Zhilong Huang
Shibo Huang
Raoshan Luo
Weiming Liang- The First Affiliated Hospital of Guangxi University of Science and Technology, Guangxi University of Science and Technology, Liuzhou, Guangxi, China
Introduction: There is still controversy on whether or not robot-assisted colorectal surgery (RACS) have advantages over laparoscopic-assisted colorectal surgery(LACS).
Materials and methods: The four databases (PubMed, Embase, Web of Science and Cochrane Library)were comprehensively searched for randomized controlled trials (RCTs) comparing the outcomes of RACS and LACS in the treatment of colorectal cancer from inception to 22 July 2023.
Results: Eleven RCTs were considered eligible for the meta-analysis. Compared with LACS,RACS has significantly longer operation time(MD=5.19,95%CI: 18.00,39.82, P<0.00001), but shorter hospital stay(MD=2.97,95%CI:−1.60,−0.33,P = 0.003),lower conversion rate(RR=3.62,95%CI:0.40,0.76,P = 0.0003), lower complication rate(RR=3.31,95%CI:0.64,0.89,P=0.0009),fewer blood loss(MD=2.71,95%CI:−33.24,−5.35,P = 0.007),lower reoperation rate(RR=2.12, 95%CI:0.33,0.96,P=0.03)and longer distal resection margin(MD=2.16, 95%CI:0.04,0.94, P = 0.03). There was no significantly difference in harvested lymph nodes, the time of first flatus, the time of first defecation,the time of first resume diet, proximal resection margin, readmission rates, mortalities and CRM+ rates between two group.
Conclusions: Our study indicated that RACS is a feasible and safe technique that can achieve better surgical efficacy compared with LACS in terms of short-term outcomes.
Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42023447088.
1 Introduction
Colorectal surgery is widely used worldwide for benign and malignant lesions, including colorectal cancer(CRC). Colorectal cancer is the third most common cancer worldwide with an estimated annual incidence of 10,000 worldwide and the second leading cause of cancer deaths (1). At present, epidemiological studies have shown that the incidence of colorectal cancer is also gradually increasing in young people (2). The management of CRC is multidisciplinary; Surgery remains the most effective treatment, however, it is only available for patients with early stage cancer, while chemotherapy, targeted therapy, immunotherapy, surgery, and radiation are commonly used for advanced CRC (3–6).
At present, colorectal resection is still the main treatment strategy for colorectal cancer. Decades of development have proved that laparoscopic surgery is feasible and effective in the treatment of CRC, which greatly improves patient outcomes and does not have negative effects in terms of oncology and safety, and is considered as the gold standard treatment for colorectal cancer (7–11).
Robotics has flourished in recent years and the development of robotic surgery is considered as a major innovation in modern medicine since it offers an alternative to surgical methods in different situations (12). Robot-assisted technology is also widely used in colorectal cancer surgery, where robots offer many advantages over laparoscopic-assisted colorectal surgery(LACS), such as three-dimensional vision, 7° wrist-like motion, tremor filtration, motion scaling, better ergonomics, and less fatigue. These technical advantages can help overcome the drawbacks of LACS, such as two-dimensional vision, limited flexibility, and tremor (13). But in terms of clinical efficacy, conclusions of previous studies were conflicting on whether or not robot-assisted colorectal surgery (RACS) have advantages over LACS. Some studies declared that laparoscopic surgery was more advantageous, providing a high quality of colorectal resection, minimizing the damage to the tissue and organs of the surrounding tissue (14–17). However, other studies reported that clinical outcomes of RACS were better than those of traditional laparoscopic surgery (18–22).
Systemic reviews and meta-analysis had been performed to compare RACS and LACS.A meta-analysis showed that the two methods had similar clinical outcomes (23), but other meta-analysis declared that RACS had advantages regarding surgical efficacy and morbidity compared to LACS (24, 25). However, due to the shortage of strict inclusion criteria, a large amount of low evidence level RACS studies such as retrospective studies was included in above studies, which might resulted in probably unreliable conclusions.
Therefore, we conducted a systemic review and meta-analysis inclusion of only randomized controlled trials with high level of evidence. Our study aimed to compare the efficacy and safety of RACS and LACS in the treatment of colorectal cancer. These results may help provide high level evidence to support patients and physicians in their choice of CRC surgery.
2 Materials and methods
2.1 Search strategy
This meta-analysis was reported in accordance with the Preferred Reporting Project for Systematic Review and Meta-Analysis (PRISMA) 2020 guidelines (26, 27). This study was registered at PROSPERO under registration number CRD42023447088.The databases of PubMed, Embase, Web of science, and the Cochrane Library were systematically searched for papers published up to July 21, 2023. The MeSH terms “colorectal tumor”,”rectal tumor”,”colon tumor”,”laparoscopic”,”robot” as well as “randomized controlled trial” the free word “robot” and other relevant keywords were used in the search. The details of the searching record in four databases were shown in Supplement Tables 1–4.
2.2 Inclusion and exclusion criteria
Search strategies are developed in accordance with the PICOS principles (28) and then screened according to inclusion and exclusion criteria. Inclusion criteria were as follows (1): a randomized controlled trial comparing RACS with LACS for the treatment of patients with colorectal cancer (2); full-text articles reporting at least one of the following outcomes: operative time, hospital stays, blood loss, number of harvested lymph nodes, time of first flatus, time of first autonomous urination, time of first defecation, time of first resume diet,proximal resection margin, distal resection margin, rates of conversion to other surgery, complication rates, reoperation rates and mortality. Exclusion criteria were (1): other types of articles, such as conference abstracts yearbook, case reports, publications, letters, meta-analyses, reviews, retrospective studies, pharmacological intervention, animal studies and protocols (2); The full text cannot be obtained (3); Data duplication (4); Data could not be extracted for meta-analysis.
2.3 Data extraction
The study was divided into two phases with two independent investigators (L.H. and S.H.) reading the title and abstract, and then reading the full text. Differences were resolved by inviting a third investigator (Y.H.). Data retrieved included first author’s name, year, country, sample size, intervention, control, male ratio, age, treatment, body mass index, outcome, operative time, hospital stays, blood loss, number of harvested lymph nodes, time of first flatus, time of first autonomous urination, time of first defecation, time of first resume diet, proximal resection margin, distal resection margin, rates of conversion to other surgery, complication rates, reoperation rates and mortality.
2.4 Risk of bias assessment
The risk of bias was assessed using the Cochrane Risk of Bias tool (29) by two independent reviewers(L.H. and S.H.),according to the following domains: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective reporting and others bias. The controversial results were resolved by group discussion if there were discrepancies.
2.5 Statistical analysis
The selection duplicate removal of studies included was conducted using EndNote (Version 20; Clarivate Analytics). All analyses were performed using Review manager 5.3(Cochrane Collaboration, Oxford, UK). Continuous variables were compared using weighted mean difference (WMD) with a 95% confidence interval (CI). Relative ratio (RR) with 95% CI were used to compare binary variables. The medians and interquartile ranges of continuous data were converted to the mean and standard deviation. Statistical heterogeneity between included studies was calculated using the Cochrane ‘Sq test and the I2 index (I2 >50% indicating high heterogeneity). When there is high heterogeneity among studies, the random effects model is adopted, otherwise the fixed effects model is adopted (29). P value < 0.05 was considered statistically significant. Begg’s method was used to test the publication bias among various studies and to draw a funnel plot. Finally, a sensitivity analysis was performed to determine the impact of individual studies on the aggregated results and to test the reliability of the results.
3 Results
3.1 Identify eligible studies
The selection process of the study was present in Figure 1. A total of 1831 records were retrieved from the four databases and 539 duplicate records were deleted before screening. Then, 1292 records were screened and 1258 were excluded. 34 reports were assessed as qualified and 23 were excluded (unable to extract data =18; Non-rct =3; Data duplication =2). Finally, we included 11 RCTS (Figure 1).
Figure 1 Flow chart of literature search strategies.
3.2 Study characteristics
Table 1 shows the characteristics of the included RCTS. Four studies were from South Korea (30, 31, 35, 39), three from Europe (34, 40, 41), one from Egypt (33), and three from China (32, 36, 37). In these 11 randomized controlled trials, 1,656 participants received RACS and 1,759 received LACS.
Table 1 Characteristics of the included studies.
3.3 Risk of Bias assessment
The results of the risk of bias assessment are summarized in Figure 2. Among the 11 studies, an adequate randomized sequence was generated in 11 studies, appropriate allocation concealment was reported in 6 studies, the blinding of participants was clear in no study, the blinding of outcome assessors was reported in 2 studies, outcome data were complete in 11 studies, 11 studies had no selective reporting, and 10 studies had no other bias (Figure 2).
Figure 2 Risk of bias assessment for the included studies.
3.4 Clinical outcomes
All results of the meta-analysis for clinical outcomes were summarized in Table 2.
Table 2 Results of the meta-analysis.
3.4.1 Operative time (min)
Operative time was reported in nine RCTs (30–37, 40). The pooled results showed a significant difference between RACS and LACS, with LACS having a shorter surgical time than RACS(MD=5.19,95%CI:18.00,39.82, P<0.00001;I 2 = 95%, PQ<0.00001) (Figure 3A).
Figure 3 Forest plot of the meta-analysis for clinical outcomes. (A) Operative time. (B) Length of stay. (C) Blood loss. (D) The number of harvested lymph nodes.
3.4.2 Length of stay (days)
Length of stay was reported in eight RCTs (30–32, 34, 36, 37, 39, 40). The difference between RACS and LACS was statistically significant, with RACS having a shorter hospital stay than LACS.(MD=2.97,95%CI:−1.60,−0.33, P = 0.003;I 2 = 95%;PQ<0.00001) (Figure 3B).
3.4.3 Blood loss (ml)
Seven randomized controlled trials reported blood loss between RACS and LACS (31–33, 35–37, 39). There was a significant difference between RACS and LACS, with RACS having lower blood loss than LACS(MD=2.71,95%CI:−33.24,−5.35, P = 0.007;I 2 = 97%, PQ< 0.00001) (Figure 3C).
3.4.4 The number of harvested lymph nodes
Nine randomized controlled trials reported the number of lymph nodes harvested between RACS and LACS (30–33, 35–37, 39, 40). There was no statistically significant difference between RACS and LACS(MD=1.70,95%CI:−0.09,1.31,P=0.09;I 2 = 79%,PQ< 0.00001) (Figure 3D).
3.4.5 Conversion to other surgery
Ten RCTS reported conversion rates for open surgery between RACS and LACS (30, 31, 33–37, 39–41). There is a significant difference between RACS and LACS, and the conversion rate of RACS is lower(RR=3.62,95%CI:0.40,0.76,P = 0.0003;I 2 = 0%,PQ=0.63) (Figure 4A).
Figure 4 Forest plot of the meta-analysis for clinical outcomes. (A) Conversion. (B) Complications. (C) CRM+.
3.4.6 Complications
Eleven RCTS reported complication rates between RACS and LACS (30–37, 39–41). There was a significant difference in the complication rate between RACS and LACS, with RACS having a lower complication rate(RR=3.31,95%CI:0.64,0.89,P = 0.0009;I 2 = 26%,PQ=0.21) (Figure 4B).
3.4.7 CRM+
Six studies showed CRM+ (30–32, 35, 36, 40) rates; RACS and LACS had no significant difference in the occurrence of CRM+(RR=1.94, 95%CI:0.49,1.00,P = 0.05;I 2 = 0%,PQ=0.81) (Figure 4C).
3.4.8 Proximal resection margin (cm)
Seven studies reported the Proximal resection margin of RACS and LACS (30, 31, 33–37). There were no significant differences between RACS and LACS(MD=1.14, 95%CI:-1.16,0.31,P = 0.25;I 2 = 95%,PQ<0.00001) (Figure 5A).
Figure 5 Forest plot of the meta-analysis for clinical outcomes. (A) Proximal resection margin. (B) Distal resection margin.
3.4.9 Distal resection margin (cm)
Distal resection margin of RACS and LACS was reported in six studies (30, 31, 33–36). There were significant differences between RACS and LACS. RACS improved the distal incisal margin better than LACS(MD=2.16, 95%CI:0.04,0.94,P = 0.03;I 2 = 92%,PQ<0.00001) (Figure 5B).
3.4.10 The time of first flatus (days)
Seven randomized controlled trials reported first exhaust time between RACS and LACS (30–34, 36, 37). The difference between RACS and LACS was not statistically significant (MD=0.88,95%CI:−0.59,0.23,P = 0.38;I 2 = 99%,PQ< 0.00001) (Figure 6A).
Figure 6 Forest plot of the meta-analysis for clinical outcomes. (A) Time of first flatus. (B) Time of first autonomous urination. (C) Time of first defecation. (D) Time of first resume diet.
3.4.11 The time of first autonomous urination (days)
Four randomized controlled trials reported first urination days between RACS and LACS (32, 34, 36, 37). There was no statistically significant difference between RACS and LACS(MD=1.59, 95%CI:−2.01,0.21,P=0.19;I 2 = 99%,PQ< 0.00001) (Figure 6B).
3.4.12 The time of first defecation (days)
Two randomized controlled trials reported first defecation days for RACS and LACS (31, 36). There was no statistically significant difference between RACS and LACS(MD=1.44, 95%CI:−0.80,0.12,P=0.15;I 2 = 64%,PQ= 0.10) (Figure 6C).
3.4.13 The time of first resume diet (days)
Six studies reported the time to resume diet between RACS and LACS (30–32, 34, 36, 37). There was no statistically significant difference between RACS and LACS(MD=1.77,95%CI:−0.82,0.04, P=0.08;I 2 = 97%, PQ< 0.00001) (Figure 6D).
3.4.14 Reoperation rates
Four studies reported reoperation rates between RACS and LACS (33, 36, 37, 39). The difference between RACS and LACS was statistically significant, and the reoperation rate of RACS was lower than that of LACS(RR=2.12, 95%CI:0.33,0.96,P=0.03;I 2 = 0%,PQ= 0.96) (Figure 7A).
Figure 7 Forest plot of the meta-analysis for clinical outcomes. (A) Reoperation rates. (B) Readmission rates. (C) Death rates.
3.4.15 Readmission rates
Four randomized controlled trials reported readmission rates between RACS and LACS (33, 36, 37, 39). There was no statistically significant difference between RACS and LACS(RR=1.46, 95%CI:0.41,1.14,P=0.15;I 2 = 4%,PQ= 0.37) (Figure 7B)
3.4.16 Death rates
Five randomized controlled trials reported mortality between RACS and LACS (32, 33, 36, 37, 40), with no statistically significant difference between RACS and LACS(RR=0.97,95%CI:0.24,1.62,P=0.33;I 2 = 0%,PQ=0.91) (Figure 7C).
3.4.17 Complete rates of TME
Eight studies have reported the integrity of total mesorectal resection of RACS and LACS (30–33, 35–37, 40). There was statistical significance between RACS and LACS, and the complete resection rate of RACS was higher(RR=2.76, 95%CI:1.01,1.08,P=0.006;I 2 = 5%,PQ=0.39) (Figure 8).
Figure 8 Forest plot of the meta-analysis for complete rates of TME.
3.5 Sensitivity analysis
Sensitivity analysis was performed on conversion rate, complication rate, CRM+ rate and number of lymph node dissection (Supplementary Material). Sensitivity analysis shows that the results of conversion rate and CRM+ rate are robust. The sensitivity analysis was carried out by excluding literatures one by one. Although the results of complication incidence changed, the results were still robust from the whole point of view. The sensitivity analysis of the number of lymph node dissection was carried out, and the results were all changed after deleting the literatures. After observing the data changes, the literature (37) with the greatest difference in selective changes was removed one by one, and the results showed no change, indicating that the heterogeneity came from this literature.
3.6 Publication bias
The main indicators in this review included conversion rates and complication rates. Eleven randomized trials reported complication rates and ten studies reported conversion rates. Funnel plots were conducted to examine the presence of significant publication bias. Bilateral symmetric funnel plots of conversion rates show that no significant evidence of publication bias is observed (Figure 9A). Bilateral symmetric funnel plots of complication rates showed that no significant evidence of publication bias was observed (Figure 9B).
Figure 9 Funnel plot. (A) Conversion rates. (B) complication rates.
4 Discussion
Colorectal resection is considered as the gold standard treatment for colorectal cancer (8–10). In recent year, as a relatively new platform for minimally invasive surgery, RACS has been proposed as an alternative to LACS (12). However, previous studies comparing the clinical outcomes of RACS with LACS has not been sufficient to prove the benefits of RACS. Some of previous reviews and meta-analysis included non-randomized and observational studies in the meta-analysis which posed a risk of bias (23, 25, 38). Another meta-analysis included only RCTs, but only six studies was selected, leading to a relatively small number of patients and limited outcomes (24). In the present study,11 RCTs was included, and a high quality meta-analysis was conducted to compare outcomes of RACS versus LACS in the treatment of colorectal cancer.
According to the present meta-analysis, RACS reduces complication rates, blood loss, conversion rates, reoperation rates and hospital stay, and provides better distal margin results as compared to the LACS cohort. Previous study has reported similar results (18–22, 38). RACS has several advantages over LACS. Different from the four-degrees-of-freedom instruments in LACS, the seven-degrees-of-freedom robotic arms in RACS allow surgeons to perform more meticulous and precise procedure (42). Besides, high-quality 3-dimensional imaging with magnification, better ergonomic, stable platform of camera controlled by surgeons and free moving multi-joint forceps were provided in RACS (43). In mininvasive surgery, the delicate handling of RACS provides safer surgical procedure and more efficient tumor resection compared with LACS (44). Multi-articulated instrument of RACS allows surgeons to carefully manipulate the blood vessels, rapidly control and minimize bleeding (45).
Our results declared that RACS has a longer surgical duration than LACS. This is likely due to several factors including of docking time, more technically demanding procedures like intracorporeal suturing and learning curve (46). Previous studies (25, 38, 47–49)reported that RACS had longer operation time compared to LACS, which is consistent with our results (38, 48, 49). With regard to surgical time, along with surgeons becoming more familiar with the robot, the learning curve decreases and the differences seen will gradually balance out (50, 51). Rausa et al. (52) reported that surgery time could be influenced by a surgeon’s learning curve, and the operative time in RACS became similar to that of LACS in right-sided hemicolectomy for cancer after 21 cases.
In terms of harvested lymph nodes, time of first flatus, time of first defecation, time of first resume diet,proximal resection margin, readmission rates, mortalities and CRM+ rates, our study reported no statistical difference between RACS and LACS. In theory, longer surgery times are associated with harmful outcomes and may lead to longer hospital stays and increased conversion rates, but previous studies have shown lower conversion rates (38, 50, 53) and shorter hospital stays (38, 54, 55). Several studies have reported that robotic surgery produces similar perioperative outcomes to conventional laparoscopic surgery (56, 57). In addition, some previous studies have also shown that compared with LACS, RACS has less blood loss, fewer complications, and lower mortality, bleeding and intestinal obstruction rates (55).
To our knowledge, the present meta-analysis included the largest number of randomized controlled trials comparing outcomes of RACS versus LACS in the treatment of colorectal cancer, which could result in relatively robust conclusion. Besides, supplementary sensitivity analyses were performed to strengthen our results and overcome the risk of baseline confounding regarding short-term outcomes presenting with high heterogeneity, supporting our findings from the primary analysis. The findings of our study provide valuable insights into the clinical outcomes of colorectal surgical approaches which contribute to clinical practice and research. However, we acknowledge the possible limitations of our study. First of all, we failed to control the confounding factors such as the type of colorectal procedures, the level of expertise of surgeons involved and total versus hybrid robotic surgery. Though Da Vinci Surgical System (Intuitive Surgical, California) was used in all these trials (Table 1), we failed to identify if there were different models of the same device, which might be considered as a bias. Second, long-term outcomes such as 5-year overall survival were not analyzed because of the short follow-ups of the studies included. Third, trials published as abstract or presented at conferences were removed, which may potentially introduce publication bias to our findings. Forth, the number of RCTs included was still relatively small due to the strictest criteria, which result in a relatively small number of patients, and the impact of RACS may be overestimated compared to studies with large samples.
In conclusion, our study indicated that RACS is a feasible and safe technique that can achieve better surgical efficacy compared with LACS in terms of short-term outcomes. Except of longer operation time, RACS has obvious advantage in hospital stay, conversion rate, complication rate, blood control, reoperation rate and distal margin results. However, large sample and long follow-up randomized clinical trials comparing RACS with LACS are still necessary to better demonstrate the advantages of RACS for colorectal cancer.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Author contributions
WL: Funding acquisition, Writing – original draft, Writing – review & editing. ZH: Data curation, Writing – original draft. SH: Data curation, Formal Analysis, Writing – original draft. YH: Conceptualization, Investigation, Writing – original draft. RL: Methodology, Visualization, Writing – original draft.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Scientific Research Foundation of Guangxi University of Science and Technology (20Z13) and the Guangxi Natural Science Foundation (AD19245017).
Acknowledgments
Everyone who contributed significantly to this study has been listed.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2023.1273378/full#supplementary-material
Supplementary Table 1 | The details of the searching record in Medline.
Supplementary Table 2 | The details of the searching record in CENTRAL.
Supplementary Table 3 | The details of the searching record in Embase.
Supplementary Table 4 | The details of the searching record in Web of Science.
References
1. International Agency for Research on Cancer, World Health Organisation. Cancer today. In: Cancer fact sheets. (International Agency for Research on Cancer of World Health Organization). (2020). Available at: https://gco.iarc.fr/today/data/factsheets/cancers/10_8_9-Colorectum-fact-sheet.pdf.
2. Sehgal M, Ladabaum U, Mithal A, Singh H, Desai M, Singh G. Colorectal Cancer Incidence after Colonoscopy at Ages 45-49 or 50-54 Years. Gastroenterology (2021) 160(6):2018–28.e13. doi: 10.1053/j.gastro.2021.02.015
3. Gascón-Navarro JA, de la Torre-Aguilar MJ, Fernández-Ramos JA, Torres-Borrego J, Pérez-Navero JL. Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital. Ital J Pediatr (2021) 47(1):228. doi: 10.1186/s13052-021-01176-4
4. Sacks D, Baxter B, Campbell BCV, Carpenter JS, Cognard C, Dippel D, et al. Multisociety consensus quality improvement revised consensus statement for endovascular therapy of acute ischemic stroke. Int J Stroke: Off J Int Stroke Soc (2018) 13(6):612–32. doi: 10.1177/1747493018778713
5. Labianca R, Nordlinger B, Beretta GD, Mosconi S, Mandalà M, Cervantes A, et al. Early colon cancer: esmo clinical practice guidelines for diagnosis, treatment and follow-up. Ann oncology: Off J Eur Soc Med Oncol (2013) 24 Suppl 6:vi64–72. doi: 10.1093/annonc/mdt354
6. Glynne-Jones R, Wyrwicz L, Tiret E, Brown G, Rödel C, Cervantes A, et al. Rectal cancer: esmo clinical practice guidelines for diagnosis, treatment and follow-up. Ann oncology: Off J Eur Soc Med Oncol (2017) 28(suppl_4):iv22–40. doi: 10.1093/annonc/mdx224
7. Reza MM, Blasco JA, Andradas E, Cantero R, Mayol J. Systematic review of laparoscopic versus open surgery for colorectal cancer. Br J Surg (2006) 93(8):921–8. doi: 10.1002/bjs.5430
8. Kuhry E, Schwenk W, Gaupset R, Romild U, Bonjer J. Long-term outcome of laparoscopic surgery for colorectal cancer: A cochrane systematic review of randomised controlled trials. Cancer Treat Rev (2008) 34(6):498–504. doi: 10.1016/j.ctrv.2008.03.011
9. Fujii S, Tsukamoto M, Fukushima Y, Shimada R, Okamoto K, Tsuchiya T, et al. Systematic review of laparoscopic vs open surgery for colorectal cancer in elderly patients. World J Gastrointest Oncol (2016) 8(7):573–82. doi: 10.4251/wjgo.v8.i7.573
10. Morneau M, Boulanger J, Charlebois P, Latulippe JF, Lougnarath R, Thibault C, et al. Laparoscopic versus open surgery for the treatment of colorectal cancer: A literature review and recommendations from the comité De L’évolution des pratiques en oncologie. Can J Surg J canadien chirurgie (2013) 56(5):297–310. doi: 10.1503/cjs.005512
11. Conticchio M, Papagni V, Notarnicola M, Delvecchio A, Riccelli U, Ammendola M, et al. Laparoscopic vs. Open mesorectal excision for rectal cancer: are these approaches still comparable? A systematic review and meta-analysis. PloS One (2020) 15(7):e0235887. doi: 10.1371/journal.pone.0235887
12. Nacul MP. Laparoscopy & Robotics: A historical parallel. Rev do Colegio Brasileiro Cirurgioes (2020) 47:e20202811. doi: 10.1590/0100-6991e-20202811
13. Kim CW, Kim CH, Baik SH. Outcomes of robotic-assisted colorectal surgery compared with laparoscopic and open surgery: A systematic review. J Gastrointestinal surgery: Off J Soc Surg Alimentary Tract (2014) 18(4):816–30. doi: 10.1007/s11605-014-2469-5
14. Guillou PJ, Quirke P, Thorpe H, Walker J, Jayne DG, Smith AM, et al. Short-term endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (Mrc clasicc trial): multicentre, randomised controlled trial. Lancet (London England) (2005) 365(9472):1718–26. doi: 10.1016/s0140-6736(05)66545-2
15. Jayne DG, Thorpe HC, Copeland J, Quirke P, Brown JM, Guillou PJ. Five-year follow-up of the medical research council clasicc trial of laparoscopically assisted versus open surgery for colorectal cancer. Br J Surg (2010) 97(11):1638–45. doi: 10.1002/bjs.7160
16. Jeong SY, Park JW, Nam BH, Kim S, Kang SB, Lim SB, 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(7):767–74. doi: 10.1016/s1470-2045(14)70205-0
17. van der Pas MH, Haglind E, Cuesta MA, Fürst A, Lacy AM, Hop WC, et al. Laparoscopic versus open surgery for rectal cancer (Color ii): short-term outcomes of a randomised, phase 3 trial. Lancet Oncol (2013) 14(3):210–8. doi: 10.1016/s1470-2045(13)70016-0
18. Chen ST, Wu MC, Hsu TC, Yen DW, Chang CN, Hsu WT, et al. Comparison of outcome and cost among open, laparoscopic, and robotic surgical treatments for rectal cancer: A propensity score matched analysis of nationwide inpatient sample data. J Surg Oncol (2018) 117(3):497–505. doi: 10.1002/jso.24867
19. Sun Z, Kim J, Adam MA, Nussbaum DP, Speicher PJ, Mantyh CR, et al. Minimally invasive versus open low anterior resection: equivalent survival in a national analysis of 14,033 patients with rectal cancer. Ann Surg (2016) 263(6):1152–8. doi: 10.1097/sla.0000000000001388
20. Speicher PJ, Englum BR, Ganapathi AM, Nussbaum DP, Mantyh CR, Migaly J. Robotic low anterior resection for rectal cancer: A national perspective on short-term oncologic outcomes. Ann Surg (2015) 262(6):1040–5. doi: 10.1097/sla.0000000000001017
21. Baek SJ, Al-Asari S, Jeong DH, Hur H, Min BS, Baik SH, et al. Robotic versus laparoscopic coloanal anastomosis with or without intersphincteric resection for rectal cancer. Surg Endoscopy (2013) 27(11):4157–63. doi: 10.1007/s00464-013-3014-4
22. Yamaguchi T, Kinugasa Y, Shiomi A, Tomioka H, Kagawa H, Yamakawa Y. Robotic-assisted vs. Conventional laparoscopic surgery for rectal cancer: short-term outcomes at a single center. Surg Today (2016) 46(8):957–62. doi: 10.1007/s00595-015-1266-4
23. Ravindra C, Igweonu-Nwakile EO, Ali S, Paul S, Yakkali S, Teresa Selvin S, et al. Comparison of non-oncological postoperative outcomes following robotic and laparoscopic colorectal resection for colorectal Malignancy: A systematic review and meta-analysis. Cureus (2022) 14(7):e27015. doi: 10.7759/cureus.27015
24. Yang L, Fang C, Bi T, Han J, Zhang R, Zhou S. Efficacy of robot-assisted vs. Laparoscopy surgery in the treatment of colorectal cancer: A systematic review and meta-analysis. Clinics Res Hepatol Gastroenterol (2023) 47(7):102176. doi: 10.1016/j.clinre.2023.102176
25. Cuk P, Kjær MD, Mogensen CB, Nielsen MF, Pedersen AK, Ellebæk MB. Short-term outcomes in robot-assisted compared to laparoscopic colon cancer resections: A systematic review and meta-analysis. Surg Endoscopy (2022) 36(1):32–46. doi: 10.1007/s00464-021-08782-7
26. Page MJ, Mckenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. J Clin Epidemiol (2021) 134:178–89. doi: 10.1016/j.jclinepi.2021.03.001
27. Swartz MK. Prisma 2020: an update. J Pediatr Health care: Off Publ Natl Assoc Pediatr Nurse Associates Practitioners (2021) 35(4):351. doi: 10.1016/j.pedhc.2021.04.011
28. Aslam S, Emmanuel P. Formulating a researchable question: A critical step for facilitating good clinical research. Indian J Sex Transm Dis AIDS (2010) 31(1):47–50. doi: 10.4103/0253-7184.69003
29. Cumpston MS, JMcKenzie JE, Welch VA, Brennan SE. Strengthening systematic reviews in public health: guidance in the Cochrane Handbook for Systematic Reviews of Interventions, 2nd edition. J Public Health (2022) 44(4):e588–92. doi: 10.1093/pubmed/fdac036
30. Baik SH, Kwon HY, Kim JS, Hur H, Sohn SK, Cho CH, et al. Robotic versus laparoscopic low anterior resection of rectal cancer: short-term outcome of a prospective comparative study. Ann Surg Oncol (2009) 16(6):1480–7. doi: 10.1245/s10434-009-0435-3
31. Kim MJ, Park SC, Park JW, Chang HJ, Kim DY, Nam BH, et al. Robot-assisted versus laparoscopic surgery for rectal cancer: A phase ii open label prospective randomized controlled trial. Ann Surg (2018) 267(2):243–51. doi: 10.1097/sla.0000000000002321
32. Tang B, Gao GM, Zou Z, Liu DN, Tang C, Jiang QG, et al. [Efficacy comparison between robot-assisted and laparoscopic surgery for mid-low rectal cancer: A prospective randomized controlled trial]. Zhonghua wei chang wai ke za zhi = Chin J gastrointestinal Surg (2020) 23(4):377–83. doi: 10.3760/cma.j.cn.441530-20190401-00135
33. Debakey Y, Zaghloul A, Farag A, Mahmoud A, Elattar I. Robotic-assisted versus conventional laparoscopic approach for rectal cancer surgery, first Egyptian academic center experience, rct. Minimally Invasive Surg (2018) 2018:5836562. doi: 10.1155/2018/5836562
34. Jiménez Rodríguez RM, Díaz Pavón JM, de la Portilla de Juan F, Prendes Sillero E, Hisnard Cadet Dussort JM, Padillo J. [Prospective randomised study: robotic-assisted versus conventional laparoscopic surgery in colorectal cancer resection]. Cirugia Espanola (2011) 89(7):432–8. doi: 10.1016/j.ciresp.2011.01.017
35. Park JS, Lee SM, Choi GS, Park SY, Kim HJ, Song SH, et al. Comparison of laparoscopic versus robot-assisted surgery for rectal cancers: the colrar randomized controlled trial. Ann Surg (2023) 278(1):31–8. doi: 10.1097/sla.0000000000005788
36. Feng Q, Yuan W, Li T, Tang B, Jia B, Zhou Y, et al. Robotic versus laparoscopic surgery for middle and low rectal cancer (Real): short-term outcomes of a multicentre randomised controlled trial. Lancet Gastroenterol Hepatol (2022) 7(11):991–1004. doi: 10.1016/s2468-1253(22)00248-5
37. Feng Q, Tang W, Zhang Z, Wei Y, Ren L, Chang W, et al. Robotic versus laparoscopic abdominoperineal resections for low rectal cancer: A single-center randomized controlled trial. J Surg Oncol (2022) 126(8):1481–93. doi: 10.1002/jso.27076
38. Ng KT, Tsia AKV, Chong VYL. Robotic versus conventional laparoscopic surgery for colorectal cancer: A systematic review and meta-analysis with trial sequential analysis. World J Surg (2019) 43(4):1146–61. doi: 10.1007/s00268-018-04896-7
39. Park JS, Kang H, Park SY, Kim HJ, Woo IT, Park IK, et al. Long-term oncologic after robotic versus laparoscopic right colectomy: A prospective randomized study. Surg Endoscopy (2019) 33(9):2975–81. doi: 10.1007/s00464-018-6563-8
40. Jayne D, Pigazzi A, Marshall H, Croft J, Corrigan N, Copeland J, et al. Effect of robotic-assisted vs conventional laparoscopic surgery on risk of conversion to open laparotomy among patients undergoing resection for rectal cancer: the rolarr randomized clinical trial. Jama (2017) 318(16):1569–80. doi: 10.1001/jama.2017.7219
41. Corrigan N, Marshall H, Croft J, Copeland J, Jayne D, Brown J. Exploring and adjusting for potential learning effects in rolarr: A randomised controlled trial comparing robotic-assisted vs. Standard laparoscopic surgery for rectal cancer resection. Trials (2018) 19(1):339. doi: 10.1186/s13063-018-2726-0
42. Szold A, Bergamaschi R, Broeders I, Dankelman J, Forgione A, Langø T, et al. European association of endoscopic surgeons (Eaes) consensus statement on the use of robotics in general surgery. Surg Endoscopy (2015) 29(2):253–88. doi: 10.1007/s00464-014-3916-9
43. Teljeur C, O’Neill M, Moran PS, Harrington P, Flattery M, Murphy L, et al. Economic evaluation of robot-assisted hysterectomy: A cost-minimisation analysis. BJOG: an Int J Obstet Gynaecol (2014) 121(12):1546–53. doi: 10.1111/1471-0528.12836
44. Kim HJ, Choi GS, Park JS, Park SY, Lee HJ, Woo IT, et al. Selective lateral pelvic lymph node dissection: A comparative study of the robotic versus laparoscopic approach. Surg Endoscopy (2018) 32(5):2466–73. doi: 10.1007/s00464-017-5948-4
45. Najarian S, Fallahnezhad M, Afshari E. Advances in medical robotic systems with specific applications in surgery–a review. J Med Eng Technol (2011) 35(1):19–33. doi: 10.3109/03091902.2010.535593
46. de’Angelis N, Lizzi V, Azoulay D, Brunetti F. Robotic versus laparoscopic right colectomy for colon cancer: analysis of the initial simultaneous learning curve of a surgical fellow. J Laparoendosc Adv Surg Tech Part A (2016) 26(11):882–92. doi: 10.1089/lap.2016.0321
47. Chok AY, Zhao Y, Tan IE, Au MKH, Tan E. Cost-effectiveness comparison of minimally invasive, robotic and open approaches in colorectal surgery: A systematic review and bayesian network meta-analysis of randomized clinical trials. Int J Colorectal Dis (2023) 38(1):86. doi: 10.1007/s00384-023-04361-5
48. Wee IJY, Kuo LJ, Ngu JC. The impact of robotic colorectal surgery in obese patients: A systematic review, meta-analysis, and meta-regression. Surg Endoscopy (2019) 33(11):3558–66. doi: 10.1007/s00464-019-07000-9
49. Wilder FG, Burnett A, Oliver J, Demyen MF, Chokshi RJ. A review of the long-term oncologic outcomes of robotic surgery versus laparoscopic surgery for colorectal cancer. Indian J Surg (2016) 78(3):214–9. doi: 10.1007/s12262-015-1375-8
50. Yang Y, Wang F, Zhang P, Shi C, Zou Y, Qin H, et al. Robot-assisted versus conventional laparoscopic surgery for colorectal disease, focusing on rectal cancer: A meta-analysis. Ann Surg Oncol (2012) 19(12):3727–36. doi: 10.1245/s10434-012-2429-9
51. Fung AK, Aly EH. Robotic colonic surgery: is it advisable to commence a new learning curve? Dis Colon Rectum (2013) 56(6):786–96. doi: 10.1097/DCR.0b013e318285b810
52. Rausa E, Kelly ME, Asti E, Aiolfi A, Bonitta G, Bonavina L. Right hemicolectomy: A network meta-analysis comparing open, laparoscopic-assisted, total laparoscopic, and robotic approach. Surg Endoscopy (2019) 33(4):1020–32. doi: 10.1007/s00464-018-6592-3
53. Law WL, Foo DCC. Comparison of short-term and oncologic outcomes of robotic and laparoscopic resection for mid- and distal rectal cancer. Surg Endoscopy (2017) 31(7):2798–807. doi: 10.1007/s00464-016-5289-8
54. Tam MS, Abbass M, Abbas MA. Robotic-laparoscopic rectal cancer excision versus traditional laparoscopy. JSLS: J Soc Laparoendoscopic Surgeons (2014) 18(3):e2014.00020. doi: 10.4293/jsls.2014.00020
55. Sheng S, Zhao T, Wang X. Comparison of robot-assisted surgery, laparoscopic-assisted surgery, and open surgery for the treatment of colorectal cancer: A network meta-analysis. Medicine (2018) 97(34):e11817. doi: 10.1097/md.0000000000011817
56. Prete FP, Pezzolla A, Prete F, Testini M, Marzaioli R, Patriti A, et al. Robotic versus laparoscopic minimally invasive surgery for rectal cancer: A systematic review and meta-analysis of randomized controlled trials. Ann Surg (2018) 267(6):1034–46. doi: 10.1097/sla.0000000000002523
Keywords: robot-assisted colorectal surgery, laparoscopic-assisted colorectal surgery, colorectal cancer, randomized controlled trial, complication
Citation: Huang Z, Huang S, Huang Y, Luo R and Liang W (2023) Comparison of robotic-assisted versus conventional laparoscopic surgery in colorectal cancer resection: a systemic review and meta-analysis of randomized controlled trials. Front. Oncol. 13:1273378. doi: 10.3389/fonc.2023.1273378
Received: 14 August 2023; Accepted: 25 September 2023;
Published: 26 October 2023.
Edited by:
Pasquale Cianci, Azienda Sanitaria Localedella Provincia di Barletta Andri Trani (ASL BT), ItalyReviewed by:
Mario Pacilli, University of Foggia, ItalyAltamura Amedeo, Pia Fondazione di Culto e Religione Card. G. Panico, Italy
Vincenzo Lizzi, Azienda Ospedaliero-Universitaria Ospedali Riuniti di Foggia, Italy
Copyright © 2023 Huang, Huang, Huang, Luo and Liang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Weiming Liang, TGlhbmd3bTIyQGljbG91ZC5jb20=
†These authors have contributed equally to this work