Is Laparoscopic Complete Mesocolic Excision and Central Vascular Ligation Really Necessary for All Patients With Right-Sided Colon Cancer?

Gyung Mo Son; In Young Lee; Yoon Suk Lee; Bong-Hyeon Kye; Hyeon-Min Cho; Je-Ho Jang; Chang-Nam Kim; Kil Yeon Lee; Suk-Hwan Lee; Jun-Gi Kim

doi:10.3393/ac.2021.00955.0136

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Review Is Laparoscopic Complete Mesocolic Excision and Central Vascular Ligation Really Necessary for All Patients With Right-Sided Colon Cancer?: Gyung Mo Son¹, In Young Lee¹, Yoon Suk Lee², Bong-Hyeon Kye³, Hyeon-Min Cho³, Je-Ho Jang⁴, Chang-Nam Kim⁴, Kil Yeon Lee⁵, Suk-Hwan Lee⁶, Jun-Gi Kim^2,7, On behalf of The Korean Laparoscopic Colorectal Surgery Study Group; Annals of Coloproctology 2021;37(6):434-444.
DOI: https://doi.org/10.3393/ac.2021.00955.0136
Published online: December 8, 2021

¹Department of Surgery, Pusan National University Yangsan Hospital, Pusan National University School of Medicine,Yangsan, Korea

²Department of Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

³Division of Colorectal Surgery, Department of Surgery, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea

⁴Department of Surgery, Daejeon Eulji Medical Center, Eulji University School of Medicine, Daejeon, Korea

⁵Department of Surgery, Kyung Hee University College of Medicine, Seoul, Korea

⁶Department of Surgery, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea

⁷Department of Surgery, Pyeongtaek St. Mary’s Hospital, Pyeongtaek, Korea

Correspondence to: Jun-Gi Kim, M.D., Ph.D., Emeritus Professor Department of Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea Tel: +82-2-2258-2876, Fax: +82-2-595-2822, E-mail: 'jgkim@catholic.ac.kr'

• Received: November 5, 2021 • Revised: November 15, 2021 • Accepted: November 15, 2021

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Abstract
INTRODUCTION
MESOCOLIC PLANE SURGERY
LONGITUDINAL EXTENT OF COLON RESECTION
CENTRAL VASCULAR LIGATION
ONCOLOGICAL NECESSITY OF COMPLETE MESOCOLIC EXCISION WITH CENTRAL VASCULAR LIGATION
NOVEL TECHNOLOGY OF LYMPH NODE MAPPING
EVOLUTION OF CANCER METASTASIS THEORY
CONCLUSION
ARTICLE INFORMATION
Acknowledgments
REFERENCES

Abstract

Colon cancer treatment is on the way to evolution over several decades. The minimally invasive surgery has improved postoperative short-term outcomes. Adjuvant chemotherapy has prolonged the survival of advanced colon cancer patients. Hohenberger proposed the noble concept of complete mesocolic excision (CME) which consists of 3 components: plane surgery, sufficient longitudinal bowel resection, and central vascular ligation (CVL). Mesocolic plane surgery shares the same surgical principle of total mesorectal excision, which is maintaining the intact mesothelial envelope. However, there remain debates about the extent of bowel resection and the level of CVL for maximizing lymph node dissection. There is no solid clinical evidence for the oncological necessity and benefit of extended radical dissection in right hemicolectomy. CME with CVL based on open surgery has been adopted in laparoscopic surgery. So, it is also necessary to look at how the CME could be transformed and successfully implanted in the laparoscopic era. Recent rapid advances in surgical technology and cancer biology are preparing for fundamental changes in cancer surgery. In this study, we reviewed the history, oncological necessity, and compatibility of CME for the right hemicolectomy in the laparoscopic era and outline the new perspectives on the evolution of cancer surgery.
Keywords: Colonic neoplasms; Colectomy; Mesocolon; Laparoscopy; Lymph node excision

INTRODUCTION

Colon cancer is one of the most common gastrointestinal cancers. As national cancer screening program is widely conducted, the early diagnosis rate of colon cancer patients is increasing. In the past, more than half of the patients with colon cancer had lymph node metastasis; however recently, the proportion of stage I and II colon cancer patients has increased with early detection [1].

Colon cancer treatment has undergone rapid development over the past several decades. The minimally invasive surgery has improved postoperative short-term outcomes, such as pain, recovery of bowel movement, and length of hospital stay [2]. Adjuvant chemotherapy has prolonged the survival of stage III and stage II patients with high-risk factors [3].

In 1982, total mesorectal excision (TME) was presented by Bill Heald of the United Kingdom as meticulous sharp dissection along the embryologic plane to remove micrometastatic foci that had spread in the mesorectum. As a result, the local recurrence rate of rectal cancer, which previously reached 40%, was reduced to less than 10%. This has been accepted as the most important surgical revolution of the modern century, showing that oncologic benefits can be obtained through improvement of surgical quality in the field of rectal cancer [4].

In 2009, Hohenberger et al. [5] of Erlangen University in Germany proposed the noble concept of complete mesocolic excision (CME) which consists of 3 components: plane surgery, sufficient longitudinal bowel resection, and central vascular ligation (CVL).

Mesocolic plane surgery of CME shares the same surgical principle of TME, which is maintaining the intact mesothelial envelope surrounding the lymphatics to avoid the spread of cancer cells [5]. However, there remain debates about the extent of bowel resection and the level of CVL for maximizing lymph node dissection. There is no solid clinical evidence for the oncological necessity and benefit of extended radical dissection, including central lymph node dissection, in right hemicolectomy.

Originally, CME was performed on the basis of open surgery, which completely exposed the superior mesenteric vascular structure and removed the central lymph nodes. So, it is also necessary to look at how the CME could be transformed and successfully implanted in the laparoscopic era. Recently, cancer biology is on way of evolution to help us deeper understand the mechanism of cancer metastasis, which is gradually approaching as great wave of fundamental change in cancer surgery.

In this article, we reviewed the history, oncological necessity, and compatibility of CME for the right hemicolectomy in the laparoscopic era and outline the new perspectives on evolution of cancer surgery that reflect the advances in surgical technology and cancer biology.

MESOCOLIC PLANE SURGERY

CME as mesocolic plane surgery has similar concept to TME as maintaining the intact mesocolic plane using the sharp dissection along Toldt’s fascia. In the pathologic study comparing the quality of mesocolic plane surgery, West et al. [5] and Philip Quirke [6] showed a statistically significant survival difference in the intact mesocolon group compared to the incomplete mesocolon group with exposure of the muscularis propria. Although high-quality evidence is lacking due to the paucity of randomized controlled trials (RCT) for CME, surgeons have strong beliefs about the importance of mesocolic plane surgery and its potential oncological benefits. In the meta-analysis, CME has continued to derive excellent oncological results (Table 1) [7-10].

In traditional colon cancer surgery, Turnbull’s no-touch technique had been widely accepted as a principle of surgical treatment to prevent cancer cell spillage, even if there is no solid evidence supporting this inspirational principle. In surgical training, professor’s emphasis had been placed on the embryological surgical plan, Toldt’s fascia, acting as a landmark for hemicolectomy. Born in Austria in 1840, Carl Florian Toldt was appointed professor of anatomy at the University of Vienna and later professor at the German University in Prague, Hungary. Over 100 years ago, Toldt asserted that the mesocolon could be separated from the retroperitoneum with a thin fascia [11]. However, Frederick Treves of the United Kingdom, a great leader in surgical anatomy at that time, argued that cadaveric research demonstrated that the mesocolon was merged into the retroperitoneum and could not be anatomically separated. The argument continued for a long time until the end of the 20th century. However, with the surgeon’s recognition of the existence of the mesocolon, Toldt’s fascia has maintained its reputation as a landmark of dissection for colectomy in the real surgical field. Recently, electron microscopy has proven that Toldt’s fascia is composed of multiple mesothelial cell layers. Intensive studies by Cullingan et al. [12, 13] in Dublin, Ireland, on the structure of the mesocolon ended the 100-year debate between Toldt and Treves. Therefore, as Hogan and Winter [14] argued, CME had been built on the basis of a long history of colon surgery with careful mesocolic dissection along Toldt’s fascia. However, it was only in the 21st century that the surgical society coined the term CME as a novel and attractive nomenclature to describe the long tradition of mesocolic plane surgery.

The conceptualization of CME could provide standardized surgical quality and enable objective analysis through quantification of surgical treatment. Mesocolic plane surgery enables the quantitative evaluation of surgical quality through pathological evaluation. The mesorectal dissection quality of TME can be evaluated by pathologists as an analysis index for surgical quality and as an indicator of the oncological prognosis [15]. Therefore, CME could be accepted as a pathologic assessment tool for the evaluation of oncologic dissection quality, and it is already serving as an opportunity to standardize and improve surgical quality. This can be said to be an inevitable developmental stage necessary for the improvement and standardization of surgery in the era of evidencebased medicine.

LONGITUDINAL EXTENT OF COLON RESECTION

Hohenberger’s CME could secure a proximal resection margin of approximately 10 cm from the ileocecal valve and a distal resection margin of 10 cm or more on the distal side of the tumor to excise sufficient longitudinal length of colon [14].

Radical resection was based on the long-standing surgeon’s belief of the curative surgery with sufficient longitudinal margin. Grinnell [16], a surgeon and pathologist working at Columbia University in New York in the 1940s, proved the existence of tumor emboli in the lymphatic channels as a pathological tissue and confirmed the spread of cancer cells along the lymphatic chains. Furthermore, when the lymph nodes around the cancer were occupied by cancer cells and the lymphatic flow was blocked, retrograde lymphatic backflow occurred through the paracolic lymph node, and metastasis could reach the distant paracolic lymph node from primary tumors more than 10 cm. Therefore, vertical lymphatic flow toward the apical lymph node as well as retrograde horizontal lymphatic flow along the longitudinal axis of the colon was suggested as important pathways for lymph node metastasis [17].

Due to the observation of these lymph node metastasis patterns, it was argued that it was crucial to secure sufficient proximal and distal resection margins for radical resection and to perform high ligation along the feeding vessel as much as possible. This anatomical and pathological study of colorectal cancer metastasis pattern raised great expectations that curative surgery could be possible with extended radical resection for cancer patients suffering from a very low survival rate in the early 20th century. The expectation and hope for such a curative cancer operation led to enthusiasm for extended radical resection among brave and passionate surgeons. However, in the 1960s, the long-term survival results of extended radical resection were reported as comparable to those of segmental resection for colon cancer [18].

Disappointingly, there was no survival benefit of extended radical resection. In particular, most patients who had radical resection for the apical lymph node metastasis did not survive by critical cancer recurrence [19]. Based on these disappointing long-term survival results, central lymph node involvement was considered as the gate of systemic metastasis in which surgical salvage was impossible. As a result, when extended radical resection failed to salvage colon cancer patients, surgeons’ enthusiasm for extended radical resection began to diminish in the Western surgical society.

CME with CVL and the Japanese D3 lymph node dissection are very similar concepts, but there is a difference of longitudinal length in the proximal and distal resection margins between the 2 surgical methods. In Japan, most metastatic foci were distributed within 5 cm of the tumor in the pathologic study of metastatic lymph node location, so it has been considered sufficient to secure a resection margin of 5 cm on both sides. Therefore, in pathologic specimens from Erlangen and Tokyo resected bowel length, mesenteric area, and harvested lymph nodes were higher in the German CME group than Japanese D3 group. However, there was no difference in the long-term oncologic outcomes of colorectal cancer between the 2 study groups [20, 21]. In addition, there are many studies that showed that there was no significant difference in the therapeutic effect of conventional radical resection and extended radical resection for colon cancer surgery [22-25].

Therefore, maintaining the intact mesocolic plane in CME is accepted as an important factor, but long resection margin greater than 10 cm from the primary tumor can be considered selectively depending on the location of the tumor, its relationship to the feeding vessel, and the spread of lymph node metastasis (Fig. 1).

CENTRAL VASCULAR LIGATION

CVL is performed for completion of mesocolon resection extending to mesenteric vascular root on the superior mesenteric artery (SMA) and superior mesenteric vein (SMV). For radical lymph node dissection, vascular ligation should be performed at the origin of the feeding arteries, the ileocolic, right colic, and middle colic arteries in right-sided colon cancer. This CVL is similar to the concept of D3 dissection in the Japanese Society of Cancer of the Colon and Rectum (JSCCR) guidelines [26].

The lymphatic pathway of the colon was published in detail by Jamieson and Dobson [27-29] at Leeds University in the United Kingdom in the early 20th century. They injected Prussian blue into the colon wall of cadavers and observed the dye flowing along the lymphatics and staining the lymph nodes. In these studies, they showed that colon cancer cells could spread out of the colon wall to regional lymph nodes, highlighting the need for radical lymph node dissection [27-29]. In a recent study using cadavers, Spasojevic et al. [30] divided the right, anterior, and posterior sections of D3 area around the SMV and SMA trunk to collect and count the associated lymph nodes. They found that 3 to 5 lymph nodes were present anterior and posterior to the SMV and SMA trunk, respectively. Therefore, as posterior dissection of the SMV and ileocolic artery retraction is required to remove all the main lymph nodes around the ileocolic artery root, the argument is that a more enlarged SMV dissection is necessary for true D3 dissection.

Unlike the manifest anatomical concept of CVL, the clinical definition of CVL is ambiguous and the surgical standard has not been established. The various surgical techniques used the different surgical landmarks to determine the boundary of main lymph node dissection depending on surgeon’s expertise and preference. The level of CVL could be classified as the right side of the SMV, the interface between the SMV and SMA, or the left border of the SMA [31]. However, disagreements about the optimal CVL level to achieve patient safety and oncological radicality remain unresolved.

Interestingly, it has been reported that even if CME was described in the operation report, there were many cases in which true ligation was not achieved at the feeding artery root depending on the variation in the mesenteric vasculature. Kaye et al. [32] analyzed postoperative computed tomography (CT) scan to examine the remaining ileocolic artery stumps in patients who underwent right hemicolectomy. The arterial stump on CT angiography might be assumed that the apical lymph node dissection might be insufficient in some patients. Therefore, since true D3 dissection is sometimes really difficult to perform, most surgeons consider D3 dissection to be complete even if performing arterial ligation on the right side of the SMV, especially in laparoscopic CME.

In real surgical practice, the most common procedure implementing CVL is based on Gillot’s concept of a surgical trunk of SMV. In 1964, Gillot [33] in France had named the area on the right side of the SMV between the gastrocolic trunk and the ileocolic vein as the surgical trunk as an anatomical landmark. Since lymphatics from the right colon collect in the surgical trunk and drain into the central lymphatic system, radical lymph node dissection for locoregional control that included the surgical trunk area was accepted. In 1995, Toyota et al. [34] explained that lymphatic flow in the right-sided colon forms a lymphatic chain on the right lateral side of the SMV that runs along the periportal lymphatics, with some lymphatic connections extending to the SMA lymph node at the root of the middle colic artery. Therefore, they said that D3 dissection can be sufficiently achieved by dissecting the central lymph node from the right lateral and anterior sides of the SMV.

Here, we can recognize that there is a practical gap between the anatomical concept of CVL and the clinically accepted scope of D3 dissection. It remains unclear whether it is sufficient to dissect the lymph nodes around the surgical trunk, or whether the extended dissection of both the anterior and posterior SMA is necessary for true D3 dissection. Until now, there is no solid clinical evidence for the oncological necessity and benefit of extended radical dissection, including central lymph node dissection, in right hemicolectomy (Fig. 2).

In the current ongoing RCTs, the definitions of D2 and D3 are almost the same as those in the JSCCR guidelines. In the COLD study, D3 node dissection is performed to expose the anterior surface of the SMV. In addition, vascular ligation should be performed at the arterial root by exposing the space between the SMA and SMV and performing SMA visualization. In the RELARC study, D3 dissection exposes the SMV anterior surface, but the boundary between the SMA and SMV is the delamination line. Therefore, anterior dissection of the SMA is not included in the D3 dissection. Even in this prospective study, the clear anatomical extent of D3 dissection is somewhat different. Nevertheless, surgeons expect that the long-term outcome of ongoing RCTs will provide a definite guideline for reasonable application of CVL in the near future (Table 2).

Compatibility of laparoscopic CME with CVL

Minimally invasive surgery has brought about a great change in the field of colon cancer surgery [35-37].

With laparoscopic or robotic surgery, faster postoperative recovery, reduced pain, and a quick return to daily life became possible. The large-scale RCTs, including the COST, COLOR, and MRC-CLASICC trials, gave clear answers to questions about whether long-term oncological outcomes did not deteriorate after laparoscopic surgery. These studies proved that laparoscopic surgery is an oncologically safe procedure for colon cancer [38-40].

Actually, CME with CVL was designed as an open surgery because it requires extended radical vascular dissection. Hence, there are still doubts as to whether CME with CVL can be safely performed in laparoscopic surgery. Since the approach for mesenteric dissection and CVL in laparoscopic surgery is different from that of open surgery, various laparoscopic surgical techniques have been devised like a bottom-up, cranial-caudal, or arterial first approach [41-48]. In a recent meta-analysis, laparoscopic CME had comparable outcomes in harvested lymph nodes, longitudinal bowel length, mesenteric area, and vertical margin to open CME. In addition, long-term survival was not different between laparoscopic and open CME. Therefore, laparoscopic CME could also be performed safely with acceptable oncological outcomes [49-51].

As the surgeons’ understanding of mesenteric vascular variation deepened and D3 dissection was actively attempted in the daily surgical practice field, it was found that various anomalies of the feeding artery and draining vein were quite common in the right colon region. The ileocolic artery is present in almost all patients; in 40%, it passes anteriorly to the SMV and travels to the right and in 60%, it branches from the SMA and proceeds posteriorly to the SMV [41, 52-54].

According to the definition of manifest D3 dissection in the JSCCR guidelines and the concept of CME with CVL, vascular ligation should be performed at the root of the feeding artery. If the ileocolic artery proceeds posteriorly to the SMV, the ileocolic root could be found after drastic retraction of fully mobilized SMV. Since laparoscopic surgery approaches the anterior chamber of the mesentery, dissection of the central lymph node anterior to the SMV and SMA can be performed relatively easily. Ligation of the ileocolic arterial root can be performed where the artery crosses the anterior chamber of SMV. However, dissecting the posterior SMV, retracting it to the left, and removing the central lymph node posterior to the SMV is a quite difficult operation. Dissection to the posterior surface of the SMV must be a dangerous operation that can cause crucial vascular injury [55, 56]. In a recent study, the risk of vascular injury was 3-fold higher in the CME surgical group with full exposure to SMV [57]. Furthermore, the excessive SMA denuding can also cause damage to the autonomic nerve plexus supplying the small intestine, resulting in postoperative sequelae, such as diarrhea [34].

Because lymphatic flow in the right colon gathers from the surgical trunk on the right side of the SMV, and the lymph nodes anterior to the SMA are mainly connected with the lymphatics in the jejunum, SMA dissection beyond the anterior surface of the SMV is not required for lymph node dissection for right colon cancer [34]. Therefore, complete SMV dissection is usually beyond the scope of D3 lymph node dissection.

Literally, strict CVL can be detrimental overtreatment in patients without suspected metastatic lymph node on D3 area. That just increases the risk of vascular and neural damage to variant branch complex of the SMV. Furthermore, there is no clear oncologic benefit for strict CVL as an essential procedure. Therefore, complete CVL should be performed selectively by experienced surgeons in patients with suspected metastasis on the central lymph node [58, 59].

ONCOLOGICAL NECESSITY OF COMPLETE MESOCOLIC EXCISION WITH CENTRAL VASCULAR LIGATION

The number and location of involved lymph nodes and the metastatic lymph node ratio are known to be significant prognostic factors. In Japan, after colon resection, a surgeon extracts the lymph nodes from the specimen and marks the location of the resection. In a study on the metastatic lymph node distributions, D3 lymph node involvement showed a poorer prognosis than D1 lymph nodes [60]. In contrast, in some studies, the number of lymph nodes involved reflected more important clinical prognosis than the location of lymph node metastasis. Most patients with central lymph node involvement already have paracolic lymph node metastasis, and in these cases, apical lymph node metastasis tends to be considered clinically distant metastasis [61]. Therefore, in the presence of multiple lymph node metastases, lymph node involvement number and location are considered as definite poor prognostic factor. Interestingly, single lymph node metastasis has a very good prognosis. Even if a single lymph node metastasis is skip metastasis in the main lymph node area, a good prognosis can be expected regardless of location. This is homogenous to surgical resection, which has a curative therapeutic effect in single distant metastasis [62].

Surgeons need to determine whether to expand lymph node dissection with preoperative imaging. The diagnostic accuracy of preoperative CT is limited in predicting lymph node metastasis. Although the size, round shape, and heterogeneous texture of the lymph nodes increase the likelihood of metastatic lymph nodes, CT scans are not reliable for preoperative lymph node staging because metastatic nodes smaller than 3 to 5 mm are also commonly found. As the depth of the tumor invasion increases, the risk of lymph node metastasis increases [63]. Preoperative CT has negligible accuracy in diagnosing T1–2; however, the diagnosis rate of T3–4 is quite reliable. Therefore, the preoperative T stage plays an important role in determining the extent of lymph node dissection. Since the probability of D3 lymph node metastasis in T3–4 is high as 10%, the JSCCR guidelines recommend D3 dissection in T3–4 patients [27].

Although surgeons are currently performing radical lymph node resections, scientific evidence for the therapeutic benefit of extended radical lymph node dissection is lacking. The radicality of lymph node dissection can be assessed by the number of harvested lymph nodes along with the location of lymph node dissection. In patients with nonmetastatic colon cancer, the higher the number of harvested lymph nodes, the better the oncological prognosis. The ratio of the involved lymph nodes to the harvested lymph nodes was identified as a strong prognostic indicator in stage III patients [64, 65]. Although it is true that the removal of more lymph nodes by extended radical lymph node dissection is reflecting favorable prognosis, it requires considerable caution in interpreting this correlation as a cause-and-effect relationship. The number of harvested lymph nodes is not only related to resection radicality but also to tumor factors such as tumor size, T status, lymphocyte infiltration, and poorly differentiated microsatellite instability. The size of the hospital, surgeon’s expertise, and pathological evaluation protocol are also related. The patient’s age, body mass index, and the presence of a chronic bowel infection or inflammatory condition also affect the harvested lymph nodes [66, 67]. It is interesting to note that the number of harvested lymph nodes is related to these various factors, and since these factors are also affecting prognosis, it is difficult to conclude that a large number of harvested lymph nodes is the cause of the positive prognosis.

The scientific mechanism remains unclear to prove that a better oncological prognosis with an increase in the number of harvested lymph nodes. Until now, several possible reasons are being investigated.

First, the most notable reason was the effect of adjuvant chemotherapy on staging migration. The prognosis was better in the patient group with 20 or more resected lymph nodes than in patients with fewer than 5 harvested lymph nodes [68, 69]. The pathological diagnosis of metastatic lymph nodes may not have been possible due to insufficient lymph node dissection, and thus the treatment opportunity for adjuvant chemotherapy may have been missed. Appropriate chemotherapy with sufficient lymph node dissection may lead to improved survival rates resulting from more accurate nodal staging. The effect of staging migration, which has been considered the most important cause to date, has been minimized in several studies [70]. A population-based colon cancer registry study in Canada reported that the number of harvested lymph nodes has increased in recent years, but the proportion of metastatic lymph nodes has not changed [68]. Therefore, the therapeutic effect of harvested lymph node numbers may be achieved by different mechanisms.

Second, radical resection may have a therapeutic effect by removing occult metastatic lymph nodes. In pathological evaluations of lymph nodes, metastasis of cancer cells is usually evaluated by hematoxylin and eosin staining in 1 to 2 sections. In this conventional pathological lymph node evaluation protocol, occult metastasis could not be detected. Nodes that appear negative for metastases in hematoxylin and eosin staining revealed isolated tumor cells or micrometastases in 30% of cases when immunohistochemical staining using pan-cytokeratin was performed. Real-time polymerase chain reaction (RT-PCR) can increase occult metastatic lymph node detection by up to 40%. However, the pathological methodology for occult metastatic lymph nodes detection is still diverse and not standardized. Additional analyses, such as immunofluorescence staining and RT-PCR, require a large amount of medical resources. Some studies show contradictory results about patient’s prognoses with isolated tumor cells [71]. This is likely to be the result of a change in the level of oncological threat posed by the isolated tumor cells according to the patient’s immune response, rather than the therapeutic effect of micrometastasis resection itself [72].

Third, harvested lymph node number can be interpreted as an indicator of the patient’s immune response to colon cancer. The greater the lymphocyte infiltration in the tumor and the more tumor antigen expression relating to microsatellite instability, the greater the immune response and the immunological defense against cancer. A strong immune response may be manifested by an increase in the number of harvested lymph nodes after surgery [73]. Since various questions about the therapeutic effect of harvested lymph nodes remain, contemporary surgeons are still performing radical D3 dissection, and the oncological necessity of CME with CVL remains valid to date.

NOVEL TECHNOLOGY OF LYMPH NODE MAPPING

Recently, fluorescence-guided lymph node mapping (FLNM) has been developed as a promising surgical approach for image-guided surgery and has been approved the effect of increasing the number of harvested lymph nodes. When fluorescence dye, indocyanine green (ICG), is injected into the colonic wall, it enters the lymphatic drainage system from the distal perivascular space [74]. In colon cancer surgery, FLNM helps the surgeon visualize the lymphatic pathway to perform a more accurate dissection of the lymph nodes, especially around the main surgical trunk. Interestingly, the FLNM technique can increase the total number of harvested lymph nodes [75, 76]. When visualizing the lymph nodes and lymphatic drainage pathway directly, the surgeon can dissect lymph nodes much more radically. When a fluorescent lymph node is found in the extraterritorial area outside the conventional radical dissection plane, a surgeon can extend the dissecting plane selectively for complete fluorescent lymph node removal. From an oncological point of view, at least 12 lymph nodes should be retrieved to evaluate the pathological stage of cancer so that patients can receive appropriate chemotherapy after surgery. The FLNM procedure is beneficial in harvesting more than 12 lymph nodes, and it can function as a surgical safety tool for the retrieval of an adequate number of lymph nodes for proper pathological staging [77].

Sentinel lymph node (SLN) mapping is a preliminary procedure for determining radical or selective lymph node dissection. It is an established technique in breast cancer and malignant melanoma to reduce postoperative complications due to radical resection. The concept of the SLN is the initial drainage of hypothetical lymph nodes from primary cancer. In many fields of cancer treatment, radioisotopes, blue dyes, and fluorescence dyes are used. The success rate of lymph node mapping using blue dye or radioisotopes is not satisfactory [78]. With the development of near-infrared camera systems, FLNM has been adopted for the detection of SLNs. The success rate of FLNM through colonoscopic submucosal ICG injection was over 90% [77].

In breast cancer and malignant melanoma, lymphatic drainage has a conduit or funnel-shaped pattern passing through 1 or 2 sentinel nodes as the first echelon lymph nodes, and metastatic cancer cells can spread into the second and third echelon lymph nodes. However, in colon cancer, lymphatic flow can be spread through various routes through the complex lymphatic network rather than through a linear connection, SLN mapping has many limitations in assessing the overall condition of lymph node metastasis [79].

There are still many questions to be answered, but further advances in fluorescence image-guided surgery could establish the basis for SLN mapping and enable the determination of expansion of radical lymphadenectomy, especially in early colon cancer.

EVOLUTION OF CANCER METASTASIS THEORY

The concept of cancer metastasis has rapidly evolved in recent years. According to the linear progression theory proposed by William Stewart Halsted more than 100 years ago, cancer cells of primary tumors reach the apical lymph node along the adjacent lymph node pathway, which leads to distant metastasis [80, 81]. This linear metastasis pathway has been established as a fundamental concept in the current TNM staging. It is also a prognostic factor that accurately reflects the prognosis of most patients. However, skip metastasis, which occurs in 4% to 5% of patients, is an exception to the linear progression model. It is difficult to explain why distant metastasis still occurs in 20% to 30% of patients undergoing successful radical resection in the early stage [82]. Although the linear metastasis model is a concept that supports the therapeutic effect of curative radical resection, the oncologic results that radical resection itself does not achieve superior oncological outcomes compared to segmental resection raises doubts about the drawback of the radical resection.

In recent studies on metastasis, a parallel progression theory has been proposed whereby cancer cell metastasis already occurs at an early stage [83]. In colon cancer, micrometastasis of lymph nodes, circulating cancer cells in the peripheral blood, and micrometastasis of bone marrow are also found in the early stage, and such early micrometastasis causes poor prognosis. In addition, by analyzing cancer cell lines of metastatic foci as well as primary tumors, it was found that they consist of polyclonal cancer cells, not monoclonal cell line. This means that the polyclonal cancer cells of the primary tumor undergo seeding in multiple, continuous waves of metastasis [84]. The fact that cancer cells constituting primary tumors and metastatic lesions are heterogenous, polyclonal populations with genetically variable mutations explains why surviving cancer cells cause recurrence even after chemotherapy.

This polyclonal cancer cell population is a phenomenon that results from parallel progression. The recent understanding of this mechanism of cancer metastasis has heralded a change in the future of cancer treatment. The role of extended radical resection, which is currently being applied for locoregional cancer control, could be changed to improve the accuracy of the molecular pathologic diagnosis. In addition, the evaluation of circulating tumor cells in peripheral blood, circulating cell-free DNA, and micrometastasis of the bone marrow can be used to predict cancer metastasis and prognosis, as well as characterizing heterogeneous cancer cells through single-cell DNA sequencing [85]. Furthermore, by analyzing various gene mutations in the polyclonal cancer cell population, strategies for patient-tailored treatment can be established.

CONCLUSION

In conclusion, CME as mesocolic plane surgery is considered as one of oncologic surgical principles. The anatomical landmark for CVL is ambiguous and the oncological benefit is not yet clear. The ongoing RCTs will provide the answer for the necessity and radicality of CVL. The advances in surgical technology and cancer biology will come to the surgical society as a great wave demanding fundamental reformation of radical cancer surgery in the near future.

ARTICLE INFORMATION

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

Acknowledgments

The Authors thank to all members of The Korean Laparoscopic Colorectal Surgery Study Group in the Korean Society of Coloproctology.

Fig. 1.

Grouping of the retrieved lymph nodes (LN). Adapted from Yang et al. [31], according to the Creative Commons License of open access.

Fig. 2.

Lymphatics of the right colon. a, superior mesenteric vein; b, superior mesenteric artery; c, main nodes; d, middle colic artery; e, middle colic vein; f, right colic artery and vein; g, ileocolic artery and vein; h, superior mesenteric node; i, Henle’s gastrocolic trunk; j, right gastroepiploic vein. Adapted from Toyota et al. [34], with permission of Wolters Kluwer Health, Inc.

Table 1.

Short-term and long-term outcomes of CME and non-CME for colon cancer surgery comparing by meta-analysis

Study	Year	No. of patients	CME vs. non-CME	Complication^a	Lymph node yield^b	Bowel length^b	Local recurrence^a	DFS^a	OS^a
Kong et al. [7]	2021	25,886	14,431 (56.2)	3 (1.56–5.76)	NA	0.29 (–0.24–0.82)	0.66 (0.52–0.83)	0.82 (0.77–0.87)	1.16 (0.89–1.66)
Kong et al. [7]	2021	25,886	11,455 (43.8)	P = 0.006	NA	P = 0.283	0.66 (0.52–0.83)	P < 0.001	P = 0.335
Crane et al. [8]	2021	26,640	13,830 (51.9)	1.06 (0.97–1.14)	6.82 (6.4–7.25)	0.16 (0.01–0.30)	NA	0.67 (0.52–0.86)	0.78 (0.64–0.95)
Crane et al. [8]	2021	26,640	12,810 (48.1)	P = 0.189	P < 0.001	P = 0.52	NA	P < 0.001	P = 0.011
Díaz-Vico et al. [9]	2021	18,989	9,883 (52.0)	1.13 (1.04–1.22)	SMD, 0.76 (0.66–0.85)	NA	0.32 (0.24–0.51)	1.10 (1.04–1.17)	1.05 (1.02–1.08)
Díaz-Vico et al. [9]	2021	18,989	9,106 (48.0)	1.13 (1.04–1.22)	SMD, 0.76 (0.66–0.85)	NA	0.32 (0.24–0.51)	1.10 (1.04–1.17)	1.05 (1.02–1.08)
De Simoni et al. [10]	2021	1,871	649 (34.7)	1.13 (0.88–1.47)	9.17(4.67–13.68)	NA	NA	1.99 (1.29–3.07)	1.41 (10.6–1.89)
De Simoni et al. [10]	2021	1,871	1,222 (65.3)	P = 0.31	P = 0.0001	NA	NA	P = 0.002	P = 0.02

Values are presented as number only, number (%), aodds ratio (95% confidence interval [CI]), or bweighted mean difference (95% CI).

CME, complete mesocolic excision; DFS, disease-free survival rate; OS, overall survival; NA, not applicable.

Table 2.

Ongoing prospective clinical trials for CME with CVL

Trial name	Year of registration	Registration	Country	Design	No. of patients	Intervention	Control	Primary endpoint
RELARC	2016	NCT02619942	China	Prospective multicenter-RCT	1,072	CME	D2 dissection	3-year DFS
COMET	2016	ISRCTN45051056	United Kingdom	Multicentre cluster RCT	80	CME	Standard right colectomy	Size of resection specimen, number of lymph nodes present
SLRC	2016	NCT02942238	China	RCT	582	Laparoscopic CME	Open D3 dissection	3-year DFS
COLD	2017	NCT03009227	Russia	Multicentre RCT	780	D3 dissection	D2 dissection	5-year OS
RESECTAT	2017	NA	Germany	Prospective open registry-based	1,000	CME	Standard right colectomy	NA
RICON	2017	NCT03200834	Ukraine	RCT	239	D3 dissection	D2 dissection	5-year OS
REK	2018	NCT03776591	Norway	RCT	126	Laparoscopic CME	Open D3 dissection	30-day complications
PIONEER	2019	NCT03992599	South Korea	Prospective, multi-institutional, single arm	250	Modified CME	NA	3-year DFS

CME, complete mesocolic excision; CVL, central vascular ligation; RCT, randomized controlled trials; DFS, disease-free survival rate; OS, overall survival rate; NA, not applicable.

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