Comparison of Methods for Removing Large Benign Broad-based Epithelial Neoplasms of the Colon: ESD and EMR.

Objective of the study: to prospectively compare the immediate, immediate and remote results of endoscopic mucosal resection through an endoscope and endoscopic submucosal dissection performed for non-invasive large-sized (20 mm or more) broad-based epithelial lesions of the colon. Study objectives: 1. To evaluate the accuracy of ultra-high-resolution colonoscopy in white, ultra-clear and narrow-spectrum light with magnification in predicting the histological structure and risks of invasion of large-sized broad-based epithelial lesions of the colon. 2. To conduct a comparative assessment of the accuracy of angio-CT/MRI, probe EUS and second-generation narrow-band endoscopy with magnification in determining the depth of invasion and the probability of lymphoregional metastasis of superficial epithelial neoplasms of the colon with malignancy. 3. To evaluate the effectiveness of endoscopic ultrasound in predicting submucosal fibrosis and its impact on surgical treatment tactics, and to compare the obtained data with the intraoperative picture using the fibrosis classification scale. 4. To conduct a comparative assessment of the completeness (in one block/in parts; R0/R1) and depth of resection of large-sized epithelial lesions of the colon on a broad base according to endoscopic and morphological criteria in EMR and ESD. 5. To study the immediate results of EMR and ESD, including conversion and intervention refusal factors. 6. To determine the risk factors for recurrence after endoscopic removal of large epithelial neoplasms of the colon and to develop an algorithm for their diagnosis and prevention 7. To assess possible intra- and postoperative complications during endoscopic removal of large epithelial neoplasms (bleeding, perforation, postcoagulation syndrome) of the colon using the AGREE endoscopic complication scale and to develop methods for their prevention and treatment. 8. To assess the effectiveness of the RDI regimen both for the prevention of an intraoperative source of bleeding and for detecting a source of bleeding during EMR/ESD 9. To study comparative indicators of the number of tumor recurrences in the immediate and late periods after endoscopic intervention (from 6 months to 5 years), and the effect of the EMR method and additional ablation of the edges of the wound bottom on the incidence of recurrent formations General characteristics of the clinical study. Design: prospective, randomized, controlled study. It is planned to include at least 110 patients in the study until statistically reliable indicators are obtained for all analyzed parameters, who will undergo EMR or ESD for large-sized (20-60mm) non-invasive epithelial formations of the colon on a broad base. The method of choosing the operation will be determined using a random number generator (randomizer). Patient inclusion criteria: 1. Patient with benign non-invasive epithelial formations of the colon on a broad base (Is and II types), 20-60mm in size 2. Age ≥ 18 years. 3. Signed informed voluntary consent for colonoscopy and removal of formations using the studied methods. Patient exclusion criteria: 1. More than one large epithelial formation on a broad base 2. Colon formations less than 20 and more than 60 mm 3. Recurrent nature of the formation. 4. Reasonable suspicion of the presence of an invasive formation (cancer), including with invasion into the submucosal layer based on the results of preoperative assessment (NICE - 3; JNET - 3; Kudo - Vn). 5. The presence of a widespread malignant tumor in any part of the colon. 6. Use of other methods of endoscopic removal of the formation. 7. IBD. 8. Infectious disease requiring systemic therapy 9. Patient on hemodialysis 10. Uncorrectable coagulopathy (INR\> 1.5), inability to discontinue antithrombotic drugs. 11. Refusal to participate in the study. 12. General contraindications to endoscopic examination. All patients were randomly divided into 2 main groups (using a randomizer) using block stratification randomization: EMR Group and ESD Group. https://randomus.ru/quick?from=1\&to=110\&count=55\&norepeat=1\&sort=1 ESD (55) patients with numbers: 5, 6, 7, 9, 13, 16, 17, 18, 19, 22, 24, 25, 28, 29, 30, 32, 33, 35, 36, 37, 38, 40, 42, 44, 47, 49, 50, 51, 58, 59, 62, 64, 65, 69, 70, 74, 75, 76, 77, 78, 79, 81, 85, 89, 93, 94, 95, 96, 98, 99, 103, 105, 106, 108, 110 Other patients - EMR (55): 1,2,3,4,8,10,11,12,14,20,21,23,26,27,31,34,39,41,43,45,46,48,52,53,54,55,56,57,60,61,63,66,67,68,71,72,73,80,83,84,86,87,88,90,91,92,97,100,101,102,104, 109 In the EMR group, it is planned to additionally divide patients into 2 main groups (using a randomizer) using block stratification randomization: EMR Group and EMR + Group ablation. https://randomus.ru/quick?from=1\&to=56\&count=28\&norepeat=1\&sort=1 EMR +APC (28 patients): 2, 5, 6, 7, 11, 12, 18, 19, 22, 24, 26, 28, 30, 32, 34, 35, 37, 38, 39, 41, 42, 43, 44, 45, 46, 47, 50, 51 The rest are EMR (28 patients) It is planned to evaluate the following patient characteristics: 1. Gender. 2. Age. 3. Taking aspirin (or analogs) and/or indirect anticoagulants 4. The degree of concomitant pathology, expressed in the concept of surgical-anesthesiological risk according to the ASA scale. 5. History of abdominal surgery 6. History of inflammatory diseases of the abdominal organs, including diverticulitis, usually leading to the formation of adhesions involving the colon, The following characteristics of the study are planned to be assessed: 1. Nature of preparation (compliance/non-compliance with the recommended diet; drug(s) used, split preparation or not, time from the last dose to the start of colonoscopy), quality of preparation (according to the Boston scale). 2. Presence of sedation (Yes/No). 3. Use of a distal cap (Yes/No). The following endoscopic characteristics of the epithelial formation are planned to be assessed: 1. Localization (according to anatomical landmarks), preferably indicating the number of haustra from significant landmarks; as well as on the fold, through the fold in the interfold space. 2. Size of the formation (mm) using a ruler; 3. Type according to the Paris Classification of Epithelial Neoplasia and the Classification of Laterally Spreading Tumors; 4. Assessment of the surface microstructure according to NICE, JNET, WASP, Kudo. 5. Assessment of invasion and submucosal fibrosis using EUS probes The following characteristics of EMR and ESD are planned to be assessed: 1. Method of removal (EMR with injection of a high-osmolar solution (gelofusin) into the submucosal layer or ESD); 2. Removal time (from the moment the loop is brought into the field of view until complete removal of the formation or from the beginning of the incision); 3. Method of removal (in fragments or as a single block, ESD or combined ESD, or impossibility of removal); 4. Completeness of removal according to high-resolution endoscopy, virtual chromoscopy and magnification at the end of the intervention (within healthy tissue/no), which will be confirmed by taking a biopsy (4 fragments) from the edges of the resection wound after EMR 5. Evaluate the EUS data with intraoperative data and pathomorphological conclusion data regarding the presence of fibrosis and neoplasm invasion. 6. Removal of the specimen (removed/lost) and the reason for loss. 7. Use of prophylactic clipping (Yes/No) and indications for its use: deep post-resection defect (up to and including the muscular layer); intestinal perforation; inability to achieve hemostasis; for social reasons (doctor, relatives...) 8. After performing EMR, use a randomizer to select a method for preventing recurrence of the formation in the group - ablation with the tip of the loop and a control group where ablation will not be performed 9. Type and nature of adverse events according to the AGREE scale 10. In case of damage to the wall of the colon, it will be assessed according to the scale of damage to the wall of the colon and, depending on this, the treatment tactics will be selected. It is planned to evaluate the following characteristics in the postoperative period: 1. The presence of abdominal pain syndrome (Yes/No) 2. Temperature Yes/No (within 24 hours, above 37.2). 3. Type, time of occurrence and nature of adverse events (bleeding, perforation, postcoagulation syndrome). 4. Type of observation after removal (outpatient/inpatient). If inpatient, for how long. 5. Compliance with a diet in the postoperative period (yes/no). 6. Use of antibiotics (yes/no). 7. Use of hemostatics (yes/no). 8. If postcoagulation syndrome is suspected - assessment of C reactive protein, assessment of leukocytes in the blood It is planned to assess the following morphological characteristics of the formation: 1. Fragmentation of the formation (yes/no) 2. Histological structure of the formation (examination of the removed specimen, according to the WHO and Vienna classification). 3. Morphological assessment of the completeness of removal (assessment of the specimen) - R0 - no cells of the formation along the resection line, R1 - there are cells of the formation along the resection line, Rx - the formation is removed in fragments or the status of the resection boundaries cannot be determined. 4. Morphological assessment of the edges of the p/o wound after EMR - 4 tissue fragments - one from each edge Technique of endoscopic intervention. To prepare for colonoscopy, it is recommended to: adhere to a low-residue diet for 2 days (the 3rd and 2nd day before the endoscopic intervention); drink only clear liquids the day before; use full-volume PEG-based drugs (Fortrans) or a low-volume sulfate-based drug (Eziclen) in split mode. After visualization of the formation, its localization is assessed, its type according to the Paris classification of epithelial neoplasia, its size compared to the diameter of the catheter ("shirt") of the loop and the polypectomy loop itself in the open state. (If technically possible, welcome(the use of an endoscopic ruler is required). The nature of the surface of the formation is assessed in white light, in TXI mode, and using virtual chromoscopy according to NICE, WASP; with magnification - according to JNET and, if necessary, according to Kudo with a 0.5-1.0% indigo carmine solution. If the selection criteria are met, randomization is performed and the formation is removed either by the ESD or EMR method. EMR technique. 3-4 ml of a high-osmolar solution or saline solution stained with indigo carmine is injected into the submucosal layer under the formation. The formation is removed with the surrounding mucous membrane (at least 5 mm from the edge of the formation) using the standard diathermic polypectomy loop available to the operator. The formation is removed using electric current in the EndocatQ mode (ensuring alternating cutting and coagulation under the control of a processor built into the electrical unit). After removal of the formation, the resection site is examined in white light, then virtual chromoscopy (NBI), and then examination with magnification. The examination results are recorded in the scientific protocol separately, and are assessed as a whole. The criteria for visual removal of the formation within healthy tissues is the absence of visible fragments of the formation. If residual tissue of the formation is detected, they are removed using the same technique. If the removal of residual tissue of the formation was performed by another method, indicate which one and why. After the final assessment of the edges of the post-resection wound, 1 fragment is taken from each edge for morphological confirmation of R0 resection in the vertical edge (4 fragments in total) After EMR, in half of the cases (according to the instructions of the randomized recording), ablation of the edges with a polypectomy loop is performed. The removed formation is extracted using a snare loop, if removed in parts, then all fragments, if possible, are extracted through the aspiration channel of the endoscope, for large fragments, a snare loop is used. A specimen not sent for morphological examination is considered lost. ESD technique. After assessing the boundaries of the formation, a mark is made on it, retreating at least 5 mm from the edge, then a circular or semicircular incision of the mucosa will be made, after which the formation will be removed by dissection of the submucosal layer using a scarecrow knife, a knife with a ceramic head at the end in EndocutQ mode, spray-coag swift-coag. The ESD technique - tunnel method, where feasible, will also be used. The essence of the technique is a semilunar incision of the mucous membrane, retreating from the marks, and creating a tunnel under the formation to the proximal edge of the marks, with subsequent cutting off of the formation along the edges. The removed neoplasm is extracted and stretched on the plate. After removal, the edges and bottom of the wound are assessed, if necessary, prophylactic coagulation of visible vessels and clipping are performed. Terminology (complications). Complications (adverse events) will be considered as occurring during the intervention (intraoperative), if they develop from the moment of insertion of the colonoscope until its removal. Otherwise, complications will be regarded as postoperative. Perforation during the examination is diagnosed when the "target" symptom is detected - the presence of an additional ring-shaped structure at the bottom of the wound and/or during endoscopic visualization of a through defect in the organ wall. Delayed perforation will be defined as the development of symptoms of peritoneal irritation and free gas in the abdominal cavity in the patient and/or the detection of a perforation hole in the area of removal of the formation during surgical revision. Immediate (intraoperative) bleeding is bleeding that has not stopped within 4 minutes (the norm of hemostasis for capillary bleeding /from a finger/ according to Duke: onset after 2 minutes, end after 4 minutes) after removal of the formation and requiring one of the methods of endoscopic hemostasis (injection of adrenaline solution and/or coagulation (including ARS) and/or clipping. Delayed bleeding is blood in the stool and unstable vital signs and/or a drop in hemoglobin ≥ 2 g / dl. Postcoagulation syndrome is defined as the presence of abdominal pain and/or leukocytosis in the patient, an increase in C reactive protein and/or fever (more than 37.2) and/or symptoms of peritoneal irritation in the case of: 1. The absence of these symptoms before the manipulation and other reasons for their appearance 2. The absence of free gas in the abdominal cavity and/or detection perforation in the area of removal of the formation during surgical revision. Methodology for morphological examination of preparations. After the preparation is removed in single fragments, it is fixed in a straightened state on a tight footrest. In the case of removal of the formation in fragments, the extracted fragments are also fixed in the above-mentioned manner, if possible. After fixation, the preparation is placed in a 10% formalin solution and delivered to the pathological anatomy department. After 24 hours of fixation, the specimen is removed from formalin. Then the size of the formation is measured and parallel sections are made every 2-3 mm, which are placed in cassettes and undergo a standard procedure for preparing paraffin blocks, after which paraffin sections are made every 3-4 μm and a routine procedure for staining with hematoxylin and eosin. During the histological description of the specimen, it is planned to note the following parameters: number of fragments; size of the formation; its morphological type and differentiation; presence of a muscular plate of the mucosa, presence and thickness of submucosal tissue, diameter of the largest vessel in the sample; presence of formation tissues along the horizontal and vertical boundaries of the formation. R0 is understood as the absence of formation cells along the border (vertical and horizontal) of the coagulation line The morphological classification of the formation will be carried out according to the WHO classification and the Vienna classification (see Appendix). When evaluating biopsies from the edges of the wound, the presence/absence of residual tissue of the formation (adenoma and/or adenocarcinoma and/or serrated formation) in the biopsy is indicated. Documentation and computer statistical data processing. A separate medical record will be filled out for each patient in a closed database on the Internet. Required - endophotographs of the formation before its removal and the wound after the end of the intervention, allowing to evaluate the parameters included in the analysis. Statistical processing of the obtained data will be performed by the method of variation statistics with the calculation of the arithmetic mean, standard deviation, standard error of the mean and the reliability criterion (p). Differences at a significance level of 95% at p\<0.05 are considered reliable. In order to check the significance of the difference between the means in different groups by comparing the variances of these groups, it is planned to use the methods of ANOVA (from the English ANalysis Of VAriance) analysis of variance. The Pearson correlation coefficient will be calculated to assess the presence or absence of a linear relationship between two variables and the tightness of this relationship. Calculations are planned to be made using the statistical section of the Microsoft Office Excel spreadsheet software package.