Literature DB >> 35706787

Endoscopic resection for colorectal laterally spreading tumors in East Asian countries: a systematic review.

Jinguo Liu1, Yujin He2, Zhaojun Wang1, Shuo Zhang3.   

Abstract

Background: To assess the efficacy and safety of different endoscopic resection methods for colorectal laterally spreading tumors (LSTs) in East Asian countries.
Methods: A literature search was performed in PubMed, Embase, Cochrane Library and Web of Science databases. Colorectal LSTs of the included studies were resected with endoscopic mucosal resection (EMR) and/or endoscopic submucosal dissection (ESD). The main outcomes involved rates of en bloc resection, R0 resection, adverse events and recurrence.
Results: A total of 20 studies were finally included in the present study. The total number of lesions were 3,903 (EMR: 1,230, ESD: 2,673). EMR-en bloc resection was obtained in 395/591 (66.8%), with ESD-en bloc resection reported in 2,020/2,265 (89.2%) [odds ratio (OR) 0.244, P<0.0001, 95% confidence interval (CI): 0.197-0.304]. EMR-R0 resection was achieved in 409/547 (74.8%), which was lower than that of ESD (1,895/2,241, 84.6%) (OR 0.541, P<0.0001, 95% CI: 0.432-0.677). Bleedings occurred more frequently in EMR than in ESD group (10.4% vs. 3.1%, OR 3.559, P<0.0001, 95% CI: 2.618-4.836). Rates of perforations in EMR and ESD were 0.4% and 4.1% (OR 0.099, P<0.0001, 95% CI: 0.036-0.27). Recurrence of EMR was higher than ESD group (6.3% vs. 1.0%, OR 6.732, P<0.0001, 95% CI: 3.751-12.082). Discussion: Endoscopic resections of colorectal LSTs are safe and effective. ESD leads to higher rates of en bloc and R0 resection, as well as lower rates of bleeding and recurrence, but it has a high risk of perforation, compared with EMR. 2022 Translational Cancer Research. All rights reserved.

Entities:  

Keywords:  Endoscopic mucosal resection (EMR); colorectal laterally spreading tumors (colorectal LSTs); endoscopic submucosal dissection (ESD)

Year:  2022        PMID: 35706787      PMCID: PMC9189166          DOI: 10.21037/tcr-21-2074

Source DB:  PubMed          Journal:  Transl Cancer Res        ISSN: 2218-676X            Impact factor:   0.496


Introduction

Colorectal cancer (CRC) remains a major health burden with high incidence and mortality worldwide. CRC ranked third in incidence and second in mortality in 2018 among all cancers (1). In East Asian countries, the incidence and mortality of CRC in Japan ranked 4/2 and 3/1 in male/female, respectively (2), which ranked both third in Korea (3) and both fifth in China (4). The early identification and removal of lesions had been shown to reduce the mortality of CRC (5). Laterally spreading tumors (LSTs) were defined as flat, broad-based lesions with a lateral diameter at least 10 mm (6) that were disposed to locate in colorectum. Based on the endoscopic morphology, LSTs were classified into two categories, either granular type (LST-G), with homogenous and nodular mixed subtypes, or non-granular type (LST-NG), with flat elevated and pseudodepressed subtypes (6,7). LSTs might evolve into high-grade intraepithelial neoplasms with an incidence from 20.9% to 33.8% (8,9). Hence, early detection and resection of colorectal LSTs is vital for the prevention and treatment of carcinogenesis. Endoscopic treatments were widely accepted because of its minimally invasive methods, rapid recovery and low cost compared with surgery. Endoscopic mucosal resection (EMR) was first described in Japan in the early 1990s, and it was suitable for the majority of gastrointestinal superficial neoplasms (10). If lesions were larger than 15–20 mm or non-lifting, the lesions were resected by piecemeal EMR (EPMR) without en bloc resection, which possibly resulted in a high rate of local recurrence (11). Endoscopic submucosal dissection (ESD) was developed years later to provide R0 resection regardless of the size of tumor and a more precise histopathological assessment, but it was considered technically more difficult to perform and associated with a higher rate of adverse events, such as bleeding and perforation (11,12). The ideal endoscopic method is cost effective with a high rate of curative resection and a low risk of adverse events, minimizing the need for recurrent interventions (13). EMR is widely used in the world, but ESD is always limited to East Asian countries. A previous systematic review showed that western endoscopists had a lower level of experience in ESD with an increasing heterogeneity (14). Our study is aimed to evaluate the efficacy and safety of EMR and ESD for colorectal LSTs in East Asian countries. We present the following article in accordance with the PRISMA reporting checklist (available at https://tcr.amegroups.com/article/view/10.21037/tcr-21-2074/rc).

Methods

Study selection

The public databases (PubMed, Embase, Cochrane library, and Web of Science) were retrieved by two investigators using the terms: (endoscopic submucosal dissection) And (colorectal laterally spreading tumor) And (China) or (Korea) or (Japan), (endoscopic mucosal resection) And (colorectal laterally spreading tumor) And (China) or (Korea) or (Japan). The initial search results were verified between two investigators with the contents, and duplicate literatures were excluded. Disagreements were judged by a third investigator. If there was no difference, the two investigators then screened potential studies by reviewing titles and abstracts (). The study was registered with PROSPERO (CRD42021226966).
Figure 1

Study flow diagram.

Study flow diagram.

Inclusion criteria

The inclusion criteria were: endoscopic changes based on the characteristics of LST; lesions resected by EMR and/or ESD; randomized control trials (RCTs) or observational studies (both prospective and retrospective) published in English up to June 2021; the clinical outcomes including at least one of en bloc resection rate, R0 resection rate, follow-up periods, recurrence rate and adverse events.

Exclusion criteria

The exclusion criteria were: insufficient or unreliable data about outcome variables (e.g., letters, case reports, comments); duplicated studies or multiple reports on the same study; data not available to be extracted; anus-associated lesions; the clinical outcomes of studies with EMR + ESD or multiple lesions (including LSTs) were not described separately.

Data extraction

The data were extracted by one investigator and confirmed by another investigator, which included first author, publication year, country, design, EMR/ESD, lesion number, en bloc resection rate, R0 resection rate, adverse events, follow-up periods and recurrence rate (). Disagreements were judged by a third investigator.
Table 1

The characteristics of the included studies

Author, yearCountryDesignEMR/ESDLesions numberEn bloc resection rate (n/%)R0 resection rate (n/%)Adverse events (n/%)Follow-up periods (months)Recurrence rate (n/%)
BleedingsPerforations
Huang et al., 2009 (15)ChinaMonocentric retrospectiveEMR111 (EMR 103)46/44.7 (EPMR 57)99/96.1 [margin (+) 4]11/10.703–2611/10.7
Son et al., 2019 (16)KoreaMulticentric retrospectiveEMR275 (EMR 275)239/86.9 (EPMR 36)221/80.422/8.01/0.3NRNR
Tanaka et al., 2001 (17) JapanMonocentric retrospectiveEMR120 (EMR 81)41/50.6 (EPMR 40)18/22.216/19.81/1.21.2–13.56/7.4
Kim et al., 2014 (18)KoreaCross-sectional retrospectiveEMR80 (EMR 44)7/15.9NR2/4.50NR17/39.4
Jung et al., 2019 (19)KoreaMulticentric retrospectiveEMR8862/70.571/81.614/15.90NRNR
ESD119104/87.4102/90.39/7.63/2.5NRNR
Terasaki et al., 2012 (20)JapanMonocentric retrospectiveEMR70NRNR5/7.11/1.43–35.31/1.4
ESD61NRNR7/11.503–35.30
Osera et al., 2017 (21)JapanMonocentric retrospectiveEMR275NRNRNRNR3–121/0.4
ESD382323/84.5303/79.312/3.118/4.73–322/0.5
Hong et al., 2018 (22)KoreaMulticentric retrospectiveEMR294NDSNDS29/9.91/0.3NRNR
ESD209NDSNDS11/5.35/2.5NRNR
Lian et al., 2018 (23)ChinaMonocentric retrospectiveESD143125/87.4119/83.22/1.45/3.56–120
Bae et al., 2016 (24)KoreaMonocentric retrospectiveESD153142/92.8121/79.15/3.314/9.26–890
Jeong et al., 2019 (25)KoreaMulticentric retrospectiveESD210187/89.0180/85.711/5.24/1.9NRNR
Yue et al., 2019 (26)ChinaMonocentric prospectiveESD138NR128/92.74/2.92/1.43–122/1.4
Youk et al., 2016 (27)KoreaMulticentric prospectiveESD195194/99.5147/75.4NDSNDSNRNR
Jung et al., 2015 (28)KoreaMonocentric retrospectiveESD163152/93.3150/92.04/2.514/8.6NRNR
He et al., 2019 (29)ChinaMonocentric retrospectiveESD162161/99.3NR1/0.61/0.66–310
Tang et al., 2016 (30)ChinaMonocentric retrospectiveESD3633/91.732/88.91/2.83/8.36–432/5.6
Nishiyama et al., 2010 (31)JapanMonocentric retrospectiveESD204177/86.8158/77.52/1.020/9.812–760
Cong et al., 2016 (32)ChinaMonocentric retrospectiveESD177147/83.1144/81.46/3.44/2.36–3611/6.2
BleedingsPerforations
Sakamoto et al., 2017 (33)JapanMonocentric retrospectiveESD5349/92.548/90.12/3.82/3.8NRNR
Toyonaga et al., 2010 (34)JapanMonocentric retrospectiveESD268266/99.3263/98.11/0.46/2.26.5–85.20

En bloc resection was defined as the lesion removed as a whole. R0 resection was defined as the pathological specimen with a free margin, both laterally and vertically. Bleeding included early bleeding after EMR/ESD within 24 hours and delayed bleeding beyond the first 24 hours after the procedure. Perforation included intraoperative and postoperative perforation, which was diagnosed by endoscopy or radiograph. EMR, endoscopic mucosal resection; ESD, endoscopic submucosal dissection; EPMR, piecemeal EMR; NR, not reported; NDS, not described separately.

En bloc resection was defined as the lesion removed as a whole. R0 resection was defined as the pathological specimen with a free margin, both laterally and vertically. Bleeding included early bleeding after EMR/ESD within 24 hours and delayed bleeding beyond the first 24 hours after the procedure. Perforation included intraoperative and postoperative perforation, which was diagnosed by endoscopy or radiograph. EMR, endoscopic mucosal resection; ESD, endoscopic submucosal dissection; EPMR, piecemeal EMR; NR, not reported; NDS, not described separately.

Quality of study

The Newcastle-Ottawa Scale for Cohort Studies, consisted of selection, comparability and outcome, was used to assess the quality of the included studies. Each study had a total score with a maximum of 13 points (). The specific criteria (14) were representativeness of the exposed cohort (yes+: retrospective studies; yes++: prospective studies; yes+++: RCTs), comparability (studies comparing EMR with ESD), assessment of outcome (yes: more than one outcomes are not included; yes+: one of the included outcomes was not reported; yes++: all outcomes were reported), and follow-up long enough (yes++: follow up more than 12 months; yes+: follow up 6–12 months; yes: follow up 1–6 months).
Table 2

Risk of bias in the included studies according to the Newcastle-Ottawa scale

AuthorSelectionComparability on the basis of design or analysisOutcomeScore
Representativeness of the exposed cohortSelection of the non-exposed cohortAscertainment of exposureDemonstration outcome not present at startAssessment of outcomeFollow-up long enoughAdequacy of follow-up
HuangYes+NoYesYesNoYes++YesYes9
SonYes+NoYesYesNoYesNoNo5
TanakaYes+NoYesYesNoYes++YesNo8
KimYes+NoYesYesNoYesNoNo5
JungYes+NoYesYesYesYesNoNo6
TerasakiYes+NoYesYesYesYesYesYes8
OseraYes+NoYesYesYesYesYesYes7
HongYes+NoYesYesYesYesNoNo6
LianYes+NoYesYesNoYes++Yes+Yes10
BaeYes+NoYesYesNoYes++Yes+Yes10
JeongYes+NoYesYesNoYesNoNo5
YueYes++NoYesYesNoYes+YesYes9
YoukYes++NoYesYesNoYesNoNo6
JungYes+NoYesYesNoYesNoNo5
HeYes+NoYesYesNoYes+YesYes8
TangYes+NoYesYesNoYes++Yes+Yes10
NishiyamaYes+NoYesYesNoYes++Yes++Yes11
CongYes+NoYesYesNoYes++Yes+Yes10
SakamotoYes+NoYesYesNoYesNoNo5
ToyonagaYes+NoYesYesNoYes++Yes+Yes10

Score: no =0; yes =1; yes+ =2; yes++ =3.

Score: no =0; yes =1; yes+ =2; yes++ =3.

Statistical analysis

SPSS software was used for statistical analysis (SPSS version 21, IBM Inc; Armonk, NY, United States). Pooled rates of each outcome were calculated. Differences in en bloc resection and R0 resection rates of EMR and ESD, as well as adverse events and recurrence rates, were evaluated by Chi-square test. Chi-square for trend was used to evaluate heterogeneity. The risk of bias in each study was assessed by the Newcastle-Ottawa Scale for Cohort Studies. All P values were two-sided, and P<0.05 was considered statistically significant.

Results

Numbers and lesions of the included studies

The initial search exhibited a total of 309 studies (EMR: 128, ESD: 181). After removing duplicate records, 191 studies were included (EMR: 71, ESD: 120), which were screened by reading the titles and abstracts. Of these, 30 studies were retrieved by reading the full text carefully and 20 studies (EMR: 4, ESD: 12 and 4 articles including EMR and ESD) were included finally (): 5 monocentric, 14 multicentric and 1 Cross-sectional; 18 retrospective and 2 prospective; 6 studies in China, 6 in Japan and 8 in Korea. Number of all lesions were 3,903 (EMR: 1,230, ESD: 2,673) ().

En bloc and R0 resection rates

En bloc resection rate was reported in all EMR studies, in 1/4 of EMR + ESD (1 not described separately, 1 not reported about EMR and 1 not reported both EMR and ESD), and in 11/12 of ESD. En bloc resection rate of EMR () was reached in 395/591 (66.8%, exclusive of lesions not described separately and not reported), with en bloc resection rate of ESD () reported in 2,020/2,265 (89.2%) [odds ratio (OR) 0.244, P<0.0001, 95% confidence interval (CI): 0.197–0.304].
Figure 2

Endoscopic mucosal resection (EMR) procedure. (A) 2.0 cm × 2.5 cm, rectum, laterally spreading tumor-non-granular type (LST-NG) with flat elevated subtype; (B) LST-NG after submucosal injection of sodium hyaluronate, methylene blue and glycerol fructose solution (1:1:4); (C) endoscopic snare resection; (D) closure with titanium clips.

Figure 3

Endoscopic submucosal dissection (ESD) procedure. (A) 3.0 cm × 3.5 cm, rectum, laterally spreading tumor-granular type (LST-G) with nodular mixed subtype; (B) submucosal injection with Sodium hyaluronate, methylene blue and glycerol fructose solution (1:1:4) and a circumferential mucosal incision using a Jet bipolar needle knife (Jet B-knife); (C) submucosal dissection with a Jet B-knife; (D) titanium clips closing wound; (E) en bloc resected specimen.

Endoscopic mucosal resection (EMR) procedure. (A) 2.0 cm × 2.5 cm, rectum, laterally spreading tumor-non-granular type (LST-NG) with flat elevated subtype; (B) LST-NG after submucosal injection of sodium hyaluronate, methylene blue and glycerol fructose solution (1:1:4); (C) endoscopic snare resection; (D) closure with titanium clips. Endoscopic submucosal dissection (ESD) procedure. (A) 3.0 cm × 3.5 cm, rectum, laterally spreading tumor-granular type (LST-G) with nodular mixed subtype; (B) submucosal injection with Sodium hyaluronate, methylene blue and glycerol fructose solution (1:1:4) and a circumferential mucosal incision using a Jet bipolar needle knife (Jet B-knife); (C) submucosal dissection with a Jet B-knife; (D) titanium clips closing wound; (E) en bloc resected specimen. R0 resection rate was obtained in 3/4 studies about EMR, in 1/4 about EMR+ESD, and in 11/12 about ESD. R0 resection rate was achieved in 409/547 (74.8%) with EMR and in 1,895/2,241 (84.6%) with ESD (OR 0.541, P<0.0001, 95% CI: 0.432–0.677).

Adverse events and follow-up periods

Adverse events occurred in 18/20 studies, including bleeding and perforation. Bleedings occurred in 99/955 (10.4%) with EMR and in 78/2,478 (3.1%) with ESD (OR 3.559, P<0.0001, 95% CI: 2.618–4.836). Perforations in EMR and ESD were in 4/955 (0.4%) and in 101/2,478 (4.1%), respectively (OR 0.099, P<0.0001, 95% CI: 0.036–0.27). Follow-up periods were described in 2/4 EMR studies (ranging from 1.2 to 26 months), in 2/4 EMR + ESD (3 to 35.3 months), and in 8/12 ESD (3 to 89 months), respectively.

Recurrence rate

Recurrence rate was described in 3/4 EMR studies, in 2/4 EMR + ESD, and in 8/12 ESD, which was associated with follow-up periods. Recurrence rate of EMR occurred in 36/573 (6.3%), while the rate of ESD appeared in 17/1,724 (1.0%) (OR 6.732, P<0.0001, 95% CI: 3.751–12.082).

The risk of bias

The risk of bias was small in 6/20 studies with a score ≥10, moderate in 14/20 studies with a score ranging from 5 to 9. The average score was 7.65 (). On account of the stringency of the inclusion criteria, the studies were expected to be homogeneous. Chi-square for trend exhibited P>0.05 suggesting little heterogeneity among the included studies.

Discussion

In the present study, ESD was associated with higher rates of en bloc resection (89.2% vs. 66.8%) and R0 resection (84.6% vs. 74.8%) and a lower risk of bleeding (3.1% vs. 10.4%), resulting in a lower risk of recurrence (1.0% vs. 6.3%) with adequate follow-up periods (3–89 months), but it was accompanied by a higher risk of perforation (4.1% vs. 0.4%) compared with EMR. These outcomes were similar to the previous meta-analyses (35,36). Zhao et al. (35) included 3,062 lesions (EMR: 1,906; ESD: 1,156) compared with EMR, in which ESD had higher rates of en bloc resection and R0 resection, with a lower risk of recurrence and perforation (95.0%, 93.2%, 0.5%, 2.4% vs. 42.8%, 71.9%, 15.9%, 1.8% respectively), but with no significant difference of bleeding (3.5% vs. 4.2%). Although the included studies of this meta-analysis all came from East Asian countries, it was mainly about single-center retrospective studies, and in our study, 5 monocentric and 14 multicentric studies were included. In addition, in EMR group, we included 3 multicentric studies with high rate of bleeding (8.0%, 15.9%, and 9.9% respectively) resulting in a high bleeding rate (10.4%). Russo et al. (36) showed higher rates of R0 resection and perforation in ESD group, a lower risk of bleeding and recurrence (93.6%, 5.9%, 2.8%, 1.1% vs. 84.0%, 1.2%, 9.6%, 12.6% respectively) compared with EMR, but with no significant difference of en bloc resection (97.5% vs. 99.5%). En bloc resection rate of EMR was primarily associated with the size of lesions, which was difficult to be achieved with the lesions ≥20 mm (11). In the present study, the size of lesions was larger than these from non-East Asian countries extracted by Russo et al, leading to a lower rate of en bloc resection. These findings revealed that ESD had a priority for colorectal LSTs, and EMR was also an option with a lower risk of perforation. The resected lesions with ESD were evidently more than EMR in our study, which revealed that endoscopists in East Asia had a higher tendency to ESD for colorectal LSTs. Colonoscopy and endoscopic resection of colorectal neoplasia had reduced the incidence and mortality of CRC (37). ESD was an established endoscopic resection method in Asian countries, especially East Asia, which was increasingly practiced in Europe and the United States for removal of early cancers and large lesions. In the United States, accumulating evidence had found that colorectal neoplasms without signs of deep submucosal invasion or advanced cancer could be resected by ESD, and colorectal neoplasms confined to the mucosa (M) was considered as the criterion standard for no risk for lymph node metastasis (38). The indication criteria of ESD in Japan consisted of intramucosal carcinoma or carcinoma with slight submucosal invasion (SM1, invasion ≤1,000 µm or less than one-third of the submucosa), size with no matter and any macroscopic type (39). In addition, EPMR, a segmental resection method, had some disadvantages in resecting large colorectal tumors owing to incomplete horizontal and vertical margins, and it was difficult to assess invasion depth and lymphovascular invasion. Moreover, EPMR led to significantly higher rates of recurrence compared with en bloc resection (10–20% compared with 1–2% by ESD, OR 8.2) (14,40). Popularization of ESD in East Asian countries was mainly owing to the high incidence and mortality of CRC. Factors limiting ESD application included equipment requirements, technical difficulties, higher costs, longer hospital stay, higher risk of adverse events, etc. Equipment requirements just demanded a carbon dioxide (CO2) insufflator and some cutting tools compared with EMR. Zhang et al. (41) exhibited a learning curve for ESD in the United States, which revealed operators would be proficient in ESD after ~250 cases. ESD was always accompanied by longer hospital stays and higher costs, but compared with surgery, ESD had the advantage of reducing financial savings (42). Moreover, a lower risk of recurrence after ESD was reached, which also decreased costs in the long run. In our study, we found the perforation rates after ESD were higher than EMR, which could be coped with endoscopic titanium clip with little surgical intervention. However, ESD always had a longer procedure time, increasing the difficulty of patient tolerance and the risk of adverse events. Our research had some limitations. Our study focused on East Asian countries without adequate representation worldwide. The risk of moderate bias was the majority of the included studies without a RCT study, which declined the evidence level of this study. For colorectal LST-NGs with a higher recurrence rate after ESD (43), the recurrence rate in our study did not distinguish different endoscopic morphological types. Follow-up periods of the eight included articles were not reported, which also influenced the judgment of recurrence rate. The location and size of colorectal LSTs were not conducted in our study, which affected clinical outcomes and needed further research.

Conclusions

EMR is a safe and effective endoscopic resection technique for colorectal LSTs less than 20mm, but the major limitation remains a high risk of recurrence and an inaccurate histologic evaluation of piecemeal specimens. ESD is a reliable and highly profitable method for larger colorectal LSTs to achieve a higher resection rate, a lower recurrence rate, and an accurate pathological evaluation, but with a higher risk of perforation.
  43 in total

Review 1.  Nonpolypoid neoplastic lesions of the colorectal mucosa.

Authors:  Shin ei Kudo; René Lambert; John I Allen; Hiroaki Fujii; Takahiro Fujii; Hiroshi Kashida; Takahisa Matsuda; Masaki Mori; Hiroshi Saito; Tadakazu Shimoda; Shinji Tanaka; Hidenobu Watanabe; Joseph J Sung; Andrew D Feld; John M Inadomi; Michael J O'Brien; David A Lieberman; David F Ransohoff; Roy M Soetikno; George Triadafilopoulos; Ann Zauber; Claudio Rolim Teixeira; Jean François Rey; Edgar Jaramillo; Carlos A Rubio; Andre Van Gossum; Michael Jung; Michael Vieth; Jeremy R Jass; Paul D Hurlstone
Journal:  Gastrointest Endosc       Date:  2008-10       Impact factor: 9.427

2.  Endoscopic submucosal dissection for laterally spreading tumors in the rectum ≥40 mm.

Authors:  X W Tang; Y T Ren; J Q Zhou; Z J Wei; Z Y Chen; B Jiang; W Gong
Journal:  Tech Coloproctol       Date:  2016-04-06       Impact factor: 3.781

3.  Early Outcomes of Endoscopic Submucosal Dissection for Colorectal Neoplasms According to Clinical Indications.

Authors:  Eui-Gon Youk; Dae Kyng Sohn; Chang Won Hong; Seong Dae Lee; Kyung Su Han; Byung Chang Kim; Hee Jin Chang; Mi-Jung Kim
Journal:  Dis Colon Rectum       Date:  2016-05       Impact factor: 4.585

Review 4.  Endoscopic mucosal resection and endoscopic submucosal dissection for colorectal lesions: A systematic review.

Authors:  Antonella De Ceglie; Cesare Hassan; Benedetto Mangiavillano; Takahisa Matsuda; Yutaka Saito; Lorenzo Ridola; Pradeep Bhandari; Federica Boeri; Massimo Conio
Journal:  Crit Rev Oncol Hematol       Date:  2016-06-16       Impact factor: 6.312

5.  What is the cost of endoscopic submucosal dissection (ESD)? A medico-economic study.

Authors:  Martin Dahan; Emmanuelle Pauliat; Sandra Liva-Yonnet; Sonia Brischoux; Romain Legros; Arnaud Tailleur; Paul Carrier; Aurélie Charissoux; Virginie Valgueblasse; Véronique Loustaud-Ratti; Abdelkader Taibi; Sylvaine Durand-Fontanier; Denis Valleix; Denis Sautereau; Sébastien Kerever; Jérémie Jacques
Journal:  United European Gastroenterol J       Date:  2018-10-28       Impact factor: 4.623

Review 6.  AGA Institute Clinical Practice Update: Endoscopic Submucosal Dissection in the United States.

Authors:  Peter V Draganov; Andrew Y Wang; Mohamed O Othman; Norio Fukami
Journal:  Clin Gastroenterol Hepatol       Date:  2018-08-02       Impact factor: 11.382

7.  Treatment of large colorectal neoplasms by endoscopic submucosal dissection: a European single-center study.

Authors:  Andrzej Białek; Jan Pertkiewicz; Katarzyna Karpińska; Wojciech Marlicz; Dariusz Bielicki; Teresa Starzyńska
Journal:  Eur J Gastroenterol Hepatol       Date:  2014-06       Impact factor: 2.566

8.  Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.

Authors:  Freddie Bray; Jacques Ferlay; Isabelle Soerjomataram; Rebecca L Siegel; Lindsey A Torre; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2018-09-12       Impact factor: 508.702

9.  Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2019 for the treatment of colorectal cancer.

Authors:  Yojiro Hashiguchi; Kei Muro; Yutaka Saito; Yoshinori Ito; Yoichi Ajioka; Tetsuya Hamaguchi; Kiyoshi Hasegawa; Kinichi Hotta; Hideyuki Ishida; Megumi Ishiguro; Soichiro Ishihara; Yukihide Kanemitsu; Yusuke Kinugasa; Keiko Murofushi; Takako Eguchi Nakajima; Shiro Oka; Toshiaki Tanaka; Hiroya Taniguchi; Akihito Tsuji; Keisuke Uehara; Hideki Ueno; Takeharu Yamanaka; Kentaro Yamazaki; Masahiro Yoshida; Takayuki Yoshino; Michio Itabashi; Kentaro Sakamaki; Keiji Sano; Yasuhiro Shimada; Shinji Tanaka; Hiroyuki Uetake; Shigeki Yamaguchi; Naohiko Yamaguchi; Hirotoshi Kobayashi; Keiji Matsuda; Kenjiro Kotake; Kenichi Sugihara
Journal:  Int J Clin Oncol       Date:  2019-06-15       Impact factor: 3.402

10.  Management of colorectal laterally spreading tumors: a systematic review and meta-analysis.

Authors:  Pedro Russo; Sandra Barbeiro; Halim Awadie; Diogo Libânio; Mario Dinis-Ribeiro; Michael Bourke
Journal:  Endosc Int Open       Date:  2019-01-30
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