The prognostic value of the preoperative c-reactive protein/albumin ratio in ovarian cancer
- Yubo Liu†1,
- Shengfu Chen†2, 3,
- Chengyu Zheng2,
- Miao Ding2,
- Lan Zhang2,
- Liangan Wang2,
- Meiqing Xie2Email author and
- Jianhua Zhou1Email author
© The Author(s). 2017
Received: 22 August 2016
Accepted: 22 March 2017
Published: 21 April 2017
Inflammation plays an important role in the pathogenesis of ovarian cancer. This study sought to investigate the association between the preoperative c-reactive protein/albumin ratio (CRP/Alb) and oncological outcomes in ovarian cancer patients.
Two hundred patients with histologically verified ovarian cancer between June 2006 and July 2012 were retrospectively reviewed. Overall survival was evaluated by the Kaplan–Meier method and log-rank test. The significance of risk factors for overall survival was evaluated with the Cox proportional hazards model. Additionally, area under the receiver operating characteristic curve (AUC) was used to compare the predictive ability of CRP/Alb, Glasgow Prognostic Score (GPS), modified GPS (mGPS), neutrophil lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR), prognostic index (PI) and prognostic nutritional index (PNI).
The optimal cutoff value of CRP/Alb was 0.68. Increased CRP/Alb (≥0.68) was associated with advanced stage, residual tumor, ascites, elevated serum carbohydrate antigen(CA)-125 level, GPS, and mGPS (all p < 0.05). Patients with high CRP/Alb had poor overall survival compared to those with low CRP/Alb (p < 0.001). Multivariable analysis showed that CRP/Alb (Hazard Ratio (HR) 1.330, 95% confidence interval (CI) 1.131–1.564, p = 0.001), tumor stage (HR 1.577, 95% CI 1.189–2.091, p = 0.002), residual tumor (HR 2.337, 95% CI 1.518–3.597, p < 0.001) and age (HR 1.017, 95% CI 1.000–1.035, p = 0.046) were independent prognostic factors for overall survival. Additionally, the CRP/Alb showed greater AUC values at 1 year (0.692), 3 years (0.659), and 5 years (0.682) than GPS, mGPS and PNI.
The CRP/Alb is a novel independent marker of poor prognosis among ovarian cancer patients and shows superior prognostic ability compared to the established inflammation-based prognostic indices.
KeywordsC-reactive protein/albumin ratio Inflammation-based prognostic score Ovarian cancer Prognosis
Ovarian cancer has the highest death rate among all gynecological malignancies worldwide . Primary cytoreductive surgery alone or in combination with adjuvant chemotherapy is now widely advocated as the standard treatment for ovarian cancer patients . Nevertheless, despite the improvement in surgical procedures and the development of adjuvant therapy such as platinum-based chemotherapy, neoadjuvant chemotherapy, intraperitoneal hyperthermic therapy and molecular targeted therapies, the long-term survival is still poor [3, 4]. Ovarian cancer is a heterogeneous disease, and the prognosis is variable. Some patients may experience better clinical outcomes than others . Therefore, the identification of factors that could help to predict the prognosis and individualize the treatment according to the stratification of risks may improve the survival of ovarian cancer patients.
In fact, ovarian cancer has been found to be closely related to inflammation [6, 7]. Firstly, ovulation itself is a natural inflammatory process involving ovarian cortex cyclical rupture and healing, which is regarded as an underlying factor of ovarian cancer [8, 9]. Secondly, patients who suffer endometriosis or pelvic inflammatory disease have an increase in the subsequent risk of ovarian cancer [10, 11]. In contrast, oral contraceptives inhibiting ovulation reduce the risk of ovarian cancer . Additionally, tubal ligation or hysterectomy has been proven to offer protection against ovarian cancer by preventing the retrograde spread of proinflammatory factors from the lower genital tract to the ovaries [10–12]. Furthermore, anti-inflammatory therapy can reduce the risk of ovarian cancer and extend the survival of ovarian cancer patients [13, 14]. Given the close relationship between inflammation and ovarian cancer, several inflammation-based prognostic indices have been constructed to predict the clinical outcome. To date, the Glasgow Prognostic Score (GPS) , neutrophil lymphocyte ratio (NLR)  and platelet lymphocyte ratio (PLR)  were reported to display prognostic value in ovarian cancer patients.
The C-reactive protein/albumin ratio (CRP/Alb), consisting of CRP and albumin, was initially used to assess the outcome of patients with acute medical admissions and sepsis [18, 19]. Recently, the prognostic ability of CRP/Alb has been reported in patients with hepatocellular carcinoma , gastric cancer  and esophageal squamous cell carcinoma [22, 23]. Elevated preoperative CRP/Alb has been associated with the poor survival of patients with the aforementioned cancers. However, up to now, no study has been conducted to clarify the clinical significance and prognostic value of this marker in ovarian cancer.
Therefore, in this study, we retrospectively investigated the impact of preoperative CRP/Alb on the overall survival (OS) in ovarian cancer and compared the predictive value of CRP/Alb, GPS, mGPS, NLR, PLR, prognostic index (PI) and prognostic nutritional index (PNI).
Written informed consents for their information to be stored and used in the hospital database were obtained prior to data collection, and the study was approved by the ethics committee of the Sun Yat-sen University Cancer Center. The study was conducted in accordance with the Declaration of Helsinki to protect personal data.
This retrospective analysis was conducted on patients pathologically diagnosed with ovarian cancer at Sun Yat-sen University Cancer Center in Guangzhou, China, between June 2006 and July 2012. All the patients were included in this study based on the following criteria: (a) histologically confirmed ovarian cancer; (b) available serum CRP and albumin levels at diagnosis; (c) adequate clinico-pathological and follow-up data; (d) no clinical evidence of infection or other inflammatory conditions; and (e) no second malignancies or multiple primary malignancies. Finally, 200 patients diagnosed with ovarian cancer were enrolled in our study. The patients were treated with hysterectomy, bilateral salpingo-oophorectomy, pelvic and/or paraaortic lymphadenectomy, appendectomy, and omentectomy. Patients with stage Ic to IV disease received platinum-based chemotherapy following surgery. Patient charts were reviewed to obtain age, preoperative laboratory measurements, postoperative tumor characteristics and time of death or time of last follow-up from the hospital database at the Sun Yat-sen University Cancer Center and pathological records from the Institute of Pathology at the same institution. OS time was defined as the interval between the date of operation and the date of death or the last follow-up. Patient follow-up was maintained until death or the cutoff date of December 2014. The clinico-pathological and full blood count data before initial treatment were obtained.
Pearson’s χ2 test was used to examine the correlations of CRP/Alb value with clinico- pathological parameters. The ROC curve was calculated, and the Youden index (maximum (sensitivity + specificity-1))  was used to determine the optimal cutoff value for CRP/Alb, PNI, NLR, PLR and CA-125. All patients were divided into two different groups (high or low CRP/Alb ratio group) according to the optimal cutoff value of CRP/Alb. The Kaplan–Meier method was used to plot the survival curves, and the log-rank test was used to compare the differences between the subgroups. A univariate and multivariate analysis was performed for the prognostic factors using the Cox proportional hazard model, with significant variables (p < 0.05) in univariate mode being further analyzed in the multivariate Cox proportional hazards mode. Area under receiver operating characteristics curve (AUC) analyses were performed using MedCalc statistical software version 15.2.1 (MedCalc Software bvba, Ostend, Belgium). Other analyses were performed using SPSS version 13.0 (Chicago, Illinois, USA). Statistical significance was set at p < 0.05 (two-tailed).
A total of 200 subjects were studied, with a median age of 53 years (range 18–83 years). A total of 110 (55%) patients had an elevated CRP concentration (10 mg/L), and 22 (11%) patients had hypoalbuminemia (albumin <35 g/L) prior to surgery. Of the 22 patients with hypoalbuminemia, 21 (95.45%) had an elevated CRP concentration. According to clinical criteria, almost all the patients (192) received platinum-based chemotherapy.
Inflammation-based prognostic scores
C-reactive protein/albumin (CRP/Alb)
C-reactive protein/albumin ≤ 0.68
C-reactive protein/albumin > 0.68
Glasgow Prognostic Score (GPS)
CRP(≤ 10 mg/L) and albumin(≥ 35 g/L)
CRP(≤ 10 mg/L) and albumin(< 35 g/L)
CRP(>10 mg/L) and albumin(≥ 35 g/L)
CRP(>10 mg/L) and albumin(< 35 g/L)
The modified GPS
CRP(≤ 10 mg/L) and albumin(≥ 35 g/L)
CRP(≤ 10 mg/L) and albumin(< 35 g/L)
CRP(>10 mg/L) and albumin(< 35 g/L)
Neutrophil lymphocyte ratio(NLR)
Neutrophil count: lymphocyte count < 2.5
Neutrophil count: lymphocyte count ≥ 2.5
Platelet lymphocyte ratio(PLR)
plt count: lymphocyte count ≤ 165
plt count: lymphocyte count > 165
Prognostic nutritional index(PNI)
Albumin(g/L) + 5 × total lymphocyte count × 109/L ≥ 48
Albumin(g/L) + 5 × total lymphocyte count × 109/L < 48
CRP(≤ 10 mg/L) and white cell count(≤ 11 × 109/L)
CRP(≤ 10 mg/L) and white cell count(> 11 × 109/L)
CRP(>10 mg/L) and white cell count(≤ 11 × 109/L)
CRP(>10 mg/L) and white cell count(> 11 × 109/L)
Relationship between CRP/alb and clinico-pathological factors
The correlation between clinicopathological factors and CRP/Alb ratio in ovarian cancer patients (n = 200)
No. of patients
≤ 2 cm
> 2 cm
≤ 10 mg/L
> 10 mg/L
Impact of inflammatory scores as predictors of OS
Univariate and multivariate analysis of potential prognostic factors for overall survival
Age(years) (≤ 50 vs >50)
FIGO Stage(I vs II vs III vs IV)
Grade(G1 vs G2 vs G3)
Residual tumor (≤2 cm vs >2 cm)
Ascites(yes vs no)
Comparison of the predictive ability
Comparison of the diagnostic performance of several inflammation-based prognostic indices in predicting mortality
One year follow-up
Three years follow-up
Five years follow-up
The present study demonstrated that increased CRP/Alb predicted the poor prognosis of OS in ovarian cancer patients. Moreover, compared to the established inflammation-based prognostic indices GPS, mGPS and PNI, CRP/Alb displayed superior prognostic ability. These results are consistent with previous studies identifying CRP/Alb as predictors of outcome in hepatocellular carcinoma , gastric cancer  and esophageal squamous cell carcinoma [22, 23].
C-reactive protein (CRP) is an important acute phase response protein produced mainly by hepatocytes, whose levels rise in response to inflammation . Mc Sorley et al. reported that high circulating CRP levels may subsequently promote ovarian cancer . This conclusion was supported by a meta-analysis . Hefler et al. found that elevated CRP is associated with chemical resistance and poor survival in patients with ovarian cancer . The underlying mechanism is that CRP can accelerate angiogenesis based on increased circulating levels of vascular growth factors and circulating interleukin in cancer patients [29, 30].
Albumin is also produced by the liver, which helps to maintain intravascular oncotic pressure, facilitate the transport of substances and scavenge free radicals. It is now considered an indicator of malnutrition. Hypoalbuminemia is related to a sustained systemic inflammatory response, either from the tumor itself or as a host response . Several studies have suggested that the progression of hypoalbuminemia is secondary to the serum elevation of CRP, as many cancer patients with hypoalbuminemia already have increased serum CRP levels [32, 33]. Malnutrition, in turn, is related to poor prognosis in patients with cancer . Several previous studies reported that pre-operative low serum albumin levels are an independent predictor of poor survival in ovarian cancer [35, 36]. Improvement in nutritional status is associated with better survival in ovarian cancer  and other tumors . One of the reasons is that the presence of a systemic inflammatory response and the concomitant nutritional decline reduces patient tolerance to treatment toxicities and patient compliance with active treatment .
CRP/Alb, which is obtained from the combination of CRP and albumin, may reflect both the inflammatory and nutritional state in cancer patients. Therefore, the presence of a chronic systemic inflammatory response and progressive nutritional decline is reflected by the elevated CRP/Alb, ultimately resulting in reduced survival.
Previous studies have established some possible prognostic factors in ovarian cancer. In particular, the adverse effect of postoperative residual tumor mass, tumor grade, peritoneal dissemination, and histological subtype on patients’ OS has been found in previously published studies . By univariate analysis, we have shown that tumor stage, postoperative residual tumor, histological subtype, ascites, CRP, hypoalbuminemia and age, as well as CRP/Alb, GPS, mGPS, PLR, PNI and PI, are predictors of OS in ovarian cancer. However, by using a Cox regression model of multivariate analysis, we found that only CRP/Alb remained as an independent prognostic marker for poor survival in patients with ovarian cancer along with residual disease, tumor stage and age, suggesting that CRP/Alb has a substantial impact on patient outcome. Surprisingly, albumin is no longer an independent predictor of OS, and age is a marginally significant predictor of OS (p = 0.046), conflicting with a recent study . The reason for this difference is that our study included CRP/Alb. In fact, when CRP/Alb was excluded, albumin became an independent risk factor for OS (data not shown), indicating that CRP/Alb is a more powerful predictor than preoperative albumin. We noted that CRP/Alb correlated significantly with advanced tumor stage, residual tumor, increased CA-125 levels and the presence of ascites, suggesting that increased CRP/Alb may correlate with a more aggressive disease phenotype.
On established prognostic factors, postoperative residual tumor mass and ovarian tumor stage have been shown to be the most reliable predictors of outcome in ovarian cancer . Similar to other studies, while CRP/Alb was a significant predictor of OS in patients with ovarian cancer, residual tumor mass and tumor stage remained significantly more powerful predictors of survival, as the Hazard Ratio for residual tumor and tumor stage were 2.337 and 1.577, respectively, compared with the HR of 1.330 for CRP/Alb by multivariate analysis. Further, we analyzed the prognostic value of CRP/Alb combined with tumor stage and residual tumor mass. The combined effect was greater than the individual effect of either variable alone, indicating that CRP/Alb may be the complementary factor for tumor stage and residual tumor mass in predicting the survival in patients with ovarian cancer.
The prognostic significance of preoperative CA-125 levels in ovarian cancer remains controversial at present. A few publications have described an association between CA-125 levels before surgery and survival. Paramasivam et al. reported patients with early-stage ovarian cancer and a preoperative serum CA-125 more than 30 U/mL were significantly associated with impaired survival . Similar results were found by Kumar et al. . However, some studies failed to show a correlation between preoperative CA-125 and prognosis. Mury et al. concluded that the specificity of CA-125 to predict surgical outcome is low, and the prognostic value is questionable . Chi et al. reported that preoperative CA-125 did not predict the primary cytoreductive outcome of patients with advanced ovarian cancer . In the present study, we also could not define a reasonable cutoff value of CA-125 to predict survival outcome due to its low specificity. In addition, although CA-125 was correlated to overall survival in univariate analysis, it was no longer an independent predictor in multivariable analysis. Therefore, we inferred that the main value of CA-125 may be useful in monitoring disease recurrence instead of prognosis.
In addition, it is important to examine whether a new prognostic system is at least equivalent or superior to other current validated prognostic scoring systems. We, therefore, compared the prognostic ability of CRP/Alb with other established inflammation-based prognostic scores, such as GPS, mGPS NLR, PI, PLR and PNI. In the context of ovarian cancer, AUC analysis has shown that CRP/Alb was superior to other inflammation-based prognostic scores in terms of predictive accuracy, which is consistent with several previous studies in hepatocellular carcinoma , gastric cancer  and esophageal squamous cell carcinoma [22, 23].
To the best of our knowledge, this is the first study to investigate whether CRP/Alb is useful for predicting postoperative outcome in ovarian cancer patients, and we analyzed all seven of these parameters for the first time. Our results suggest that preoperative serum CRP/Alb might serve as a potentially clinically valuable marker in patients with ovarian cancer. Firstly, CRP/Alb has the advantage of being simple to measure, routinely available and well standardized. Secondly, increased CRP/Alb might correlate with a more aggressive disease phenotype, possibly using it to screen a subset of patients with bad prognosis requiring intense therapy. Thirdly, CRP/Alb displays superior prognostic ability compared to other inflammation-based scoring systems. Finally, CRP/Alb may be a complementary factor for tumor stage and residual tumor mass in predicting the survival in patients with ovarian cancer.
Although the present study shows the strong independent prognostic value of the CRP/Alb in ovarian cancer patients, the retrospective nature and the relatively small sample size from a single center should be acknowledged as potential limitations. However, the strict inclusion and exclusion criteria and the level of statistical significance achieved for the prognostic traits tested in our series leave little doubt about the reliability and reproducibility of our findings.
Preoperative CRP/Alb derived from routine blood tests is an independent prognostic marker in patients with ovarian cancer. Moreover, compared to other inflammation-based prognostic scores, it shows superior prognostic ability. Therefore, clinically, CRP/Alb may be used as a complementary factor to stratify ovarian cancer patients into different prognostic groups for tailored treatment.
Area under receiver operating characteristics curve
C-reactive protein/albumin ratio
International federation of gynecologists and obstetricians
The modified glasgow prognostic score
Neutrophil lymphocyte ratio
Platelet lymphocyte ratio
Prognostic nutritional index
This work was supported by Grant 163 from Key Laboratory of Malignant Tumor Molecular Mechanism and Translational Medicine of Guangzhou Bureau of Science and Information Technology; Grant K1809001 from the Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes; Guangdong Natural Science Fund (2015A030310083). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
The datasets during and/or analysed during the current study available from the corresponding author on reasonable request.
CSF and LYB drafted the manuscript. LYB, CSF, ZCY, DM and ZL participated in the clinical data collecting of patients. CSF and LYB performed the statistical analysis. WLA, XMQ and ZJH helped in the verification of patients’ data and revised the manuscripts. CSF, LYB, XMQ and ZJH conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Written informed consents for their information to be stored and used in the hospital database were obtained prior to data collection and the study was approved by the ethics committee of the Sun Yat-sen University Cancer Center. The study was conducted in accordance with the Declaration of Helsinki to protect the personal data.
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