Journal List > Korean J Gastroenterol > v.65(5) > 1007369

Kim, Ahn, Park, Park, Kim, Baek, Lee, and Park: Long-term Outcomes of Laparoscopic versus Open Surgery for Rectal Cancer: A Single-center Retrospective Analysis

Abstract

Background/Aims

Laparoscopic surgery has been proven to be an effective alternative to open surgery in patients with colon cancer. However, data on laparoscopic surgery in patients with rectal cancer are insufficient. The aim of this study was to compare the long-term outcomes of laparoscopic and open surgery in patients with rectal cancer.

Methods

A total of 307 patients with rectal cancer who were treated by open and laparoscopic curative resection at Kosin University Gospel Hospital (Busan, Korea) between January 2002 and December 2011 were reviewed retrospectively.

Results

Regarding treatment, 176 patients underwent an open procedure and 131 patients underwent a laparoscopic procedure. The local recurrence rate after laparoscopic resection was 2.3%, compared with 5.7% after open resection (p=0.088). Distant metastases occurred in 6.9% of the laparoscopic surgery group, compared with 24.4% in the open surgery group (p<0.001). In univariate analysis, age (≥75 years vs. ≤60 years), preoperative staging, surgical approach (open vs. laparoscopic), elevated initial CEA level, elevated follow-up CEA level, number of positive lymph nodes, and postoperative chemotherapy affected overall survival and disease free survival. However, in multivariate analysis, the surgical approach apparently did not affect long-term oncologic outcome.

Conclusions

In this study, long-term outcomes after laparoscopic surgery for rectal cancer were not inferior to those after open surgery. Therefore, laparoscopic surgery would be an alternative operative tool to open resection for rectal cancer, although further investigation is needed.

References

1. Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011; 61:69–90.
crossref
2. Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin. 2014; 64:9–29.
crossref
3. Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010; 127:2893–2917.
crossref
4. Kapiteijn E, Kranenbarg EK, Steup WH, et al. Total mesorectal excision (TME) with or without preoperative radiotherapy in the treatment of primary rectal cancer. Prospective randomised trial with standard operative and histopathological techniques. Dutch ColoRectal Cancer Group. Eur J Surg. 1999; 165:410–420.
5. Sauer R, Becker H, Hohenberger W, et al. German Rectal Cancer Study Group. Preoperative versus postoperative chemoradiotherapy for rectal cancer. N Engl J Med. 2004; 351:1731–1740.
crossref
6. Clinical Outcomes of Surgical Therapy Study Group. A comparison of laparoscopically assisted and open colectomy for colon cancer. N Engl J Med. 2004; 350:2050–2059.
7. Buunen M, Veldkamp R, Hop WC, et al. Colon Cancer Laparoscopic or Open Resection Study Group. Survival after laparoscopic surgery versus open surgery for colon cancer: long-term outcome of a randomised clinical trial. Lancet Oncol. 2009; 10:44–52.
8. Jayne DG, Guillou PJ, Thorpe H, et al. UK MRC CLASICC Trial Group. Randomized trial of laparoscopic-assisted resection of colorectal carcinoma: 3-year results of the UK MRC CLASICC Trial Group. J Clin Oncol. 2007; 25:3061–3068.
crossref
9. Lacy AM, García-Valdecasas JC, Delgado S, et al. laparoscopy-assisted colectomy versus open colectomy for treatment of non- metastatic colon cancer: a randomised trial. Lancet. 2002; 359:2224–2229.
10. Delaney CP, Chang E, Senagore AJ, Broder M. Clinical outcomes and resource utilization associated with laparoscopic and open colectomy using a large national database. Ann Surg. 2008; 247:819–824.
crossref
11. Kemp JA, Finlayson SR. Outcomes of laparoscopic and open colectomy: a national population-based comparison. Surg Innov. 2008; 15:277–283.
crossref
12. da Luz Moreira A, Mor I, Geisler DP, Remzi FH, Kiran RP. Laparoscopic resection for rectal cancer: a case-matched study. Surg Endosc. 2011; 25:278–283.
crossref
13. Lujan J, Valero G, Biondo S, Espin E, Parrilla P, Ortiz H. Laparoscopic versus open surgery for rectal cancer: results of a prospective multicentre analysis of 4,970 patients. Surg Endosc. 2013; 27:295–302.
crossref
14. Ng SS, Lee JF, Yiu RY, et al. Laparoscopic-assisted versus open total mesorectal excision with anal sphincter preservation for mid and low rectal cancer: a prospective, randomized trial. Surg Endosc. 2014; 28:297–306.
crossref
15. Seshadri RA, Srinivasan A, Tapkire R, Swaminathan R. Laparoscopic versus open surgery for rectal cancer after neoadjuvant chemoradiation: a matched case-control study of short-term outcomes. Surg Endosc. 2012; 26:154–161.
crossref
16. Jeong SY, Park JW, Nam BH, et al. Open versus laparoscopic surgery for mid-rectal or low-rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): survival outcomes of an open- label, non-inferiority, randomised controlled trial. Lancet Oncol. 2014; 15:767–774.
17. van der Pas MH, Haglind E, Cuesta MA, et al. COlorectal cancer Laparoscopic or Open Resection II (COLOR II) Study Group. Laparoscopic versus open surgery for rectal cancer (COLOR II): short-term outcomes of a randomised, phase 3 trial. Lancet Oncol. 2013; 14:210–218.
crossref
18. Ng SS, Leung KL, Lee JF, et al. Laparoscopic-assisted versus open abdominoperineal resection for low rectal cancer: a prospective randomized trial. Ann Surg Oncol. 2008; 15:2418–2425.
crossref
19. Chiang JM, Hsieh PS, Chen JS, Tang R, You JF, Yeh CY. Rectal cancer level significantly affects rates and patterns of distant metastases among rectal cancer patients post curative-intent surgery without neoadjuvant therapy. World J Surg Oncol. 2014; 12:197.
crossref
20. Tarantino I, Warschkow R, Worni M, et al. Elevated preoperative CEA is associated with worse survival in stage I-III rectal cancer patients. Br J Cancer. 2012; 107:266–274.
crossref
21. Das P, Skibber JM, Rodriguez-Bigas MA, et al. Predictors of tumor response and downstaging in patients who receive preoperative chemoradiation for rectal cancer. Cancer. 2007; 109:1750–1755.
crossref
22. Baik SH, Gincherman M, Mutch MG, Birnbaum EH, Fleshman JW. Laparoscopic vs open resection for patients with rectal can,!cer: comparison of perioperative outcomes and long-term survival. Dis Colon Rectum. 2011; 54:6–14.
crossref
23. Braga M, Frasson M, Vignali A, Zuliani W, Capretti G, Di Carlo V. Laparoscopic resection in rectal cancer patients: outcome and cost-benefit analysis. Dis Colon Rectum. 2007; 50:464–471.
crossref
24. Laurent C, Leblanc F, Wütrich P, Scheffler M, Rullier E. Laparoscopic versus open surgery for rectal cancer: long-term oncologic results. Ann Surg. 2009; 250:54–61.
25. Lujan J, Valero G, Hernandez Q, Sanchez A, Frutos MD, Parrilla P. Randomized clinical trial comparing laparoscopic and open surgery in patients with rectal cancer. Br J Surg. 2009; 96:982–989.
crossref
26. Irvin TT. Prognosis of colorectal cancer in the elderly. Br J Surg. 1988; 75:419–421.
crossref
27. Mulcahy HE, Patchett SE, Daly L, O'Donoghue DP. Prognosis of elderly patients with large bowel cancer. Br J Surg. 1994; 81:736–738.
crossref
28. Colorectal Cancer Collaborative Group. Surgery for colorectal cancer in elderly patients: a systematic review. Lancet. 2000; 356:968–974.
29. Vironen JH, Sainio P, Husa AI, Kellokumpu IH. Complications and survival after surgery for rectal cancer in patients younger than and aged 75 years or older. Dis Colon Rectum. 2004; 47:1225–1231.
crossref

Fig. 1.
Comparison of overall survival (OS) and disease-free survival (DFS) according to preoperative staging between open surgery group and laparoscopic surgery group. (A) Stage 1. (B) Stage 2. (C) Stage 3.
kjg-65-273f1.tif
Fig. 2.
Comparison of overall survival (OS) and disease-free survival (DFS) according to tumor location between open surgery group and laparoscopic surgery group. (A) Upper (11–15 cm from anal verge). (B) Middle (6–10 cm from anal verge). (C) Lower (≤5 cm from anal verge).
kjg-65-273f2.tif
Table 1.
Patient Characteristics
Characteristic Open (n=176) Laparoscopy (n=131) p-value
Gender     0.153
 Male 89 (50.6) 77 (58.8)  
 Female 87 (49.4) 54 (41.2)  
Age (yr) 59 (22–85) 61 (33–88) 0.252
Location     0.002
 Lower (≤5 cm from anal verge) 45 (25.6) 26 (19.8)  
 Middle (6–10 cm from anal verge) 84 (47.7) 45 (34.4)  
 Upper (11–15 cm from anal verge) 47 (26.7) 60 (45.8)  
Preoperative staging     0.056
 I 33 (18.8) 40 (30.5)  
 II 45 (25.6) 29 (22.1)  
 III 98 (55.7) 62 (47.3)  
Neoadjuvant CCRT     0.293
 Yes 26 (14.8) 14 (10.7)  
 No 150 (85.2) 117 (89.3)  
Adjuvant chemotherapy     0.008
 Yes 130 (73.9) 78 (59.5)  
 No 46 (26.1) 53 (40.5)  

Values are presented as n (%) or mean (range).

CCRT, concurrent chemoradiotherapy.

Table 2.
Pathological Data
Variable Open (n=176) Laparoscopy (n=131) p-value
Completeness of resection     0.304
 Complete 163 (92.6) 126 (96.2)  
 Partially complete 12 (6.8) 4 (3.1)  
 Incomplete 1 (0.6) 1 (0.8)  
Histology     0.846
 Well differentiated 44 (28.0) 36 (27.5)  
 Moderately differentiated 118 (63.0) 88 (67.2)  
 Poorly differentiated 10 (6.6) 5 (3.8)  
 Mucinous 4 (2.4) 2 (1.5)  
Circumference resection margin     0.951
 Positive 7 (4.0) 4 (3.1)  
 Negative 122 (69.3) 67 (51.1)  
 Missing data 47 (26.7) 60 (45.8)  
Number of harvested lymph nodes      
 Total group 13.0 (0–48.0) 12.0 (0–83.04) 0.946
 Missing data 4 5  
Number of positive lymph nodes      
 Total group 2.62±4.45 1.39±2.52 0.003
 Missing data 4 4  
Distance to proximal resection margin (cm)      
 Total group 13.5 (1.5-40.0) 10.0 (0.8-33.0) <0.001
 Missing data 11 5  
Distance to distal resection margin (cm)      
 Total group 2.0 (0–10.0) 3.0 (0–8.5) 0.181
 Missing data 11 5  

Values are presented as n (%), median (range), n only, or mean±SD.

Table 3.
Postoperative Recurrence according to Surgical Procedure
  Total (n=307) Open (n=176) Laparoscopy (n=131) p-value
Period of performance of operation       <0.001
 January 2002-December 2004 47 (15.3) 43 (24.4) 4 (3.0)  
 January 2005-December 2007 99 (32.2) 85 (48.3) 14 (10.7)  
 January 2008-December 2011 161 (52.5) 48 (27.3) 113 (86.3)  
Duration of follow-up (mo) 44 (8–142) 51 (8–142) 40 (11–135) <0.001
Time to recurrence (mo) 18 (5–136) 20 (5–136) 11 (5–37) 0.076
Recurrence after operation       <0.001
 Local recurrence 13 (4.3) 10 (5.7) 3 (2.3) 0.088
 Distant recurrence 52 (16.9) 43 (24.4) 9 (6.9) <0.001
 No recurrence 242 (78.8) 123 (69.9) 119 (90.8)  
Site of distant recurrence       0.958
 Liver 13 (4.2) 10 (5.7) 3 (2.3)  
 Lungs 20 (6.5) 17 (9.7) 3 (2.3)  
 Bone 3 (1.0) 3 (1.7) 0 (0)  
 Lymph nodes 2 (0.7) 2 (1.1) 0 (0)  
 Peritoneum 4 (1.3) 3 (1.7) 1 (0.8)  
 Ovary 1 (0.4) 1 (0.6) 0 (0)  
 Multiple organ involvement 9 (2.9) 7 (4.0) 2 (1.5)  

Values are presented as n (%) or median (range).

Table 4.
Univariate Analysis of Overall Survival and Disease-free Survival
Factor Overall Survival
Disease-free Survival
Hazard ratio (95% CI) p-value Hazard ratio (95% CI) p-value
Age (yr)        
 60-74 vs. ≤60 1.46 (0.88-2.44) 0.144 1.51 (0.94-2.44) 0.091
 ≥75 vs. ≤60 2.47 (1.08-5.67) 0.033 3.79 (1.85-7.77) <0.001
Male vs. female 1.21 (0.78-1.89) 0.404 1.31 (0.84-2.04) 0.232
Open vs. laparoscopic surgery 1.94 (1.14-3.28) 0.014 2.09 (1.24-3.52) 0.006
Tumor location        
 Middle vs. lower 1.62 (0.89-2.92) 0.114 1.60 (0.89-2.90) 0.120
 Upper vs. lower 1.08 (0.57-2.08) 0.807 1.04 (0.54-1.99) 0.910
Stage 2 vs. stage 1 3.29 (1.22-8.93) 0.019 3.45 (1.27-9.36) 0.015
Stage 3 vs. stage 1 6.19 (2.48-15.45) <0.001 5.59 (2.24-13.97) <0.001
Histology (well/moderate vs. poorly/mucinous) 0.94 (0.38-2.32) 0.887 0.85 (0.34-2.11) 0.727
Completeness of resection (R1/R2 vs. R0) 2.00 (0.96-4.16) 0.063 1.98 (0.95-4.12) 0.067
Positive CRM 0.86 (0.67-1.10) 0.234 0.83 (0.64-1.06) 0.138
Number of harvested LNs 0.99 (0.97-1.02) 0.787 1.00 (0.97-1.03) 0.983
Number of positive LNs 1.17 (1.12-1.23) <0.001 1.15 (1.11-1.20) <0.001
Distance to proximal RM 0.99 (0.96-1.02) 0.558 0.99 (0.96-1.02) 0.622
Distance to distal RM 1.01 (0.89-1.14) 0.861 0.99 (0.88-1.12) 0.882
Elevated initial CEA level 3.12 (1.97-4.95) <0.001 2.91 (1.84-4.60) <0.001
Elevated follow-up CEA level 3.46 (2.59-4.61) <0.001 3.69 (2.76-4.93) <0.001
Preoperative CCRT 0.82 (0.44-1.51) 0.519 0.93 (0.50-1.72) 0.810
Postoperative chemotherapy 0.18 (0.08-0.39) <0.001 0.19 (0.09-0.41) <0.001

CRM, circumferential resection margin; LNs, lymph nodes; RM, resection margin; CCRT, concurrent chemoradiotherapy.

Table 5.
Multivariate Analysis of Overall Survival and Disease-free Survival
Factor Overall Survival
Disease-free Survival
Hazard ratio (95% CI) p-value Hazard ratio (95% CI) p-value
Age (yr)        
 60-74 vs. ≤60 1.46 (0.88-2.44) 0.144 1.41 (0.85-2.35) 0.186
 ≥75 vs. ≤60 2.47 (1.08-5.67) 0.033 3.30 (1.43-7.63) 0.005
Open vs. laparoscopic surgery 1.06 (0.57-1.98) 0.845 1.49 (0.78-2.85) 0.222
Stage 2 vs. stage 1 0.73 (0.12-4.48) 0.732 0.43 (0.07-2.73) 0.369
Stage 3 vs. stage 1 0.99 (0.17-6.05) 0.998 0.46 (0.07-2.92) 0.412
Number of positive LNs 1.19 (1.12-1.27) <0.001 1.14 (1.07-1.21) <0.001
Elevated initial CEA level 2.16 (1.29-3.60) 0.003 1.76 (1.06-2.91) 0.029
Elevated follow-up CEA level 3.68 (2.59-5.23) <0.001 3.72 (2.63-5.26) <0.001
Postoperative chemotherapy 0.29 (0.13-0.67) 0.004 0.20 (0.09-0.49) <0.001

LNs, lymph nodes.

TOOLS
Similar articles