Association between Preoperative Leukocytosis and Pathological Features of Colorectal Cancers

  1. Reza Hajebi ,
  2. Hadi Ahmadi Amoli ,
  3. Hossein Zabihi Mahmoudabadi ,
  4. Ehsan Rahimpour ,
  5. Khosro Najjari ,
  6. Elham Nazar

Vol 6 No 1 (2021)

DOI 10.31557/apjcb.2021.6.1.43-47

Abstract

Background: Using hematologic profiles including leukocyte count have been considered as prognostic factor for some cancers. We have been assessed the predictive value of leukocytosis before surgery in colorectal cancers.
Methods: This cross-sectional study has been conducted on patients with colorectal cancer who underwent surgery from 2017 to 2019 in Sina hospital, Tehran. The patients were divided in two groups based on high and low leukocyte count before surgery.
Results: A total of 84 patients were studied with colorectal cancers including 46 males (55.4%) and 37 females (44.6%) with the average age of 55.2 (± 13.63) years. 36.1% of patients had leukocytosis in laboratory data before surgery. There was a significant association between tumor’s grade and the incidence of leukocytosis before surgery (P <0.001). The existence of leukocytosis is highly associated with poorly differentiated tumor. Also, the relationship between the location of the tumor and leukocytosis was seen which the location was distal, the possibility of leukocytosis decreased significantly (P <0.005).
Conclusion: Our findings suggest that the location of the tumor and its degree of tumor differentiation are related with leukocytosis. This current study by considering leukocytosis before surgery aimed to use this variable as a prognostic factor in patients with colorectal cancer alongside with other variables.

Introduction

Colorectal cancer is one of the most common cancers among societies, highly affected by lifestyle. A number of risk factors for colorectal cancer have been recognized such as lack of physical activity, obesity, low use of vegetables and fruits, and smoking [1-6]. Prognostic factors are indicators affecting the overall results of treatment whereas predictive factors are those affecting the response to intervention or any specific treatment [7-8]. Using predictive factors, especially for high risk patients such as those with cancer which require more attention and precise treatments, was considered for appropriate treatment approaches with fewer side effects for patients [9-10]. Changes in blood parameters including anemia, leukopenia, leukocytosis, and thrombocytosis in most malignancies have been well studied and considered as a part of paraneoplastic syndromes.

Paraneoplastic syndromes include non-metastatic systematic manifestations which observe in many malignancies and have negative alter on the prognosis. These non-metastatic manifestations almost always occur in all malignancies, but their patterns in each cancer are different [11]. Many of patients who have abnormality in hematology profile even before the diagnosis is established. Other paraneoplastic syndroms develop during treatment course and related with the progression or regression of the tumor [12-14]. Among paraneoplastic syndromes, leukocytosis (mainly granulocytosis) is more prevalent in non-hematologic malignancies. About 10 percent of patients with non-hematologic malignancies have leukocytosis. This percentage is higher in tumors of lung, head and neck, pancreas, brain, and melanoma. Granulocytosis connect to paraneoplastic leukemoid reaction which observes with the increased presence of mature neutrophils and some other related forms [15]. Based on recent studies suggest that using hematology profiles including leukocyte count has been considered as prognostic factors in some cancers [16-20]. Hematology profile test is cheap, easy to use, and available in all surgery centers. Particularly during the hospitalization of patients, is suitable to use it [21- 22]. In this study, we report the association between preoperative leukocytosis and pathological features of colorectal cancers based on data from the 2017 to 2019 in Sina hospital, Tehran, Iran. The purpose of this study is to investigate prognostic value of leukocytosis before surgery in colorectal cancers.

Materials and Methods

This is a cross-sectional study included patients with colorectal cancers who were treated in Sina hospital affiliated to Tehran University of Medical Sciences from 2017 to 2019. Inclusion criteria for the study were patients with colorectal cancer (confirmed by pathology result) that underwent surgery with curative goal. Exclusion criteria were the incomplete medical record files, loss of patients during follow up, and patients with abscess, obstruction, and patients who had neoadjuvant chemoradiation’s side effects. Recorded variables for each patient were age, sex, tumor location and pathologic characteristic of the tumor after resection (depth of invasion, lymph node status, lymphovascular invasion, perineural invasion, tumor differentiation grade). Laboratory findings were assessed such as Carcinoembryonic antigen (CEA) and complete blood cell count (CBC) by Electrochemiluminescence assay and blood cell analyzer (Sysmex KX21), respectively. Based on the amount of leukocyte (higher or lower than 10000/µl), patients were divided into two groups of leukocytosis and non-leukocytosis, respectively. Other factors including tumor stage, its degree, its anatomical location as well as CEA levels were compared between two groups.

Statistical analysis of the results was performed by using SPSS-16 software (SPSS Inc, Chicago, Illinois, USA). Descriptive and statistical analysis was done. Results were presented as mean ± standard deviation (SD) for quantitative variables and were summarized by absolute frequencies and percentages for categorical variables. The association between the variables and leukocytosis was examined using by Chi-square test. All statistical tests were 2-sided and P-value less than 0.05 were considered significant.

Results

The database query returned 179 patients. We excluded 96 patients due to mentioned exclusion criteria. The remaining 83 patients were evaluated which including 46 males (55.4%) and 37 females (44.6%) with mean age of 55 years and standard deviation of 13.6 years (42-68 years). According to TNM (tumor, node and metastasis system in all its versions) staging: 3 (3.6%), 17 (20.4%), 55 (66.2%), and 8 (9.6%) of patients’ tumor was in T1, T2, T3, and T4, respectively. 49 (59%) patients had no lymph node invasion, but 34 (41%) had lymph node invasion. Metastasis was present in 3 (3.6%) patients while 80 (96.4%) patients had no detectable metastases. Staging of tumor in 14 (16.8%), 35(42.1%), 33(39.7%), and 3 (3.6%)

patients was stage I, stage II, stage III, and stage IV, respectively. Tumor differentiation grading consist of 11(13.2%), 57(68.6%), and 15 (18%) patients with poor, moderate, and well differentiated features, respectively. Location of the tumor in 30 (36.1%), 5 (6%), 27 (32.5%), and 21 (25.3%) patients was in right colon, transverse colon, left colon, and rectum, respectively. Histologic tumor types consist of 85.5% with classic adenocarcinoma and 14.5% with mucinous adenocarcinoma, respectively. Mean White blood cell (WBC) count before surgery was 8880 (±4051.7)/ml, ranging from 2500 to 19800/ ml. Mean Hemoglobin (Hbg) level was 11.59 (±1.6) gr/ dl, ranging from 8.2 to16 gr/dl. Mean platelet count was 305602 (±119267.8)/ml, ranging from 12500 to 673000/ ml. Increased CEA level was about 17 (28.8%) ng/ml in patients.

There was no statistically significant difference in lymphovascular and perineural invasion between the two groups (P-value>0.05). There was no statistically significant difference in tumor staging and presence of metastasis between the two groups (P-value>0.05).

There was statistically significant difference in grade of the differentiation tumor between two groups (P-value<0.05). Leukocytosis has been seen in 6.7% of well differentiated tumors, in 35.1% of moderately differentiated tumors and in 81.8% of poorly differentiated tumors. Chi-square test had shown statistically significant correlation between the differentiation of tumor and the existence of leukocytosis (p<0.001).

Other important finding of the current study was the correlation between leukocytosis and location of the tumor. Data analysis showed that the percentage of tumors accompanied with leukocytosis in right colon cancer and transverse was 60%, in left colon was 22.2% and in rectum was 14.3%. Chi-square test have shown that presence of leukocytosis had a significant decrease from right colon towards rectum (p<0.005) (Tables 1).

Table 1: Tumor Characteristics Based on the Existence or Lack of Leukocytosis.

Patients’ Groups P-value
Without Leukocytosis (n=53) With Leukocytosis (n=30)
Based on the tumor staging (TNM) T1 3 (8.5%) 0 (0.0%) 0.595
T2 10 (18.8%) 7 (23.3%)
T3 35 (66%) 20 (66.6%)
T4 5 (9.4%) 3 (10%)
Lymph invasion based on TNM staging system N0 34 (64.1%) 15 (50%) 0.361
N1 11 (20.7%) 7 (23.3%)
N2 8 (15%) 8 (26.6%)
Presence of Tumor Metastasis M0 52 (98.1%) 28 (93.3%)
M1 1 (1.8%) 2 (6.6%) 0.262
Lymphovascular invasion Positive 8 (15%) 4 (13.3%) 0.827
Negative 45 (49%) 26 (86.7%)
Tumor Staging I 12 (22.6%) 2 (6.6%) 0.216
II 22 (41.5%) 13 (43.3%)
III 18 (33.9%) 13 (43.3%)
IV 1 (1.8%) 2 (6.6%)
Differentiation of tumor well 14 (25.2%) 1 (3.3%) 0.000*
moderate 37 (69.8%) 20 (66.6%)
poor 2 (3.6%) 9 (30%)
location of tumor Right colon 13 (24.5%) 17 (56.6%) 0.001*
Transverse colon 1 (1.8%) 4 (13.2%)
Left colon 21 (39.6%) 6 (20%)
Rectum 18 (33.9%) 3 (10%)
Tumor histology adenocarcinoma 42 (79.2%) 29 (96.6%)
mucus adenocarcinoma 11 (20.7%) 1 (3.4%) 0.030*

*A p-value<0.05 is considered statistically significant.

There was no statistically significant mean between other hematologic findings and CEA level with our variables (Tables 2).

Table 2: CEA Level Changes in two Groups.

Without Leukocytosis (34) With Leukocytosis (25) P-value
CEA changes Normal 24 (70.5%) 18 (72%) 0.906
Increased 10 (29.5%) 7 (28%)

Discussion

Several studies have been conducted on factors affecting the prognosis of colorectal cancers. In these studies, age, sex, location of the tumor, size of the tumor, differentiation degree of the tumor, cancer stage, and the symptoms of disease have been assessed as prognostic factors for colorectal cancer [23]. Several studies regarded hematologic indexes consist of leukocytosis as a predictive factor for prognosis and mortality of the patients which was recognized in majority of solid tumors [21-22]. In a study by Qiu et al. the level of WBC, platelets and hemoglobin in patients with breast, hepatocellular, nasopharyngeal, oropharyngeal, gastric, cervix, endometrial, renal cell, and lung cancers was assessed which showed only leukocytosis can be an independent prognostic factor in patients with cervix cancer [22]. Studies showed that patients with cervix cancer who had leukocytosis (WBC count>10,000/ml), had lower treatment success and survival comparing to those without leukocytosis. Moreover, these patients had a higher activity of immune system comparing to groups without leukocytosis. Leukocytosis before surgery along with other variables such as the stage of disease, tumor diameter, and histology grade of tumor are the main prognostic factors in the patients and can be used for determination of the patients with poor prognosis [11]. In a study by Banerjee et al. it had been shown that leukocytosis in prior treatment of anal cancer was associated with lower life expectancy and survival. It seems that hematologic indexes can be used as the potential prognostic factors. This study showed that leukocytosis in the patients related with decreased two-year survival and disease free survival. Also, the patients with accompanying anemia and leukocytosis had more decreased survival than the patients with only leukocytosis [17]. The current study demonstrates that leukocytosis is related to the location of tumor and degree of tumor differentiation which associated with poor prognosis. In a study by Nakshabendi et al. was conducted on patients with colorectal cancer which showed WBC to Hbg ratio was high and considered as concurrency of anemia (Hbg<10gr/dl) and leukocytosis. The ratio was higher in patients with right colon cancer about 55% while in those with left colon cancer was about 10% which the difference was statistically significant. Such studies had shown that patients with right colon cancer were more prone to develop leukocytosis and anemia [19] which is similar to our findings. Qiu et al. study established that anemia and thrombocytosis before treatment were independent prognostic factors for patients’survival in advanced stages of the disease. In addition, the synergistic effect of anemia and thrombocytosis decreased the survival of the patients more than each one alone [21]. Several studies compared leukocytosis, anemia, and thrombocytosis between patients with colorectal cancers and patients with benign colorectal lesions including benign colorectal polyps. These results showed hematologic indexes were significantly higher among patients with colorectal cancers, especially in advanced stages of the disease [23].

The current study by considering leukocytosis before surgery aimed to use this variable as a prognostic factor in the patients with colorectal cancer alongside with other variables. Our results show that the leukocytosis is related to the location and degree of tumor differentiation. Right colon cancer has more prominent leukocytosis than the other site and poorly differentiated tumor has more leukocytosis than well and moderately differentiated tumor. Unfortunately, our study has some limitations including limited sample size and we couldn’t differentiate WBCs because all samples hadn’t differential count. Also, for the reason that large disparities exist between population in cancer incidence, sign, and survival, further studies in Iran with larger scale in several main surgery center is recommended.

In conclusion, based on current study, the location and differentiation degree of the tumor is associated with the existence or lack of leukocytosis. The existence of leukocytosis is highly associated with tumor in the right colon as well as poor differentiation degree of tumor. So, we can use CBC test as prognostic factor easily.

Acknowledgments

Conflict of Interest

None declared.

References


  1. Global Cancer Statistics, 2002 Parkin D. M., Bray F., Ferlay J., Pisani P.. CA: A Cancer Journal for Clinicians.2005;55(2). CrossRef
  2. International variation Parkin Donald M. Oncogene.2004;23(38). CrossRef
  3. International Trends in Colorectal Cancer Incidence Rates Center Melissa M., Jemal Ahmedin, Ward Elizabeth. Cancer Epidemiology Biomarkers & Prevention.2009;18(6). CrossRef
  4. Cancers of the colon and rectum Giovannucci E, Wu K. Cancer epidemiology and prevention.2006;3:809.
  5. Smoking and Colorectal Cancer Botteri Edoardo, Iodice Simona, Bagnardi Vincenzo, Raimondi Sara, Lowenfels Albert B., Maisonneuve Patrick. JAMA.2008;300(23). CrossRef
  6. Modifiable risk factors for colon cancer Giovannucci Edward. Gastroenterology Clinics of North America.2002;31(4). CrossRef
  7. The Nutrition Transition: An Overview of World Patterns of Change Popkin Barry M.. Nutrition Reviews.2004;62. CrossRef
  8. Impact of haemoglobin levels on the outcome of cancers treated with chemotherapy Van Belle Simon Jean-Pierre, Cocquyt Véronique. Critical Reviews in Oncology/Hematology.2003;47(1). CrossRef
  9. Predictive factors of response to cisplatin-based chemotherapy and the relation of response to survival in patients with metastatic urothelial cancer Sengeløv Lisa, Kamby Claus, Geertsen Poul, Andersen Lisbeth Juhler, von der Maase Hans. Cancer Chemotherapy and Pharmacology.2000;46(5). CrossRef
  10. Prediction of Prognosis Following Fludarabine Used as Secondary Therapy for Chronic Lymphocytic Leukemia Keating M. J., Smith T. L., Lerner S., O'brien S., Robertson L. E., Kantarjian H., Freireich E. J.. Leukemia & Lymphoma.2000;37(1-2). CrossRef
  11. The prognostic significance of leukocytosis in cervical cancer Garcia-Arias A., Cetina L., Candelaria M., Robles E., Dueñas-González A.. International Journal of Gynecologic Cancer.2007;17(2). CrossRef
  12. Effects of Epoetin Alfa on Hematologic Parameters and Quality of Life in Cancer Patients Receiving Nonplatinum Chemotherapy: Results of a Randomized, Double-Blind, Placebo-Controlled Trial Littlewood T. J., Bajetta E., Nortier J. W.R., Vercammen E., Rapoport B.. Journal of Clinical Oncology.2001;19(11). CrossRef
  13. Etiology and outcome of extreme leukocytosis in 758 nonhematologic cancer patients Granger John M., Kontoyiannis Dimitrios P.. Cancer.2009;115(17). CrossRef
  14. An update on the etiology and diagnostic evaluation of a leukemoid reaction Sakka Vissaria, Tsiodras Sotirios, Giamarellos-Bourboulis Evangelos J., Giamarellou Helen. European Journal of Internal Medicine.2006;17(6). CrossRef
  15. Hypercalcemia–leukocytosis syndrome associated with lung cancer Hiraki Akio, Ueoka Hiroshi, Takata Ichiro, Gemba Kenichi, Bessho Akihiro, Segawa Yoshihiko, Kiura Katsuyuki, Eguchi Kenji, Yoneda Toshiyuki, Tanimoto Mitsune, Harada Mine. Lung Cancer.2004;43(3). CrossRef
  16. Tumor-related leukocytosis is linked with poor prognosis in patients with lung carcinoma Kasuga Ikuma, Makino Shigeru, Kiyokawa Hiroshi, Katoh Harubumi, Ebihara Yoshiro, Ohyashiki Kazuma. Cancer.2001;92(9). CrossRef
  17. The prognostic signficance of pretreatment leukocytosis in patients with anal cancer treated with radical chemoradiotherapy or radiotherapy Banerjee R, Roxin G, Eliasziw M, Joseph K, Buie D, Doll C. Journal of Clinical Oncology.2012;30(4_suppl):656.
  18. Pretreatment leukocytosis is an indicator of poor prognosis in patients with cervical cancer Mabuchi Seiji, Matsumoto Yuri, Isohashi Fumiaki, Yoshioka Yasuo, Ohashi Hiroshi, Morii Eiichi, Hamasaki Toshimitsu, Aozasa Katsuyuki, Mutch David G., Kimura Tadashi. Gynecologic Oncology.2011;122(1). CrossRef
  19. The predictive value of concurrent anaemia and leukocytosis in the diagnosis of colorectal cancer Nakashabendi I, Dawodu J, Lee F, Russell R, Mikhail M, Dragenscu J. Gastroenterology.1998;114:A652.
  20. Preoperative leukocytosis, anemia and thrombocytosis are associated with poor survival in non-small cell lung cancer Tomita M, Shimizu T, Hara M, Ayabe T, Onitsuka T. Anticancer research.2009;29(7):2687-2690.
  21. Impact of pretreatment hematologic profile on survival of colorectal cancer patients Qiu Miao-zhen, Yuan Zhong-yu, Luo Hui-yan, Ruan Dan-yun, Wang Zhi-qiang, Wang Feng-hua, Li Yu-hong, Xu Rui-hua. Tumor Biology.2010;31(4). CrossRef
  22. Incidence of anemia, leukocytosis, and thrombocytosis in patients with solid tumors in China Qiu Miao-zhen, Xu Rui-hua, Ruan Dan-yun, Li Zhuang-hua, Luo Hui-yan, Teng Kai-yuan, Wang Zhi-qiang, Li Yu-hong, Jiang Wen-qi. Tumor Biology.2010;31(6). CrossRef
  23. Multivariate regression analysis of prognostic factors in colorectal cancer Zuli Y, Jianping W, Lei W, Wenguang D, Yihua H, Jianzhang Q, et al . The Chinese-German Journal of Clinical Oncology.2003;2(3):149-152.

Copyright

© Asian Pacific Journal of Cancer Biology , 2021

Author Details

Reza Hajebi
Department of surgery, Sina Hospital, Tehran University of Medical Sciences, Iran

Hadi Ahmadi Amoli
Department of surgery, Sina Hospital, Tehran University of Medical Sciences, Iran

Hossein Zabihi Mahmoudabadi
Department of surgery, Sina Hospital, Tehran University of Medical Sciences, Iran

Ehsan Rahimpour
Department of surgery, Sina Hospital, Tehran University of Medical Sciences, Iran

Khosro Najjari
Department of surgery, Sina Hospital, Tehran University of Medical Sciences, Iran

Elham Nazar
Department of Pathology, Sina Hospital, Tehran University of Medical Sciences, Iran
elhamnazar@yahoo.com

How to Cite

1.
Hajebi R, Ahmadi Amoli H, Zabihi Mahmoudabadi H, Rahimpour E, Najjari K, Nazar E. Association between Preoperative Leukocytosis and Pathological Features of Colorectal Cancers. apjcb [Internet]. 21Mar.2021 [cited 22Dec.2024];6(1):43-7. Available from: http://waocp.com/journal/index.php/apjcb/article/view/631
  • Abstract viewed - 0 times
  • PDF (FULL TEXT) downloaded - 0 times
  • Xml downloaded - 0 times