Open Access

Effect of anesthetic methods on postoperative CD3+, CD4+ and CD4+CD25+ in patients with lung cancer undergoing radical operation

  • Authors:
    • Shuang Fu
    • Pi-Sheng Qu
    • Shu-Nv Cai
  • View Affiliations

  • Published online on: September 7, 2018     https://doi.org/10.3892/ol.2018.9416
  • Pages: 6547-6551
  • Copyright: © Fu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Effects of anesthesia methods on immune function in patients with lung cancer undergoing radical operation were investigated. A total of 122 patients undergoing radical resection of lung cancer who were treated in Zhejiang Cancer Hospital from September 2013 to April 2016 were randomly divided into the combined anesthesia group and the intravenous anesthesia group, with 61 cases in each group. The patients in the combined anesthesia group were given intravenous combined epidural anesthesia. Patients in the intravenous anesthesia group were given intravenous anesthesia. The change of CD3+, CD4+ and CD4+CD25+ at time-point T0 (before anesthesia), T1 (the time of anesthesia), T2 (after operation), T3 (24 h after operation), T4 (72 h after operation) were compared between the two groups. The levels of CD3+, CD4+ and CD4+CD25+ at T1, T2, T3 and T4 in the combined anesthesia group were higher than that in the intravenous anesthesia group (P<0.05). Αfter starting anesthesia, the levels of CD3+, CD4+ and CD4+CD25+ began to decrease in both groups. The levels of CD3+, CD4+ and CD4+CD25+ at T2 and T1 were lower than those at T0 (P<0.05). The levels of CD3+, CD4+ and CD4+CD25+ at T2 were lower than T1 (P<0.05). After T3, the levels of CD3+, CD4+ and CD4+CD25+ began to increase in both groups. Τhe levels of CD3+, CD4+ and CD4+CD25+ at T3 and T4 were higher in both groups than those at T2 and T1 (P<0.05), and the levels of CD3+, CD4+ and CD4+CD25+ at T4 were higher in both groups than those at T3, but the levels of CD3+, CD4+ and CD4+CD25+ at T3 and T4 were lower than those at T0 (P<0.05). Intravenous combined epidural anesthesia can maintain a relatively stable immune function compared with simple intravenous anesthesia patients.

Introduction

Lung cancer is a malignant tumor with the highest mortality rate in the world, with a prevalence of approximately 2–3:1 in men and women (1). With industrial development, the incidence and mortality rate of lung cancer are still rising (2). Radical operation is the main treatment of lung cancer and is the only way to cure lung cancer at present. However, it causes severe trauma to the body and intense stimulation to the organ, which can easily lead to a strong stress response in the body and cause a decrease in immune function. While the autoimmune function of patients with lung cancer is lower than healthy people, which is one of the important factors leading to the not ideal results in radical resection of lung cancer treatment (35).

Anesthesia is one of the most important auxiliary means of surgery. Appropriate anesthesia has a decisive significance in maintaining vital signs of patients and in helping perioperative patients (6). However, the current use of various narcotic drugs is not ideal, in order to improve this deficiency, combined anesthesia came into being (7). Combined anesthesia, also known as balanced anesthesia, is the combination of two or more narcotic drugs or anesthesia method in order to improve perioperative analgesia effect and surgical conditions (8). Combined general epidural anesthesia is currently the main method of combined anesthesia, it can reduce the use of anesthetic drugs in surgery, can improve the analgesic effect, reduce side effects and adverse reactions, improve surgical safety, and also eliminate the fear and tension of patients, reduce stress response, improve patient immune function (9,10).

The purpose of this study was to investigate the effects of intravenous combined epidural anesthesia on patients with lung cancer undergoing radical surgery and to investigate the effects of intravenous combined epidural anesthesia on immune function in patients with lung cancer by dynamically monitoring the changes of CD3+, CD4+ and CD4+CD25+.

Materials and methods

Patients

A total of 122 patients undergoing radical resection of lung cancer treated in Zhejiang Cancer Hospital (Hangzhou, China) from September 2013 to April 2016 were randomly divided into two groups: Combined anesthesia group and intravenous anesthesia group, 61 cases in each group. Patients in the combined anesthesia group received intravenous combined epidural anesthesia. Patients in the intravenous anesthesia group were given intravenous anesthesia alone. Inclusion criteria were: Patients in Zhejiang Cancer Hospital pathology department; no past history of tumor, diagnosed and received a series of tests and treatment in Zhejiang Cancer Hospital, willing to cooperate with medical staff in Zhejiang Cancer Hospital. Exclusion criteria were: Patients with other cardiovascular and cerebrovascular diseases, patients with other gastrointestinal diseases, patients who were transferred midway through the course of treatment or taking antibiotics not prescribed by Zhejiang Cancer Hospital or those who had been treated in a non-hospital setting for rehabilitation. This study was approved by the Zhejiang Cancer Hospital Ethics Committee. Written informed consents were collected and signed by the patients.

Treatment method

Intravenous anesthesia group was given simple intravenous anesthesia. Combined anesthesia group was given intravenous combined epidural anesthesia. All patients were given intramuscular injection of midazolam (0.05 mg/kg, H10980025; Jiangsu Enhua Pharmaceutical Co., Ltd., Xuzhou, China) and atropine (0.5 mg/patient, H44024022; Guangdong Nanguo Pharmaceutical Co., Ltd., Zhanjiang, China) for 30 min before entering the operating room, and GT6800-12 monitor (Hunan Yimin Sunshine Technology Co., Ltd., Hunan, China) was used for monitoring of vital signs and timely establishment of venous fluid path. Anesthesia was induced by intravenous injection of fentanyl (2 µg/kg, H42022076; Yichang Renfu Pharmaceutical Co., Ltd., Yichang, China) and propofol (2 mg/kg, H20163040; Xi'an Libang Pharmaceutical Co., Ltd.). After the patient lost consciousness, atracurium (0.5 mg/kg, H20090202; Zhejiang Xianju Pharmaceutical Co., Ltd., Zhejiang, China) was given until the patient's vital signs became stable and then tracheal intubation was performed.

Intravenous anesthesia: Intravenous target-controlled infusion of remifentanil (0.02 µg/kg/min, H20143314; Yichang Renfu Pharmaceutical Co., Ltd.) combined with propofol (0.05 µg/kg/min) maintaining anesthesia until 10 min prior to surgery with intermittent administration of atracurium (0.1 mg/kg).

Intravenous combined epidural anesthesia: After endotracheal intubation, epidural puncture was performed in the waist 5 to the waist 6 or waist 6 to the waist 7 levels of local administration of 1% lidocaine (5 ml, H41023668; Sui Cheng Pharmaceutical Co., Ltd.). Intraoperative target-controlled infusion of propofol (0.05 µg/kg/min) was performed to maintain anesthesia while administering 0.375% ropivacaine every 30 min (5 ml, H20113381; Guangdong Jiabo Pharmaceutical Co., Ltd., Guangzhou, China) till 10 min before the end of the surgery, and atracurium was given intermittently (0.1 mg/kg).

Observation indicators

Peripheral blood samples were collected before anesthesia (T0), immediately after anesthesia (T1), after operation (T2), 24 h after operation (T3) and 72 h after operation (T4), and CD3+, CD4+ and CD4+CD25+ levels were detected at all 5 time-points using a MACSQuant flow cytometer from Gene Tech Co., Ltd. (Hong Kong, China).

Statistical analysis

Statistical methods: SPSS 22.0 software (IBM Corp., Armonk, NY, USA) was used for statistical analysis. Enumeration data were expressed as n (%) and were examined by χ2 test. Measurement data were expressed as mean ± SD. Comparison between multiple groups was done using One-way ANOVA test followed by post hoc test (Least Significant Difference). P<0.05 for the difference was considered statistically significant.

Results

General information

There were 122 patients in line with the inclusion criteria, 61 cases in intravenous anesthesia group. There were 36 male and 25 female patients, mean age 53.5±6.4 years, 61 cases of joint anesthesia group, including 38 males and 23 females, mean age 54.3±6.6 years (Table I). There was no significant difference in gender proportion and average age between the two groups (P>0.05). Body mass index, operation time and preoperative life parameters of two groups of patients showed no difference (P>0.05).

Table I.

Clinical data comparison of two groups.

Table I.

Clinical data comparison of two groups.

ItemsIntravenous anesthesiaCombined anesthesiat/χ2 valueP-value
No. of patients6161
Sex 0.3710.711
  Male3638
  Female2523
Age (years)53.5±6.454.3±6.60.6800.498
BMI (kg/m2)24.82±10.1325.17±10.460.1880.851
Operation time (min)81.13±12.5681.75±12.720.2710.787
Preoperative diastolic blood pressure (mmHg)78.25±7.3378.36±7.450.0820.934
Preoperative systolic blood pressure (mmHg)133.46±14.12133.17±13.690.1150.909
Preoperative heart rate (beats/min)78.29±9.1778.48±9.360.1130.910
Analysis of T0, T1, T2, T3 and T4 CD3+ levels in the groups

There was no difference in CD3+ level at T0 between the two groups (P>0.05). CD3+ levels at T1, T2, T3 and T4 were significantly higher in the combined anesthesia group than those in the intravenous anesthesia group (P<0.05). The level of CD3+ at T2 and T1 was lower than that at T0 (P<0.05), and the level of CD3+ at T2 was lower than that at T1 (P<0.05). After T3, the level of CD3+ increased in both groups; the levels of CD3+ at T3 and T4 were higher in both groups than those in T2 and T1 (P<0.05). The levels of CD3+ at T4 were higher than those at T3 in both groups (P<0.05). All CD3+ levels at T3 and T4 were lower than T0 in both groups (P<0.05) (Table II).

Table II.

CD3+ level analysis at T0, T1, T2, T3 and T4 (%).

Table II.

CD3+ level analysis at T0, T1, T2, T3 and T4 (%).

ItemsIntravenous anesthesiaCombined anesthesiat-valueP-value
No. of patients6161
T0a62.03±10.1561.79±10.160.1310.896
T1b50.13±8.1456.58±8.384.312<0.001
T2c46.14±6.9453.28±7.485.465<0.001
T3d48.25±8.1557.97±8.676.380<0.001
T4e52.24±8.1361.59±8.486.216<0.001

[i] The levels of CD3+ at T1b, T2c, T3d, T4e in both groups were significantly lower than those in T0a (P<0.05). The levels of CD3+ at T2c were significantly lower than those at T1b (P<0.05). The levels of CD3+ at T3d and T4e in both groups were higher than those at T1b, T2c; the levels of CD3+ at T4e in both groups were higher than those at T3d (P<0.05).

Analysis of CD4+ levels in two groups at T0, T1, T2, T3 and T4

There was no significant difference in CD4+ level between two groups at T0 (P>0.05). CD4+ levels at T1, T2, T3 and T4 were significantly higher in the combined anesthesia group than those in the intravenous anesthesia group (P<0.05). After the start of anesthesia, CD4+ levels of both groups started to decrease. CD4+ levels at T2 and T1 were lower than those at T0 (P<0.05), and CD4+ levels at T2 were lower than those at T1 (P<0.05). After T3, the levels of CD4+ in both groups began to increase (P<0.05); the levels of CD4+ in both groups at T3 and T4 were higher than those at T2 and T1 (P<0.05). The levels of CD4+ at T4 were higher in both groups than those at T3 (P<0.05), but the level of CD4+ at T3 and T4 were lower than those at T0 (P<0.05) (Table III).

Table III.

CD4+ level analysis at T0, T1, T2, T3 and T4 (%).

Table III.

CD4+ level analysis at T0, T1, T2, T3 and T4 (%).

ItemsIntravenous anesthesiaCombined anesthesiat-valueP-value
No. of patients6161
T0a39.12±7.0439.17±7.010.0390.969
T1b30.03±6.1934.22±6.733.579<0.001
T2c26.13±6.3231.82±6.914.746<0.001
T3d30.97±5.1235.88±5.385.163<0.001
T4e34.01±4.8437.69±5.134.075<0.001

[i] The levels of CD4+ at T1b, T2c, T3d, T4e in both groups were significantly lower than those in T0a (P<0.05). The levels of CD4+ at T2c were significantly lower than those at T1b (P<0.05). The levels of CD4+ at T3d and T4e in both groups were higher than those at T1b, T2c; the levels of CD4+ at T4e in both groups were higher than those at T3d (P<0.05).

Analysis of CD4+CD25+ levels in two groups at T0, T1, T2, T3 and T4

There was no significant difference in CD4+CD25+ level between the two groups at T0 (P>0.05). CD4+CD25+ levels at T1, T2, T3 and T4 were significantly higher in the combined anesthesia group than those in the intravenous anesthesia group (P<0.05). After the start of anesthesia, CD4+CD25+ levels of both groups started to decrease, and CD4+CD25+ levels at T2 and T1 were lower than those at T0 (P<0.05), and CD4+CD25+ levels at T2 were lower than those at T1 (P<0.05). After T3, the levels of CD4+CD25+ in both groups began to increase (P<0.05); the levels of CD4+CD25+ in both groups at T3 and T4 were higher than those at T2 and T1 (P<0.05). The levels of CD4+CD25+ at T4 were higher in both groups than those at T3 (P<0.05), but the level of CD4+CD25+ at T3 and T4 were lower than those at T0 (P<0.05) (Table IV). Changes of CD3+, CD4+ and CD4+CD25+ are shown in Figs. 13.

Table IV.

CD4+CD25+ level analysis at T0, T1, T2, T3 and T4 (%).

Table IV.

CD4+CD25+ level analysis at T0, T1, T2, T3 and T4 (%).

ItemsIntravenous anesthesiaCombined anesthesiat-valueP-value
No. of patients6161
T0a7.83±1.257.79±1.170.1830.856
T1b5.40±1.466.24±1.912.7290.007
T2c4.77±0.755.73±0.627.705<0.001
T3d5.25±0.846.21±1.015.708<0.001
T4e5.83±1.027.22±1.137.132<0.001

[i] The levels of CD4+CD25+ at T1b, T2c in both groups were significantly lower than those in T0a (P<0.05). The levels of CD4+CD25+ at T2c were significantly lower than those at T1b (P<0.05). The levels of CD4+CD25+ at T3d and T4e in both groups were higher than those at T1b, T2c; the levels of CD4+CD25+ at T4e in both groups were higher than those at T3d (P<0.05).

Discussion

Different methods of surgery and anesthesia often cause different degrees of stress response in the patients. Due to individual differences, patients also experience different ranges of stress response (11). Stress response within a certain range can enhance the body's immune function, stimulate cell metabolism to speed up and improve the body's resistance to external stimuli, but the stress response exceeding the bodys limit will seriously hinder the treatment of patients with prognosis, and it will inhibit immune function of the body, causing cell and organ damage in patients (12,13). Cellular immunity plays an important role in the anti-inflammatory and antitumor responses of the body (14). This study explored the effects of different anesthesia on the cellular immune function in patients undergoing radical resection of lung cancer, in order to provide reference for the choice of anesthesia in surgical treatment opinion.

CD3+ is a mature T lymphocyte, which can prompt the body's cellular immune function status; CD4+ is a helper T cells, which is the most important hub to regulate the immune response; CD4+CD25+ is a subset of T cells, which plays an important role in the body inflammation and immune response (15,16). The results of this study showed that the levels of CD3+, CD4+ and CD4+CD25+ in the two groups were lower than those before the operation, but the levels of CD3+, CD4+ and CD4+CD25+ in the patients receiving intravenous combined epidural anesthesia were significantly higher than those in the simple intravenous anesthesia. After surgery, two groups of patients with varying degrees of CD3+, CD4+ and CD4+CD25+ levels were restored. Patients receiving intravenous composite epidural anesthesia were significantly better than those who received intravenous anesthesia alone, indicating that patients receiving intravenous composite epidural anesthesia had more stable intraoperative immunologic function and better postoperative immune function recovery. This may be related to intravenous compound epidural anesthesia on the inhibition of the stability of the autonomic nervous system; epidural anesthesia can change autonomic nerve function (17), and stabilize the autonomic nervous system, improve the level of peripheral neurotransmitters, effectively improve the anesthesia of T Lymphocyte inhibition, maintain patients with perioperative cellular immune function stability and balance (18). Ropivacaine is an anesthetic with small fat-soluble and relatively diminished absolute efficacy. It blocks motor and sensory nerves independently during maintenance anesthesia and relieves stress stimulation of body anesthesia, surgery and postoperative pain (19). Some studies (20) showed that intraoperative continuous maintenance of ropivacaine in patients with T lymphocyte response was significantly higher. Chen et al (21) in the study also showed that the general anesthesia combined with epidural anesthesia can effectively improve the patient's immune function. Kun et al (22) also reported in the study that systemic combined epidural anesthesia has a weaker NK cell suppressive effect in gastric cancer surgery compared with pure general anesthesia, which helps to maintain perioperative immune function in patients. Their findings are similar to ours, but because of the short duration of our study, we were unable to assess the longer duration of immune function and adverse events. Therefore, the findings and conclusions of this study need more research and data for confirmation.

In conclusion, intravenous combined epidural anesthesia can maintain a relatively stable immune function of patients compared to simple intravenous anesthesia.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

SF wrote the manuscript and treated the patients. PSQ detected CD3+, CD4+ levels. SNC treated the patients and helped with detection of CD4+CD25+ levels. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of Zhejiang Cancer Hospital (Hangzhou, China). Patients who participated in this research, signed the informed consent and had complete clinical data.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References

1 

Rizvi NA, Hellmann MD, Snyder A, Kvistborg P, Makarov V, Havel JJ, Lee W, Yuan J, Wong P, Ho TS, et al: Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer. Science. 348:124–128. 2015. View Article : Google Scholar : PubMed/NCBI

2 

Lortet-Tieulent J, Soerjomataram I, Ferlay J, Rutherford M, Weiderpass E and Bray F: International trends in lung cancer incidence by histological subtype: Adenocarcinoma stabilizing in men but still increasing in women. Lung Cancer. 84:13–22. 2014. View Article : Google Scholar : PubMed/NCBI

3 

Brahmer J, Reckamp KL, Baas P, Crinò L, Eberhardt WE, Poddubskaya E, Antonia S, Pluzanski A, Vokes EE, Holgado E, et al: Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer. N Engl J Med. 373:123–135. 2015. View Article : Google Scholar : PubMed/NCBI

4 

Herbst RS, Baas P, Kim DW, Felip E, Pérez-Gracia JL, Han JY, Molina J, Kim JH, Arvis CD, Ahn MJ, et al: Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): A randomised controlled trial. Lancet. 387:1540–1550. 2016. View Article : Google Scholar : PubMed/NCBI

5 

Horn L, Spigel DR, Vokes EE, Holgado E, Ready N, Steins M, Poddubskaya E, Borghaei H, Felip E, Paz-Ares L, et al: Nivolumab versus docetaxel in previously treated patients with advanced non-small-cell lung cancer: Two-year outcomes from two randomized, open-label, phase III trials (CheckMate 017 and CheckMate 057). J Clin Oncol. 35:3924–3933. 2017. View Article : Google Scholar : PubMed/NCBI

6 

Chen C, Li M, Wang K, Shen J, Yang L, Bu X and Gao G: Protective effect of combined general and regional anesthesia on postoperative cognitive function in older arthroplasty patients. Int J Clin Exp Med. 10:15453–15458. 2017.

7 

Zhang CH, Ma WQ, Yang YL, Dong FT, Wang HM and Wei HM: Effect of the intraoperative wake-up test in sevoflurane-sufentanil combined anesthesia during adolescent idiopathic scoliosis surgery: A randomized study. J Clin Anesth. 25:263–267. 2013. View Article : Google Scholar : PubMed/NCBI

8 

Segal D, Awad N, Nasir H, Mustafa S and Lowenstein L: Combined spinal and general anesthesia vs. general anesthesia for robotic sacrocervicopexy: A randomized controlled trial. Int Urogynecol J. 25:369–374. 2014. View Article : Google Scholar : PubMed/NCBI

9 

Tsukamoto A, Serizawa K, Sato R, Yamazaki J and Inomata T: Vital signs monitoring during injectable and inhalant anesthesia in mice. Exp Anim. 64:57–64. 2015. View Article : Google Scholar : PubMed/NCBI

10 

Browning RM, Fellingham WH, O'Loughlin EJ, Brown NA and Paech MJ: Prophylactic ondansetron does not prevent shivering or decrease shivering severity during cesarean delivery under combined spinal epidural anesthesia: A randomized trial. Reg Anesth Pain Med. 38:39–43. 2013. View Article : Google Scholar : PubMed/NCBI

11 

Zhao J and Mo H: The impact of different anesthesia methods on stress reaction and immune function of the patients with gastric cancer during peri-operative period. J Med Assoc Thai. 98:568–573. 2015.PubMed/NCBI

12 

Hu LG, Pan JH, Li J, Kang F and Jiang L: Effects of different doses of sufentanil and remifentanil combined with propofol in target-controlled infusion on stress reaction in elderly patients. Exp Ther Med. 5:807–812. 2013. View Article : Google Scholar : PubMed/NCBI

13 

Wang L, Yuan R, Yao C, Wu Q, Christelle M, Xie W, Zhang X, Sun W, Wang H and Yao S: Effects of resolvin D1 on inflammatory responses and oxidative stress of lipopolysaccharide-induced acute lung injury in mice. Chin Med J (Engl). 127:803–809. 2014.PubMed/NCBI

14 

Kirchheiner K, Czajka-Pepl A, Ponocny-Seliger E, Scharbert G, Wetzel L, Nout RA, Sturdza A, Dimopoulos JC, Dörr W and Pötter R: Posttraumatic stress disorder after high-dose-rate brachytherapy for cervical cancer with 2 fractions in 1 application under spinal/epidural anesthesia: Incidence and risk factors. Int J Radiat Oncol Biol Phys. 89:260–267. 2014. View Article : Google Scholar : PubMed/NCBI

15 

Ma C, Kesarwala AH, Eggert T, Medina-Echeverz J, Kleiner DE, Jin P, Stroncek DF, Terabe M, Kapoor V, ElGindi M, et al: NAFLD causes selective CD4(+) T lymphocyte loss and promotes hepatocarcinogenesis. Nature. 531:253–257. 2016. View Article : Google Scholar : PubMed/NCBI

16 

Pentcheva-Hoang T, Simpson TR, Montalvo-Ortiz W and Allison JP: Cytotoxic T lymphocyte antigen-4 blockade enhances antitumor immunity by stimulating melanoma-specific T-cell motility. Cancer Immunol Res. 2:970–980. 2014. View Article : Google Scholar : PubMed/NCBI

17 

Liu J, Cui F, Li S, Chen H, Shao W, Liang L, Yin W, Lin Y and He J: Nonintubated video-assisted thoracoscopic surgery under epidural anesthesia compared with conventional anesthetic option: A randomized control study. Surg Innov. 22:123–130. 2015. View Article : Google Scholar : PubMed/NCBI

18 

Zhang Y, Guan Z, Reader B, Shawler T, Mandrekar-Colucci S, Huang K, Weil Z, Bratasz A, Wells J, Powell ND, et al: Autonomic dysreflexia causes chronic immune suppression after spinal cord injury. J Neurosci. 33:12970–12981. 2013. View Article : Google Scholar : PubMed/NCBI

19 

Marhofer D, Kettner SC, Marhofer P, Pils S, Weber M and Zeitlinger M: Dexmedetomidine as an adjuvant to ropivacaine prolongs peripheral nerve block: A volunteer study. Br J Anaesth. 110:438–442. 2013. View Article : Google Scholar : PubMed/NCBI

20 

Chloropoulou P, Iatrou C, Vogiatzaki T, Kotsianidis I, Trypsianis G, Tsigalou C, Paschalidou E, Kazakos K, Touloupidis S and Simopoulos K: Epidural anesthesia followed by epidural analgesia produces less inflammatory response than spinal anesthesia followed by intravenous morphine analgesia in patients with total knee arthroplasty. Med Sci Monit. 19:73–80. 2013. View Article : Google Scholar : PubMed/NCBI

21 

Chen WK, Ren L, Wei Y, Zhu DX, Miao CH and Xu JM: General anesthesia combined with epidural anesthesia ameliorates the effect of fast-track surgery by mitigating immunosuppression and facilitating intestinal functional recovery in colon cancer patients. Int J Colorectal Dis. 30:475–481. 2015. View Article : Google Scholar : PubMed/NCBI

22 

Kun L, Tang L, Wang J, Yang H and Ren J: Effect of combined general/epidural anesthesia on postoperative NK cell activity and cytokine response in gastric cancer patients undergoing radical resection. Hepatogastroenterology. 61:1142–1147. 2014.PubMed/NCBI

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Spandidos Publications style
Fu S, Qu P and Cai S: Effect of anesthetic methods on postoperative CD3+, CD4+ and CD4+CD25+ in patients with lung cancer undergoing radical operation. Oncol Lett 16: 6547-6551, 2018
APA
Fu, S., Qu, P., & Cai, S. (2018). Effect of anesthetic methods on postoperative CD3+, CD4+ and CD4+CD25+ in patients with lung cancer undergoing radical operation. Oncology Letters, 16, 6547-6551. https://doi.org/10.3892/ol.2018.9416
MLA
Fu, S., Qu, P., Cai, S."Effect of anesthetic methods on postoperative CD3+, CD4+ and CD4+CD25+ in patients with lung cancer undergoing radical operation". Oncology Letters 16.5 (2018): 6547-6551.
Chicago
Fu, S., Qu, P., Cai, S."Effect of anesthetic methods on postoperative CD3+, CD4+ and CD4+CD25+ in patients with lung cancer undergoing radical operation". Oncology Letters 16, no. 5 (2018): 6547-6551. https://doi.org/10.3892/ol.2018.9416