Open Access
CC BY-NC-ND 4.0 · Endosc Int Open 2022; 10(06): E874-E897
DOI: 10.1055/a-1794-0635
Review

Efficacy and safety of endoscopic duodenal stent versus endoscopic or surgical gastrojejunostomy to treat malignant gastric outlet obstruction: systematic review and meta-analysis

Rajesh Krishnamoorthi
1   Department of Gastroenterology and Hepatology, Virginia Mason Medical Center, Seattle, Washington, United States
,
Shivanand Bomman
1   Department of Gastroenterology and Hepatology, Virginia Mason Medical Center, Seattle, Washington, United States
,
Petros Benias
2   Division of Gastroenterology, Zucker School of Medicine at Hofstra/Northwell, North Shore University Hospital, Manhasset, New York, United States
,
Richard A. Kozarek
1   Department of Gastroenterology and Hepatology, Virginia Mason Medical Center, Seattle, Washington, United States
,
Joyce A. Peetermans
3   Endoscopy Division, Boston Scientific Corporation, Marlborough, Massachusetts, United States
,
Edmund McMullen
3   Endoscopy Division, Boston Scientific Corporation, Marlborough, Massachusetts, United States
,
Ornela Gjata
3   Endoscopy Division, Boston Scientific Corporation, Marlborough, Massachusetts, United States
,
Shayan S. Irani
1   Department of Gastroenterology and Hepatology, Virginia Mason Medical Center, Seattle, Washington, United States
› Institutsangaben
 

Abstract

Background and study aims Malignant disease accounts for up to 80 % of gastric outlet obstruction (GOO) cases, which may be treated with duodenal self-expanding metal stents (SEMS), surgical gastrojejunostomy (GJ), and more recently endoscopic-ultrasound-guided gastroenterostomy (EUS-GE). These three treatments have not been compared head-to-head in a randomized trial.

Methods We searched the Embase and MEDLINE databases for studies published January 2015−February 2021 assessing treatment of malignant GOO using duodenal SEMS, endoscopic (EUS-GE) or surgical (laparoscopic or open) GJ. Efficacy outcomes assessed included technical and clinical success rates, GOO recurrence and reintervention. Safety outcomes included procedure-related bleeding or perforation, and stent-related events for the duodenal SEMS and EUS-GE arms.

Results EUS-GE had a lower rate of technical success (95.3%) than duodenal SEMS (99.4 %) or surgical GJ (99.9%) (P = 0.0048). For duodenal SEMS vs. EUS-GE vs. surgical GJ, rates of clinical success (88.9 % vs. 89.0 % vs. 92.3 % respectively, P = 0.49) were similar. EUS-GE had a lower rate of GOO recurrence based on limited data (P = 0.0036), while duodenal SEMS had a higher rate of reintervention (P = 0.041). Overall procedural complications were similar (duodenal SEMS 18.7 % vs. EUS-GE 21.9 % vs. surgical GJ 23.8 %, P = 0.32), but estimated bleeding rate was lowest (P = 0.0048) and stent occlusion rate was highest (P = 0.0002) for duodenal SEMS.

Conclusions Duodenal SEMS, EUS-GE, and surgical GJ showed similar clinical efficacy for the treatment of malignant GOO. Duodenal SEMS had a lower procedure-related bleeding rate but higher rate of reintervention.


Introduction

Malignant disease accounts for an estimated 50 % to 80 % of cases of gastric outlet obstruction (GOO), with pancreatic cancer being the most common associated malignancy (15 %–20 %) [1]. Patients with GOO may experience progressively worsening nausea, vomiting, weight loss, abdominal pain and severe dehydration [2]. Because patients with GOO secondary to an unresectable malignancy have limited life expectancy, palliative treatment prioritizes symptom resolution (especially relief of vomiting and return to oral intake) and minimization of hospital stays, complications and reinterventions [1].

Palliative interventions for GOO include open or laparoscopic surgical gastrojejunostomy (GJ), duodenal stenting using self-expanding metal stents (SEMS), and endoscopic gastroenterostomy (EUS-GE). Surgical GJ and SEMS are the two most common palliative treatment options for patients with malignant GOO [2]. A 2019 meta-analysis of data from 27 studies including 2354 patients with malignant GOO found similar technical and clinical success rates for surgical GJ and duodenal stenting, with shorter mean time to resumption of oral intake for patients who received stenting [2]. However, because stenting was associated with shorter survival time (mean difference 43 days) and higher rates of stent‑related complications, reobstruction and reintervention compared to surgical GJ, the authors concluded that surgical GJ was preferable for patients with a long life expectancy and good performance status [2]. A 2018 meta-analysis of the same treatments analyzed only three randomized controlled trials (RCTs) including 84 patients after exclusion of many studies for low-quality data [1]. This analysis confirmed that compared to surgical GJ, patients receiving duodenal stenting had a faster return to oral intake, shorter mean hospital stay, increased recurrence of symptoms and increased reintervention rate, while quality of life and survival could not be analyzed due to insufficient adequate-quality data [1].

Since 2015 [3], endoscopic ultrasound-guided gastroenterostomy (EUS-GE) has been studied for the management of GOO. A meta-analysis of 12 studies published through 2018 including 285 patients concluded that EUS-GE is effective and safe for patients with malignant GOO, estimating 92 % technical success, clinical success in 90 % of patients, symptom recurrence or unplanned reintervention in 9 % and adverse events (AEs) in 12 % [4]. Subsequently, a 2020 multicenter study of 45 patients showed lower technical (86.7 %) and clinical (73.3 %) success rates with AEs in 12 patients (26.7 %), including five fatal AEs that occurred at one center [5].

The above treatments have been studied in observational studies and 2-arm randomized trials. No clinical trials have included all three treatments in a head-to-head comparison. To address this evidence gap, we conducted a systematic review and meta-analysis comparing the efficacy and safety of duodenal SEMS versus EUS-GJ versus surgical GJ in observational studies.


Methods

Search strategy

An expert librarian conducted searches of the Embase and MEDLINE databases (via Embase.com) to identify studies published in English between January 2015 and February 2021 (eTable 1). January 2015 was chosen as the search start date because EUS-GE (newest of the three treatments) was first documented for the management of GOO in human patients in 2015 [3]. RCTs, retrospective and prospective cohort studies, case-control studies, and case series that assessed endoscopic duodenal stenting or endoscopic or surgical GJ for malignant GOO were included. We excluded in vitro or animal studies, reviews or editorials, and publications that reported on < 10 patients, had article text in a non-English language, or had study populations that were clearly overlapping or had suspected overlap based on common authors and study sites with overlapping enrollment dates. In cases of overlap, we retained the study/studies with the most comprehensive data on the outcomes of interest that were mutually exclusive with all other included studies. If some but not all arms of a comparative study showed overlap with another publication, the arm(s) with overlap were excluded but the arm(s) without overlap were retained for the analysis.


Data extraction and assessment for risk of bias

For all manuscripts identified by the literature search, two authors (RK, SB) independently reviewed studies for eligibility and/or extracted data from selected publications for preidentified efficacy and safety endpoints. Discrepancies were resolved after review by a third author (PB) and consensus decision after discussion among the entire author group. Baseline information consisted of study characteristics (year published, country of origin, study design, sample size), patient characteristics (age, sex), treatment and treatment subgroup (e. g., type of stent, subcategory of surgery). Reasons for study exclusion were documented.

The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were used to conduct this analysis [6]. The Newcastle-Ottawa Scale (NOS) was employed (author SB) to review the methodologic quality of non-randomized studies and assess for bias. An adapted NOS was used that assessed the selection and representativeness of the study population (eTable 2) and the ascertainment of outcomes and exposures. Items from the NOS that made comparative assessments (e. g. exposed vs. non-exposed cohorts) were removed, as they did not apply to single-arm studies. This adaptation of the NOS has been used previously [7] [8] [9], and for the purposes of this study, one question (“Were other important diagnoses excluded?”) was replaced by another question (“Was follow-up long enough for outcomes to occur? Reported adequate follow-up time”) to make it more appropriate for this systematic review. Yes/no responses were required for each of five questions, and the quality of each study was ranked as good (5 yes responses), moderate (4 yes responses), or poor ( ≤ 3 yes responses).


Endpoint assessment and definition

Efficacy outcomes assessed were “technical success” and “clinical success” as defined by the reporting authors, pre- and postprocedural Gastric Outlet Obstruction Scoring System (GOOSS) score [10] (no oral intake = 0, liquids only = 1, soft solids = 2, low-residue or full diet = 3), recurrence of GOO, and reintervention (for any reason) during the study period.

Safety outcomes assessed were overall adverse event rate, procedure-related bleeding and perforation, and for the duodenal stent and EUS-GE arms: stent migration, patency, occlusion, ingrowth and overgrowth. In many cases, procedure-related deaths were not distinguished from all-cause deaths, and some studies were designed to follow all patients until death. Therefore, as a surrogate of procedure-related deaths, we only extracted deaths described in the AEs section since this location in the paper suggested the authors thought the death could be procedure-related.

In some articles, some outcomes were only reported for technically successful cases. To avoid inflated estimates (e. g. clinical success only reported for technically successful cases) or exclusion of AEs in failed cases, all reported events were extracted, using denominators reflecting the entire study population.


Statistical methods

Efficacy and safety outcomes were assessed using a random-effects meta-analysis to estimate the proportion of patients with the measure or mean of the measure. Since the number of comparative studies was small and those studies were retrospective, both arms from all comparative studies were treated as independent studies and combined with non-comparative studies. The arcsine transformation was used to compute weighted pooled random-effects estimates for all endpoints. For endpoints with three treatment groups, pairwise comparisons between treatments were done with a Bonferroni adjustment. A sensitivity analysis was performed including only studies with “good” quality ratings. Heterogeneity was assessed across studies using the I2 statistic [11]. Funnel plots were created to assess for publication bias across studies. The Begg and Mazumdar rank correlation test of funnel plot asymmetry and Egger’s linear regression test of funnel plot asymmetry were also used to assess publication bias [12] [13]. All meta-analyses were performed using R (version 3.6.1); SAS (version 9.4, SAS Inc., Cary, North Carolina, United States) was used for plotting and all other analyses.



Results

Study selection and patient characteristics

Study and patient characteristics are summarized in [Table 1]. The systematic literature search identified 451 unique articles, of which 61 studies representing 5772 subjects met the inclusion criteria ([Fig. 1]). In total, 390 articles were excluded ([Fig. 1]), most often for the wrong indication (including benign GOO) or being unrelated to the search objectives (n = 211), or because they were a review article or editorial (n = 65), case report or had < 10 patients (36), in vitro or animal study (32) or not available in English language (31). Fifty-two eligible studies were retrospective; and nine were prospective, including two randomized studies comparing covered SEMS to uncovered SEMS.

Table 1

Publications and extracted data.

First author

Year

Country

Study design

Treatment

Treatment subgroup

No. of Cases

Age
[mean± SD]

Males
(x/n)

Chiu [32]

2015

UK

Retrospective

SEMS

Uncovered

18

70 median (range 46–85)

8/18

JW Kim [33]

2015

South Korea

Retrospective

SEMS

Uncovered

38

68.9 ± 10.2

18/38

SEMS

Covered

29

68.5 ± 11.2

11/29

SH Kim [34]

2015

South Korea

Retrospective

SEMS

27 Covered stents, 29 uncovered

56

69 mean (range 52–91)

36/56

H Lee [35]

2015

South Korea

Prospective randomized; WAVE partially covered SEMS vs uncovered SEMS

SEMS

Partially covered

51

57.9 ± 12.5

34/51

SEMS

Uncovered

51

58.7 ± 10.8

36/51

JE Lee [23]

2015

South Korea

Retrospective

SEMS

60 Uncovered, 7 partially covered

67

61.2 ± 12.7

41/67

SEMS

80 Uncovered; eight partially covered

88

64.4 ± 12.8

61/88

D Oh [36]

2015

South Korea

Retrospective

SEMS

Partially covered

20

64.5 median (range 39–85)

11/20

SY Oh [37]

2015

USA

Retrospective

SEMS

NS

196

65.4 median (IQR 59.4–74.2)

102/196

SEMS

NS

96

70.4 median (IQR 61.0–79.2)

55/96

Park [24]

2015

South Korea

Retrospective

SEMS

Mixed (141 uncovered, 76 covered)

217

60.7 ± 13.3

162/217

Surgical

Mixed

39

61.7 ± 13.3

34/39

Sato [38]

2015

Japan

Retrospective

SEMS

Uncovered

61

64.0 ± 10.3

35/61

Trotter [39]

2015

UK

Retrospective

SEMS

NS

29

Fiori [40]

2016

Italy

Prospective, not randomized

SEMS (arm excluded for overlap)[1]

Mixed covered and uncovered[1]

72[1]

71[1]

46/70[1]

Surgical

Open

30

70

19/30

Grunwald [41]

2016

USA

Retrospective

SEMS

NS

100

69.7

43/100

Itoi [42]

2016

Japan, India, USA

Prospective

EUS-GJ (EPASS) with LAMS

EUS-GJ

20

Jung [43]

2016

South Korea

Retrospective

SEMS

Fully covered

SEMS

Partially covered

SEMS

Uncovered

SEMS

Mixed

220

63 median (IQR 15–90)

125/220

Kato [44]

2016

Japan

Retrospective

SEMS

Uncovered

46

SEMS

Uncovered

79

SEMS

Uncovered

125

70.2 mean (range 38–97)

71/125

Khan [45]

2016

China

Prospective

SEMS

Uncovered

30

65 mean (range 40–90)

18/30

Kobayashi [46]

2016

Japan

Retrospective

SEMS

Uncovered

71

67.6 (range: 31–92)

43/71

Lye [47]

2016

Singapore

Retrospective

SEMS

Uncovered

24

79.5 median (range 49–92)

11/24

Surgical

Open

30

Okuwaki [48]

2016

Japan

Retrospective

SEMS

Uncovered

14

72 median (IQR 69–79)

9/14

SEMS

Uncovered

17

71 median (IQR 66–75)

8/17

J-H Park (1) [49]

2016

South Korea

Retrospective

SEMS

Partially covered

125

61 mean (range 25–89)

81/125

SEMS

Partially covered

68

62 mean (range 36–91)

48/68

J-H Park (2) [50]

2016

South Korea

Retrospective propensity score-matched

SEMS

Dual stent consisting of outer partially covered stent and inner bare stent

74

62.1 ± 13.8

57/74

Surgical

Mixed

74

61.1 ± 12.1

55/74

Rademacher [51]

2016

Germany

Retrospective

SEMS

NS

62

70.5 median (range 63–81)

35/62

Sasaki [52]

2016

Japan

Prospective

SEMS

Uncovered

39

69.2 ± 13.3

25/39

Shin [53]

2016

South Korea

Retrospective

SEMS

Mixed

124

71.8 median (range 42–97)

70/122

Tsauo [54]

2016

South Korea

Retrospective

SEMS

Partial

75

61.7 ± 10.9

45/75

Surgical

Mixed

32

63.4 ± 9.6

21/32

Yamao [55]

2016

Japan

Retrospective

SEMS

Mixed covered and uncovered

278

71.7 ± 11.4

163/278

Bulut [56]

2017

Turkey

Retrospective

SEMS

Uncovered

53

58.7 ± 15.07

33/53

Chen [30]

2017

USA, Japan (EUS-GJ)
USA (SEMS)

Retrospective

SEMS

NS

52

64 ± 13.2

32/52

EUS-GJ

EUS-GJ

30

70 ± 13.3

17/30

Hori [57]

2017

Japan

Retrospective

SEMS

Uncovered

126

74 median (range 39–101)

160/252

SEMS

Covered

126

Jang [58]

2017

South Korea

Retrospective

SEMS

NS

99

58.8 ± 13.2

67/99

Surgical

Mixed

45

58.9 ± 11.4

36/45

Khashab [59]

2017

USA, Japan

Retrospective

EUS-GJ
(arm excluded for overlap)[1]

30[1]

70 ± 13.3[1]

17/30[1]

Surgical

Open

63

68 ± 9.6

32/63

Kim [60]

2017

South Korea

Retrospective

SEMS

Partially covered

18

71.2 ± 10.0

9/18

Ojima [61]

2017

Japan

Retrospective

Surgical

Open

23

67 median (range 45–85)

15/23

Surgical

Lap

30

71 median (range 52–85)

20/30

Perez-Miranda [62]

2017

USA, Spain, France

Retrospective

EUS-GJ[1]

EUS-GJ[1]

25[1]

63.9[1]

11/25[1]

Surgical

Lap, with conversion to open at surgeon's discretion

29

75.8

22/29

Takahara [63]

2017

Japan

Retrospective

SEMS

Partially covered

41

67 median (range 35–89)

26/41

Tanaka [64]

2017

Japan

Retrospective

Surgical

lap

43

67 median (range 43–83)

29/43

Tsauo [65]

2017

South Korea

Retrospective

SEMS

Dual stent consisting of outer partially covered stent and inner bare stent

40

56.8 ± 10.6

23/40

Ye [66]

2017

Taiwan

Retrospective

SEMS

Uncovered

87

71.1 ± 14.6

58/87

Yoshida [67]

2017

Japan

Retrospective

SEMS

Uncovered

23

70 (range 48–87)

15/23

Surgical

Mixed (28 open, 2 lap)

30

63.5 (range 46–72)

16/30

SEMS

Uncovered

23

70 (range 48–87)

15/23

Bekheet [68]

2018

South Korea

Retrospective

SEMS

Covered

55

60.6 (range 38–89)

35/55

Choi [69]

2018

South Korea

Retrospective

SEMS (Bonastent Wing)

Partially covered

63

65.0 (range 58.5–75.0)

44/63

Leiyuan [70]

2018

China

Retrospective

SEMS

NS

29

64.6 ± 14.2

19/29

Surgical

Lap

34

59.8 ± 15.5

21/34

Uemura [71]

2018

Japan

Retrospective

SEMS

Uncovered

64

72 (range 43–90)

32/64

Surgical

Open

35

68 (range 47–87)

12/35

Yukimoto [72]

2018

Japan

Retrospective

SEMS

Uncovered

38

73.0 median (IQR 65.0–79.0)

23/38

Surgical

Open

27

75.0 median (IQR 66.0–81.5)

18/27

Ge [22]

2019

USA

Prospective

SEMS

Uncovered

78

65.7 ± 12.6

47/78

EUS-GJ

EUS-GJ

22

66.4 ± 9.2

9/22

Jang [73]

2019

USA

Retrospective

SEMS

Uncovered

183

66.2 ± 14.3

90/183

Surgical

Mixed

127

67.5 ± 11.1

80/127

Kerdsirichairat [74]

2019

USA

Retrospective

EUS-GJ

malignant

48

65 median for all

28/57 for all

EUS-GJ[1]

Benign[1]

9[1]

Kumar [75]

2019

India

Retrospective

SEMS

NS

90

56.4 ± 11.7

43/90

SEMS

NS

24

56.9 ± 11.6

12/24

Ramos [76]

2019

Brazil

Retrospective

Surgical

Gastric partitioning

30

67.5 ± 13.4

22/30

Surgical

Conventional GJ

30

64.3 ± 12.7

19/30

Ratone [77]

2019

France

Retrospective

SEMS

Uncovered

220

67.2 ± 13.9

123/220

Sterpetti [78]

2019

Italy

Prospective

SEMS

87

71

57/87

Alcala-Gonzalez [79]

2020

Spain

Retrospective

SEMS

Uncovered

36

68 median (IQR 53–83)

20/36

Kastelijn [5]

2020

The Netherlands, Germany, Spain, Italy

Retrospective

EUS-GJ

EUS-GJ

45

69.9 ± 12.3

22/45

Miwa [80]

2020

Japan

Prospective

SEMS

Uncovered

31

70 median (range 52–90)

19/31

Mo [81]

2020

South Korea

Retrospective

SEMS

61 Uncovered, 29 covered initially

90

72.1 (range 31–96)

59/90

Wu [82]

2020

Taiwan

Retrospective

SEMS

Uncovered

71

63 ± 16

36/71

SEMS

Uncovered

32

62 ± 12

17/30

Xu [83]

2020

China

Retrospective

EUS-GJ

EUS-GE

36

69.0 ± 12.8

17/36

Yildirim [84]

2020

Turkey

Retrospective

Surgical

Open

37

68.7 ± 14.4

25/37

Surgical

Mixed (2 lap, 14 open)

16

62.7 ± 10.2

11/16

Hindryckx [85]

2021

Belgium

Retrospective

EUS-GJ

EUS-GJ

6

Kouanda [86]

2021

USA

Retrospective

EUS-GJ

EUS-GJ

36

70.4 ± 11.8

20/36

Surgical

Open

14

71.5 ± 15.6

8/14

Yamao [87]

2021

Japan

Prospective randomized

SEMS

Covered

182

73.5 median (range 35–97)

98/182

SEMS

Uncovered

184

72 median (range 43–96)

107/184

SEMS, self-expanding metal stent; EUS-GJ, endoscopic ultrasound-guided gastrojejunostomy.

1 Trial arms were excluded due to overlap with one or more other studies.


Zoom
Fig. 1 Flow diagram of literature search and study selection.

Patients who were treated with EUS-GJ were significantly older than patients who were treated with duodenal SEMS or surgical GJ (mean age 69.1 for EUS-GJ, 64.2 for duodenal SEMS, 64.3 years for surgical GJ, P = 0.0004) The EUS-GJ treatment group had a lower proportion of males than the surgical GJ group (50.3 % vs. 65.6 %, P = 0.0042 for pairwise comparison). The preprocedural GOOSS scores were similar among groups (0.62 for duodenal SEMS vs. 0.60 for EUS-GJ vs. 0.68 for surgical GJ, P = 0.7783).


Study quality

All 61 publications were assessed for quality with the modified NOS. Thirty-eight studies were judged to have good quality, 17 moderate quality, and six poor quality (eTable 2).


Assessment of heterogeneity

Heterogeneity was found in the analyses endpoints (eTable 3). There was heterogeneity in the EUS-GE and SEMS groups for technical success, stent migration, and death reported in AE section, in the Surgical GJ and SEMS groups for clinical success, reintervention, procedure-related complications, and pre- and postprocedural GOOSS score, and for the SEMS group only for bleeding, recurrence of GOO, stent occlusion, ingrowth, and overgrowth. No heterogeneity was found in the analyses of perforation and patency for any group.


Efficacy outcomes

Technical success

Forty-four of 61 (72.1 %) studies reported rates of procedural technical success. Consistent with its more recent development, EUS-GE was reported to have a significantly lower rate of technical success than the other two treatments (pooled rates 95.3 % for EUS-GE vs. 99.4 % for duodenal SEMS [P = 0.0495 for pairwise comparison] and 95.3 % for EUS-GE vs. 99.9 % for surgical GJ [P = 0.0060 for pairwise comparison]) ([Table 2]).

Table 2

Summary of efficacy and safety meta-analytic outcomes for three treatments for malignant gastric outlet obstruction.

Duodenal SEMS

EUS-GJ

Surgical GJ

P value[1]

N studies

N patients

% (95 % CI)

N studies

N patients

% (95 % CI)

N studies

N patients

% (95 % CI)

Efficacy outcomes

  • Technical success

45

4413

99.4 %
(98.9 % to 99.8 %)

8

245

95.3 %
(89.3 % to 98.9 %)

13

564

99.9 %
(99.5 % to 100.0 %)

0.0048

  • Clinical success

45

4590

88.9 %
(86.7 % to 90.9 %)

8

245

89.0 %
(82.3 % to 94.3 %)

13

588

92.3 %
(86.9 % to 96.3 %)

0.49

  • Preprocedural GOOSS score

27

2655

0.62
(0.50 to 0.73)

2

65

0.60
(0.44 to 0.76)

6

215

0.68
(0.52 to 0.83)

0.78

  • Postprocedural GOOSS score

19

2184

2.27
(2.12 to 2.41)

2

59

2.57
(1.83 to 3.32)

5

180

2.20
(1.48 to 2.92)

0.71

  • Recurrence of GOO

11

573

28.7 %
(19.7 % to 38.6 %)

1

25

4.0 %
(0.0 % to 15.0 %)

8

342

16.9 %
(11.6 % to 23.0 %)

0.0036

  • Reintervention

33

2963

20.3 %
(16.9 % to 23.9 %)

4

129

11.2 %
(4.9 % to 19.6 %)

9

418

12.6 %
(6.6 % to 20.1 %)

0.041

Safety outcomes

  • Any procedure-related adverse event

43

4285

18.7 %
(14.7 % to 23.1 %)

6

189

21.9 %
(16.3 % to 28.1 %)

16

746

23.8 %
(18.6 % to 29.5 %)

0.32

  • Bleeding

25

2854

1.7 %
(0.9 % to 2.7 %)

4

141

2.9 %
(0.2 % to 8.6 %)

9

412

5.2 %
(3.2 % to 7.5 %)

0.0048

  • Perforation

24

2823

1.6 %
(1.1 % to 2.3 %)

3

105

2.8 %
(0.0 % to 10.7 %)

3

170

2.0 %
(0.0 % to 7.3 %)

0.88

  • Stent migration

33

3451

4.8 %
(3.6 % to 6.1 %)

4

116

2.4 %
(0.0 % to 10.1 %)

0

---

---

0.45

  • Stent occlusion

22

1993

12.9 %
(7.9 % to 18.8 %)

3

69

0.5 %
(0.0 % to 4.2 %)

0

---

---

0.0002

  • Tissue ingrowth

22

2172

10.9 %
(7.5 % to 14.8 %)

1

24

4.2 %
(0.0 % to 15.6 %)

0

---

---

0.22

  • Stent patency

3

140

85.9 %
(79.7 % to 91.2 %)

0

---

---

0

---

---

---

  • Tissue overgrowth

20

1962

5.5 %
(4.1 % to 7.1 %)

0

---

---

0

---

---

---

  • Laparoscopic complication

0

---

---

0

---

---

5

196

16.1 %
(6.8 % to 28.2 %)

---

  • Deaths reported in AE section

26

2151

0.8 %
(0.2 % to 1.7 %)

4

151

1.7 %
(0.0 % to 8.7 %)

8

421

0.9 %
(0.1 % to 2.9 %)

0.89

  • Total unique studies or patients

47

4711

---

8

243

---

18

818

---

SEMS, self-expanding metal stent; EUS-GJ, endoscopic ultrasound-guided gastrojejunostomy; GOO, gastric outlet obstruction; GOOSS, Gastric Outlet Obstruction Scoring System; AE, adverse event.

1 P value for comparison of duodenal SEMS vs. EUS-GJ vs. surgical GJ.



Clinical success

Five distinct definitions of “clinical success” were documented among 51 of 61 (83.6 %) studies that reported this endpoint. The most common definition was improved clinical symptoms (especially obstructive symptoms and vomiting) and/or improved oral intake or GOOSS score (19 studies), followed by change in GOOSS score (18), followed by improved oral intake (12), improved oral intake and hospital discharge (1), and resolution of GOO symptoms (intractable vomiting necessitating gastric drainage) the day after stent implantation (1). Pooled rates of “clinical success” were similar among the three treatments, with 88.9 % for duodenal SEMS, 89.0 % for EUS-GE, and 92.3 % for surgical GJ (P = 0.49) ([Fig. 2a], [Table 2]). Among studies reporting outcomes for laparoscopic GJ alone, open surgical GJ alone, or mixed laparoscopic or surgical GJ, rates of clinical success were similar (96.6 % vs. 85.9 % vs. 93.8 % respectively, P = 0.2903).

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Fig. 2a Analysis of efficacy outcomes. Outcomes for clinical success.
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Fig. 2a Analysis of efficacy outcomes. Outcomes for clinical success.
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Fig. 2b Analysis of efficacy outcomes. Outcomes for preprocedural GOOSS score.
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Fig. 2c Analysis of efficacy outcomes. Outcomes for postprocedural GOOSS score.
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Fig. 2d Analysis of efficacy outcomes. Outcomes for recurrence of GOO.
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Fig. 2e Analysis of efficacy outcomes. Outcomes for reintervention.

Pre-procedure and post-procedure GOOSS score

Pooled estimates of mean preprocedural GOOSS score 0.62 for duodenal SEMS, 0.60 for EUS-GE, and 0.68 for surgical GJ, reflecting minimal oral intake before treatment ([Fig. 2b], [Table 2]). Estimated mean postprocedural GOOSS scores exceeded two for all three treatments (2.27 for duodenal SEMS, 2.57 for EUS-GE, and 2.20 for surgical GJ), suggesting that most patients were able to eat solid food after treatment ([Fig. 2c], [Table 2]).


Recurrence of GOO

Recurrence of GOO in the EUS-GE group (4.0 %, 95 % CI 0.0 % to 15.0 %) was significantly lower than for duodenal SEMS (28.7 %, 95 % CI 19.7 % to 38.6 %; P = 0.0040 for pairwise comparison) and similar to surgical GJ (16.9 %, 95 % CI 11.6 % to 23.0 %; P = 0.11 for pairwise comparison) ([Fig. 2d], [Table 2]). Only one EUS-GE study (N = 25 patients) was included in this comparison, while 11 studies of duodenal SEMS (573 patients) and eight studies of surgical GJ (342 patients) were represented.


Reintervention

Rates of reintervention (for any reason) during the study period were lower for EUS-GE (11.2 % among 129 patients in four studies) and surgical GJ (12.6 % among 418 patients in nine studies) than for duodenal SEMS (20.3 % among 2963 patients in 33 studies) (P = 0.041 for comparison of all three treatments, pairwise comparisons did not show significant differences) ([Fig. 2e], [Table 2]).



Safety outcomes

Any procedure-related serious adverse event

The pooled rate of any procedure-related serious adverse event was similar among the three treatments, i. e. 18.7 %, 95 % CI 14.7 % to 23.1 % for SEMS vs. 21.9 %, 95 % CI 16.3 % to 28.1 % for EUS-GE vs. 23.8 %, 95 % CI 18.6 % to 29.5 % for surgical GJ (P = 0.32) ([Fig. 3a], [Table 2]). Among studies reporting outcomes for laparoscopic GJ alone, open surgical GJ alone, or mixed laparoscopic or open surgical GJ, rates of procedure-related complications were similar (17.6 % vs. 26.9 % vs. 19.3 % respectively, P = 0.1340).

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Fig. 3a Analysis of safety outcomes. Outcomes for any procedure-related adverse event.
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Fig. 3a Analysis of safety outcomes. Outcomes for any procedure-related adverse event.
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Fig. 3b Analysis of safety outcomes. Outcomes for bleeding.
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Fig. 3c Analysis of safety outcomes. Outcomes for perforation.
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Fig. 3d Analysis of safety outcomes. Outcomes for stent migration.
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Fig. 3e Analysis of safety outcomes. Outcomes for e tissue ingrowth.
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Fig. 3f Analysis of safety outcomes. Outcomes for stent occlusion.
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Fig. 3g Analysis of safety outcomes. Outcomes for stent patency.
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Fig. 3h Analysis of safety outcomes. Outcomes for tissue overgrowth.
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Fig. 3i Analysis of safety outcomes. Outcomes for deaths reported in AE section.

Bleeding

The bleeding rate associated with duodenal SEMS (1.7 %, 95 % CI 0.9 % to 2.7 %) was similar to the rate for EUS-GE (2.9 %, 95 % CI 0.2 % to 8.6 %; P = 0.999 for pairwise comparison) and lower than the rate for surgical GJ (5.2 %, 95 % CI 3.2 % to 7.5 %; P = 0.0033 for pairwise comparison) ([Fig. 3b], [Table 2]).


Perforation

Perforation rates were similar among the three treatments, with 1.6 % for duodenal SEMS, 2.8 % for EUS-GE, and 2.0 % for surgical GJ (P = 0.88) ([Fig. 3c], [Table 2]).



Stent-related outcomes

Duodenal SEMS and EUS-GE were reported to have similar rates of stent migration (4.8 % vs. 2.4 % respectively, P = 0.45) ([Fig. 3d], [Table 2]) and tissue ingrowth (10.9 % vs. 4.2 % [based on one study of EUS-GE], P = 0.22) ([Fig. 3e], [Table 2]), while stent occlusion was significantly higher for duodenal SEMS (12.9 % vs. 0.5 % respectively, P = 0.0002) ([Fig. 3f], [Table 2]).

Stent patency (85.9 %) ([Fig. 3g], [Table 2]) and tissue overgrowth (5.5 %) ([Fig. 3h], [Table 2]) were adequately reported for duodenal SEMS but not for EUS-GE.


Deaths reported in adverse events section

Using deaths reported in the AEs section of the articles as a surrogate of procedure-related deaths, all three interventions were associated with a similar risk (EUS-GE [1.7 %], vs. duodenal SEMS [0.8 %], and surgical GJ [0.9 %] [P = 0.89]) ([Fig. 3i], [Table 2]).


Sensitivity analysis

In a sensitivity analysis including 43 studies (33 SEMS, 6 EUS-GE, four surgical GJ) rated as good quality, statistically significant differences from the main analysis included: no significant difference in technical success (99.4 % vs. 95.2 % vs. 99.6 %, P = 0.097) and reintervention (18.9 % vs. 11.2 % vs. 23.4 %, P = 0.082), and a significant difference in preprocedural GOOSS score (0.59 vs. 0.60 vs. 1.07, P = 0.037) among the SEMS, EUS-GJ and surgical GJ arms respectively.


Publication bias

Publication bias was suggested by a significant Begg and Mazumdar test (p ≤ 0.10) with continuity correction for technical success in duodenal SEMS and surgical GJ, procedure-related complications for EUS-GE and surgical GJ, and overgrowth for duodenal SEMS (eTable 4). The Egger test showed a lack of symmetry of the funnel plots (eFigures 1A–1M) for technical success (surgical GJ), reintervention (surgical GJ), procedure-related complications (EUS-GE and surgical GJ), bleeding (duodenal SEMS), perforation (EUS-GE), migration (EUS-GJ), overgrowth (duodenal SEMS), and preprocedural and postprocedural GOOSS score (duodenal SEMS for both measures).



Discussion

In this systematic review and meta-analysis of 61 studies including 5772 patients with malignant GOO, duodenal SEMS, EUS-GE and surgical GJ were found to achieve similar rates of clinical success and similar improvement in dietary intake. EUS-GE was reported to have the lowest rate of technical success and (based on one study) lowest recurrence of GOO, while duodenal SEMS had the highest rate of reintervention. Overall procedure-related AEs were similar among the treatments, but duodenal SEMS had a lower bleeding rate than the other two treatments and a higher rate of stent occlusion than EUS-GE.

Surgical GJ for GOO evolved from an open procedure performed for a patient with a duodenal ulcer in 1884 [14], to the introduction of laparoscopic GJ in 1992 [15]. Laparoscopic GJ has shown improved morbidity and mortality rates compared with the open surgical approach [16], for which delayed gastric emptying rates of 20 % or more and overall complication rates of 25 % to 35 % have been reported [1]. Endoscopic duodenal stenting using SEMS was described in the early 1990 s as a minimally invasive treatment for malignant GOO [17]. While periprocedural outcomes for duodenal stenting are favorable, high reocclusion rates increase the risk of obstruction and need for reintervention over time [18]. A 2020 multicenter prospective study of EUS-GE reported a high rate of AEs including five fatalities [5]. However, because the deaths were reported at one center, these results might be more reflective of an early phase of procedural training than of long-term expected outcomes at centers with endoscopists who are familiar with the technique [19].

Our findings are consistent with the 2021 American Gastroenterology Association Clinical Practice Update on the Optimal Management of the Malignant Alimentary Tract Obstruction [20]. This expert review advised that for surgical candidates with GOO having life expectancy greater than 2 months and good functional status, surgical GJ should be considered, preferably using a laparoscopic approach [20]. EUS-GE was considered an acceptable alternative to surgical GJ depending on the endoscopist’s experience, while patients who are not candidates for surgical or endoscopic GE should be considered for an enteral stent [20]. Similarly, the European Society of Gastrointestinal Endoscopy (ESGE) currently recommends EUS-GE performed in an expert setting for malignant GOO, as an alternative to enteral stenting or surgery [21]. EUS-GE is a newer procedure requiring advanced endoscopist expertise; therefore should currently be limited to specialized endoscopy centers with high procedural volume and endoscopists trained in this advanced therapeutic EUS approach. Our results reflect the early stage of EUS-GE procedural development, including its significantly lower reported rate of technical success and higher (but not significantly) rate of deaths reported in the AEs sections of eligible articles. After wider dissemination and increasing familiarity among endoscopists, EUS-GE could potentially be used more frequently as a less invasive approach compared to surgery.

There are several considerations that go into selection of what treatment approach is chosen for an individual patient with malignant GOO. Reviewing the cross-sectional imaging (ideally a CT scan) to evaluate for proximity of the small bowel to the stomach, and quantity of intervening ascites (which, should give pause at least with early use of EUS-GE) [22]. Carcinomatosis with ascites predicts unfavorable long-term clinical outcomes in patients undergoing SEMS placement for malignant GOO [23] [24], and a large amount of ascites is currently considered by some to be an absolute contraindication to EUS-GE [25]. Both covered and uncovered enteral SEMS have been utilized in the management of malignant GOO, although, covered SEMS are not universally available worldwide (unavailable in the US, while available in Asia and Europe). Compared to covered SEMS, uncovered duodenal SEMS are generally thought to have lower risk of migration and lower risk of impacting biliary and pancreatic drainage when it covers the papilla, but have higher risk of reobstruction from tumor ingrowth [26] [27]. Hence, the following factors could be considered in the choice of covered vs uncovered SEMS: 1) anticipated life expectancy and aggressiveness of the tumor; 2) extraluminal vs intraluminal tumors (tumor ingrowth is less of a problem in extrinsic tumors); 3) location of the tumor relative to the papilla; and 4) availability by region/country.

Life expectancy greater than 2 to 3 months should encourage the selection of an EUS-GE, due to its lower rates of reintervention, and although not borne out in this meta-analysis, a likely higher rate of initial clinical success as reported in some previous studies and based on our experience [22] [28]. For patients with combined obstruction of the bile duct and duodenum (common occurrence in periampullary malignancies) at centers with adequate endoscopic expertise, EUS-GE may have an advantage over endoscopic stenting because the site of intervention is away from the tumor site [29]. Therefore, the problem of reocclusion of the stent as a result of tumor overgrowth or ingrowth is unlikely compared to endoscopic enteral stenting [30]. In summary, when expertise is available, EUS-GE can be used in most cases for the treatment of malignant GOO as a less invasive alternative to surgery. However, patients with anticipated short survival, widespread metastasis, diffuse malignant infiltration of the gastric wall, or uncontrolled ascites are better approached with SEMS. Surgery can be reserved for patients with expected prolonged survival in whom less invasive procedures are not feasible or have failed.

Our study has strengths and limitations. In the absence of a 3-arm RCT, this meta-analysis compares the two most common palliative treatments for malignant GOO (duodenal stenting using SEMS and surgical GJ), as well as the newer EUS-GE procedure. Our eligibility criteria were relatively generous to include sufficient data to compare all three treatments. While this allowed an informative review, the quality of some studies included may be lower than reviews with stricter inclusion criteria [1]. Baseline characteristics among the three treatment arms were not equal for age and proportion of males; however, similarity of preprocedural GOOSS scores suggested that patients in all three treatment arms had similarly low levels of oral intake at baseline. Our analysis focused on palliative treatment of symptoms associated with malignant GOO, not on the treatment of associated conditions such as biliary obstruction, which is estimated to occur in 40 % to 92 % of patients with malignant GOO [31]. EUS-GE can be performed using at least three different techniques including direct EUS-GE, device-assisted EUS-GE, and EPASS double balloon-occluded gastrojejunostomy bypass [25]. Outcomes for specific techniques might vary compared to findings for our combined “EUS-GE” category. Time to postprocedure return to oral intake and resumption of chemotherapy, and SEMS migration rates by postprocedure chemotherapy status could not be analyzed because they were incompletely reported or not reported among studies. Because it is a newer technique, limited data on EUS-GE were available for some estimates, e. g. only one EUS-GE study was represented in the analysis of GOO recurrence. Although available in some studies, data on mortality and survival rates was usually missing or of very low quality as has been reported previously [1]. Therefore, our estimated mortality rates may have low generalizability. Incomplete reporting (e. g. outcomes reported only in technically successful cases or other patient subgroup) was also a barrier to comprehensive data on all outcomes.


Conclusions

Duodenal SEMS, EUS-GE and surgical GJ achieve similar rates of clinical success and improved dietary intake. Safety profiles were similar except that bleeding was less common and reintervention was more common for duodenal SEMS. Based on less data than the other two treatments, EUS-GE appears to be a promising treatment for patients with malignant GOO for whom surgery is contraindicated or less desirable.



Competing interests

Dr. Benias is a consultant for Boston Scientific and Fujifilm. Dr. Kozarek receives research support from Boston Scientific and the National Institutes of Health. Dr. Peetermans, Mr. McMullen and Ms. Gjata are full-time employees of Boston Scientific Corporation. Dr. Irani is a consultant for Boston Scientific and Gore.

Acknowledgements

The authors acknowledge Boston Scientific employees Margaret Gourlay, MD, MPH, and Jennifer Olson, PhD, for assistance in preparation of the manuscript. The data, analytic methods, and study materials for this study may be made available to other researchers in accordance with the Boston Scientific Data Sharing Policy (http://www.bostonscientific.com/en-US/data-sharing-requests.html).

Supplementary material


Corresponding author

Rajesh Krishnamoorthi, MD
Virginia Mason Medical Center – GI
1100 9th Ave
Seattle, WA 98101
United States   
Fax: +1-206-223-2319   

Publikationsverlauf

Eingereicht: 14. Oktober 2021

Angenommen nach Revision: 13. Januar 2022

Artikel online veröffentlicht:
10. Juni 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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Rüdigerstraße 14, 70469 Stuttgart, Germany


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Fig. 1 Flow diagram of literature search and study selection.
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Fig. 2a Analysis of efficacy outcomes. Outcomes for clinical success.
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Fig. 2a Analysis of efficacy outcomes. Outcomes for clinical success.
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Fig. 2b Analysis of efficacy outcomes. Outcomes for preprocedural GOOSS score.
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Fig. 2c Analysis of efficacy outcomes. Outcomes for postprocedural GOOSS score.
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Fig. 2d Analysis of efficacy outcomes. Outcomes for recurrence of GOO.
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Fig. 2e Analysis of efficacy outcomes. Outcomes for reintervention.
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Fig. 3a Analysis of safety outcomes. Outcomes for any procedure-related adverse event.
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Fig. 3a Analysis of safety outcomes. Outcomes for any procedure-related adverse event.
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Fig. 3b Analysis of safety outcomes. Outcomes for bleeding.
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Fig. 3c Analysis of safety outcomes. Outcomes for perforation.
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Fig. 3d Analysis of safety outcomes. Outcomes for stent migration.
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Fig. 3e Analysis of safety outcomes. Outcomes for e tissue ingrowth.
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Fig. 3f Analysis of safety outcomes. Outcomes for stent occlusion.
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Fig. 3g Analysis of safety outcomes. Outcomes for stent patency.
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Fig. 3h Analysis of safety outcomes. Outcomes for tissue overgrowth.
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Fig. 3i Analysis of safety outcomes. Outcomes for deaths reported in AE section.