Introduction
Endoscopic mucosal resection (EMR) is a well-defined technique for the removal of precancerous lesions. It involves submucosal injection of fluid underneath a lesion, which lifts it away from the muscular layer, facilitates easier snaring of flat or sessile lesions, reduces the risk of thermal transmural trauma, and identifies lesions with submucosal invasion or scarring, probably not amenable to endoscopic removal [1].
Several studies and meta-analyses in recent years have addressed the efficacy of EMR in treating large polyps within the colorectum, by assessing the recurrence rate, the number of follow-up endoscopic procedures needed to treat the residual lesion, the need for surgery after EMR, and the complication rates [2,3]. The EMR recurrence rate has been reported to be as high as 45% [4]. Many factors that contribute to this are discussed in this article, but one significant issue is that a piecemeal dissection is required for lesions greater than 20 mm. In contrast, the technique of endoscopic submucosal dissection (ESD) for lesions provides en bloc specimens, which facilitate the accurate histopathological assessment of submucosal invasion, and has a significantly lower recurrence rate. However, ESD also suffers from some disadvantages compared to EMR: it is less accessible; it is significantly more time-consuming; it has higher complication rates; it is more expensive; and a long learning curve with prolonged training is required to master the technique, even for highly skilled endoscopists.
EMR has been an established technique for the last 25 years and the literature has recently provided high quality meta-analyses and data from prospective studies on its efficacy. Over this period, there have been modifications in the technique in an attempt to improve the outcomes of this procedure. However, comparative studies of the various modified techniques are lacking. This article reviews the variations and modified techniques of performing EMR, highlighting the differences and merits of each technique based on the current available literature.
Indications for EMR and ESD
The recent Japanese guidelines have set indications for both EMR and ESD (Tables 1 and 2) and have highlighted the need for endoscopic assessment of the lesion prior to resection to identify carcinomas and to assess the submucosal invasion depth [5]. ESD is an absolute indication for IIc or IIa+IIc lesions larger than 2 cm. In addition, it is indicated for lateral spreading tumors of non-granular type (LST-NG), larger than 2 cm, that may harbor superficial multifocal submucosal invasion in 30-56% of cases [6] (Fig. 1).
Table 1 Indications for endoscopic mucosal dissection for colorectal tumors (Japanese guidelines)
Table 2 Indications for colorectal ESD and EMR at National Cancer Centre Hospital in Japan
Non invasive patterns should be diagnosed by chromo magnification colonoscopy
Figure 1 Case 1: EMR of LST-NG in the transverse colon. (A) LST-NG-transverse colon; (B) small stiff snare to deal with central area; (C) final results; (D) 3 months post EMR
EMR, endoscopic mucosal resection; LST-NG, lateral spreading tumors of non-granular type.
These indications are led by the need for the above lesions to be removed en bloc, because of their high risk of harboring submucosal invasion. The higher incidence of submucosal fibrosis or submucosal invasion in these lesions could impede the EMR procedure, as it might lead to inadequate lifting of the lesion after the submucosal fluid injection (non-lifting sign) [2]. Additionally, piecemeal EMR may make it difficult to evaluate precisely the invasion depth and the free margins of carcinomas with less than 1000 µm submucosal invasion depth (pT1a). Accurate histopathological evaluation is essential in these cases, which carry a low metastatic risk (1.5-1.9%) in the colon and 4.2-4.5% in the rectum) and only endoscopic resection can be adequate, to prevent unnecessary surgery [7].
In the vast majority of cases referred for EMR (>90%) within the western world submucosal invasion/malignancy is not an important factor and therefore EMR can be used safely as the preferred technique [8]. Even for lateral spreading tumors of granular type (LST-G) >2 cm, piecemeal EMR is an acceptable technique in the eastern world, provided that the largest nodule that may contain carcinoma will be removed en bloc and the rest of the lesion piecemeal (planned EMR) [5] (Figs. 2 and 3).
Figure 2 Case 2: EMR of LST-G. (A) 80 mm rectal LST-G; (B) Post-EMR; (C) At 3 months post EMR
EMR, endoscopic mucosal resection; LST-G, lateral spreading tumors of granular type.
Figure 3 Case 3: EMR of LST-G
EMR, endoscopic mucosal resection; LST-G, lateral spreading tumors of granular type.
The assessment for submucosal invasion is carried out by ordinary observation, looking for surface unevenness, the presence of depression and fold convergence, by magnifying observation (pit pattern diagnosis) using dye spraying (indigo carmine, crystal violet, etc.) and image-enhancement technology (narrow-band imaging, blue-laser imaging) to assess fine surface structures and microvessels. Deep depression, an expansive appearance, a submucosal tumor-like margin or defective extension predict deep submucosal invasion in 70-80% of cases, which indicates direct referral for surgery.
The accuracy rate of discrimination between adenoma and carcinoma is between 70-90% using pit pattern observation or narrow-band imaging. If the V pit pattern is observed in a lesion with dye spraying and magnifying observation, the diagnostic accuracy of deep submucosal invasion is 90% [5].
Long-term outcomes of standard EMR
Recurrence rate
The recurrence rate following EMR is between 15-45%. Large series, however, suggest that a more realistic value is around 15-18% [9]. The recurrence if seen at follow-up endoscopy is 91% at 6 months and 98% at 12 months. Consequently, follow-up protocols for lesions vary with first follow up at 3-6 months and another at 12 months, as studies have highlighted that recurrence can occur after a normal initial follow-up endoscopy in up to 12% of cases [3,10].
The main predictors for recurrence have been shown to be piecemeal resection and large polyp size. A lesion size of greater than 20 mm has been shown to be significant (unsurprisingly, as piecemeal resection is required) [11]. One study has shown that if the lesion is 40 mm or more, there is a greater than 8-fold increase in the incidence of recurrence [9]. Of these recurrences, 91.4-93% are treated successfully after a mean number of 1.2 endoscopic treatments with either argon plasma coagulation (APC) or EMR [3,9]. There is conflicting evidence regarding the effectiveness of APC on recurrence. The reason is that whilst some meta-analyses have not identified this as a significant factor, other studies have shown a greater than 2-fold effect. The issues include the fact that many studies have not identified the use or non-use of APC within the procedure, and the context, i.e., use when clearance could not be attained or in the context of prophylaxis when clearance was achieved [12-15]. Prospective randomized trials are needed in this area. Other factors that have been identified include proximity to colonic folds and intraprocedural bleeds.
Other modalities used to reduce the recurrence rate or to treat recurrent adenomas are endoscopic mucosal ablation (EMA) and the hot avulsion (HA) technique, which are also rescue treatments for fibrotic recurrent adenomas. EMA, a novel technique for the eradication of recurrent polyps with extensive submucosal scarring, combines submucosal fluid injection with high power APC. The submucosal injection provides a safety cushion that protects the muscularis propria, as high power APC needs to be applied for the eradication of extensively scarred residual polyps. In a pilot study, EMA as a “rescue” treatment successfully eradicated 82% of fibrotic recurrent polyps [16].
HA is a new variation of the hot biopsy (HB) that is used to eradicate residual or recurrent fibrotic adenomatous tissue, especially after snare polypectomy has failed. HB forceps are used to grasp neoplastic tissue with slight traction away from the polyp base while current is applied. The main difference between HA and HB is that HB uses forced coagulation current, which can result in transmural injury, while in HA ENDOCUT I or soft coagulation current is used. Studies have shown lower recurrence rates when macroscopically visible residual adenoma, non-amenable to snare resection, is treated with HA compared to APC (10% vs. 59.3%) [17]. It is also very promising in eradicating fibrotic recurrent polyps, with a success rate of up to 100% in small case series [18,19].
Complication rates
Delayed bleeding rates have been reported to be 1.6%, 1.15-1.7%, and 0.7-2.2% for polypectomy, EMR, and ESD, respectively [20,21]. In low-volume centers, delayed bleeding rates for large lesions have been reported to be up to 25%, highlighting the need for tertiary referral.
In recent large studies, the rate of clinically significant bleeding post EMR for lesions >20 mm is 5-7% [22-24]. Risk factors for post-EMR bleeding are lesions >30 mm (odds ratio [OR] 2.5, 95% CI 1.5–4.2), proximal colon location (OR 2.3, 95% CI 1.4-4.0), or any major comorbidity at procedure (OR 1.5, 95% CI 0.9-2.6), while the use of epinephrine injection in the EMR solution (OR 0.57, 95% CI 0.32-1.0), may modestly reduce post-EMR bleeding [25]. The use of aspirin during large EMRs has been evaluated in only two studies. An observational study with 302 lesions found an OR of 6.3, but a prospective multicenter study with 1172 lesions found no significant association [23,26].
In 55% of cases of post-EMR bleeding, the bleeding stops spontaneously, whereas the rest will need endoscopic treatment and 1% will need primary embolization or surgery [28]. The prophylactic use of clips has been evaluated, and, although it seems to decrease the delayed bleeding rate, it is not cost-effective [27]. An individualized approach in cases with high risk for delayed bleeding would probably be preferential. Moreover, prophylactic endoscopic coagulation of the exposed vessels in the mucosal defect of EMR does not seem to prevent delayed bleeding [29].
Perforation rates during endoscopic resection are reported to be 0.05%, 0.58-0.8%, and 2-14% for polypectomy, EMR, and ESD, respectively [20]. In hemodynamically stable, non-immunosuppressed patients with adequately prepared bowel and no signs of generalized peritonitis, use of endoscopic clips and antibiotic administration has been reported as a favorable treatment of iatrogenic colonic perforations, with success rates ranging between 81.3% and 100% [30,31]. Over-the-scope clipping devices have shown good results, with up to 90% successful closure of perforations, although larger studies are needed to fully assess the efficacy and safety of these devices [32].
Long-term curative rates and surgical intervention
Overall surgical intervention is required after an attempted EMR in 8.3-13.5% of cases. Possible reasons are: adverse histopathology, i.e. invasive cancer following a successful EMR (3.7-4.8% of cases); 2) initial non-curative resection for various conditions, such as submucosal fibrosis, non-lifting sign and difficult positioning (2.3-8.8%); or 3) complications encountered (0.5%), such as perforation or intractable bleeding [2,9]. An important finding is that surgical referral for recurrences non-amenable to endoscopic resection after initial successful EMR is needed in only 0.2-1% of cases [3].
Modified EMR techniques
EMR-precutting (EMR-P)
EMR-P is a technique that combines ESD tools with EMR to remove larger tumors that would be difficult to snare en bloc with classic EMR. After the submucosal fluid injection, the mucosa is incised 5-10 mm away from the tumor with a flex knife. A 35-mm oval snare is then applied round the tumor at the mucosal incision site. The mucosal incision enables effective snaring without slippage of the snare.
A retrospective study that compared EMR, EMR-P and ESD for the treatment of large colorectal tumors [32] demonstrated that lesions removed by EMR and EMR-P were of similar size, whereas EMR-P compared to EMR had a significantly higher en bloc resection rate (65.2% vs. 42.9%) and complete resection rate (59.4% vs. 32.9%). The recurrence rate was 25% vs. 3%, respectively. In 90% of the recurrences the EMR had piecemeal resection. All the recurrences in the EMR group, apart from one patient who needed surgery, were successfully treated with one additional EMR. Interestingly, 15.7% of EMR, 29% of EMR-P and 37.9% of ESD cases were adenocarcinomas. Of the patients with adenocarcinoma treated with EMR, 9% underwent surgery because of uncertain margins in the histopathology, compared with 0% of those treated with EMR-P. In terms of complications, perforation rates were not significantly different, though slightly higher for EMR-P (2.9% compared to none in the EMR group).
EMR-P with a certain degree of additional submucosal dissection before snaring the lesion is the definition of hybrid/simplified ESD, or knife-assisted EMR. The complication rate for hybrid ESD seems to be similar to that of ESD and further studies are needed to establish the indications for this procedure [33]. In a recent prospective study [34], knife-assisted EMR was used to remove polyps that could not be lifted because of scar tissue. In this study, ESD was performed for approximately 10 mm around the polyp into the scar tissue before the lesion was snared. The success in polyp eradication was 90%, with no perforations, but there was a delayed bleeding rate of 5%.
Overall, it was highlighted that the technique can be useful in cases where carcinoma is suspected and, in the absence of ESD, en bloc resection is required to prevent unnecessary operation on the basis of uncertain histopathological margins. EMR-P seems to offer an intermediate method for the endoscopist who is not experienced in ESD. In the correct hands, it has good technical success rates with the advantages of a low recurrence rate and higher en bloc resection. Randomized controlled head-to-head studies are needed, as it may carry higher complication rates than traditional EMR.
Underwater EMR
This novel EMR technique was first described in 2012 [35], when polyps larger than 2 cm were snared without prior submucosal injection. Instead, the lumen was initially deflated and the polyp was totally immersed in water using a water pump. The theory behind the technique was based on an observation made during colonic endoscopic ultrasound, where it was noticed that, when the lumen is filled with water, the colonic muscularis propria remains circular and the water floats the mucosa and submucosa away from the deeper muscular layer, creating a safety cushion. Few single-center prospective studies have given good results [36]. A recent study with the largest series of 81 polyps treated with underwater EMR demonstrated en bloc resection in two thirds of the cases. Successful EMR with no macroscopic residual tissue was demonstrated in all cases [37] and no recurrence was seen at 3-month follow up.
In another recent prospective study, lesions between 2 and 4 cm were removed en bloc with a 33-mm snare. The study design was based on the observation that water immersion results in less distension of the bowel lumen, contraction of the adenomatous tissue, and reduction of the haustral folds, enabling the snare to capture a larger mucosal surface even in lesions straddling a fold. In 55% of cases, complete en bloc resections was achieved and no recurrence was seen in these cases. In those that needed piecemeal resection, the recurrence rate was 5% at 4-6-month follow up [38].
Almost 200 underwater EMRs have been performed in a few prospective studies to date. Interestingly, no perforation has been reported. The main complication is delayed bleeding in 0.5-5%, with no need of transfusion or intervention [39]. Intraprocedural bleeding was rare and minor and usually ceased spontaneously. Interestingly, this study confirms a previous report where the use of heated water at 37°C to fill the lumen reduced bowel peristalsis [40].
The underwater EMR technique appears to be a promising method of EMR, given the significantly low rates of adverse events reported, the reduction in procedure time, the possible cost-effectiveness and the short learning curve [39]. In addition, there is a possibility that larger lesions can be removed en bloc, leading to negligible recurrence rates. The disadvantages of the technique are the need for good bowel preparation and the poor views when there is vigorous bleeding. Large multicenter studies are needed to determine the efficacy and complications of the technique.
Cap-assisted EMR (C-EMR)
C-EMR is a modified technique in which a transparent plastic mucosectomy cap is mounted on the tip of the colonoscope. At its distal end, the cap has a gutter that positions the open polypectomy snare. The polyp is lifted with submucosal fluid injection and the cap is placed against the polyp. Mild suction is applied to make the polyp fill half of the cap. The snare is closed round the aspirated mucosa and the lesion is resected.
C-EMR has been used for EMRs in the upper gastrointestinal tract, mainly the stomach and esophagus; however, the use of this method in the colon is not popular, given the possible entrapment of muscularis propria in the cap with consequent perforation. In the largest study to date, 255 cases of C-EMR performed in lesions larger than 2 cm were evaluated [41]. The median diameter of the resected specimens was 13 mm (range 12-16). All polyps were removed piecemeal. The median size of the LSTs was 30 mm (range 20-100) and of the sessile polyps 25 mm (range 20-80). APC was used for residual tissues in 22.3% of the cases. The recurrence rate after a median period of 12.1 (5.5-71.2) months was 4% and the recurrent polyps were treated endoscopically with APC or EMR in one session.
Intraprocedural bleeding occurred in 7.4% and was managed endoscopically. No delayed bleeding and no perforations occurred. Conio et al highlighted the need for controlled suction to prevent perforation and commented that in many cases suction is not necessary, as pressure against the lesion causes its protrusion into the cap.
The advantages of C-EMR were confirmed in a recent retrospective study that included 124 polyps [42], 60% of which were larger than 2 cm. The decision to use C-EMR was made case by case, as it is considered the best method for flat polyps in difficult locations. Of the polyps included, 45% were flat polyps, 14% were polyps involving the ileocecal valve (ICV), and 5% were polyps involving the appendiceal orifice.
During a median follow up of 4.2 months (range 1.6-46.8 months), the recurrence rate after a successful C-EMR was 1.2%, while for all attempted C-EMRs polyp removal was successful in 91%. The reasons for failure were an inadequate grasp of the polyp (scarring/carcinoma) and difficult position and/or size.
The perforation rate was 3.9%, of which 2 cases needed surgery and the rest were managed endoscopically with endoclips. Perforation rates in previous studies with small numbers of patients were 2.5-4%. There was 3.9% intraprocedural bleeding and 2.4% delayed bleeding managed endoscopically.
The cap seems to offer better visualization of the operative field and the possibility of resecting lesions located in difficult places. The cap is advantageous in interhaustral lesions and lesions involving the ICV, as the exposure of the lesion is greater, helping keep the ileum distended and facilitating the placement of the snare.
Despite the fact that C-EMR was used as a technique for piecemeal EMR in all the above studies, the recurrence rate is low, probably because of the improved visualization of the field and the suction of normal mucosa along with the lesions at the margins of the lesion. The technique needs adequate training, as it has shown increased perforation rates in non-experienced hands. Most of the perforations occurred in the first quarter of the period included in the study as the endoscopist gained experience [41].
Endoscopic submucosal resection with band ligation (ESMR-L)
This modified EMR technique has been used to remove small rectal neuroendocrine tumors. A multi-band ligation device is mounted on the colonoscope. Submucosal saline solution is injected beneath the tumor to reduce the risk of perforation. The lesion is then aspirated into the ligation device and an elastic band is deployed. The snared lesion is then resected below the band.
Carcinoid tumors less than 1 cm in the rectum have a low risk of metastatic disease and local treatment is considered curative. As the carcinoid extends to the submucosa, resection techniques must aim for complete resection. The use of a ligation device in the esophagus has shown a maximum thickness of submucosa resected up to 1200 µm (median 800 µm, range 500-1200) [43].
The efficacy of ESMR-L in resecting small rectal carcinoids has been compared to that of standard EMR and ESD. Complete resection with histopathologically negative margins has been reported in 94.3-100% of ESMR-L vs. 75.7-80% of EMR cases [44,45]. ESMR-L has shown equivalent complete resection rates to those of ESD (100% vs. 92%, respectively), while offering the advantages of a shorter procedural duration and shorter (if any) hospital admission [46].
No perforations occurred in all the above studies. The results of a recent meta-analysis confirm that treatment of rectal carcinoid tumors with ESD or ESMR-L is superior to EMR, and that the efficacy of ESMR-L is equivalent to ESD treatment [47].
Concluding remarks
Classic EMR, especially in tertiary centers, can successfully remove more than 90% of the polyps. Any variation of the technique should aim to resolve specific problems where classic EMR is not successful, such as submucosal fibrosis, polyps in difficult locations, or superficial submucosal invasion. The variations discussed are promising, but large studies are needed before they can be widely adopted.