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Pakistan Journal of Medical Sciences logoLink to Pakistan Journal of Medical Sciences
. 2023 Sep-Oct;39(5):1473–1477. doi: 10.12669/pjms.39.5.7090

Effect of laparoscopic complete mesocolic excision combined with immunotherapy and its impact on immune function and tumor markers in elderly patients with colon cancer

Tao Zhang 1,, Qian Lin 2, Zhi Liu 3, Hua Yang 4
PMCID: PMC10480738  PMID: 37680796

Abstract

Objective:

To determine the effect of laparoscopic complete mesocolic excision combined with immunotherapy and its impact on immune function and tumor markers in elderly patients with colon cancer.

Methods:

This is a clinical comparative study. Eighty elderly patients with colon cancer hospitalized in the No.2 Hospital of Baoding from May 2020 to May 2022 were randomly divided into two groups, with 40 cases in each group. Patients in the study group received laparoscopic complete mesocolic resection combined with ubenimex orally. While patients in the control group received routine open surgery. The surgical indexes, surgical complications, and the changes of immune molecules and tumor markers before and after treatment were compared between the two groups.

Results:

The amount of intraoperative bleeding, retention time of drainage tube and postoperative length of stay in the hospital in the study group were significantly better than those in the control group (p=0.000). The incision length of the study group was significantly shorter than that of the control group, the number of lymph nodes removed during the operation was significantly higher than that of the control group, and the incidence of surgical complications was significantly lower than that of the control group (p<0.05). After treatment, the levels of immune molecules in the study group were remarkably higher than those in the control group (p<0.05), while the levels of tumor markers were much lower than those in the latter group (p=0.000).

Conclusion:

Laparoscopic complete mesocolic excision combined with immunotherapy exhibits a superior therapeutic effect to traditional open surgery in elderly patients with colon cancer, and is worthy of clinical promotion.

KEYWORDS: Laparoscopic complete mesocolic excision, Immunotherapy, Colon cancer in the elderly, Immune function, Tumor markers

INTRODUCTION

With the changes in living and dietary habits of the public, colon cancer has become the second most common cancer in the world, with a gradual increase in its incidence.1,2 Surgery is still the primary approach for the treatment of colon cancer.3 Mesocolic excision has gradually become the standard radical operation for colon cancer, which can significantly improve the prognosis of colon cancer patients.4 At present, laparoscopic-assisted surgery has been widely adopted for colon cancer.5 Laparoscopic complete mesocolic excision has a larger surgical margin than that of traditional radical surgery.

Besides, due to its high difficulty of detection and diagnosis in the early stage, these patients may lose the best opportunity for surgery and experience significantly compromised therapeutic effects. Meanwhile, elderly patients have low immunity, slow postoperative recovery, and high risk of serious surgical complications than young patients.6 At the same time, there are few studies on the effect and safety of laparoscopic complete mesocolic excision combined with postoperative immunotherapy in elderly patients. Accordingly, the present study was performed to evaluate the effect of laparoscopic complete mesocolic excision combined with immunotherapy and its impact on immune function and tumor markers in elderly patients with colon cancer.

METHODS

This is a clinical comparative study. Eighty elderly patients with colon cancer hospitalized in the No.2 Hospital of Baoding from May 2020 to May 2022 were randomly divided into two groups, with 40 cases in each group. They’re existed comparability between the two groups as there was no significant difference in the comparison of general data between groups (Table-I). This study has been approved by the medical ethics committee of Ethical Approval: The No.2 Hospital of Baoding (No.:2041ZF014; date: March 20, 2021), and written informed consent was obtained from all participants.

Table-I.

Comparison of general data between the two groups (χ̅±S) n=40.

Study group Control group t/χ2 p
Male (n %) 23 (57.50%) 25 (62.50%) 0.208 0.648
Age (years) 69.83±3.17 69.53±3.42 0.407 0.685
BMI (kg/m2) 34.32±4.34 34.09±3.54 0.257 0.798
Course of disease (years) 1.78±0.70 1.68±0.73 0.626 0.533
Tumor site 0.474 0.491
Left 14 (35.00%) 17 (42.50%)
Right 26 (65.00%) 23 (57.50%)
Tumor stage
I 8 (20.00%) 9 (22.50%) 0.075 0.785
II 14 (35.00%) 15 (37.50%) 0.054 0.816
III 18 (45.00%) 16 (40.00%) 0.205 0.651
ECOG score 0.3±0.54 0.68±0.66 0.372 0.711

p>0.05.

Inclusion criteria:

  • Patients aged 65-75 years old.

  • Patients who met the diagnostic criteria of colon cancer and had surgical indications.7

  • Patients with complete relevant data.

  • Patients who agreed to be included in the study and provided the written informed consent and those agreed by family members.

  • Patients who agreed to be followed up.

Exclusion criteria:

  • Patients with severe mental disorders who cannot cooperate to complete the study.

  • Patients with other serious underlying diseases that cannot be corrected and cannot tolerate surgery.

  • Patients with severe infectious diseases.

  • Patients with other malignant tumors.

  • Patients with an estimated survival time of <six months.

  • Patients with previous abdominal surgery.

  • Patients with distant metastasis of tumor.

Patients in the study group received laparoscopic complete mesocolic excision combined with immunotherapy. Via tracheal intubation under general anesthesia, the operation was started through a medial approach by using the four-hole method. After that, the ileocolic blood vessels, the gastrocolonic venous trunk and the branches of the middle colonic artery were severed from the root of the blood vessels, after which the mesenteric lymph nodes were dissected. Further sharp dissection was made along the visceral layer of fascia around the mesocolon and the avascular area between spaces to completely remove the tumor, blood vessels and visceral fascia around lymph nodes.

For left colon cancer, a sharp dissection was carried out for the visceral fascia covering the descending colon and sigmoid colon as well as the parietal fascia covering perirenal fat, ureter, etc. After the recovery of food intake after operation, patients were provided with oral ubenimex (30 mg, once a day). Meanwhile, patients in the control group were given open surgery, with the same surgical margin and operation as those in the study group. Postoperative routine treatment in this group included nutritional supplements, correction of water and electrolyte, supplementation of albumin, etc.

Observation indicators:

(1) Surgical indicators were compared and analyzed between the two groups, including average operation time, total amount of intraoperative bleeding, extraction time of drainage tube, postoperative length of stay in the hospital. (2) The number of dissected lymph nodes intraoperatively was compared and analyzed between the two groups. (3) Occurrence of surgical complications was also compared between the study group and the control group. (4) As for the comparative analysis of immune molecules and tumor markers, venous blood was collected from each group before operation and three months after operation. Further detection was performed focusing on immune molecules of CD3+, CD4+, CD8+ and CD4+/CD8+ and tumor markers of serum colon cancer-specific antigen 2 (CCSA-2), pleiotropic growth factor (pleiotrophin, PTN) and soluble interleukin two (SIL2) to compare and analyze the changes of these indicators before and after treatment. The maximum follow-up time for patients in both groups was three months. And case data collection ceased in May 2022.

Statistical analysis:

All data were statistically analyzed using SPSS 20.0 software. The measurement data were presented in the form of (±S). Two independent samples t-test and paired t-test were respectively used for inter- and intra-group analyses. The comparison of rate adopted c2 test. P<0.05 was used to indicate the existence of a statistically significant difference.

RESULTS

As shown in Table-II, the study group had significantly less amount of intraoperative bleeding, as well as a shorter retention time of drainage tube and postoperative length of stay in the hospital than those in the control group (p=0.000). The incision length was obviously shorter in the study group than that in the control group (p=0.000).

Table-II.

Comparison of surgical indicators between the two groups (χ̅±S) n=40.

Groups Operation time (min) Amount of bleeding (ml)* Retention time of drainage tube (d)* Postoperative length of stay (d)* Incision length (cm)*
Study group 161.38±8.51 86.50±5.57 3.65±0.80 7.75±1.26 6.30±0.56
Control group 158.60±5.29 110.85±3.61 4.85±0.77 12.83±1.15 11.15±0.48
t 1.752 23.209 6.827 18.834 41.313
p 0.084 0.000 0.000 0.000 0.000
*

p<0.05.

The comparative analysis of the difference in the number of dissected lymph nodes intraoperatively between the two groups suggests that it was significantly higher in the study group than that in the control group, with consistent results observed based on the subgroup analyses according to different tumor stages and tumor sites (p<0.05, Table-III). According to the comparative analysis, the incidence of surgical complications in the study group was much lower than that in the control group, and the difference was statistically significant (p=0.032; Table-IV).After treatment, the levels of CD3+, CD4+ and CD4+/CD8+ were obviously higher in the study group than those in the control group (p<0.05, Table-V).After treatment, the levels of CCSA-2, PTN and SIL2 were obviously lower in the study group when compared with those in the control group (p=0.000, Table-VI).

Table-III.

Comparison of the number of dissected lymph nodes intraoperatively between the two groups (χ̅±S) n=40.

Groups Stage I* Stage II* Stage III* Left colon* Right colon*
Study group 15.88±2.37 16.50±1.84 19.85±2.48 18.48±1.69 22.05±1.34
Control group 14.65±1.99 14.63±1.33 15.75±2.10 16.95±1.72 18.43±2.54
t 2.504 5.219 7.992 3.990 7.983
p 0.014 0.000 0.000 0.000 0.000
*

p<0.05.

Table-IV.

Comparison of the incidence of surgical complications between the two groups (χ̅±S) n=40.

Groups Incision infection Lung infection Venous thrombosis of lower limbs Lymphorrhagia Intestinal obstruction Poor wound healing Incidence rate (%)*
Study group 0 1 1 1 2 0 5 (12.50%)
Control group 3 0 3 1 4 2 13 (32.50%)
c2 4.588
p 0.032
*

p<0.05.

Table-V.

Comparison of T lymphocyte subset level in two groups before and after treatment (χ̅±S) n=40.

Indicators Study group Control group t p
CD3+ (%) Before treatment 43.03±5.49 42.97±6.22 0.048 0.962
After treatment* 47.80±6.37 44.13±6.15 2.621 0.011
CD4+ (%) Before treatment 27.28±4.09 27.01±3.83 0.302 0.764
After treatment* 35.68±4.64 31.22±4.76 4.243 0.000
CD8+ (%) Before treatment 21.62±3.70 21.08±3.70 0.653 0.516
After treatment 22.25±3.73 22.32±3.90 0.082 0.935
CD4+/CD8+ Before treatment 1.27±0.10 1.29±0.07 1.149 0.254
After treatment* 1.62±0.16 1.41±0.15 5.992 0.000
*

p <0.05.

Table-VI.

Comparison of tumor marker levels between the two groups before and after treatment (χ̅±S) n=40.

Indicators Study group Control group t p
CCSA-2 (mg/L) Before treatment 122.48±7.53 119.89±7.47 1.545 0.126
After treatment* 62.74±8.14 73.65±7.26 6.323 0.000
PTN (ng/L) Before treatment 183.65±7.24 180.55±7.44 1.887 0.063
After treatment* 112.06±5.31 139.81±5.72 22.480 0.000
SIL2 (U/L) Before treatment 2.27±0.76 2.30±0.42 0.218 0.828
After treatment* 1.12±0.27 1.59±0.35 6.653 0.000
*

p <0.05.

DISCUSSION

In our study, the number of dissected lymph nodes intraoperatively in the study group was significantly higher than that in the control group, regardless of different tumor stages or tumor sites (p=0.00), which may be attributed to the amplification effect of laparoscopy. Meanwhile, the study group was discovered to have a smaller amount of intraoperative bleeding, as well as a shorter retention time of drainage tube, length of stay in the hospital postoperatively and postoperative incision length. In addition, the incidence of complications in the study group was obviously lower than that in the control group.

It has been recognized that there is an intimate association between the levels of postoperative tumor markers and the risk of tumor recurrence.8 SIL2 can inhibit the immune function of the body; PTN is a pleiotropic growth factor and has a variety of biological functions that can cause tumor cell metastasis and proliferation.9 CCSA-2 plays an important role in evaluating the prognosis of diseases, which is a colon cancer-specific molecule.10 In the present study, the levels of CCSA-2, PTN and SIL2 in the study group were lower than those in the control group after treatment. These data further reveal that compared with open radical surgery, laparoscopic surgery can remove tumor tissues more thoroughly, and also has a lower risk of postoperative recurrence.

Colon cancer is featured by relatively higher clinical morbidity and mortality, and high incidence in elderly men.11 Surgery has been accepted clinically as the major approach to treating colon cancer.12 Through the resection of the tumor primarily, the traditional radical resection of colon cancer may cause the extrusion and then the spread of tumor tissues during intraoperative separation and resection, leading to a greater risk of postoperative recurrence.13 Significantly, complete mesocolic excision is a novel therapeutic option surgically, with significant clinical effects.14 With the assistance of a laparoscope, it may provide a clear field of vision for a surgical operation with minimal damage to the patients, exhibiting advantages of less intraoperative bleeding, short hospital stay, low complications, etc.15

Previous research16 has reported that the number of dissected lymph nodes during colon cancer surgery was an independent factor affecting the clinical prognosis of patients with colon cancer. The use of a laparoscope can magnify the field of vision to display the local anatomical visual field more clearly, which can facilitate the identification of blood vessels to assist in the dissociation of the root of blood vessels and dissection of lymph nodes, eventually protecting the surrounding adjacent tissue structures, and reducing secondary damages of surgery.

Enhancement of immunity and body resistance is of great significance for the postoperative rehabilitation of elderly patients.17 Ubenimex is a new generation of immunopotentiator that can enhance immune function, which can can be used cooperatively or jointly for the treatment of patients with various solid tumors.18 Yang et al. suggested that ubenimex also had a certain direct antitumor effect.19 At the same time, ubenimex, an inhibitor of CD13, can be used as an immune adjuvant to improve the immune state of patients.20 Similarly, in our study, after treatment, the levels of CD3+, CD4+ and CD4+/CD8+ were obviously elevated in the study group than those in the control group (p<0.05), which confirmed significant improvement in the cellular immune function of patients after applying immunotherapy jointly.

Limitations:

However, the small sample size and the lack of follow-up are two major limitations of our study. Our future research will be continued by including more samples, having follow-ups, and further exploring the impact of the therapeutic scheme on the long-term effect and survival of patients. Through relevant studies, we hope to realize a more comprehensive evaluation of its long-term therapeutic effect so that more patients can benefit from this treatment.

CONCLUSION

Findings in our study supported that laparoscopic complete mesocolic excision combined with immunotherapy has a superior therapeutic effect to traditional open surgery in elderly patients with colon cancer. Simultaneously, this therapeutic schedule also has a certain effect on improving the cellular immune function of patients, reducing the levels of tumor markers and the incidence of postoperative complications.

Authors’ Contributions:

TZ and QL: Carried out the studies, participated in collecting data, and drafted the manuscript, are responsible and accountable for the accuracy and integrity of the work.

ZL: Performed the statistical analysis and participated in its design.

HY: Participated in acquisition, analysis, or interpretation of data and draft the manuscript.

All authors read and approved the final manuscript.

Footnotes

Conflicts of interest: None.

Source of funding: This study is supported by Baoding Science and technology plan project task (No.: 2141ZF195).

REFERENCES

  • 1.Wen J, Min X, Shen M, Hua Q, Han Y, Zhao L, et al. ACLY facilitates colon cancer cell metastasis by CTNNB1. J Exp Clin Cancer Res. 2019;38(1):401. doi: 10.1186/s13046-019-1391-9. doi: 10.1186/s13046-019-1391-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bukhari MH, Coppola D, Nasir A. Clinicopathologic analysis of primary gastroenteropancreatic poorly differentiated neuroendocrine carcinoma;A ten year retrospective study of 68 cases at Moffit Cancer Center. Pak J Med Sci. 2020;36(2):265–270. doi: 10.12669/pjms.36.2.1336. doi: 10.12669/pjms.36.2.1336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Ding S, Ma H, Wang G, Yu Z, Li K, Huang A. Effect of Remifentanil Combined Anesthesia on Cytokines and Oxidative Stress in Patients undergoing Laparoscopic Surgery for Colon Cancer. J Coll Physicians Surg Pak. 2019;29(1):8–11. doi: 10.29271/jcpsp.2019.01.8. doi: 10.29271/jcpsp.2019.01.8. [DOI] [PubMed] [Google Scholar]
  • 4.Kim JC, Lee JL, Yoon YS, Kim CW, Park IJ, Lim SB. Robotic left colectomy with complete mesocolectomy for splenic flexure and descending colon cancer, compared with a laparoscopic procedure. Int J Med Robot. 2018;14(5):e1918. doi: 10.1002/rcs.1918. doi: 10.1002/rcs.1918. [DOI] [PubMed] [Google Scholar]
  • 5.Siani LM, Lucchi A, Berti P, Garulli G. Laparoscopic complete mesocolic excision with central vascular ligation in 600 right total mesocolectomies:Safety, prognostic factors and oncologic outcome. Am J Surg. 2017;214(2):222–227. doi: 10.1016/j.amjsurg.2016.10.005. doi: 10.1016/j.amjsurg.2016.10.005. [DOI] [PubMed] [Google Scholar]
  • 6.Kwak HD, Ju JK, Lee SY, Kim CH, Kim YJ, Kim HR. The relation between oncologic outcomes and metastatic lymph node location following laparoscopic resection of stage III colon cancer. Int J Colorectal Dis. 2019;34(4):667–673. doi: 10.1007/s00384-019-03245-x. doi: 10.1007/s00384-019-03245-x. [DOI] [PubMed] [Google Scholar]
  • 7.Benson AB, Venook AP, Al-Hawary MM, Cederquist L, Chen YJ, Ciombor KK, et al. NCCN Guidelines Insights:Colon Cancer, Version 2.2018. J Natl Compr Canc Netw. 2018;16(4):359–369. doi: 10.6004/jnccn.2018.0021. doi: 10.6004/jnccn.2018.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Herrera M, Berral-Gonzalez A, Lopez-Cade I, Galindo-Pumarino C, Bueno-Fortes S, Martín-Merino M, et al. Cancer-associated fibroblast-derived gene signatures determine prognosis in colon cancer patients. Mol Cancer. 2021;20(1):73. doi: 10.1186/s12943-021-01367-x. doi: 10.1186/s12943-021-01367-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Korsbakke K, Dahlback C, Karlsson N, Zackrisson S, Buchwald P. Tumor and nodal staging of colon cancer:accuracy of preoperative computed tomography at a Swedish high-volume center. Acta Radiol Open. 2019;8(12):2058460119888713. doi: 10.1177/2058460119888713. doi: 10.1177/205846011988∉. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Abdel-Latif RT, Wadie W, Abdel-Mottaleb Y, Abdallah DM, El-Maraghy NN, El-Abhar HS. Reposition of the anti-inflammatory drug diacerein in an in-vivo colorectal cancer model. Saudi Pharm J. 2022;30(1):72–90. doi: 10.1016/j.jsps.2021.12.009. doi: 10.1016/j.jsps.2021.12.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Argiles G, Tabernero J, Labianca R, Hochhauser D, Salazar R, Iveson T, et al. Localised colon cancer:ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31(10):1291–1305. doi: 10.1016/j.annonc.2020.06.022. doi: 10.1016/j.annonc.2020.06.022. [DOI] [PubMed] [Google Scholar]
  • 12.Zhao J, Kang Z, Xie W, Lin H, Liu Y. Effects of Depth of Anesthesia Monitored by IoC on Patients Undergoing Laparoscopic Radical Resection of Colorectal Cancer. Mol Ther Methods Clin Dev. 2020;18:304–311. doi: 10.1016/j.omtm.2020.05.032. doi: 10.1016/j.omtm.2020.05.032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Verkuijl SJ, Jonker JE, Trzpis M, Burgerhof JGM, Broens PMA, Furnee EJB. Functional outcomes of surgery for colon cancer:A systematic review and meta-analysis. Eur J Surg Oncol. 2021;47(5):960–969. doi: 10.1016/j.ejso.2020.11.136. doi: 10.1016/j.ejso.2020.11.136. [DOI] [PubMed] [Google Scholar]
  • 14.Koh FH, Tan KK. Complete mesocolic excision for colon cancer:is it worth it? J Gastrointest Oncol. 2019;10(6):1215–1221. doi: 10.21037/jgo.2019.05.01. doi: 10.21037/jgo.2019.05.01. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ogun E, Ekrem UA, Yuksel C, Serdar C, Basceken SI, Umit M, et al. Laparoscopic Gastric Resection for Gastric Cancer:Is Intracorporeal Anastomosis Necessary? Pak J Med Sci. 2020;36(6):1177–1182. doi: 10.12669/pjms.36.6.1915. doi: 10.12669/pjms.36.6.1915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Wells KO, Senagore A. Minimally Invasive Colon Cancer Surgery. Surg Oncol Clin N Am. 2019;28(2):285–296. doi: 10.1016/j.soc.2018.11.004. doi: 10.1016/j.soc.2018.11.004. [DOI] [PubMed] [Google Scholar]
  • 17.Nguyen TH, Tran HX, Thai TT, La DM, Tran HD, Le KT, et al. Feasibility and Safety of Laparoscopic Radical Colectomy for T4b Colon Cancer at a University Hospital in Vietnam. Biomed Res Int. 2020;2020:1762151. doi: 10.1155/2020/1762151. doi: 10.1155/2020/1762151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Wang Y, Pang B, Zhang R, Fu Y, Pang Q. Ubenimex induces apoptotic and autophagic cell death in rat GH3 and MMQ cells through the ROS/ERK pathway. Drug Des Devel Ther. 2019;13:3217–3228. doi: 10.2147/DDDT.S218371. doi: 10.2147/DDDT.S218371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Yang YK, Shen DD, He P, Du LD, Wan DJ, Wang P, et al. Chemically synthesized LYRM03 could inhibit the metastasis of human breast cancer MDA-MB-231 cells in vitro and in vivo. Bioorg Med Chem Lett. 2019;29(14):1719–1726. doi: 10.1016/j.bmcl.2019.05.027. doi: 10.1016/j.bmcl.2019.05.027. [DOI] [PubMed] [Google Scholar]
  • 20.Guo Q, Jing FJ, Qu HJ, Xu W, Han B, Xing XM, et al. Ubenimex Reverses MDR in Gastric Cancer Cells by Activating Caspase-3-Mediated Apoptosis and Suppressing the Expression of Membrane Transport Proteins. Biomed Res Int. 2019;2019:4390839. doi: 10.1155/2019/4390839. doi: 10.1155/2019/4390839. [DOI] [PMC free article] [PubMed] [Google Scholar]

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