in predicting patient complete response to chemotherapy with a cut-off of 100 IU/ml*days and an accuracy of 82% .
Longitudinal Serum CA125 and Ovarian Cancer Survival
Table 9 summarizes the epidemiologic studies on the association between longitudinal CA125 levels and survival in ovarian cancer.
The first study was a multicentric study , carried out to assess the prognostic value of the CA125 change after the first and the second courses of induction chemotherapy. CA125 determination of all patients was carried out before each cycle of chemotherapy (on average each 3 weeks). The data from this study showed that early CA125 change induced by the first chemotherapy courses was strongly correlated both with the probability of achieving pathological complete response after chemotherapy and with survival duration. In another study  the relationship between survival and early changes in the serum level of the CA125 antigen in patients with advanced ovarian cancer was assessed. While pretreatment CA125 values did not correlate with survival, the concentration of CA125 8 weeks after initiation of therapy was a powerful independent prognostic factor.
Epithelial ovarian cancer is fairly common with high rates in Scandinavia, intermediate rates in Western Europe and North America and low rates in the developing countries and in Japan. The 5-year survival rate is less than 40% . A variety of biomarkers have been developed to monitor growth of ovarian cancer and to detect disease at an early interval . Amongst them CA125 has been the most extensively studied and clinically utilized serum tumor marker. As a clinical tool, prognostic markers like CA125 may potentially help individualizing treatment within subgroups of patients. Serum levels of CA125 are used to monitor responses to chemotherapy, relapse, and disease progression in ovarian cancer patients [31, 75]. Levels of CA125 can be elevated in the serum before clinical development of primary and recurrent ovarian carcinoma . It is now widely accepted that the tumor marker CA125 is a predictive and prognostic factor in CA125 positive ovarian cancers.
In the diagnosis of the disease, prognosis and monitoring of treatment CA125 serum concentration has been established as a tool of great importance. An important characteristic of CA125 is the ability to reflect changes in tumor mass during chemotherapy or in the follow-up period after completion of therapy . The postoperative serum CA125 level is an independent prognostic factor in patients with invasive ovarian cancer , and CA125 tumor marker half-life (t1/2) and tumor marker doubling time (DT) are often used as kinetic parameters for the evaluation of clinical response and follow-up of patients with ovarian cancer . Serum CA125 half-life during early chemotherapy is an independent prognostic factor for both the achievement of a pathologically complete response and the survival of patients with advanced epithelial ovarian cancer , and several studies report that the greatest difference in progression rate was found at a t1/2 of 20 days [44, 51, 68, 69, 73]. While CA125 levels at the time of diagnosis are of limited prognostic significance, CA125 measurements are now performed almost routinely during the course of chemotherapy. Decreasing levels of CA125 after cytoreductive surgery and during initial chemotherapy courses have been used as an indicator of clinical outcome . Despite general acceptance that CA125 is a prognostic marker, it remains unclear as to how accurately serial CA125 measurements can predict long-term overall survival in patients with advanced ovarian cancer .
The present review summarizes findings from studies assessing the relationship between serum CA125 levels and survival in ovarian cancer. All studies that evaluated the relationship between prechemotherapy, post chemotherapy, during chemotherapy, preoperative, postoperative absolute serum CA125 levels, CA125 half-life, nadir CA125 levels, time to reach nadir level and survival in ovarian cancer were included in this review. Also studies evaluating the relationship between a new kinetic parameter AUC (Area under the Curve) as well as the longitudinal studies on CA125 and survival in ovarian cancer have also been reviewed.
Most studies reviewed had retrospective study design. To date, only four prospective investigations have been conducted, of which two [41, 62] had very few cases (n < 55), indicating limited power to detect associations. Prospective studies are the preferred study design, as they are less susceptible to various types of biases and provide the best risk estimates. Thus, further prospective investigations are needed for clearly understanding the relationship between serum CA125 levels and survival in ovarian cancer. Also most of the studies reviewed lack information in the relative risk estimates associated with different CA125 levels.
There have been earlier attempts by Hogdall  and Gadducci et al.  to review the literature on CA125 and ovarian cancer survival. Review by Hogdall addressed recently reported progress in CA125 as a prognostic marker in patients with ovarian cancer. It primarily focused on recent publications on the topic and excluded some studies on CA125 levels during chemotherapy, time to reach nadir level and CA125 AUC levels. Another very informative review by Gadducci et al. focused on all serum and tissue biomarkers in ovarian cancer and not just CA125. Also, it failed to include all available studies on CA125 possible because the focus of the paper was not just CA125. The present review we believe provides a very comprehensive evaluation on the existing literature on the prognostic role of CA125 in ovarian cancer.
We conclude that although the results from different studies are sometimes contradictory, serum CA125 level is a strong prognostic factor for overall survival and progression free survival in ovarian cancer. There is an inverse relationship between serum CA125 levels and survival in ovarian cancer. A decreasing level generally indicates a positive response to cancer therapy while an increasing level indicates tumor recurrence and poor survival. Future research on this subject should focus on prospective longitudinal studies evaluating the impact of changes in serum CA125 levels on survival.
Chan JK, Cheung MK, Husain A, Teng NN, West D, Whittemore AS, Berek JS, Osann K: Patterns and progress in ovarian cancer over 14 years. Obstet Gynecol 2006, 108: 521–528. 10.1097/01.AOG.0000231680.58221.a7
Hartge P, Whittemore AS, Itnyre J, McGowan L, Cramer D: Rates and risks of ovarian cancer in subgroups of white women in the United States. The Collaborative Ovarian Cancer Group. Obstet Gynecol 1994, 84: 760–764.
Quirk JT, Natarajan N: Ovarian cancer incidence in the United States, 1992–1999. Gynecol Oncol 2005, 97: 519–523. 10.1016/j.ygyno.2005.02.007
Hannibal CG, Cortes R, Engholm G, Kjaer SK: Survival of ovarian cancer patients in Denmark: Excess mortality risk analysis of five-year relative survival in the period 1978–2002. Acta Obstet Gynecol Scand 2008, 1–9.
van Dalen A, Favier J, Burges A, Hasholzner U, de Bruijn HW, Dobler-Girdziunaite D, Dombi VH, Fink D, Giai M, McGing P, Harlozinska A, Kainz C, Markowska J, Molina R, Sturgeon C, Bowman A, Einarsson R: Prognostic significance of CA 125 and TPS levels after 3 chemotherapy courses in ovarian cancer patients. Gynecol Oncol 2000, 79: 444–450. 10.1006/gyno.2000.5982
Bast RC Jr: Status of tumor markers in ovarian cancer screening. J Clin Oncol 2003, 21: 200s-205s. 10.1200/JCO.2003.01.068
Hoskins WJ: Prospective on ovarian cancer: why prevent? J Cell Biochem Suppl 1995, 23: 189–99. 10.1002/jcb.240590926
Crawford SM, Peace J: Does the nadir CA125 concentration predict a long-term outcome after chemotherapy for carcinoma of the ovary? Ann Oncol 2005, 16: 47–50. 10.1093/annonc/mdi012
Eisenkop SM, Spirtos NM, Friedman RL, Lin WC, Pisani AL, Perticucci S: Relative influences of tumor volume before surgery and the cytoreductive outcome on survival for patients with advanced ovarian cancer: a prospective study. Gynecol Oncol 2003, 90: 390–396. 10.1016/S0090-8258(03)00278-6
McGuire WP, Hoskins WJ, Brady MF, Kucera PR, Partridge EE, Look KY, Clarke-Pearson DL, Davidson M: Cyclophosphamide and cisplatin compared with paclitaxel and cisplatin in patients with stage III and stage IV ovarian cancer. N Engl J Med 1996, 334: 1–6. 10.1056/NEJM199601043340101
Ozols RF, Bundy BN, Greer BE, Fowler JM, Clarke-Pearson D, Burger RA, Mannel RS, DeGeest K, Hartenbach EM, Baergen R: Phase III trial of carboplatin and paclitaxel compared with cisplatin and paclitaxel in patients with optimally resected stage III ovarian cancer: a Gynecologic Oncology Group study. J Clin Oncol 2003, 21: 3194–3200. 10.1200/JCO.2003.02.153
Hoskins P, Eisenhauer E, Vergote I, Dubuc-Lissoir J, Fisher B, Grimshaw R, Oza A, Plante M, Stuart G, Vermorken J: Phase II feasibility study of sequential couplets of Cisplatin/Topotecan followed by paclitaxel/cisplatin as primary treatment for advanced epithelial ovarian cancer: a National Cancer Institute of Canada Clinical Trials Group Study. J Clin Oncol 2000, 18: 4038–4044.
Jacobs IJ, Skates SJ, MacDonald N, Menon U, Rosenthal AN, Davies AP, Woolas R, Jeyarajah AR, Sibley K, Lowe DG, Oram DH: Screening for ovarian cancer: a pilot randomised controlled trial. Lancet 1999, 353: 1207–1210. 10.1016/S0140-6736(98)10261-1
Rapkiewicz AV, Espina V, Petricoin EF III, Liotta LA: Biomarkers of ovarian tumours. Eur J Cancer 2004, 40: 2604–2612. 10.1016/j.ejca.2004.05.021
Tuxen MK, Soletormos G, Dombernowsky P: Tumor markers in the management of patients with ovarian cancer. Cancer Treat Rev 1995, 21: 215–245. 10.1016/0305-7372(95)90002-0
Abstracts of the first scientific workshop of the Early Detection Research Network. September 2000 Dis Markers 2001, 17: 3–38.
Bast RC Jr, Badgwell D, Lu Z, Marquez R, Rosen D, Liu J, Baggerly KA, Atkinson EN, Skates S, Zhang Z, Lokshin A, Menon U, Jacobs I, Lu K: New tumor markers: CA125 and beyond. Int J Gynecol Cancer 2005,15(Suppl 3):274–81. 10.1111/j.1525-1438.2005.00441.x
Meyer T, Rustin GJ: Role of tumour markers in monitoring epithelial ovarian cancer. Br J Cancer 2000, 82: 1535–1538. 10.1054/bjoc.2000.1174
Hogdall E: Cancer antigen 125 and prognosis. Curr Opin Obstet Gynecol 2008, 20: 4–8. 10.1097/GCO.0b013e3282f2b124
Bast RC Jr, Feeney M, Lazarus H, Nadler LM, Colvin RB, Knapp RC: Reactivity of a monoclonal antibody with human ovarian carcinoma. J Clin Invest 1981, 68: 1331–1337. 10.1172/JCI110380
Bast RC Jr, Klug TL, St John E, Jenison E, Niloff JM, Lazarus H, Berkowitz RS, Leavitt T, Griffiths CT, Parker L, Zurawski VR Jr, Knapp RC: A radioimmunoassay using a monoclonal antibody to monitor the course of epithelial ovarian cancer. N Engl J Med 1983, 309: 883–887. 10.1056/NEJM198310133091503
Nustad K, Bast RC Jr, Brien TJ, Nilsson O, Seguin P, Suresh MR, Saga T, Nozawa S, Bormer OP, de Bruijn HW, Nap M, Vitali A, Gadnell M, Clark J, Shigemasa K, Karlsson B, Kreutz FT, Jette D, Sakahara H, Endo K, Paus E, Warren D, Hammarstrom S, Kenemans P, Hilgers J: Specificity and affinity of 26 monoclonal antibodies against the CA 125 antigen: first report from the ISOBM TD-1 workshop. International Society for Oncodevelopmental Biology and Medicine. Tumour Biol 1996, 17: 196–219. 10.1159/000217982
Markman M: Optimizing primary chemotherapy in ovarian cancer. Hematol Oncol Clin North Am 2003, 17: 957–68. viii 10.1016/S0889-8588(03)00058-3
Kenemans P, van Kamp GJ, Oehr P, Verstraeten RA: Heterologous double-determinant immunoradiometric assay CA 125 II: reliable second-generation immunoassay for determining CA 125 in serum. Clin Chem 1993, 39: 2509–2513.
Hogdall EV, Christensen L, Kjaer SK, Blaakaer J, Kjaerbye-Thygesen A, Gayther S, Jacobs IJ, Hogdall CK: CA125 expression pattern, prognosis and correlation with serum CA125 in ovarian tumor patients. From The Danish "MALOVA" Ovarian Cancer Study. Gynecol Oncol 2007, 104: 508–515. 10.1016/j.ygyno.2006.09.028
Rustin GJ, Nelstrop AE, Tuxen MK, Lambert HE: Defining progression of ovarian carcinoma during follow-up according to CA 125: a North Thames Ovary Group Study. Ann Oncol 1996, 7: 361–364.
Rustin GJ, Marples M, Nelstrop AE, Mahmoudi M, Meyer T: Use of CA-125 to define progression of ovarian cancer in patients with persistently elevated levels. J Clin Oncol 2001, 19: 4054–4057.
Bast RC Jr, Xu FJ, Yu YH, Barnhill S, Zhang Z, Mills GB: CA 125: the past and the future. Int J Biol Markers 1998, 13: 179–187.
Menon U, Jacobs IJ: Ovarian cancer screening in the general population. Curr Opin Obstet Gynecol 2001, 13: 61–64. 10.1097/00001703-200102000-00009
Verheijen RH, Mensdorff-Pouilly S, van Kamp GJ, Kenemans P: CA 125: fundamental and clinical aspects. Semin Cancer Biol 1999, 9: 117–124. 10.1006/scbi.1998.0114
Yin BW, Lloyd KO: Molecular cloning of the CA125 ovarian cancer antigen: identification as a new mucin, MUC16. J Biol Chem 2001, 276: 27371–27375. 10.1074/jbc.M103554200
Skates SJ, Menon U, MacDonald N, Rosenthal AN, Oram DH, Knapp RC, Jacobs IJ: Calculation of the risk of ovarian cancer from serial CA-125 values for preclinical detection in postmenopausal women. J Clin Oncol 2003, 21: 206s-210s. 10.1200/JCO.2003.02.955
Nossov V, Amneus M, Su F, Lang J, Janco JM, Reddy ST, Farias-Eisner R: The early detection of ovarian cancer: from traditional methods to proteomics. Can we really do better than serum CA-125? Am J Obstet Gynecol 2008,199(3):215–23. 10.1016/j.ajog.2008.04.009
Helzlsouer KJ, Bush TL, Alberg AJ, Bass KM, Zacur H, Comstock GW: Prospective study of serum CA-125 levels as markers of ovarian cancer. JAMA 1993, 269: 1123–1126. 10.1001/jama.269.9.1123
Duffy MJ, Bonfrer JM, Kulpa J, Rustin GJ, Soletormos G, Torre GC, Tuxen MK, Zwirner M: CA125 in ovarian cancer: European Group on Tumor Markers guidelines for clinical use. Int J Gynecol Cancer 2005, 15: 679–691. 10.1111/j.1525-1438.2005.00130.x
Rustin GJ, Bast RC Jr, Kelloff GJ, Barrett JC, Carter SK, Nisen PD, Sigman CC, Parkinson DR, Ruddon RW: Use of CA-125 in clinical trial evaluation of new therapeutic drugs for ovarian cancer. Clin Cancer Res 2004, 10: 3919–3926. 10.1158/1078-0432.CCR-03-0787
Markman M, Federico M, Liu PY, Hannigan E, Alberts D: Significance of early changes in the serum CA-125 antigen level on overall survival in advanced ovarian cancer. Gynecol Oncol 2006, 103: 195–198. 10.1016/j.ygyno.2006.02.024
Riedinger JM, Wafflart J, Ricolleau G, Eche N, Larbre H, Basuyau JP, Dalifard I, Hacene K, Pichon MF: CA 125 half-life and CA 125 nadir during induction chemotherapy are independent predictors of epithelial ovarian cancer outcome: results of a French multicentric study. Ann Oncol 2006, 17: 1234–1238. 10.1093/annonc/mdl120
Gronlund B, Dehn H, Hogdall CK, Engelholm SA, Jorgensen M, Norgaard-Pedersen B, Hogdall EV: Cancer-associated serum antigen level: a novel prognostic indicator for survival in patients with recurrent ovarian carcinoma. Int J Gynecol Cancer 2005, 15: 836–843. 10.1111/j.1525-1438.2005.00145.x
Gadducci A, Zola P, Landoni F, Maggino T, Sartori E, Bergamino T, Cristofani R: Serum half-life of CA 125 during early chemotherapy as an independent prognostic variable for patients with advanced epithelial ovarian cancer: results of a multicentric Italian study. Gynecol Oncol 1995, 58: 42–47. 10.1006/gyno.1995.1181
Ron IG, Inbar M, Gelernter I, Lewysohn O, Ayalon D, Dale J, Chaitchik S: Use of CA-125 response to predict survival parameters of patients with advanced ovarian carcinoma. Acta Obstet Gynecol Scand 1994, 73: 658–662. 10.3109/00016349409013462
Davidson NG, Khanna S, Kirwan PH, Bircumshaw D: Prechemotherapy serum CA125 level as a predictor of survival outcome in epithelial carcinoma of the ovary. Clin Oncol (R Coll Radiol) 1991, 3: 32–36.
Rustin GJ, Gennings JN, Nelstrop AE, Covarrubias H, Lambert HE, Bagshawe KD: Use of CA-125 to predict survival of patients with ovarian carcinoma. North Thames Cooperative Group. J Clin Oncol 1989, 7: 1667–1671.
Burg ME, Lammes FB, van Putten WL, Stoter G: Ovarian cancer: the prognostic value of the serum half-life of CA125 during induction chemotherapy. Gynecol Oncol 1988, 30: 307–312. 10.1016/0090-8258(88)90244-2
Kim HS, Park NH, Chung HH, Kim JW, Song YS, Kang SB: Serum CA-125 level after 6 cycles of primary adjuvant chemotherapy is a useful prognostic factor for complete responders' survival in patients with advanced epithelial ovarian cancer. Onkologie 2008, 31: 315–320. 10.1159/000131270
Juretzka MM, Barakat RR, Chi DS, Iasonos A, Dupont J, Abu-Rustum NR, Poynor EA, Aghajanian C, Spriggs D, Hensley ML, Sabbatini P: CA125 level as a predictor of progression-free survival and overall survival in ovarian cancer patients with surgically defined disease status prior to the initiation of intraperitoneal consolidation therapy. Gynecol Oncol 2007, 104: 176–180. 10.1016/j.ygyno.2006.07.027
Riedinger JM, Bonnetain F, Basuyau JP, Eche N, Larbre H, Dalifard I, Wafflart J, Ricolleau G, Pichon MF: Change in CA 125 levels after the first cycle of induction chemotherapy is an independent predictor of epithelial ovarian tumour outcome. Ann Oncol 2007, 18: 881–885. 10.1093/annonc/mdl500
Badulescu F, Badulescu A, Schenker M, Popescu CF, Stoica Z: The value of serum and tissular expression of CA 125 antigen, in evaluation of the response to second line chemotherapy for the relapsed ovarian carcinoma. Rom J Morphol Embryol 2005, 46: 329–334.
Fisken J, Leonard RC, Stewart M, Beattie GJ, Sturgeon C, Aspinall L, Roulston JE: The prognostic value of early CA125 serum assay in epithelial ovarian carcinoma. Br J Cancer 1993, 68: 140–145.
Redman CW, Blackledge GR, Kelly K, Powell J, Buxton EJ, Luesley DM: Early serum CA125 response and outcome in epithelial ovarian cancer. Eur J Cancer 1990, 26: 593–596. 10.1016/0277-5379(90)90085-8
Colakovic S, Lukic V, Mitrovic L, Jelic S, Susnjar S, Marinkovic J: Prognostic value of CA125 kinetics and half-life in advanced ovarian cancer. Int J Biol Markers 2000, 15: 147–152.
Yedema CA, Kenemans P, Voorhorst F, Bon G, Schijf C, Beex L, Verstraeten A, Hilgers J, Vermorken J: CA 125 half-life in ovarian cancer: a multivariate survival analysis. Br J Cancer 1993, 67: 1361–1367.
Osman N, O'Leary N, Mulcahy E, Barrett N, Wallis F, Hickey K, Gupta R: Correlation of serum CA125 with stage, grade and survival of patients with epithelial ovarian cancer at a single centre. Ir Med J 2008, 101: 245–247.
Petri AL, Hogdall E, Christensen IJ, Kjaer SK, Blaakaer J, Hogdall CK: Preoperative CA125 as a prognostic factor in stage I epithelial ovarian cancer. APMIS 2006, 114: 359–363. 10.1111/j.1600-0463.2006.apm_397.x
Cooper BC, Sood AK, Davis CS, Ritchie JM, Sorosky JI, Anderson B, Buller RE: Preoperative CA 125 levels: an independent prognostic factor for epithelial ovarian cancer. Obstet Gynecol 2002, 100: 59–64. 10.1016/S0029-7844(02)02057-4
Buller RE, Vasilev S, DiSaia PJ: CA 125 kinetics: a cost-effective clinical tool to evaluate clinical trial outcomes in the 1990s. Am J Obstet Gynecol 1996, 174: 1241–1253. 10.1016/S0002-9378(96)70667-1
Geisler JP, Miller GA, Lee TH, Harwood RM, Wiemann MC, Geisler HE: Relationship of preoperative serum CA-125 to survival in epithelial ovarian carcinoma. J Reprod Med 1996, 41: 140–142.
Nagele F, Petru E, Medl M, Kainz C, Graf AH, Sevelda P: Preoperative CA 125: an independent prognostic factor in patients with stage I epithelial ovarian cancer. Obstet Gynecol 1995, 86: 259–264. 10.1016/0029-7844(95)00126-C
Makar AP, Kristensen GB, Kaern J, Bormer OP, Abeler VM, Trope CG: Prognostic value of pre- and postoperative serum CA 125 levels in ovarian cancer: new aspects and multivariate analysis. Obstet Gynecol 1992, 79: 1002–1010.
Sevelda P, Schemper M, Spona J: CA 125 as an independent prognostic factor for survival in patients with epithelial ovarian cancer. Am J Obstet Gynecol 1989, 161: 1213–1216.
Moebus V: KRCGWHCHKH: Evaluation of CA125 as a prognostic and predictive factor in ovarian cancer. J Tumor Marker Oncol 1988, 3: 251–258.
Cruickshank DJ, Fullerton WT, Klopper A: The clinical significance of pre-operative serum CA 125 in ovarian cancer. Br J Obstet Gynaecol 1987, 94: 692–695.
Munstedt K, Krisch M, Sachsse S, Vahrson H: Serum CA 125 levels and survival in advanced ovarian cancer. Arch Gynecol Obstet 1997, 259: 117–123. 10.1007/BF02505319
Riedinger JM, Eche N, Basuyau JP, Dalifard I, Hacene K, Pichon MF: Prognostic value of serum CA 125 bi-exponential decrease during first line paclitaxel/platinum chemotherapy: a French multicentric study. Gynecol Oncol 2008, 109: 194–198. 10.1016/j.ygyno.2008.01.035
Gadducci A, Cosio S, Fanucchi A, Negri S, Cristofani R, Genazzani AR: The predictive and prognostic value of serum CA 125 half-life during paclitaxel/platinum-based chemotherapy in patients with advanced ovarian carcinoma. Gynecol Oncol 2004, 93: 131–136. 10.1016/j.ygyno.2003.12.043
Rosman M, Hayden CL, Thiel RP, Chambers JT, Kohorn EI, Chambers SK, Schwartz PE: Prognostic indicators for poor risk epithelial ovarian carcinoma. Cancer 1994, 74: 1323–1328. 10.1002/1097-0142(19940815)74:4<1323::AID-CNCR2820740423>3.0.CO;2-5
Hogberg T, Kagedal B: Serum half-life of the tumor marker CA 125 during induction chemotherapy as a prognostic indicator for survival in ovarian carcinoma. Acta Obstet Gynecol Scand 1990, 69: 423–429. 10.3109/00016349009013306
Hunter VJ, Daly L, Helms M, Soper JT, Berchuck A, Clarke-Pearson DL, Bast RC Jr: The prognostic significance of CA 125 half-life in patients with ovarian cancer who have received primary chemotherapy after surgical cytoreduction. Am J Obstet Gynecol 1990, 163: 1164–1167.
Hawkins RE, Roberts K, Wiltshaw E, Mundy J, Fryatt IJ, McCready VR: The prognostic significance of the half-life of serum CA 125 in patients responding to chemotherapy for epithelial ovarian carcinoma. Br J Obstet Gynaecol 1989, 96: 1395–1399.
Gard GB, Houghton CR: An assessment of the value of serum CA 125 measurements in the management of epithelial ovarian carcinoma. Gynecol Oncol 1994, 53: 283–289. 10.1006/gyno.1994.1135
Frasci G, Conforti S, Zullo F, Mastrantonio P, Comella G, Comella P, Persico G, Iaffaioli RV: A risk model for ovarian carcinoma patients using CA 125: time to normalization renders second-look laparotomy redundant. Cancer 1996, 77: 1122–1130. 10.1002/(SICI)1097-0142(19960315)77:6<1122::AID-CNCR18>3.0.CO;2-3
Mano A, Falcao A, Godinho I, Santos J, Leitao F, de Oliveira C, Caramona M: CA-125 AUC as a predictor for epithelial ovarian cancer relapse. Cancer Biomark 2008, 4: 73–81.
Mano A, Falcao A, Godinho I, Santos J, Leitao F, Oliveira C, Caramona M: CA-125 AUC as a new prognostic factor for patients with ovarian cancer. Gynecol Oncol 2005, 97: 529–534. 10.1016/j.ygyno.2005.01.040
Riman T, Persson I, Nilsson S: Hormonal aspects of epithelial ovarian cancer: review of epidemiological evidence. Clin Endocrinol (Oxf) 1998, 49: 695–707. 10.1046/j.1365-2265.1998.00577.x
O'Brien TJ, Beard JB, Underwood LJ, Dennis RA, Santin AD, York L: The CA 125 gene: an extracellular superstructure dominated by repeat sequences. Tumour Biol 2001, 22: 348–366. 10.1159/000050638
Burger RA, Darcy KM, DiSaia PJ, Monk BJ, Grosen EA, Gatanaga T, Granger GA, Wang J, Tian C, Hanjani P, Cohn DE: Association between serum levels of soluble tumor necrosis factor receptors/CA 125 and disease progression in patients with epithelial ovarian malignancy: a gynecologic oncology group study. Cancer 2004, 101: 106–115. 10.1002/cncr.20314
Tuxen MK, Soletormos G, Dombernowsky P: Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy. Br J Cancer 2001, 84: 1301–1307. 10.1054/bjoc.2001.1787
Bidart JM, Thuillier F, Augereau C, Chalas J, Daver A, Jacob N, Labrousse F, Voitot H: Kinetics of serum tumor marker concentrations and usefulness in clinical monitoring. Clin Chem 1999, 45: 1695–1707.
Peters-Engl C, Obermair A, Heinzl H, Buxbaum P, Sevelda P, Medl M: CA 125 regression after two completed cycles of chemotherapy: lack of prediction for long-term survival in patients with advanced ovarian cancer. Br J Cancer 1999, 81: 662–666. 10.1038/sj.bjc.6690744
Gadducci A, Cosio S, Tana R, Genazzani AR: Serum and tissue biomarkers as predictive and prognostic variables in epithelial ovarian cancer. Crit Rev Oncol Hematol 2009,69(1):12–27. 10.1016/j.critrevonc.2008.05.001
This study was funded by Cancer Treatment Centers of America®.
The authors declare that they have no competing interests.
DG and CGL participated in concept, design, data collection, data interpretation and writing. Both authors read and approved the final manuscript.