Abstract
Objectives. The role of complement system in predicting prognosis of gastric cancer (GC) remains obscured. This study aims to explore the incidence of complement C3 depletion and associated outcomes in GC patients. Methods. between August 2013 and December 2013, 106 patients with gastric adenocarcinoma were prospectively analyzed. Plasma levels of complement C3 and C4 were detected at baseline, one day before surgery, and postoperative day 3, respectively. Patients with low C3 levels (<0.75 mg/mL) were considered as having complement depletion (CD), while others with normal C3 levels were included as control. The 3-year overall survival (OS), disease-free survival (DFS), and other outcomes were compared between both groups, with the CD incidence explored meanwhile. Results. The CD incidence was 28.3% before surgery but increased to 37.7% after surgery. Preoperative CD was related to prolonged hospital stay (22.7 versus 19.2 day, ) and increased postoperative complications (33.3% versus 14.5%, ) and hospital costs (). Besides, postoperative C3 depletion was significantly associated with decreased 3-year OS () and DFS (). Moreover, postoperative C3 depletion and advanced tumor stage were independent predictive factors of poor prognosis. Conclusions. Complement C3 depletion occurring in gastric cancer was associated with poor short-term and long-term outcomes.
1. Introduction
Gastric cancer (GC) is the third leading cause of cancer-associated death worldwide [1]. Worse still, GC is correlated to a higher health burden in several countries such as China and Japan, where it is the most common cancer in both sexes. To date, long-term outcomes of GC in China remain quite poor due to over 80% advanced tumor stage at diagnosis and rich diversity of treatment [2]. Early diagnosis by gastroscopy and appropriate surgical treatment are essential for improved prognosis in such population. In clinical practice, some patients with identical clinical stage of cancer experience various survival times, indicating differences in GC biology [3]. Therefore, researches for investigating heterogeneity in genetic susceptibility and demographic characteristics are definitely required to understand the mechanism of gastric carcinogenesis.
Epidemiological studies have identified several risk factors for development of GC, including Helicobacter pylori (Hp) infection, high oral intake of salt-preserved foods, long-term smoking habit, and pernicious anemia [4]. Those factors are commonly related to chronic inflammation around gastric epithelium and play roles in gastric carcinogenesis [5]. It has been recognized that chronic inflammation typically caused by Hp infection is involved in GC onset, promotion, and progression [6–9].
Complement system is a collection of over 30 serum proteins that are integral to inflammatory processes and innate immunity against exogenous infection [10]. Given the insidious links between complement system and inflammation, some complement components may play partial roles in inflammation-related carcinogenesis. A previous review has suggested that complement activation could enhance innate immunity against cancer through direct tumor cell lysis or complement-dependent cytotoxicity [11]. However, other studies have indicated that complement components C5a and C3a generated by complement activation could promote tumor growth and progression [12, 13]. Taken as a whole, complement system seems to have dual effects on the carcinogenesis process.
As known to all, complement C3 is the point of convergence for three complement activation pathways. The storage of C3 in human body is abundant; however, its concentration in serum can be easily affected by infection or inflammation. Our previous studies have found that complement C3 depletion due to extensive complement activation would depress immunity and predict a poor prognosis of severe intra-abdominal infection [14, 15]. Whether such complement depletion observed during exogenous infection also occurs in GC remains unknown. In addition, the predictive value of complement C3 depletion in GC patients is not completely clear. We herein perform a prospective study in Chinese population to illustrate our hypotheses that complement C3 depletion does develop in GC patients and links to poor clinical outcomes.
2. Patients and Methods
This was a prospective cohort study of patients with GC at a tertiary level teaching hospital in southern China. Patients with pathological diagnosis of gastric carcinoma were recruited between August 2013 and December 2013. The study protocol was approved by the Institutional Review Board of our hospital and registered in ClinicalTrials.gov (NCT02425930). Written informed consents were obtained from all participants prior to any treatment.
2.1. Patients
Within the study period, consecutive patients referred or admitted to our center were screened for eligibility criteria. Inclusion criteria included the following: (1) pathological diagnosis of gastric adenocarcinoma with clinical stages of I–III based on abdominal and pelvic computed tomography (CT), (2) indication for radical gastrectomy (total or subtotal) after a multidisciplinary team (MDT) meeting, with adjuvant chemotherapy considered as a routine plan for pathologic stage IIB and above, and (3) adult age between 18 and 75 years, with no limitation of gender.
Patients with the following medical conditions were excluded from this study: another primary malignancy, cardiopulmonary dysfunction, active uncontrolled infection or psychosis, and chronic inflammatory disease (tuberculosis, Crohn’s disease, etc.) except for Hp infection; any abdominal emergency surgery due to tumor progression, history of major abdominal surgery within the last six months, or nonradical gastrectomy for palliative care; and long-term use of corticosteroids, insulin, oral antidiabetic drugs, or other drugs for obesity. Besides, those who recently received blood transfusion or continuous renal replacement therapy were also excluded from participation.
2.2. Clinical Management Schemes
As routinely practiced in China, surgical residents would interview patients and collect personal and clinical data, such as the period of chief complains, features of symptoms, percentage of weight loss and cachexia defined as the history of weight loss greater than 5% during the last three months, status of feeding, and past medical, drug, and family history. All enrolled patients would allocate a clinical tumor stage (cTNM) during the MDT meeting, which was usually held weekly on Monday morning. Of note, patients scheduled to receive neoadjuvant chemotherapy were not included in the current study. In general, patients had to wait 2–4 days after admission to receive an operation. After a curative resection, histology tumor stage (pTNM) was assessed by experienced gastrointestinal pathologists. All tumor stages were determined using the 7th edition of American Joint Committee on Cancer (AJCC) TNM staging system for gastric cancer [16].
Generally, surgical treatment, which was consisted of total or subtotal gastrectomy with R0 resection and lymphadenectomy, could be accomplished by open or laparoscopic techniques. The detailed surgical procedures were primarily determined by surgeon’s preference. After a definitive surgery, adjuvant chemotherapy, with S-1 (60 mg/m2) and oxaliplatin (85 mg/m2) as a main regimen for at least eight cycles (SOX regimen), was initiated 3-4 weeks after surgery. Specifically, postoperative radiotherapy would be considered in patients with regional positive lymph nodes or suspicious resection margin on final pathology report.
As previously described, follow-up was typically every three months for the first year after surgery, every six months for the second year, and twice a year thereafter [17]. Similar follow-up visits took place with a medical oncologist or radiation oncologist. In our clinical practice, the abdominal and pelvic contrast-enhanced CT scan was routinely performed for tumor recurrence surveillance.
2.3. Complement Levels Monitor and Study Outcomes
Peripheral blood samples were routinely collected at baseline and one day before and three days after surgery, respectively. Plasma was obtained from the centrifugation (3000, 20 min, 4°C) and immediately stored at −80°C until tested. As previously described, complement C3 and C4 levels were dynamically measured with ELISA method, with routine blood counts and biochemical analyses performed meanwhile. Patients were stratified into two groups according to preoperative levels of C3. In detail, patients, who had low levels of C3 both at admission and one day before surgery (cutoff value, 0.75 mg/mL), were assigned to complement depletion (CD) group [14]. The rest with normal C3 level at least one-shot test prior to surgery were assigned into control group. Of note, the incidence of complement C3 depletion was determined according to percentage of values below the lower reference limit (reference interval, 0.75–1.35 mg/mL).
The primary outcome of this study was the 3-year overall survival (OS) after a radical surgery. The secondary outcomes included the incidence of complement depletion, disease-free survival (DFS), incidence of postoperative complications, length of stay (LOS), and hospital expenditure. Meanwhile, several predictive factors (gender, age, body mass index, American Society of Anesthesia score, baseline C3 level, etc.) of poor prognosis in GC patients were detected using the Cox-regression analysis.
2.4. Statistical Analyses
Provided that level of significance is 5%, to have 90% power to detect a hazard ratio (HR) of 0.5 between binary intervals of plasma C3 levels with assumed one standard deviation (SD), at least 30 deaths should be observed within the follow-up period [18]. Besides, given an estimate of 30% for 3-year OS and a 10% loss of follow-up, at least 80 GC patients should be included for this study.
Descriptive statistics were employed to present demographic characteristics and oncologic outcomes. Data were expressed as means ± SD if not otherwise indicated. Survival analysis was performed using the Kaplan-Meier method and the log-rank test. The OS was calculated from the date of definitive operation to death resulting from any cause. The DFS was defined as the time interval from surgery to confirmed recurrence, occurrence of a new primary cancer, or death from any cause. Student’s -test and Mann-Whitney test were employed for continuous variables, whereas Fisher’s exact test and Chi-square test were used for categorical variables. Cox proportional hazards models were utilized to calculate HRs with 95% confidence intervals (CIs) for the relationship between complement C3 depletion and 3-year OS or DFS. All data analyses were performed using IBM® SPSS® Statistics (Statistics. 23.0; Chicago, IL). In general, two-tailed tests were used, with value < 0.05 considered statistically significant.
3. Results
Between August 2013 and December 2013, 188 patients were enrolled for eligibility, and 106 patients were finally included based on inclusion and exclusion criteria (Figure 1). Of note, ten (8.6%) patients were lost during the follow-up period. The median follow-up period of this cohort was 23 (range, 1–40) months, with an observed death rate of 29.2% (31/106) after a radical gastrectomy. The demographic and baseline characteristics of included subjects were summarized in Table 1. Briefly, the median age of this cohort was 57 (range, 23–87) years, with 61.3% of male adults included. Among those, 30 (28.3%) patients suffering from preoperative C3 depletion were assigned into CD group, with the rest into control group. Although the case number in control group was twice of that in CD group, statistical comparisons in demographic and clinical data were not significant between both groups.
3.1. The Changes of Complement Components and Correlation Analyses
As mentioned above, the function of complement system was mainly evaluated using changes of C3 levels at three time points: baseline at admission and one day before and three days after surgery. The average plasma levels of C3 and C4 at baseline were 0.87 (median, 0.87; range, 0.43–1.79) mg/mL and 0.23 (median, 0.22; range, 0.10–0.47) mg/mL, respectively. After surgery, both plasma levels declined in different degrees; however, such falling changes did not reach statistical significance compared to baseline values (). Besides, the number of patients suffering from CD increased from 30 (28.3%) at baseline to 40 (37.7%) after surgery, with 23 and 17 cases from control and CD group, respectively. Of 30 patients with preoperative CD, only 13 (43.3%) participants involving CD at first had improved plasma levels of complement C3 after surgery. There were significant differences in overall levels of C3 and C4 between CD group and control group (Figure 2). The current perioperative management for GC appeared to play minimal roles in enhancing complement function. Tumor invasive depth () and pathological stage () were not correlated to preoperative C3 depletion. In addition, body mass index (BMI), white blood cells (WBC) counts, hemoglobin, platelet (PLT) counts, plasma albumin, and total bilirubin (TB) were also not related to plasma C3 levels by a linear regression (Table 2). As a result, complement C3 depletion at admission or before surgery may be considered as an independent risk factor for predicting clinical outcomes of GC patients.
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3.2. Primary and Secondary Outcomes
In the current study, 98 (92.5%) patients received open surgery for radical gastrectomy, with the rest undergoing laparoscopic surgery. Of note, intraoperative conversion due to massive hemorrhage was observed in one (12.5%) case from the CD group. Those secondary outcomes were shown in Table 3. The median LOS was 19 (range, 10–64) days, with nine (range, 3–52) days for length of postoperative stay (LOPS). Specifically, both LOS and LOPS were significantly prolonged in the CD group compared with the control group (). Moreover, the incidence of postoperative complications was markedly increased in the CD group compared with the control group (33.3% versus 14.5%, ). In sum, 21 (19.8%) patients had various degrees of postoperative complications, with 12 for wound infection, 5 for postoperative pyrexia, 4 each for anastomotic leak and hemorrhage, and 3 for bowel obstruction. Among those, only two (9.5%) patients had to undergo unplanned reoperation for severe complications. However, no patient died in the hospital or within 30 days of operation. The total hospital expenditure was markedly increased in patients with preoperative CD compared to those without ().
Within the follow-up period, 31 (29.2%) patients died of tumor progression. Among those, 12 (38.7%) patients were in the CD group, with the others in the control group. The 3-year estimated OS rate was 51%, and the median estimated OS time for the current cohort was 26.0 (95% CI, 23.1–28.8) months. On the basis of Kaplan-Meier survival analysis, the OS time had no significant difference between both groups (, Figure 3). However, patients who developed postoperative CD would have much poorer OS than those without postoperative CD (, Figure 3). On the other hand, 35 (33%) patients developed tumor recurrence within the median follow-up period of 20.9 (range, 1–37) months. Similarly, Kaplan-Meier estimates of DFS by baseline C3 levels had no significant difference (, Figure 3), while the DFS by postoperative C3 levels appeared statistically significant (). A Cox regression using univariate analysis indicated that postoperative C3 levels, pathological T stage, N stage, and total tumor stage (pTNM), and tumor marker were associated with long-term survival (Table 4). A further analysis with stepwise multivariate regression revealed that postoperative C3 level and pTNM were independent predictive factors of poor survival in such cohort. Specifically, postoperative decreased C3 levels (<0.75 mg/mL) and advanced tumor stage (stage III/IV) were correlated with a poor prognosis for GC patients.
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4. Discussion
In the current study, 106 patients with resectable gastric cancer were prospectively followed. To our knowledge, the incidence of complement depletion for such patients was 28.3% in the beginning but increased to 37.7% after a definitive operation. Our results indicated that preoperative complement depletion was an independent risk factor during preoperative evaluation. It was associated with prolonged stay in hospital and increased postoperative complications and hospital expenses. Importantly, the 3-year OS and DFS were both decreased in patients with CD compared to those without CD. Besides, we found that postoperative CD, rather than preoperative CD, had prognostic significance for those long-term outcomes. By using Cox logistic regression analyses, postoperative CD and advanced tumor stage were independent predictive factors of a poor prognosis.
As known to all, complement system is an old member of innate immunity, which plays key roles in defending against exogenous pathogens and regulating intrinsic inflammation [15]. Its biological functions, producing numerous active effectors for immunity regulation and opsonization, are realized majorly through three activation pathways: classical, lectin, and alternative ways [19]. Nowadays, more and more evidence have demonstrated that such pathways are minutely regulated based on various plasma levels of complement components, particularly complement C3 [20]. Our previous studies have found that complement C3 exhaustion due to severe sepsis would deteriorate immunity and coagulopathy meanwhile [14, 15].
While there is great interest in complement system in various inflammation-related diseases, there have been limited studies that focus on the exhaustion of complement by-products and subsequent outcomes in cancer diseases. A recent literature review indicates that complement system definitely plays roles in carcinogenesis of certain cancers, such as bladder, cervical, and hepatocellular carcinomas [21]. To our knowledge, the current study first reported the incidence of complement depletion and its predictive value for short-term and long-term outcomes in GC.
In clinical practice, complement dysfunction is commonly underestimated or even ignored during the preoperative evaluation, as compared with tumor-related obstruction and hemorrhage, malnutrition, and coagulopathy. Hence, its role in predicting postoperative outcomes, particularly long-term results, would be completely unclear. Our study has provided a referenced CD incidence (28.3%–37.7%) in GC patients but, more importantly, offered a hint to alert complement dysfunction in the perioperative management of gastric cancer.
Based on our preliminary studies, it is believed that persistent CD due to severe intra-abdominal infection was related to a poor prognosis. Similarly, it is confirmed that postoperative CD in GC patients was associated with poor OS and DFS. However, the concrete mechanism of CD-associated cancer surveillance remains obscured. To our knowledge, the vast majority of gastric cancers grow for years and induce repeatedly chronic inflammation. Therefore, uninterrupted complement activation would be inevitable, and circulatory complement insufficiency would be predictable. In spite of intrinsic consumption, complement proteins, such as C3d, C5b-9, and S protein, would be deposited on GC cells to avoid complement-mediated cytotoxicity [22]. These possible pathways for consuming complement components might contribute to the observed CD in GC patients. On the other hand, a depressed complement activity could indirectly promote the growth of gastric cancer cells and allow distant metastasis due to resistance to immune attack [23–25]. However, it is still unknown why only a few patients would develop CD in clinical practice of GC treatment. A recent study indicates that a certain genotype of type I complement receptor (CR) is highly expressed in Chinese population and strongly associated with decreased complement activation and reduced GC risk [10].
Several limitations of this study should be addressed. First, the small sample size due to relatively short recruiting period might depress statistical power and conceal some significances of current findings. Given limited number of patients with early-stage disease, a subgroup analysis by tumor stage was failed to perform in this study. Second, other complement proteins, such as C3a, C5a, type I CR, and factor B, were not available for daily clinical tests. Exploring plasma changes of those effectors in GC will enhance our understanding of roles of complement system in cancer surveillance and inflammation. Indeed, the complement C3 depletion was not fully equal with the complement depletion, since other activation pathways did work independently without complement C3. At last, future studies with larger samples and focus on the molecular mechanism of CD-associated cancer surveillance are needed to answer the following question: “is complement good or bad for cancer patients?”
In summary, our results demonstrate that complement C3 depletion could indicate poor clinical outcomes for gastric cancer patients in China. Additionally, such depletion emerging after a definitive operation seems to be an independent predictive factor of poor long-term survival. The complement C3 depletion, whether before or after surgery, should be paid close attention in clinical surveillance of this subset population.
Ethical Approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Consent
Informed consent was obtained from all individual participants included in the study.
Conflicts of Interest
All authors have declared no potential conflicts of interest.
Authors’ Contributions
Yulong He and Yujie Yuan conceived and designed the experiments. Jinning Ye, Yufeng Ren, Jianhui Chen, and Shirong Cai performed the study. Yujie Yuan, Chuangqi Chen, Yulong He, and Min Tan analyzed the data. Jianhui Chen, Yufeng Ren, Chuangqi Chen, Yujie Yuan, and Shirong Cai contributed reagents/materials/analysis tools. Yujie Yuan, Jinning Ye, and Yulong He wrote the paper. Yujie Yuan, Yufeng Ren, and Min Tan designed the software used in analysis. Yujie Yuan and Yulong He obtained permission for clinical trials. Jinning Ye and Yufeng Ren equally contributed to this study.
Acknowledgments
This study was supported by the National Natural Science Foundation of China (no. 81401307) and Medical Science and Technology Research Fund Project in Guangdong province (A2015112). Mrs. Donglian Chen and Mrs. Lifeng Lu must be acknowledged for their dedicated works in telephone follow-up and dataset management.