High Mean Corpuscular Volume Predicts Poor Outcome for Patients With Gastroesophageal Adenocarcinoma

Background Elevated mean corpuscular volume (MCV) is associated with a diminished prognosis for various tumor entities. This study aimed to evaluate the association between preoperative serum MCV levels and both overall (OS) and disease-free survival (DFS) for patients with resectable adenocarcinomas of the esophagogastric junction (AEG). Methods This study included consecutive patients undergoing surgical resection between 1992 and 2016. Measured preoperative MCV levels were stratified into quintiles and correlated with patients’ survival and clinicopathologic characteristics. Results The study analyzed 314 patients with a median OS of 36.8 months and a median DFS of 20.6 months. The multivariate analysis showed that preoperatively elevated MCV is a significant prognostic factor for OS (hazard ratio [HR], 1.05; 95% confidence interval [CI], 1.03–1.08; P < 0.001) and DFS (HR, 1.05; 95% CI, 1.03–1.08; P < 0.001). In the subgroup analysis of neoadjuvantly treated and untreated patients, MCV remained an independent prognostic factor for OS (HR, 1.08; 95% CI, 1.04–1.12; P < 0.001) and DFS (HR, 1.07; 95% CI, 1.03–1.12; P < 0.001) in both groups. In the univariate analysis, tumor stage and differentiation, adjuvant chemotherapy, MCV, mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) were significantly correlated with diminished OS and DFS. Conclusion Preoperatively elevated MCV is an independent prognostic factor for patients with adenocarcinomas of the esophagus and the gastroesophageal junction.

(MCHC) were significantly correlated with diminished OS and DFS. Conclusion. Preoperatively elevated MCV is an independent prognostic factor for patients with adenocarcinomas of the esophagus and the gastroesophageal junction.
Esophageal cancer (EC) is the sixth most common cause of cancer-related death, causing an estimated 400,000 deaths worldwide per year. In East Asian countries, EC consists mainly of esophageal squamous cell carcinoma (ESCC), located most frequently in the proximal parts of the esophagus. 1,2 Whereas the number of ESCCs decreases in Western countries, the percentage of adenocarcinomas at the esophagogastric junction (AEG) is continuously increasing. 3 Neoadjuvant (radio)chemotherapy has emerged as the current standard treatment for locally advanced AEG. Despite the development of new therapeutic approaches combining multimodal treatment protocols and surgery, the prognosis for most patients with gastroesophageal adenocarcinoma remains poor, with 5-year overall survival rates of approximately 30%0. 4,5 To date, traditional tumorbased, histopathologic risk factors such as tumor and lymph node staging, tumor differentiation, and status of resection margin remain the only prognostic factors, available only retrospectively to surgery. In addition, these factors often are influenced by the use of neoadjuvant treatment. 6,7 Therefore, other prognostic factors available before surgery that can evaluate prognosis and treatment response are urgently needed.
Findings have shown hematologic parameters, particularly mean corpuscular volume (MCV), to be predictive markers for patients with various cancer entities. Recently, preoperatively elevated MCV, caused by alcohol abuse and acetaldehyde and folate deficiency, was shown to be an independent prognostic factor in ESCC patients. 8,9 Whereas ESCC is highly associated with alcohol and nicotine abuse, the association of alcohol consumption and the development of AEG remains unclear. [9][10][11][12][13][14] Besides alcohol abuse, folate and vitamin B12 deficiency, oxidative stress, and chemotherapy are known causes for elevation and/or changes in MCV levels in cancer patients. [15][16][17][18][19] To date, no data exist on the prognostic value of MCV for patients with gastroesophageal adenocarcinoma. In this study, we evaluated the prognostic value of preoperative MCV for patients with resectable adenocarcinomas of the esophagus and the gastroesophageal junction as well as the influence of preoperative systemic treatment on the potential prognostic value of MCV.

Blood Examinations
Laboratory factors including preoperative serum MCV, mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), red cell distribution width (RDW), and hemoglobin (Hb) were obtained within 7 days before surgery. Hematologic parameters were determined using the Coulter STKS (Coulter, Hialeah, FL, USA), the Sysmex NE-8000, or the hematology analyzer Sysmex XE-2100 (both from TOA Medical Electronics, Kobe, Japan), depending on the date of blood testing, under controlled conditions at the Department of Laboratory Medicine, Medical University of Vienna, which operates as the central laboratory of the General Hospital of Vienna, a certified (ISO 9001) and accredited (ISO 15189 since 2008) quality management system. [20][21][22] Patients We reviewed a prospectively maintained database of patients who underwent curative resection of locally advanced AEG between January 1992 and April 2016 in the Department of Surgery at the Medical University Vienna. Approval was obtained from the ethics committee of the Medical University Vienna, Austria, according to the declaration of Helsinki (EK1652/2016).
The exclusion criteria ruled out distant metastasis at the time of surgery, positive resection margin, postoperative death from a cause other than cancer or death within 30 days after surgery, known history of alcohol abuse, malignancies other than AEG, and missing preoperative levels of serum MCV, MCH, MCHC, RDW, and Hb. Blood for a complete blood count was drawn within 3 days before surgery. At that time, none of the patients showed signs of pyrexia (axillary C 37.2°C [99.0°F]) or any form of active infection or chronic inflammatory disease.
The patients' baseline clinicopathologic values were retrospectively reviewed and collected from the local database and electronic patients' records. The pathologic classification of the primary tumor, the degree of lymph node involvement, and the presence of organ metastasis were determined according to the tumor-node-metastasis (pTNM) classification of the Union for International Cancer Control (UICC), 7th edition.
Pre-and postoperatively, every patient was discussed in the interdisciplinary tumor board meeting. Patients with resectable AEG, clinical stage T1, N1-3 or T2-4a, or N0-3 received neoadjuvant treatment. Neoadjuvant chemotherapy was performed by intravenous infusion, either with oxaliplatin/capecitabine (regimen A) or cisplatine/5-fluoruracil (regimen B) according to a current study protocol. Concomitant radiation was performed according to the recommendations of the interdisciplinary tumor board based on the regimen published by Van Hagen et al. 23 (regimen C).
The rate of response to neoadjuvant treatment was classified as defined by Mandard et al. 24 The tumor location at the gastroesophageal junction was classified according to Siewert and Stein. 25 All the patients were regularly followed up with physical examination, tumor marker, and computed tomography at our outpatient clinic every 3 months for the first 2 years, then every 6 months until 5 years after surgery. Patients with missing follow-up data (lost to follow-up assessment) were excluded from analysis.

Surgery
Transhiatal extended gastrectomy (THG) was performed for the patients with AEG 2 and 3 tumors. Proximal gastrectomy (Merendino procedure) was performed for the patients presenting with stage 1 tumors located at AEG 1 or 2 in selected cases. Abdominothoracic esophageal resection (ATE) was performed for the patients with AEG 1 or 2 tumor.
All the patients were regularly followed up with physical examination, tumor marker, and computed tomography at our outpatient clinic every 3 months for the first 2 years, then every 6 months until 5 years after surgery.

Statistical Analysis
Statistical analysis was performed using the software R 3.3 (R Foundation for Statistical Computing, Vienna, Austria; www.r-project.org). Categorical variables were described by absolute and relative frequencies, and metric variables were described by mean and median minimum and maximum.
To analyze the association of hematologic parameters and other potential predictors with post-surgery overall survival (OS) or disease-free survival (DFS), hazard ratios corresponding to a one-unit increase in a predictor variable were estimated from uni-and multivariable Cox proportional hazard regression models. Separate models were calculated for the full sample and for the subgroups of patients with and without neoadjuvant therapy. For these analyses, UICC stages 1 and 2 as well as stages 3 and 4 were combined to ensure a sufficient sample size in each class. The reported p values correspond to Wald tests for the null hypothesis for a hazard ratio of 1, or in the case of UICC and AEG, for equal hazards in all factor stages. No adjustment for multiple testing was applied due to the explorative nature of the study. For visualization, preoperative MCV, MCH, MCHC, RDW, and Hb levels were stratified by sample quintiles, and Kaplan-Meier estimates of OS and DFS functions were calculated for each quintile.

RESULTS
In our prospective database containing 544 patients with resectable esophageal cancer, 314 patients with adenocarcinomas of the esophagogastric junction had data on preoperative hematologic parameters and were eligible for further investigation. Their mean age at time of surgery was 63.8 years (range, 30.7-89.5 years). The study included 255 male patients (81.2%). Of the 157 patients (50%) who underwent neoadjuvant treatment, 95 received regimen A, 51 received regimen B, and 11 received regimen C. The majority of the patients (n = 132, 43%) had clinical stage 3 disease. Of the patients receiving neoadjuvant treatment, 13 (8.3%) showed a complete response (CR).
The clinicopathologic characteristics are summarized in Table 1 For all the patients, the median OS was 36.8 months, and the median DFS was 20.6 months. The Kaplan-Meier survival analysis showed that high MCV, MCH, and MCHC all were associated with poor OS and DFS for all the patients (all P \ 0.001) ( Fig. 1a and b).
In the subgroup analysis of neoadjuvantly treated and untreated patients, elevated MCV, MCH, and MCHC remained highly associated with diminished OS and DFS as well. No significant correlation of RDW and Hb could be found for OS and DFS in any of the groups. The Cox regression analysis identified tumor stage, lymph node status, tumor differentiation, adjuvant chemotherapy, MCV, MCH, and MCHC as the significant prognostic factors for OS and DFS in all the patients.
In the subgroup analysis of neoadjuvantly treated patients, tumor stage, lymphnode status, tumor differentiation, Mandard response rate, MCV, MCH, and MCHC were significantly associated with shorter OS and DFS. In addition, sex was shown to be a significant factor for DFS in neoadjuvantly treated AEG patients.

DISCUSSION
High MCV plasma levels were significantly correlated with diminished OS and DFS, defining the preoperative MCV plasma level as an independent prognostic factor for patients with adenocarcinomas of the esophagus and the gastroesophageal junction. Besides MCV, the prognostic Anemia is common among cancer patients, and the prognostic role of hematologic parameters has been reported for a number of malignancies, including ESCC. 9 However, to date, no data exist on the correlation between MCV and the survival of patients with adenocarcinomas of the esophagus and the gastroesophageal junction. Because MCV is an indicator for the red blood cell volume, it often is used for detection of megaloblastic-or iron-deficiency anemia. Macrocytosis often is related to liver and blood disease, alcohol consumption, smoking, and vitamin B12 or folate deficiency. [26][27][28] In contrast to ESCC, no correlation exists between alcohol consumption and the development of AEG. Therefore, other reasons for elevated MCV must exist in patients with adenocarcinomas of the esophagus and the gastroesophageal junction. A potential explanation might be the location of the tumor at the gastroesophageal junction. Malignant tumors located near the cardia of the stomach, developing from chronic atrophic gastritis, could result in an impaired function of the parietal cells and therefore could lead to vitamin B12 deficiency and macrocytic anemia.
Another cause for vitamin B12 deficiency and macrocytic anemia might be malnutrition, a negative prognostic factor in various malignancies, including esophageal cancer. [29][30][31] Due to dysphagia, a common symptom of patients with adenocarcinomas of the esophagus and the gastroesophageal junction, impaired nutritional intake leads to lowered serum concentration of electrolytes, glucose, and proteins, causing decreased crystal osmotic pressure, which leads to red cell dilation (macrocytosis). 32 Recently, we showed that malnutrition and inflammation are independent prognostic factors in AEG. 31 Therefore, malnutrition and inflammation (systemic inflammatory response [SIR]) might provide another potential explanation for the association among increased MCV and cancer mortality.
Besides factors such as blood loss, hemolysis, tumor infiltration, malnutrition, and chronic cytokine-related anemia, chemotherapy and radiation are known reasons for anemia in cancer patients. 17 Neoadjuvant chemo(radio)therapy in combination with surgical resection has become the current standard regimen for locally advanced AEG. 33,34 We therefore investigated the prognostic role of hematologic parameters in a subgroup of neoadjuvantly treated patients with adenocarcinomas of the esophagus and the gastroesophageal junction. In the multivariate analysis, we found that MCV and MCH were independent prognostic factors for OS and that MCV was an independent prognostic factor for DFS in neoadjuvantly treated patients with adenocarcinomas of the esophagus and the gastroesophageal junction.       Interestingly, a number of studies have reported a prognostic benefit for patients experiencing macrocytosis during chemotherapy. 17,19 In contrast, our findings and previously published data by other study groups show that preoperative elevated serum MCV is associated with diminished patient survival. 9,15 A possible explanation might be that for patients experiencing macrocytosis during chemotherapy, not the elevated MCV, but the longer observation period until development of macrocytosis is the factor resulting in a survival benefit. On the other hand, it is remarkable that MCV was an independent prognostic factor in both of our investigated subgroups (neoadjuvantly treated and untreated patients), whereas no statistical significance could be found for UICC stage and neoadjuvant treatment.
Although our finding that UICC stage is not significantly associated with patient outcome accords well with recently published data by Anderegg et al. 35 it remains unclear why neoadjuvant treatment was not a prognostic factor for patient survival in this study. Although response rates after neoadjuvant treatment vary throughout published data (5-29%), the response rate of only 8.3% in our study was not as high as the rates reported in previously published studies. 23,36 Our finding that MCV, but not RDW or Hb, is a prognostic factor independent of other (hematologic) parameters for patients with adenocarcinomas of the esophagus and the gastroesophageal junction accords well with the data published by Yoon et al. 15 underscoring the prognostic potential of a number of possible hematologic prognostic markers.
Although we could show that MCV is an independent prognostic factor in AEG, this study had certain limitations. Besides its retrospective nature, the long observation period must be addressed. During this period, both the surgical techniques and the regimens of neoadjuvant treatment undergo significant changes. Those two points cannot be disregarded, although the surgical approach and neoadjuvant therapy were factors that did not show any significant correlation in our study.
Based on our findings, clinicians might well focus on identifying patients at high risk for early recurrence and diminished survival after surgery. The possible consequences of preoperatively elevated MCV might be that patients receive neoadjuvant treatment despite their low clinical staging and must followed up in shorter intervals after surgery or receive adjuvant chemotherapy even though they show no lymph node involvement in their pathologic staging.
Nevertheless, the mechanisms for the development of macrocytosis and therefore the background for the prognostic role of MCV are not fully understood to date. Thus, further studies investigating preoperative vitamin B12 and folate status are needed to clarify the prognostic role of MCV for patients with adenocarcinomas of the esophagus and the gastroesophageal junction.
ACKNOWLEDGMENT Open access funding provided by Medical University of Vienna. The authors thank Dr. Helmuth Haslacher for his assistance with the Materials and methods section (laboratory methods).

CONFLICT OF INTEREST
There are no conflicts of interest.
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