Evidence - Laparoscopic oncological sigmoid resection

  1. Summary of the literature

    Minimally Invasive Oncological Colon Surgery

    In the treatment of colorectal carcinomas, the surgical resection of the tumor-bearing bowel segment is essential. The fundamental oncological principle involves the central ligation of the arterial blood supply with the performance of a complete mesocolic excision (CME) and the complete removal of all lymph nodes associated with the respective bowel segment [1, 2].

    Numerous randomized controlled trials with strict inclusion and exclusion criteria and clear guidelines for the qualification of surgeons, as well as registry data and population-based studies, demonstrate the equivalence of laparoscopic colon resections (LCR) compared to conventional open resections (OCR) in the oncological setting [3-13].

    Compared to OCR, LCR shows a longer operation time, less intraoperative blood loss, reduced postoperative analgesic requirement, less postoperative bowel atony, and a shorter hospital stay [4, 6, 10, 14, 15, 16]. Extensive RCTs show no statistically significant difference in postoperative mortality between OCR and LCR [3, 4, 6,17], while population and registry-based studies report it as lower in the LCR group [8, 11, 13].

    In deciding between OCR or LCR, tumor location, low T-stage, smaller estimated tumor size, younger patient age, female gender, type of clinic, and elective setting are predictors favoring the decision for LCR [9, 11, 18].

    Even in colorectal carcinomas, the patient's prognosis depends on the number of lymph nodes removed with the resectate [1, 19]. In large RCTs, the number of lymph nodes removed in the LCR group is comparable to that in the OCR group [4-6, 15, 17].

    Many studies were conducted before the establishment of the CME principle. However, a 2017 meta-analysis showed that resections under CME standards regarding the number of lymph nodes removed and the surface area of the resected mesocolon largely maintain comparable resectate quality between LCR and OCR [20].

    There is some heterogeneity in the reported conversion rates to conventional open procedures. In large RCTs, it ranges from 11 to 25% [3-6], while in population and registry-based studies, it ranges from 5.7 to 19% [11, 21-23]. Over time, with the application of LCR, increasing surgeon experience, and experience in patient selection, the conversion rate decreases (11.8% → 8.6% [21]). In the MRC-CLASSIC trial, conversion is consistently associated with a significantly higher risk of recurrence and disease-associated mortality up to the 10-year follow-up [24]. Conversion is associated with a higher risk of postoperative complications [22].

    Risk factors for conversion include:

    • high body mass index
    • higher ASA classification
    • abdominal previous surgeries
    • male gender
    • tumor location in the transverse colon and left hemicolon

    In a 2012 study with a conversion rate of 15.8%, 20.8% of procedures were on the transverse colon, 20.7% on the left hemicolon, 15.6% on the right hemicolon, and 14.3% on the sigmoid colon [25]. Other factors influencing the conversion rate include local tumor extension and the frequency of LCRs performed in a clinic [18, 21, 26].

    Whether a new surgical procedure (here: LCR) can establish itself in the oncological setting depends on its comparability, possibly even superiority, to the currently established procedure (OCR) in terms of overall survival, disease-free survival, and recurrence rate. The initially postulated increased risks of implantation metastases of the abdominal wall (trocar insertions) and tumor cell dissemination were quickly refuted [27-29]. Large RCTs show comparability of LCR to OCR for overall survival and disease-free survival, as well as the frequency of local recurrences and distant metastases [27, 29-32]. Some registry data and population-based studies indicate a superiority of LCR over OCR, as in the work of Völkl et al [9]. However, a significant difference is only evident for stages T1 to T3, not for T4 and/or cases with lymph node metastases. Another study also describes a significant survival advantage after LCR, regardless of tumor location and T-stage [7].

    In locally advanced cases (T4a and T4b), current studies suggest that even in a T4 situation, LCR can lead to satisfactory oncological outcomes and appears safe and not inferior to OCR [9, 33, 34].

  2. Currently ongoing studies on this topic

  3. Literature on this topic

    1. German Cancer Society, German Cancer Aid (2019) AWMF S3-Guideline Colorectal Carcinoma, Long Version 2.1. AWMF Registration Number: 021/007OL

    2. Hohenberger W, Weber K, Matzel K et al (2009) Standardized surgery for colonic cancer: complete mesocolic excision and central ligation—technical notes and outcome. Colorectal Dis 11:354–364.

    3. Lacy AM, García-Valdecasas JC, Delgado S et al (2002) Laparoscopy-assisted colectomy versus open colectomy for treatment of nonmetastatic colon cancer: a randomized trial. Lancet 359:2224–2229.

    4. Nelson H, Sargent DJ, Wieand HS et al (2004) A comparison of laparoscopically assisted and open colectomy for colon cancer. N Engl J Med 350:2050–2059.

    5. Veldkamp R, Kuhry E, Hop WJC, Jeekel J, Kazemier G, Bonjer HJ, Haglind E, Pahlmann L, Cuesta MA, Msika S, Morino M, Lacy AM, Colon Cancer Laparoscopic or Open Resection Study Group (2005) Laparoscopic surgery versus open surgery for colon cancer: short-term outcomes of a randomized trial. Lancet Oncol 6:477–484.

    6. Guillou PJ, Quirke P, Thorpe H et al (2005) Short-term endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicenter, randomized controlled trial. Lancet 365:1718–1726.

    7. Benz S, Barlag H, Gerken M et al (2017) Laparoscopic surgery in patients with colon cancer: a population-based analysis. Surg Endosc 31:2586–2595.

    8. Ghadban T, Reeh M, Bockhorn M et al (2018) Minimally invasive surgery for colorectal cancer remains underutilized in Germany despite its nationwide application over the last decade. Sci Rep 8:15146.

    9. Völkel V, Draeger T, Gerken M et al (2018) Long-term oncologic outcomes after laparoscopic vs. open colon cancer resection: a high-quality population-based analysis in a Southern German district. Surg Endosc 32:4138–4147.

    10. Huang Y-M, Lee Y-W, Huang Y-J et al (2020) Comparison of clinical outcomes between laparoscopic and open surgery for left-sided colon cancer: a nationwide population-based study. Sci Rep 10:75.

    11. Zheng Z, Jemal A, Lin CC et al (2015) Comparative effectiveness of laparoscopy vs open colectomy among nonmetastatic colon cancer patients: an analysis using the National Cancer Data Base. J Natl Cancer Inst.

    12. McKay GD, Morgan MJ, Wong S-KC et al (2012) Improved short-term outcomes of laparoscopic versus open resection for colon and rectal cancer in an area health service: a multicenter study. Dis Colon Rectum 55:42–50.

    13. Kolfschoten NE, van Leersum NJ, Gooiker GA et al (2013) Successful and safe introduction of laparoscopic colorectal cancer surgery in Dutch hospitals. Ann Surg 257:916–921.

    14. Schwenk W, Haase O, Neudecker J et al (2005) Short-term benefits for laparoscopic colorectal resection. Cochrane Database Syst Rev.

    15. Ohtani H, Tamamori Y, Arimoto Y et al (2012) A meta-analysis of the short- and long-term results of randomized controlled trials that compared laparoscopy-assisted and open colectomy for colon cancer. J Cancer 3:49–57.

    16. Völkel V, Draeger T, Gerken M et al (2020) Laparoscopic surgery for colon cancer. Coloproctology 370:1453.

    17. Hewett PJ, Allardyce RA, Bagshaw PF et al (2008) Short-term outcomes of the Australasian randomized clinical study comparing laparoscopic and conventional open surgical treatments for colon cancer: the ALCCaS trial. Ann Surg 248:728–738.

    18. Stormark K, Søreide K, Søreide JA et al (2016) Nationwide implementation of laparoscopic surgery for colon cancer: short-term outcomes and long-term survival in a population-based cohort. Surg Endosc 30:4853–4864.

    19. Chang GJ, Rodriguez-Bigas MA, Skibber JM et al (2007) Lymph node evaluation and survival after curative resection of colon cancer: systematic review. J Natl Cancer Inst 99:433–441.

    20. Negoi I, Hostiuc S, Negoi RI et al (2017) Laparoscopic vs open complete mesocolic excision with central vascular ligation for colon cancer: a systematic review and meta-analysis. World J Gastrointest Oncol 9:475–491.

    21. de Neree Tot Babberich MPM, van Groningen JT, Dekker E et al (2018) Laparoscopic conversion in colorectal cancer surgery; is there any improvement over time at a population level? Surg Endosc 32:3234–3246.

    22. de Castro Duraes L, Steele SR, de Camargo MGM et al (2019) Conversion to open from laparoscopic colon resection is a marker for worse oncologic outcomes in colon cancer. Am J Surg 217:491–495.

    23. Yerokun BA, Adam MA, Sun Z et al (2016) Does conversion in laparoscopic colectomy portend an inferior oncologic outcome? Results from 104,400 patients. J Gastrointest Surg 20:1042–1048.

    24. Green BL, Marshall HC, Collinson F et al (2013) Long-term follow-up of the Medical Research Council CLASICC trial of conventional versus laparoscopically assisted resection in colorectal cancer. Br J Surg 100:75–82.

    25. Simorov A, Shaligram A, Shostrom V et al (2012) Laparoscopic colon resection trends in utilization and rate of conversion to open procedure: a national database review of academic medical centers. Ann Surg 256:462–468.

    26. Kuhry E, Bonjer HJ, Haglind E et al (2005) Impact of hospital case volume on short-term outcome after laparoscopic operation for colonic cancer. Surg Endosc 19:687–692.

    27. Kuhry E, Schwenk WF, Gaupset R et al (2008) Long-term results of laparoscopic colorectal cancer resection. Cochrane Database Syst Rev

    28. Deijen CL, Vasmel JE, de Lange-de Klerk ESM et al (2017) Ten-year outcomes of a randomized trial of laparoscopic versus open surgery for colon cancer. Surg Endosc 31:2607–2615.

    29. Fleshman J, Sargent DJ, Green E et al (2007) Laparoscopic colectomy for cancer is not inferior to open surgery based on 5-year data from the COST Study Group trial. Ann Surg 246:655–662.

    30. Bagshaw PF, Allardyce RA, Frampton CM et al (2012) Long-term outcomes of the Australasian randomized clinical trial comparing laparoscopic and conventional open surgical treatments for colon cancer: the Australasian Laparoscopic Colon Cancer Study trial. Ann Surg 256:915–919.

    31. Colon Cancer Laparoscopic or Open Resection Study Group, Buunen M, Veldkamp R, Hop WC, Kuhry E, Jeekel J, Haglind E, Pahlman L, Cuesta MA, Msika S, Morino M, Lacy A, Bonjer HJ (2009) Survival after laparoscopic surgery versus open surgery for colon cancer: long-term outcome of a randomized clinical trial. Lancet Oncol 10:44–52.

    32. Jayne DG, Thorpe HC, Copeland J et al (2010) Five-year follow-up of the Medical Research Council CLASICC trial of laparoscopically assisted versus open surgery for colorectal cancer. Br J Surg 97:1638–1645.

    33. Feinberg AE, Chesney TR, Acuna SA et al (2017) Oncologic outcomes following laparoscopic versus open resection of pT4 colon cancer: a systematic review and meta-analysis. Dis Colon Rectum 60:116–125.

    34. Liu Z-H, Wang N, Wang FQ et al (2018) Oncological outcomes of laparoscopic versus open surgery in pT4 colon cancers: a systematic review and meta-analysis. Int J Surg 56:221–233.

Reviews

Ryu HS, Kim J. Current status and role of robotic approach in patients with low-lying rectal cancer

Activate now and continue learning straight away.

Single Access

Activation of this course for 3 days.

US$9.40  inclusive VAT

Most popular offer

webop - Savings Flex

Combine our learning modules flexibly and save up to 50%.

from US$7.27 / module

US$87.34/ yearly payment

price overview

general and visceral surgery

Unlock all courses in this module.

US$14.55 / month

US$174.70 / yearly payment

  • literature search

    Literature search on the pages of pubmed.