Literature DB >> 25167797

Clinical outcomes of the endoscopic submucosal dissection of early gastric cancer are comparable between absolute and new expanded criteria.

Keun Young Shin1, Seong Woo Jeon1, Kwang Bum Cho2, Kyung Sik Park2, Eun Soo Kim2, Chang Keun Park3, Yun Jin Chung3, Joong Goo Kwon4, Jin Tae Jung4, Eun Young Kim4, Kyeong Ok Kim5, Byung Ik Jang5, Si Hyung Lee5, Jeong Bae Park6, Chang Hun Yang6.   

Abstract

BACKGROUND/AIMS: Advances in endoscopic submucosal dissection (ESD) techniques have led to the development of expanded criteria for endoscopic resection of early gas-tric cancer (EGC). The aim of this study was to evaluate the short- and long-term outcomes for ESD using indication cri-teria.
METHODS: A total of 1,105 patients underwent ESD for EGC at six medical centers. The patients were classified into the following two groups based on the lesion size, presence of ulceration and pathological review an absolute criteria group (n=517) and an expanded criteria group (n=588).
RESULTS: The curative resection rates (91.1% vs 91.3%, p=0.896) were similar in the absolute criteria group and the expanded criteria group. The en bloc resection rates (93.4% and 92.3%, respectively; p=0.488) and complete resection rates (98.3% and 97.4%, respectively; p=0.357) did not differ between the groups. The cumulative disease-free survival rates and the overall survival rates were similar between the groups (p=0.778 and p=0.654, respectively). Independent factors for the curative resection of EGC included tumor lo-cation (upper vs middle and lower, 2.632 [1.128-6.144] vs 3.497 [1.560-7.842], respectively) and en bloc resection rate 12.576 [7.442-21.250].
CONCLUSIONS: The expanded criteria for ESD in cases of EGC is comparable with the widely ac-cepted pre-existing criteria. (Gut Liver, 2015;9181-187).

Entities:  

Keywords:  Criteria; Endoscopy, gastrointesti-nal; Stomach neoplasms

Mesh:

Year:  2015        PMID: 25167797      PMCID: PMC4351024          DOI: 10.5009/gnl13417

Source DB:  PubMed          Journal:  Gut Liver        ISSN: 1976-2283            Impact factor:   4.519


INTRODUCTION

Gastric cancer is the most prevalent malignant neoplasm in Korea, and the second leading cause of cancer-related death in the world.1,2 Early gastric cancer (EGC) is defined as gastric cancer that is confined to the mucosa or submucosa (T1 cancer), irrespective of the presence of regional lymph node metastasis.3 As current growing number of health examinations and developments in endoscopic technology, more cases of EGC are being detected, corresponding to 47.4% of all gastric cancers in Korea as of 2004.4 Endoscopic mucosal resection (EMR) is widely accepted as an alternative treatment of EGC with a low risk of lymph node metastasis, as it is minimally invasive and has a good safety profile.5,6 At present, the standard guideline criteria for endoscopic resection, which were established by the Japanese Gastric Cancer Association, have been generally accepted, and as follows: a differentiated-type adenocarcinoma without ulcerative findings, of which the depth of invasion is clinically diagnosed as T1a and the diameter is ≤2 cm.7 However conventional EMR nearly always results in piecemeal resection when lesions are larger than 20 mm in diameter, and is not reliable for lesions with ulcer findings.8,9 Conventional EMR is associated with a high risk of local recurrence (2% to 35%), especially when resections are not accomplished en bloc or the margins are not clear.10 Endoscopic submucosal dissection (ESD) has been developed to dissect directly along the submucosal layer using specialized devices, and has advantage over conventional EMR for removing larger or ulcerated EGC lesions in an en bloc manner.8,11 ESD technique enabled to expand the range of criterias of endoscopic treatment in cases of EGC and Gotoda et al.12 and the Japanese Gastric Cancer Association7 recently defined expanded criteria, based on an analysis of the risk of lymph node involvement in more than 5,000 EGCs: (1) mucosal cancer without ulcer findings irrespective of tumor size, (2) mucosal cancer with ulcer findings ≤3 cm in diameter, (3) minute (<500 μm from the muscularis mucosae) submucosal invasive cancer ≤3 cm in size, and (4) undifferentiated type mucosal cancer ≤2 cm in size without ulceration. However, the outcomes of EGC patients treated by ESD that fulfilled the new expanded inclusion criteria remain uncertain. The purpose of this study was to evaluate the feasibility and efficacy of expanded criterias for ESD as a treatment of EGC and to compare it with other criteria.

MATERIALS AND METHODS

1. Patients

A total of 1,105 EGCs in 1,105 consecutive EGC patients were treated by ESD at the six hospitals in the Daegu Kyungpook area in Korea from February 2003 to May 2010. The patients were enrolled based on the criteria proposed by Gotoda et al.12 and the Japanese Gastric Cancer Association.7 EGCs which did not meet these criteria were recommended to receive a gastrectomy with removal of lymph nodes. The study was approved by the Institutional Review Board of each medical center. Before ESD, all patients provided oral and written informed consent for the procedure. We retrospectively reviewed a prospectively maintained database of all patients with EGC treated with ESD. The patients were divided into two groups according to the endoscopic findings and histopathological diagnoses. The absolute criteria A group is defined as a differentiated-type adenocarcinoma without ulcerative findings, of which the depth of invasion is clinically diagnosed as T1a and the diameter is ≤2 cm. The expanded criteria E group is defined as tumors clinically diagnosed as T1a and: (a) of differentiated-type, ulcer (−), but >2 cm in diameter (b) of differentiated-type, ulcer (+), and ≤3 cm in diameter (c) of undifferentiated-type, ulcer (−), and ≤2 cm in diameter.

2. Endoscopic submucosal dissection

The ESD procedure was carried out in a standardized way. After informed consent was obtained, the ESD was performed in patients under conscious sedation with intravenous midazolam and meperidine. The procedure was performed by experienced endoscopists who performed EMR or EMR-precutting (EMR-P) over 100 cases. To determine the resection margin, chromoendoscopy with indigo carmine or narrow-band imaging (NBI) was performed in addition to conventional white light endoscopy. And then the area at about 5 mm lateral to the lesions was marked with spotty cautery with various endoscopic knives (IT knife or hook knife; Olympus, Tokyo, Japan). Then, submucosal injection of hypertonic saline mixed with epinephrine (1:10,000) or glycerol, and sodium hyaluronate was performed to lift the lesion. The endoscope was passed to the submucosa and dissection was performed under direct vision with an endoscopic knife in the caudal direction. The resected lesion was spread to mark the orientation with pins and fixed with 10% formalin solution; it was then brought to pathology for histological evaluation and diagnosis.

3. Complications

The perforations were divided into two types: macroperforation, defined as a gross defect noted during the procedure, with extraluminal organs, fatty tissues or space visualized through the lesion endoscopically, irrespective of the presence of air accumulation in the abdomen, retroperitoneum, or mediastinum; or microperforation defined as a perforation that was invisible during procedure but was recognized as free air on a plain radiography (abdomen, retroperitoneum, mediastinum) after the procedure.13

4. Histopathological evaluation

The macroscopic lesions were classified into the elevated type and the flat/depressed type. EGC location was classified into the upper, middle, and lower third of the stomach. Ulcer was defined as mucosal defect, mucosal deformity, or converging fold by endoscopic findings, or submucosal fibrosis. Resection specimens were stretched with needles and sent for histopathological assessment and sectioned perpendicularly at 2 mm intervals. The histology was divided into differentiated adenocarcinoma (well or moderately differentiated or papillary adenocarcinoma) or undifferentiated adenocarcinoma (poorly differentiated or signet ring cell carcinoma). Tumor involvement to the horizontal and deep margins, lymphatic and vascular involvement, tumor size, and presence or absence of submucosal invasion were assessed. In cases with submucosal infiltration, invasion depth was measured and described quantitatively. En bloc resection was defined as a single resection procedure performed for a single lesion; and piecemeal resection as multiple resection procedures for a single lesion.14 The complete resection was defined as R0 resection: complete en bloc resection with vertical and horizontal margins free of neoplasia at histology. The curative resection was defined as en bloc and margin negative resection without lymphovascular involvement in the absolute and expanded criteria groups.7

5. Follow-up

The patients were followed up with an endoscopic examinations with a biopsy at 3, 6, and 12 months after ESD and then annually. To avoid case losses, we attempted to identify details by questionnaires or telephone conversation with the patients, in particular in those who delayed the follow up period. To access the presence of local recurrence or metachronous cancer, biopsy was done from the treatment-related scar or any other suspicious abnormalities. In addition, an abdominal computed tomography (CT) and/or positron emission tomography/CT was performed annually to detect lymph node and distant metastases. The cumulative disease-specific and overall survivals were estimated.

6. Statistical analysis

The significance of differences in patients’ characteristics and clinicopathological features was determined using chi-square test, Fisher exact test, the Mann-Whitney U-test, or Student t-test. Factors associated with curability of ESD were analyzed using logistic regression analysis. Odds ratios, together with 95% confidence intervals, were calculated to estimate the relative risk of noncurative resection and their associations with various parameters. Data for the long-term outcomes were calculated using the Kaplan-Meier method and analyzed by the log rank test. p-values <0.05 were considered statistically significant.

RESULTS

1. Characteristics of patients and lesions

1) Clinical features of patients

A total of 1,105 EGCs in 1,105 consecutive patients were included in our analysis and they were divided into two groups; A group (517 patients) and E group (588 patients). We targeted one EGC lesion by each person, which was the largest one or was included the highest criteria group. The E group consisted of 232 mucosal cancer without ulcer findings larger than 2 cm in tumor size, 281 mucosal cancer with ulcer findings ≤3 cm in diameter, 27 minute (<500 μm from the muscularis mucosae) submucosal invasive cancer ≤3 cm in size, and 48 undifferentiated type mucosal cancer ≤2 cm in size without ulceration (Fig. 1).
Fig. 1

Classification of patients with early gastric cancer (EGC) according to the endoscopic and histopathological diagnoses: 517 patients were in the absolute criteria group, and 588 patients were in the expanded criteria group. SM, submucosa.

The median age of the patients was 64 years (33 to 87 years) for the A group, 66 years (27 to 87 years) for the E group. All of the groups have higher distribution of men than women (Table 1). Major comorbidity included malignancies other than EGC, cerebrovascular event, cardiopulmonary diseases, chronic kidney or hepatic diseases, and hematologic diseases which result the limitation of physical activities and need periodic treatment. Patients with major comorbidities accounted for 6.4% in the A group, and 5.3% in the E group (p=0.430).
Table 1

Clinicopathological Characteristics Based on the Indication Criteria

CharacteristicAbsolute criteria group (n=517)Expanded criteria group (n=588)p-value
Age, yr64 (33–87)66 (27–87)0.143
Gender, female/male, %34.6/65.430.3/69.70.123
Macroscopic appearance<0.001
 Elevated277 (53.6)251 (42.7)
 Flat/depressed240 (46.4)337 (57.3)
Tumor size, mm<0.001
 <20517 (100.0)309 (52.6)
 20–30183 (31.1)
 >3096 (16.3)
Location0.237
 Upper24 (4.6)23 (3.9)
 Middle135 (26.1)180 (30.6)
 Lower358 (69.2)385 (65.5)
Ulcer findings<0.001
 Present0294 (50.0)
 Abscent517 (100.0)294 (50.0)
Invasion depth<0.001
 M517 (100.0)540 (91.8)
 SM1048 (8.2)
 SM200
Major comorbidity33 (6.4)31 (5.3)0.430
Delayed bleeding17 (3.3)27 (4.6)0.269
Perforation14 (2.7)18 (3.1)0.727
 Microperforation1114
 Macroperforation34

Data are presented as median (range) or number (%).

M, mucosa; SM, submucosa.

2) Characteristics of resected lesions

The most common location of the lesion was the lower third of the stomach in all groups (69.2%/65.5%, respectively). The elevated type of lesion was more common in the A group than in the E group (Table 1), and this difference was statistically significant (53.5%/42.6%, p<0.001). The mean tumor size was 12.51±0.23 mm in the A group, and 22.91±0.55 mm in the E group; The A group has significantly smaller lesion size than the E group (p<0.001). The ulcer findings by gross appearance were 50.0% in the E group.

2. Results of the ESD

1) Resectability, complete resection, and curability of ESD

The frequency of endoscopic en bloc resections was 92.9% (1,026/1,105) in all lesions; it was 93.4% in the A group, and 92.3% in the E group and there was no statistically significant difference between the groups (p=0.488) (Table 2). A complete resection rate was 97.8% (1,081/1,105) in all lesions; 98.3% in the A group, and 97.4% in the E group, however, this difference was not statistically significant (p=0.357). Of the 1,105 lesions, 1,008 (91.2%) were defined as curative; the curative resection rate was 91.1% in the A group and 91.3% in the E group, there was no statistically significant difference between the two groups (p=0.896).
Table 2

Resectability, Completeness, and Curability of Endoscopic Submucosal Dissection for Early Gastric Cancer and the Indication Criteria

Absolute criteria group (n=517)Expanded criteria group (n=588)p-value
Resectability0.488
En bloc resection483543
 Piecemeal resection3445
En bloc resection rate, %93.492.3
Completeness0.357
 Complete508573
 Incomplete915
 Complete resection rate, %98.397.4
Curability0.896
 Curative471537
 Noncurative4651
 Curative resection rate, %91.191.3

Data are presented as number.

Table 3 shows the association of various factors with curability of ESD. On univariate analysis, the location of the lesion, and the presence of ulcer and en bloc resection had a significant impact on ESD curability (p<0.001, p=0.020, and p<0.001, respectively). On a multivariate analysis, the tumor location: upper versus middle and lower, 2.632 (1.128–6.144) and 3.497 (1.560–7.842), and the presence of en bloc resection: 12.576 (7.442–21.250) were related to the curability.
Table 3

Association of Clinicopathological Characteristics of the 1,105 Early Gastric Cancer Lesions with Curability of Endoscopic Submucosal Dissection

CharacteristicUnivariate analysisMultivariate analysis


OR (95% CI)p-valueOR (95% CI)p-value
Age0.995 (0.973–1.017)0.633--
Gender
 Female1-
 Male0.666 (0.413–1.076)0.097--
Tumor size, cm
 <2.01-
 2.0–3.00.659 (0.392–1.109)0.116--
 >3.00.660 (0.335–1.299)0.229--
Tumor location
 Upper11
 Middle3.381 (1.619–7.061)0.0012.632 (1.128–6.144)0.025
 Lower5.081 (2.527–10.216)<0.0013.497 (1.560–7.842)0.002
Macroscopic appearance
 Elevated1-
 Flat/depressed1.213 (0.795–1.853)0.370--
Ulcer findings
 Absent11
 Present1.928 (1.108–3.354)0.0201.644 (0.917–2.947)0.095
Resectability
En bloc14.183 (8.491–23.693)<0.00112.576 (7.442–21.250)<0.001
 Piecemeal11

OR, odds ratio; CI, confidence interval.

2) Follow-up observations and recurrence rates

The rate of surgical treatment was 3.8% (42/1,105) in all patients; 3.5% (18/517) in the A group, and 4.1% (24/588) in the E group (Fig. 2). These 42 patients who underwent surgical treatment and the patients with a follow-up period of <1 year were excluded from the disease-free survival and overall survival analysis, and thus 1,063 patients treated by ESD were eligible for the analyses.
Fig. 2

Flowchart of patients included in this study. A total of 1,105 lesions from 1,105 patients were included in endoscopic outcomes. EGC, early gastric cancer; CR, complete resection; OP, operation; IR, incomplete resection.

The cumulative disease-free survival rates did not significantly differ between the A group and the E group (p=0.778). The 1-year disease-free rates were 99.3% in the A group, and 99.6% in the E group, and the 3-year disease-free survival rates were 98.1%, and 97.1%, respectively (Fig. 3).
Fig. 3

Kaplan-Meier estimates of disease-free survival rates in the absolute and expanded criteria groups. There were no significant between-group differences (p=0.778).

The cumulative overall survival rates did not differ significantly between the groups (Fig. 4). The 3-year overall survival rates were 99.0% in the A group, and 98.6% in the E group (p=0.654).
Fig. 4

Kaplan-Meier estimates of overall survival rates in the absolute and expanded criteria groups. There were no significant between-group differences (p=0.654).

3) Complications

Perforation occurred in 32 out of 1,105 lesions. Macroperforations occurred during ESD in seven lesions and microperforation was identified in 25 lesions. They were successfully managed by decompression of the pneumoperitoneum with an 18-gauge puncture needle and/or hemoclipping of the perforation site and with systemic antibiotics. Delayed bleeding occurred in 44 out of 1,105 lesions, and the mean time to bleeding was 98 hours after the procedure; all patients recovered with endoscopic intervention and conservative treatment, there was no need for surgical intervention. There was no difference in the frequency of delayed bleeding and perforation based on the criteria in this study (p=0.300 and p=0.688).

DISCUSSION

Endoscopic resection is less invasive and more cost-effective than surgery,10 and preserving the organ involved as well as patient quality of life. Thus, endoscopic resection has recently become an alternative treatment modality for EGC patients at low risk of lymph node metastasis or for whom surgery might be dangerous.6,10,15 Despite the expanding use of the criterias of ESD for EGC in clinical practice, the clinical outcomes for this new criterias have not been fully evaluated.7 Our study was designed to have an evidence for this clinical practice. In this present study, en bloc resection rate in the E group is similar within the A group (92.3% vs 93.4%), and the reported en bloc resection rate of ESD ranges from 91.9% to 98.6%.16–18 Some recent studies reported a significant difference in the curative resection rate between the A group and the E group (97.0% vs 90.4% and 97.1% vs 91.1%, respectively).16,17 In contrast, our study showed no statistically significant difference in the curative resection rate between the A group (91.1%) and the E group (91.3%). We think that the reason of these different results among the studies might be that our definition of ulcer was distinct from other studies. We included mucosal defect as an ulcer, which was actually defined as erosion, therefore, the proportion of our E group was higher than the other studies. According to the result of our study, erosion has no influence on the outcome of ESD in EGC patient. Another recent study evaluated the validity of expanding the criterias for ESD and reported the 1-year disease-free survival rate and the cumulative disease-free survival rate did not differ significantly between the A group and the E group.18 We also found that the cumulative disease-free survival rate did not differ significantly between the A group and E group. A recent study reported a comparable overall survival between the A group and the E group.16 Our study also found that the 3-year overall survival rates did not significantly different among the A group and the E group. Using logistic regression analysis, we assessed the impact of various factors on the curability of ESD. The location of lesion and en bloc resection were the independent factors for curative resection. One recent study reported that the tumor size larger than 3 cm, ulceration, histological type, and piecemeal resection were the unfavorable factors of curative resection.19 Our study also revealed that piecemeal resection represented an independent factor for noncurative resection. More distal location of lesion was also the favorable factor of curative resection. Macroscopic classification of the lesions was divided into the elevated type and the flat/depressed type, and was not the independent factors for curative resection. A recent study on the comparison of the outcomes of 1,627 cases EGCs after endoscopic resection based on the criteria20 reported that with the ESD method, the absolute criteria group has significantly higher rates of complete resection (97.8% vs 91.1%, p<0.001) and margin-negative status (98.8% vs 91.7%, p<0.001) than those in the expanded criteria group. They also reported the 3-year disease-specific, local recurrence-free rate 98.8% to 99.0% in the A group and 98.5% in the E group, and differences between criteria groups were not significant (p=0.547). Our 3-year local and metachronous recurrence-free survival rates were slightly lower than that (98.1% vs 97.1%, p=0.778). At a median follow-up period of 32 months, we observed 22 locally and metachronous recurrent tumors (2.1%). None of them was died in the follow-up period, and five were treated by surgery. The major complications associated with the ESD were bleeding and perforation.21 The frequency of hemorrhagic complications has been reported to be 1.5% to 24%; the variation is due to the definition used as well as the type of resected lesion reported.11,21 Immediate bleeding developed in 172 cases out of the 1,105 cases (15.6%) in this study, and delayed bleeding developed in 44 cases out of the 1,105 cases (4.0%); most of them were minor bleeding that occurred during or after the procedure without changes in the vital signs. Perforation is another major complication; the frequency of perforation has been reported to be 0% to 6.7%.16,21,22 The overall frequency of perforations found in this study was 2.9% (microperforation, 2.3%; macroperforation, 0.6%), and they were diagnosed during or after ESD, managed with endoscopic procedures and conservative treatment without the need for further surgery. There are several limitations in this study. First, this was retrospective study design, so there was potential for a selection bias. To minimize the selection bias, we included almost all patients with EGC treated by ESD who were identified within the database. Second, because the data were collected from multicenter, the ESD procedures were performed by several endoscopists. This could make differences in the indications of ESD or histopathological diagnoses. Lastly, this study has relatively short median follow-up period, so further study is needed with long-term results over 5 years and in prospective manner to establish the validity of ESD results. In conclusion, ESD was effective for treatment of expanded criteria of EGC. The rate of E group’s en bloc resection and complete resection was comparable with A group. Further prospective investigation is needed to assess the long-term prognosis and survival.
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7.  Endoscopic and oncologic outcomes after endoscopic resection for early gastric cancer: 1370 cases of absolute and extended indications.

Authors:  Ji Yong Ahn; Hwoon-Yong Jung; Kee Don Choi; Ji Young Choi; Mi-Young Kim; Jeong Hoon Lee; Kwi-Sook Choi; Do Hoon Kim; Ho June Song; Gin Hyug Lee; Jin-Ho Kim; Young Soo Park
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8.  Predictive risk factors of perforation in gastric endoscopic submucosal dissection for early gastric cancer: a large, multicenter study.

Authors:  Min Kim; Seong Woo Jeon; Kwang Bum Cho; Kyung Sik Park; Eun Soo Kim; Chang Keun Park; Hyang Eun Seo; Yun Jin Chung; Joong Goo Kwon; Jin Tae Jung; Eun Young Kim; Byeong Ik Jang; Si Hyung Lee; Kyeong Ok Kim; Chang Hun Yang
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Journal:  Gut       Date:  2008-11-10       Impact factor: 23.059

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Journal:  Surg Endosc       Date:  2015-07-09       Impact factor: 4.584

Review 2.  [Endoscopic techniques for early stage cancer of the upper and lower gastrointestinal tract : Possibilities and limitations].

Authors:  A Probst; A Ebigbo; H Messmann
Journal:  Chirurg       Date:  2018-05       Impact factor: 0.955

3.  Endoscopic submucosal dissection of gastric tumors: A systematic review and meta-analysis.

Authors:  Emmanuel Akintoye; Itegbemie Obaitan; Arunkumar Muthusamy; Olalekan Akanbi; Mayowa Olusunmade; Diane Levine
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4.  Endoscopic Indication of Endoscopic Submucosal Dissection for Early Gastric Cancer Is Not Compatible with Pathologic Criteria in Clinical Practice.

Authors:  Seong Woo Jeon; Hyun Woo Park; Yong Hwan Kwon; Su Youn Nam; Hyun Seok Lee
Journal:  Dig Dis Sci       Date:  2018-10-11       Impact factor: 3.199

5.  Diagnostic group classifications of gastric neoplasms by endoscopic resection criteria before and after treatment: real-world experience.

Authors:  Jun Hee Lee; Yang Won Min; Jun Haeng Lee; Eun Ran Kim; Hyuk Lee; Byung-Hoon Min; Jae J Kim; Kee-Taek Jang; Kyoung-Mee Kim; Cheol Keun Park
Journal:  Surg Endosc       Date:  2015-12-22       Impact factor: 4.584

6.  Enormous postoperative perforation after endoscopic submucosal dissection for duodenal cancer successfully treated with filling and shielding by polyglycolic acid sheets with fibrin glue and computed tomography-guided abscess puncture.

Authors:  Yoshiko Ohara; Kengo Takimoto; Takashi Toyonaga; Tomohiro Yamaguchi; Hiroya Sakaguchi; Fumiaki Kawara; Shinwa Tanaka; Tsukasa Ishida; Yoshinori Morita; Eiji Umegaki
Journal:  Clin J Gastroenterol       Date:  2017-11-01

7.  The Feasibility of Performing Colorectal Endoscopic Submucosal Dissection Without Previous Experience in Performing Gastric Endoscopic Submucosal Dissection.

Authors:  Dong-Hoon Yang; Gwi Hong Jeong; Yerim Song; Sang Hyoung Park; Soo-Kyung Park; Jong Wook Kim; Kee Wook Jung; Kyung-Jo Kim; Byong Duk Ye; Seung-Jae Myung; Suk-Kyun Yang; Jin-Ho Kim; Young Soo Park; Jeong-Sik Byeon
Journal:  Dig Dis Sci       Date:  2015-06-19       Impact factor: 3.199

8.  Colorectal Endoscopic Submucosal Dissection in a Western Center: Analysis of Outcomes and Safety Profile.

Authors:  João Santos-Antunes; Margarida Marques; Rui Morais; Fátima Carneiro; Guilherme Macedo
Journal:  GE Port J Gastroenterol       Date:  2021-04-09

9.  Real-life evaluation of the safety, efficacy and therapeutic outcomes of endoscopic submucosal dissection in a Western tertiary centre.

Authors:  João Santos-Antunes; Francisco Baldaque-Silva; Margarida Marques; Joanne Lopes; Fátima Carneiro; Guilherme Macedo
Journal:  United European Gastroenterol J       Date:  2018-01-23       Impact factor: 4.623

10.  Expanding indications of endoscopic submucosal dissection for early gastric cancer: hope or hype?

Authors:  Hyuk Lee; Jun Haeng Lee
Journal:  Gut Liver       Date:  2015-03       Impact factor: 4.519

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