Introduction
Gastric cancer is a common neoplasm worldwide and was the second most common malignancy
causing death in 2018 following lung cancer [1]. Since the evolution of endoscopy, including image enhanced endoscopy, facilitates
the early detection of gastric cancer, indications for minimally invasive resection
are expanding. Endoscopic submucosal dissection (ESD) is one of the standard endoscopic
treatments for superficial gastric neoplasms. However, the difficulty associated with
performing ESD of gastric lesions varies greatly depending on the location of the
lesion because the stomach has a wide lumen and unique shape. ESD of gastric lesions
in difficult locations increases the risk of adverse events and prolongs procedure
time due to slow rate of dissection. Gastric neoplasms involving the pyloric ring
is one of the difficult situations encountered in ESD of gastric lesions [2]. The working space around the pyloric ring is limited. At the duodenal bulb, the
presence of Brunner’s glands and poor mucosal elevation after injection make ESD difficult.
In the conventional method (CM), an antegrade approach creates a vertical approach
to the pyloric sphincter and the submucosal side of the dissected mucosa. After getting
over the pyloric ring, a horizontal approach in the duodenal bulb is difficult due
to the firm and high muscularis at the pyloric ring ([Fig. 1a]). Retroflexion in the duodenal bulb is one option to overcome this difficulty. However,
a vertical approach to the duodenal wall is inevitable in the area near the pyloric
sphincter. Poor maneuverability during retroflexion has the potential to cause perforation
due to the thin wall and narrow lumen of the duodenum ([Fig. 1b]). Further, retroflexion requires a slim endoscope with a small working channel that
restricts the kind of devices that can be introduced. A traction device such as the
clip-and-line method has been reported to overcome these difficulties [3]. However, traction cannot facilitate opening the submucosal layer in the duodenum,
because it cannot compress the pyloric sphincter but just pulls the lesion.
Fig. 1 The conventional method was performed as follows. a An antegrade approach gives a vertical approach at the pyloric sphincter. To avoid
the solid muscularis of the pyloric sphincter, the upward angle also leads to a vertical
approach against the submucosal side of the dissected mucosa that may damage the resected
specimen. After getting over the pyloric ring, a horizontal approach in the duodenal
bulb is impossible because the dissected mucosa falls down to the duodenal side and
the tip of the endoscope becomes unstable due to the high muscularis of the pyloric
ring. b With a retroflexed approach, maneuverability is limited in the narrow space in the
duodenal bulb. The vertical approach at the pyloric sphincter makes submucosal dissection
difficult.
We invented the pocket-creation method (PCM) to overcome the difficulties associated
with ESD and reported its usefulness in performing stable and reliable ESD [4]
[5]. In short, the PCM is characterized by a minimal mucosal incision and making a pocket
without a circumferential incision. The PCM has four major advantages: (1) preventing
leakage of injected solution, (2) applying both traction and counter-traction, (3)
conquering the tangential approach and (4) stabilization of the tip of the endoscope
in the pocket [4]. We believe that the PCM is especially helpful to overcome the above-mentioned difficult
circumstances associated with ESD of superficial gastric lesions involving the pyloric
ring ([Fig. 2], [Fig. 3], [Fig. 4], [Video 1]). In performing ESD of gastric lesions involving the pyloric ring, compressing the
pyloric sphincter is the key to accomplishing an en bloc resection. Compression can be achieved by providing traction and counter-traction
using the PCM with a small-caliber-tip transparent hood (ST-hood). The PCM prevents
migration of the mucosa being dissected into the duodenum due to a minimal mucosal
incision and enables antegrade straightforward submucosal dissection even in the duodenum
without retroflexion. The aim of this study was to clarify usefulness of the PCM for
ESD of superficial gastric neoplasms requiring duodenal submucosal dissection beyond
the pyloric ring compared to the CM.
Fig. 2 The pocket-creation method with an ST hood is performed as follows. a The duodenal side of the tumor is incised without submucosal dissection. b The gastric side is minimally incised and then dissected to make a pocket. c At the pyloric ring, stable and well-visualized submucosal dissection is enabled
by compressing the pyloric sphincter using both traction and counter-traction (red
arrows). The tip of the endoscope is effectively held by the pocket (blue arrow).
d A tunnel is created from the gastric to the duodenal sides in an antegrade manner.
Fig. 3 Schematic of the pocket-creation method viewed from above. a A mucosal incision is made on the duodenal side of the tumor to the pyloric ring.
b A minimal mucosal incision is made on the gastric side. c A large submucosal pocket is created under the tumor while compressing the pyloric
sphincter. d A tunnel is created from the gastric to the duodenal sides in an antegrade manner.
Submucosal dissection under the lesion should be completed before opening the pocket.
e The pocket is opened in a step-by-step manner working toward the distal side and
against gravity. f The remaining area is dissected and an en bloc resection is accomplished.
Fig. 4 An example of endoscopic submucosal dissection with the pocket-creation method. a A gastric elevated lesion involving the pyloric ring observed from the gastric side.
b Observed from the duodenal side with retroflexion. c First mucosal incision at the distal side in the duodenal bulb. d A minimal mucosal incision of the proximal side in the stomach. e Antegrade approach compressing the pyloric sphincter using both traction and counter-traction
by the tip of the ST-hood. f Reaching the first mucosal incision of the duodenal bulb. g Submucosal dissection of lateral side when opening the pocket. h The mucosal defect in the stomach. i The mucosal defect in the duodenum. j The mucosal side of the resected specimen. The resected specimen is 36x23 mm in size.
k The submucosal side of the resected specimen. The central depression indicates the
pyloric sphincter (arrows). l The yellow line indicates the border between the stomach and duodenum and red lines
indicate the presence of carcinoma. m The pathology is a well- to moderately-differentiated intramucosal adenocarcinoma
with negative horizontal and vertical margins and without lymphovascular invasion
or ulceration. n The duodenal mucosa has a Brunner’s gland (arrows).
Video 1 Procedure for endoscopic submucosal dissection of gastric neoplasms involving the
pyloric ring with the pocket-creation method.
Patients and methods
Study population
From October 2006 to August 2019, 2258 gastric lesions were treated with ESD at Jichi
Medical University Hospital. Of these 2258 lesions, 66 lesions in 66 patients required
duodenal submucosal dissection beyond the pyloric sphincter. We retrospectively reviewed
the medical records of these patients. The PCM was introduced in September 2014. The
CM was performed during the first period (October 2006 to August 2014) except in two
patients (CM group, n = 46) and the PCM was performed during the second period (September
2014 to August 2019, PCM group, n = 20) ([Fig. 5]). We compared the PCM group to the CM group (control group). Informed consent regarding
ESD was obtained. The Institutional Review Board approved this retrospective review
(ID#A19–255).
Fig. 5 Inclusion process for the study.
Endoscopic resection
All patients were hospitalized and underwent ESD under conscious sedation with pethidine
and midazolam. All ESD procedures were performed by expert endoscopists, defined as
an endoscopist with an experience of having performed more than 50 ESD procedures
of gastric lesions. An endoscope with a waterjet instrument (EG-450RD or EG-580RD,
Fujifilm, Tokyo, Japan) was used for submucosal dissection without retroflexion. If
retroflexion was required in the CM, an endoscope (GIF-XQ240, Olympus, Tokyo, Japan)
was used for marking, mucosal incision and submucosal dissection in the duodenum.
In the PCM, retroflexion was not required in any cases. Carbon dioxide insufflation
was used. A small-caliber-tip transparent (ST) hood (DH-15GR [conventional ST hood]
or DH-28GR [short ST hood], Fujifilm) or a cylindrical hood (D-201-10804, Olympus)
fitted to the tip of the endoscope was used. The injection solution was 0.4 % sodium
hyaluronate (MucoUp, Seikagaku, Tokyo, Japan) with 0.002 %–0.004 % indigo carmine
and 0.001 % epinephrine. We used a Flush knife BT (DK2618JB-15, Fujifilm), a DualKnife
(KD-650Q, Olympus), a SAFE Knife V (DK2518DV15, Fujifilm) or a needle knife (KD-10Q-1,
Olympus). To control bleeding during the ESD procedure, hot hemostatic forceps (HOYA
Corporation, Tokyo, Japan) were used. The electrosurgical generator used was an ICC
200 or a VIO300 D (ERBE Elektromedizin GmbH, Tübingen, Germany).
En bloc resection was defined as endoscopic resection yielding a single piece macroscopically.
An R0 resection was defined as an en bloc resection with negative pathological margins for both adenoma and adenocarcinoma.
The area of the resected specimen was calculated with the following formula: major
axis (mm)/2 × minor axis (mm)/2 × 3.14. The dissection time was defined as the time
between the initial mucosal incision and completion of the resection. The dissection
speed was calculated with the following formula: specimen area (mm2)/dissection time (minutes) [6]. Intraprocedural and delayed perforations were defined as perforations during or
after the ESD procedure, respectively. Delayed bleeding was defined as melena or hematochezia
with a decrease in hemoglobin concentration of more than 2 g/dL, requiring transfusion
or requiring endoscopic hemostasis within 14 days after ESD [7]. The primary outcome measure was the R0 resection rate, and secondary outcome measures
included the en bloc resection rate, presence of holes in the resected specimens, positive horizontal/vertical
margins, dissection speed, requirement for snare use and the incidence of adverse
events.
Statistical analysis
Stata software version 16 (StataCorp LLC, Texas, United States) was used for analysis,
and differences were considered significant when P < 0.05. Data without a normal distribution were evaluated using the Mann-Whitney
U-test. Categorical data were assessed with the chi-square test.
Results
Baseline characteristics of patients
There were no differences between the PCM and CM groups in baseline characteristics
such as location, macroscopic type and size except for the presence of an ulcer ([Table 1]). A conventional ST hood was used more often than in the PCM group compared to the
CM group, because the ST hood is essential for the PCM to obtain both traction and
counter-traction in the pocket. Traction devices were not used in any procedure.
Table 1
Baseline characteristics of patients.
|
Characteristics
|
Pocket-creation method
|
Conventional method
|
P value
|
|
Number of lesions
|
20
|
46
|
|
|
Number of patients
|
20
|
46
|
|
|
Age, median (range), years
|
73 (70–79)
|
76 (68–79)
|
0.818
|
|
Gender, male, n (%)
|
13 (65)
|
29 (63)
|
0.879
|
|
Tumor location, n (%)
|
|
|
10 (50)
|
22 (48)
|
0.871
|
|
|
2 (10)
|
4 (9)
|
0.865
|
|
|
5 (25)
|
11 (24)
|
0.925
|
|
|
3 (15)
|
9 (19)
|
0.659
|
|
Macroscopic type
|
|
|
5 (25)
|
22 (48)
|
0.083
|
|
|
15 (75)
|
24 (52)
|
|
|
Hood
|
|
|
0 (0)
|
11 (24)
|
0.017
|
|
|
15 (75)
|
21 (46)
|
0.028
|
|
|
5 (25)
|
14 (30)
|
0.654
|
|
Antiplatelet or anticoagulation
|
4 (20)
|
4 (9)
|
0.196
|
ST, small-caliber-tip.
Quality of ESD
Although no significant differences were observed in en bloc resection rates between the two groups, the PCM group had a significantly higher
R0 resection rate than the CM group (P = 0.047) ([Table 2]). There were no holes in the resected specimens in the PCM group while three lesions
(7 %) had a hole in the CM group. The dissection speed in the PCM group was faster
than in the CM group, although this difference did not reach statistical significance.
No significant differences were observed in the incidence of adverse events. All delayed
bleeding was successfully stopped by endoscopic hemostasis. No patient developed a
stricture after ESD.
Table 2
Clinical outcomes and adverse events.
|
Characteristics
|
Pocket-creation method
|
Conventional method
|
P value
|
|
Tumor diameter, median (range), mm
|
23 (13–35)
|
20 (13–35)
|
0.748
|
|
Pathologic findings, n (%)
|
|
|
0 (0)
|
1 (2)
|
0.506
|
|
|
17 (85)
|
41 (89)
|
0.637
|
|
|
1 (5)
|
3 (7)
|
0.812
|
|
|
2 (10)
|
1 (2)
|
0.161
|
|
|
2 (10)
|
0 (0)
|
0.029
|
|
|
2 (10)
|
1 (2)
|
0.161
|
|
|
1 (5)
|
1 (2)
|
0.538
|
|
|
1 (5)
|
0 (0)
|
0.126
|
|
En bloc resection, n (%)
|
20 (100)
|
45 (98)
|
0.506
|
|
R0 resection, n (%)
|
20 (100)
|
38 (83)
|
0.047
|
|
Hole in resected specimen, n (%)
|
0 (0)
|
3 (7)
|
0.242
|
|
Positive horizontal margin, n (%)
|
0 (0)
|
3 (7)
|
0.242
|
|
Positive vertical margin, n (%)
|
0 (0)
|
6 (13)
|
0.090
|
|
Positive horizontal and vertical margin, n (%)
|
0 (0)
|
1 (2)
|
0.506
|
|
Resected specimen diameter, median (range), mm
|
45 (37–53)
|
40 (31–49)
|
0.270
|
|
Dissection time, median (range), min
|
75 (58–111)
|
75 (50–115)
|
0.856
|
|
Dissection speed, median (range), mm2/min
|
16 (12–25)
|
11 (8–20)
|
0.148
|
|
Follow-up snare resection, n (%)
|
0 (0)
|
1 (2)
|
0.506
|
|
Delayed bleeding, n (%)
|
2 (10)
|
2 (4)
|
0.376
|
|
Perforation, n (%)
|
0 (0)
|
0 (0)
|
1.000
|
Discussion
This retrospective observational study demonstrates the usefulness of the PCM for
ESD of gastric lesions involving the pyloric ring. In the PCM group, the R0 resection
rate was significantly higher than that of the CM group. In the CM group, six specimens
had positive vertical margins including three with a hole, while no specimen in the
PCM group had these unfavorable events. We suspect that incorrect direction of the
endoknife caused by a firm pyloric sphincter damaged specimens being resected in the
CM group ([Fig. 1a]). We believe that the PCM with the ST hood is a useful and suitable method to accomplish
this difficult ESD by compressing the firm elevated sphincter muscle using both traction
and counter-traction in the pocket.
In this study, ESD with the CM could not accomplish an R0 resection in eight patients
(17 %). First, the mucosa being dissected gradually slides down into the duodenum
making submucosal dissection quite difficult due to the downward view in the CM. In
this case, snare resection during the last stage of ESD is necessary and adequate
margins cannot be maintained. Using a snare may damage the specimen. Second, the CM
cannot compress the pyloric sphincter because of the circumferential mucosal incision
in the stomach. In getting over the pyloric ring, the endoscope approach becomes vertical
to the sphincter and the tip of endoscope goes into the lesion resulting in cutting
of the specimen being resected ([Fig. 1]). Even if a hole is not in the specimen, a thick submucosal layer may not be obtained
with the CM. Three resected specimens in the present study had positive vertical margins.
However, the PCM accomplished an R0 resection of all lesions including two lesions
with ≥ 500-µm submucosal invasion by obtaining a thick submucosal layer.
According to the Japanese gastric cancer treatment guidelines, an R0 resection is
essential for curative resection [8]. To estimate local curability and lymph node metastases, tumor size, tumor depth,
lymphovascular invasion and vertical margin are important factors to determine next
therapeutic strategy after ESD [9]. These are mainly based on factors relating to the submucosal layer, not the mucosal
layer. Therefore, obtaining an adequate submucosal layer is important to obtain optimal
clinical outcomes. The specimen resected by the PCM has a thick submucosal layer because
the PCM enables endoscopists to select the dissection layer in the pocket by visualizing
the submucosa and stabilizes the tip of the endoscope regardless of cardiac or respiratory
movements. Applying both traction and counter-traction in the pocket provides clear
visualization and stabilization. Further, unlike the CM, the PCM enables an antegrade
approach without retroflexion by compressing the pyloric sphincter resulting in a
straightforward approach without the need for special traction devices.
ESD of gastric lesions at the pyloric ring is challenging, even for expert endoscopists.
Bae et al reported that a gastric tumor with duodenal extension is a significant factor
leading to difficult ESD [10]. In the CM, the most difficult point is the downward facing view just after getting
over the pyloric ring using an antegrade approach. A Korean study reported that the
usefulness of the retroflexed approach in the duodenum for ESD of gastric lesions
involving the pyloric ring improved the en bloc resection rate [11]. However, the retroflexed approach in the duodenal bulb suffers from limited maneuverability
in a narrow lumen that may result in mucosal injury or perforation. Therefore, submucosal
dissection using an antegrade approach compressing the sphincter muscle with the PCM
is desirable.
We recognize the acknowledged limitations of this study. This is a single-center,
retrospective observational study using historical controls. Evolution of devices
and the learning curve may influence the outcomes. Long-term outcomes including local
recurrence and survival were not evaluated. Although only expert endoscopists performed
the ESDs in this study, technical experience may be a source of bias. This study did
not include ESD with traction devices.
Conclusions
In conclusion, this is the first study reporting the advantages of the PCM for ESD
of gastric lesions involving the pyloric ring. The PCM is a unique and suitable strategy
for compressing the pyloric sphincter and enables an R0 resection. Use of the PCM
with the ST hood is a viable option to accomplish ESD for superficial gastric neoplasms
involving the pyloric ring.