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Abstract

Background:

Proton-pump inhibitors (PPIs) and potassium-competitive acid blockers (P-CABs) are recommended for erosive esophagitis (EE), with good safety and tolerance. However, it is unclear which is the best treatment option for EE.

Objectives:

This study aimed to evaluate the comparative efficacy of P-CABs and PPIs for healing EE patients, seeking an appropriate treatment choice in the 4- or 8-week treatment and standard or double dose.

Design:

A systematic review and network meta-analysis.

Data sources and methods:

Relevant databases were searched to collect randomized controlled trials of PPIs and P-CABs in the treatment of EE up to 31 May 2023. Studies on standard or double-dose PPIs or P-CABs which were published in English and assessed 4- or 8-week healing effects in EE were included. A network meta-analysis was performed to evaluate the efficacy of the treatments under the frequentist framework. Sensitivity and subgroup analyses of patients with different baseline EE were also conducted.

Results:

In all, 34 studies involving 25,054 patients and 9 PPIs, 6 P-CABs, or placebo treatment interventions were included. The pooled 4-week healing rate was significantly statistically lower than the pooled 8-week healing rate for most treatments. Besides, the higher healing rate of double-dose treatment than standard-dose treatment was not observed in the initial treatment of most drugs. The main analysis only included studies conducted for both patients with and without severe EE at baseline, and the proportion of severe EE included in the study was >10%, Keverprazan 20 mg qd ranked best with a surface under the cumulative ranking curve (SUCRA) value of 84.7, followed by Ilaprazole 10 mg qd with a SUCRA value of 82.0, for the healing rate at 8 weeks. Sensitivity analysis showed that the results were robust. Subgroup analysis showed that most P-CABs had higher healing rates than PPIs, particularly for patients with severe EE. And the healing rate of Keverprazan 20 mg qd at 8 weeks ranked best in the subgroup without or with severe EE at baseline.

Conclusion:

This study showed that an 8-week treatment seemed more effective than the 4-week treatment for healing EE patients. The healing effect of Keverprazan (20 mg qd) ranked best in 8-week treatment, for both severe and non-severe EE patients.

Trial registration:

The study protocol was registered with INPLASY (registration number INPLASY2023120053).

Plain language summary

A review and network meta-analysis of different medications for treating erosive esophagitis: potassium-competitive acid blockers and proton-pump inhibitors

Why was the study done? Proton-pump inhibitors (PPIs) and potassium-competitive acid blockers (P-CABs) are commonly used to treat Erosive esophagitis (EE) due to their good safety and tolerance. This study aimed to compare the effectiveness of P-CABs and PPIs in healing EE patients. We wanted to determine the best treatment choice in terms of the duration of treatment (4 or 8 weeks) and the dosage (standard or double-dose). What did the researchers do? The researchers searched relevant databases for randomized controlled trials that studied the use of PPIs and P-CABs in treating EE up until May 31, 2023. They included studies that evaluated the healing effects of standard or double-dose PPIs or P-CABs over a period of 4 or 8 weeks. A network meta-analysis was performed to compare the effectiveness of these treatments. They also conducted sensitivity analysis and subgroup analysis to examine the effects on patients with different levels of EE. What did the researchers find? The results showed that the healing rate after 4 weeks of treatment was significantly lower than the healing rate after 8 weeks for most treatments. Additionally, the higher healing rate observed with double-dose treatment compared to standard-dose treatment was not seen in the initial treatment of most drugs. In the main analysis, which included studies with patients both with and without severe EE at the beginning, Keverprazan 20mg qd was ranked as the most effective treatment with a healing rate of 84.7, followed by Ilaprazole 10mg qd with a healing rate of 82.0 at 8 weeks. The results were robust in sensitivity analysis. Subgroup analysis showed that most P-CABs had higher healing rates than PPIs, especially for patients with severe EE. What do the findings mean? Treating EE patients for 8 weeks was more effective than treating them for 4 weeks. Keverprazan (20mg once a day) with the 8-week treatment is the optimal method.

Keywords

erosive esophagitis network meta-analysis potassium-competitive acid blockers proton-pump inhibitors

Introduction

Gastroesophageal reflux disease (GERD) is one of the most common gastroenterological diseases, with a prevalence of 13.3% worldwide, covering all age groups and both genders.¹ GERD results from the reflux of gastric contents into the esophagus, often accompanied by symptoms such as heartburn, acid regurgitation, and dysphagia.² The symptomatic nature and high prevalence of GERD not only impact patients’ quality of life and well-being³ but also bring a huge economic burden on social medical systems.⁴

Erosive esophagitis (EE) is a severe condition of GERD, with an estimated proportion of 25–50% occurring in patients with GERD.^5,6 And EE is graded by the severity of mucosal breaks using the Hetzel–Dent,⁷ Savary–Miller,⁸ or Los Angeles scale.⁹ Without effective treatment, EE may develop into esophageal stricture, esophageal bleeding, or Barrett’s esophagus, the risk factor for esophageal adenocarcinoma.^10,11 The principal aim of treatment for patients with EE is gastric acid suppression. Currently, proton-pump inhibitors (PPIs) are the first-line drug for treating EE.¹² However, the efficacy of PPIs depends on the polymorphism of CYP2C19,¹³ and three to five dosages are needed to maximize the efficacy.¹⁴ Furthermore, PPIs need to be activated by gastric acid before they can bind to the proton pumps, and thus their onset is gradual and needs to be taken before meals.^14,15

Potassium-competitive acid blockers (P-CABs) are recent alternatives to PPIs for EE. In contrast to PPIs, P-CABs inhibit H⁺/K⁺-ATPase in a reversible and K⁺-competitive manner without any conversion.^16,17 The inhibitory effect of P-CABs is impacted less by the CYP2C19 enzyme, enabling gastric acid suppression faster and more potent.¹⁸ In addition, P-CABs are more stable in an acidic environment, water soluble, and capable of combining with both activated and inactivated proton pumps.^19,20 Several types of P-CABs, such as Vonoprazan developed by Takeda Pharmaceutical Company Ltd, in Japan,²¹ Tegoprazan developed by CJ Healthcare Corp. in South Korea,²² Keverprazan developed by Jiangsu Carephar Pharmaceutical Co. Ltd in China,²³ and Fexuprazan developed by Daewoong Pharmaceutical Co. Ltd in South Korea,²⁴ have been launched for EE treatment. In addition, PPIs or P-CABs at standard dose or double dose, if ineffective with the standard dose, are recommended in GERD guidelines or consensuses for treating EE.²⁵ However, as many types of PPIs and P-CABs are available in clinical practice, it is unclear which is the best treatment option for EE. Three meta-analyses have compared Vonoprazan and PPIs in healing GERD, but they did not include other P-CABs.^26–28

The confirmed safety and tolerance of PPIs and P-CABs have been demonstrated in clinical practice. For example, previous meta-analyses showed no significant difference in the incidence of adverse events among all PPIs, Vonoprazan, and placebo.^27,28 Some head-to-head randomized controlled trials (RCTs) have also shown that other P-CABs such as Tegoprazan, Keverprazan, and Fexuprazan had similar safety outcomes to those of some PPIs.^23,29–31 Therefore, we conducted a systematic review and network meta-analysis to evaluate the comparative efficacy of P-CABs and PPIs for healing EE patients. A subgroup analysis of patients with different baseline erosive grades would be also conducted, given that P-CABs could be more effective in patients with severe EE who could not benefit from PPIs.¹⁹ We ranked the efficacy on the 4- and 8-week healing rate of each treatment to help establish evidence-based hierarchies. In addition, the pooled 4- and 8-week healing rates were compared, to determine the optimal main outcome as well as the appropriate treatment course.

Methods

This study was conducted using the recommended method by the Cochrane Handbook for Systematic Reviews of Interventions and reported according to the PRISMA statement and the PRISMA extension for network meta-analysis.³² The study protocol was registered with INPLASY (registration number INPLASY2023120053). We have already registered it with PROSPERO, and it is under review.

Data sources and searches

PubMed, Embase, Web of Science, Cochrane Library, and Medline were searched for all years up to 31 May 2023, to identify RCTs of PPIs and P-CABs in the treatment of EE. The search terms and meshes were mainly ‘Esophagitis’, ‘Esomeprazole’, ‘Fexuprazan’, ‘Ilaprazole’, ‘Lansoprazole’, ‘Omeprazole’, ‘Pantoprazole’, ‘Rabeprazole’, ‘Tegoprazan’, ‘Vonoprazan’, and ‘Keverprazan’. More detailed terms are listed in Supplemental Material S1.

Study selection

The inclusion criteria for eligible studies were (1) Patients: patients with EE. Exclude refractory EE or resistance to previous PPI treatment. (2) Interventions and comparisons: drugs included either PPIs or P-CABs administered with the standard or double dose and placebo, excluding medications that are not yet licensed in the market. The included drugs and doses were described as follows: Esomeprazole 40 and 80 mg qd; Ilaprazole 10 and 20 mg qd; Lansoprazole 30 and 60 mg qd; Omeprazole 20 and 40 mg qd; Pantoprazole 40 and 80 mg qd; Rabeprazole 10 and 20 mg qd; Vonoprazan 20 and 40 mg qd; Tegoprazan 50 and 100 mg qd; Keverprazan 20 and 40 mg qd; and Fexuprazan 20 and 40 mg qd. (3) Outcomes: 4- or 8-week healing rate. (4) Study design: only RCTs published in English. Studies were excluded if informally published literature such as conference abstracts and academic papers, or patients received combined therapy for EE, such as two types of PPIs.

Data extraction and quality assessment

Two authors independently screened the title and abstract, reviewed the full texts, performed data extraction, and assessed the risk of bias. Disagreement was solved via discussion or consultation with the senior authors.

Study characteristics (ID, authors, year of publication), population (sample size, patient demographics, grade of EE at baseline, proportion of patients with severe EE at baseline), description of interventions (drug class, name, dose), and outcomes were extracted from each treatment group from each study. Intention-to-treat data were collected for all outcomes if available; otherwise, completer-only data were collected. The risk of bias was assessed using the Cochrane Risk of Bias Tool for randomized clinical trials.³²

Data synthesis and analysis

The network meta-analyses were performed under the frequentist framework using Stata 13 software (StataCorp, College Station, TX, USA).

Inconsistency was assessed by global Wald χ², with a p value >0.05 defined as no inconsistency, and the fixed-effects model was used; otherwise, a random-effects model with restricted maximum likelihood variance estimation was used.³³ Pairwise odds ratios (ORs) and the 95% confidence interval (95% CI) were calculated to compare the efficacy of treatments. The surface under the cumulative ranking curve (SUCRA) was used to rank the efficacy of the treatments, and the larger SUCRA indicated the better efficacy of the treatment regimen.³⁴ The funnel plot and Egger’s test of the intercept were employed to assess indications of publication bias.³⁴

To control the impact of the proportion of severe EE at baseline on the outcomes, studies were included in the main analysis if (1) they were originally conducted for both patients with and without severe EE at baseline and (2) the proportion of severe EE at baseline included in the study was >10%. Sensitivity analysis was also conducted to examine the validity and robustness of the main analysis using all studies that were originally conducted for both patients with and without severe EE at baseline. Subgroup analysis was conducted on the data of patients with or without a severe EE baseline grade, which was defined as grade 3 or higher on the Hetzel–Dent or Savary–Miller scales, or grade C or D on the Los Angeles scale.^35–39 If the study was originally conducted only for patients with or without severe EE at baseline, the data were only used in the subgroup analysis. The pooled 4- and 8-week healing rates were compared based on each treatment arm, via calculating OR and 95% CI.

Results

Study selection and characteristics

Figure 1 shows the number of included and excluded studies at each stage of the process. A total of 11,420 studies were identified from the databases, of these, 34 were eligible for analyses and included a total of 25,054 patients.^{23,29–31,40–69}

Figure 1.

Study flow diagram. Inconsistent dose: PPIs and P-CABs were not administered with the standard or double dose.

Characteristics of the eligible studies are shown in Table 1. After literature screening, the dose of Rabeprazole 10 mg bid was identified in one article. Given that Rabeprazole 10 mg bid was similar to the double dose of Rabeprazole (20 mg qd), we supplemented this dose to this study. A total of 16 treatment interventions were included, including nine PPIs (Esomeprazole 40 mg qd, Ilaprazole 10 mg qd, Lansoprazole 30 mg qd, Lansoprazole 60 mg qd, Omeprazole 40 mg qd, Omeprazole 20 mg qd, Pantoprazole 40 mg qd, Rabeprazole 10 mg bid, and Rabeprazole 20 mg qd), six P-CABs (Tegoprazan 100 mg qd, Tegoprazan 50 mg qd, Vonoprazan 20 mg qd, Vonoprazan 40 mg qd, Keverprazan 20 mg qd, and Fexuprazan 40 mg qd), and placebo. Data on the healing rate at 4 weeks were reported in 31 studies. Of these, 28 studies were originally conducted for both patients with and without severe EE at baseline but 3 studies included a proportion of less than 10% of severe EE at baseline, 2 studies only included patients without severe EE at baseline, and 1 study only included patients with severe EE at baseline.

Table 1.

Characteristics of the eligible studies.

Study ID	Study	Sample size	Treatment	Age	Male (%)	Diagnosis level	Proportion of patients with severe EE at baseline (%)	4-Week healing rate		8-Week healing rate
Study ID	Study	Sample size	Treatment	Age	Male (%)	Diagnosis level	Proportion of patients with severe EE at baseline (%)	Event	Total	Event	Total
1	Sontag et al., 1992⁴⁰	91	Omeprazole 40 mg qd	NR	NR	HD II–IV	About 50	40	91	66	91
1	Sontag et al., 1992⁴⁰	93	Omeprazole 20 mg qd	NR	NR	HD II–IV		36	93	68	93
1	Sontag et al., 1992⁴⁰	46	Placebo	NR	NR	HD II–IV		3	46	7	46
2	Hatlebakk et al., 1993⁴¹	116	Lansoprazole 30 mg qd	54.3	66.4	1–2^a	0	71	113	95	112
2	Hatlebakk et al., 1993⁴¹	113	Omeprazole 20 mg qd	55.4	65.5	1–2^a		73	112	96	111
3	Corinaldesi et al., 1995⁴²	121	Omeprazole 20 mg qd	52	62	SM II–III	18.3	83	105	96	105
3	Corinaldesi et al., 1995⁴²	120	Pantoprazole 40 mg qd	50	65	SM II–III		81	103	97	103
4	Mössner et al., 1995⁴³	95	Omeprazole 20 mg qd	55	69	SM II–III	20.3	67	86	81	86
4	Mössner et al., 1995⁴³	191	Pantoprazole 40 mg qd	53	70	SM II–III		126	170	153	170
5	Castell et al., 1996⁴⁴	422	Lansoprazole 30 mg qd	48.6	68.4	II–IV^a	34.8	335	421	367	421
5	Castell et al., 1996⁴⁴	431	Omeprazole 20 mg qd	47.5	60.3	II–IV^a		343	431	375	431
5	Castell et al., 1996⁴⁴	213	Placebo	47.6	66.7	II–IV^a		62	213	68	213
6	Mee and Rowley, 1996⁴⁵	300	Lansoprazole 30 mg qd	53.4	66.0	SM 1–4	16.6	186	300	226	300
6	Mee and Rowley, 1996⁴⁵	304	Omeprazole 20 mg qd	52.4	67.1	SM 1–4		172	304	216	304
7	Earnest et al., 1998⁴⁶	71	Lansoprazole 30 mg qd	NR	NR	II–IV^a	NR	52	71	62	71
7	Earnest et al., 1998⁴⁶	79	Lansoprazole 60 mg qd	NR	NR	II–IV^a		60	79	70	79
7	Earnest et al., 1998⁴⁶	66	Placebo	NR	NR	II–IV^a		20	66	31	66
8	Dekkers et al., 1999⁴⁷	102	Omeprazole 20 mg qd	52 ± 15.56	71.6	HD II–IV	56.9	83	102	96	102
8	Dekkers et al., 1999⁴⁷	100	Rabeprazole 20 mg qd	54 ± 15.70	53	HD II–IV		81	100	92	100
9	Vcev et al., 1999⁴⁸	60	Omeprazole 20 mg qd	NR	NR	SM 1–2	0	43	60	56	60
9	Vcev et al., 1999⁴⁸	60	Pantoprazole 40 mg qd	NR	NR	SM 1–2		46	60	57	60
10	Delchier et al., 2000⁴⁹	103	Omeprazole 20 mg qd	53 ± 15.1	39	HD II–IV	Median grade: 3.0; mean grade: 2.6	94	103	97	103
10	Delchier et al., 2000⁴⁹	103	Rabeprazole 10 mg bid	52 ± 14.3	30	HD II–IV		88	103	94	103
10	Delchier et al., 2000⁴⁹	104	Rabeprazole 20 mg qd	55 ± 15.7	45	HD II–IV		92	104	95	104
11	Kahrilas et al., 2000⁵⁰	654	Esomeprazole 40 mg qd	44.8 ± 13.0	58.7	LA A–D	26.7	496	654	615	654
11	Kahrilas et al., 2000⁵⁰	650	Omeprazole 20 mg qd	46.5 ± 13.5	61.4	LA A–D		421	650	565	650
12	Richter and Bochenek, 2000⁵¹	173	Pantoprazole 40 mg qd	49.3 ± 13.6	69.9	HD II–IV	44.5	125	173	152	173
12	Richter and Bochenek, 2000⁵¹	82	Placebo	48.3 ± 14.0	64.6	HD II–IV		11	82	27	82
13	Dupas and Houcke, 2001⁵²	235	Lansoprazole 30 mg qd	55.0 ± 14.7	75	SM II–III	17	189	235	201	235
13	Dupas and Houcke, 2001⁵²	226	Pantoprazole 40 mg qd	53.0 ± 14.5	73	SM II–III		184	226	203	226
14	Richter et al., 2001⁵³	1216	Esomeprazole 40 mg qd	NR	59.4	LA I–IV	26.4	993	1216	1139	1216
14	Richter et al., 2001⁵³	1209	Omeprazole 20 mg qd	NR	62.9	LA I–IV		831	1209	1018	1209
15	Castell et al., 2002⁵⁴	2624	Esomeprazole 40 mg qd	47.0 ± 13.0	57.4	LA A–D	24.6	2083	2624	2430	2624
15	Castell et al., 2002⁵⁴	2617	Lansoprazole 30 mg qd	47.4 ± 13.1	57.3	LA A–D		1965	2617	2324	2617
16	Howden et al., 2002⁵⁵	141	Esomeprazole 40 mg qd	46 ± 13	76	II–IV^a	39.4	108	138	123	138
16	Howden et al., 2002⁵⁵	143	Lansoprazole 30 mg qd	47 ± 12	82	II–IV^a		107	139	127	139
17	Gillessen et al., 2004⁵⁶	114	Esomeprazole 40 mg qd	54 ± 14	50	LA B–C	16.5	68	103	92	103
17	Gillessen et al., 2004⁵⁶	113	Pantoprazole 40 mg qd	53 ± 15	57	LA B–C		55	94	94	94
18	Fennerty et al., 2005⁵⁷	498	Esomeprazole 40 mg qd	47.3 ± 13.2	65.7	LA C–D	100	292	498	410	498
18	Fennerty et al., 2005⁵⁷	501	Lansoprazole 30 mg qd	47.1 ± 12.9	66.5	LA C–D		247	501	388	501
19	Labenz et al., 2005⁵⁸	1562	Esomeprazole 40 mg qd	50.6 ± 14.0	62	LA I–IV	24.4	1265	1562	1492	1562
19	Labenz et al., 2005⁵⁸	1589	Pantoprazole 40 mg qd	50.5 ± 13.8	63.7	LA I–IV		1184	1589	1462	1589
20	Pace et al., 2005⁵⁹	277	Omeprazole 20 mg qd	47.1 ± 14.9	67.7	SM I–III	29.7	213	237	231	237
20	Pace et al., 2005⁵⁹	283	Rabeprazole 20 mg qd	47.7 ± 14.2	68.6	SM I–III		212	233	228	233
21	Schmitt et al., 2006⁶¹	576	Esomeprazole 40 mg qd	47.1 ± 13.3	60.1	LA A–D	26.6	393	576	501	576
21	Schmitt et al., 2006⁶¹	572	Omeprazole 20 mg qd	46.2 ± 13.6	58.6	LA A–D		379	572	491	572
22	Vcev et al., 2006⁶²	90	Esomeprazole 40 mg qd	51.2 ± 14.5	63.3	LA I–III	31.4	70	90	83	90
22	Vcev et al., 2006⁶²	90	Pantoprazole 40 mg qd	49.4 ± 13.9	65.6	LA I–III		65	90	82	90
23	Bardhan et al., 2007⁶³	293	Esomeprazole 40 mg qd	54 ± 14	53	LA A–D	34.6	202	293	243	293
23	Bardhan et al., 2007⁶³	288	Pantoprazole 40 mg qd	53 ± 14	49	LA A–D		199	288	248	288
24	Zheng, 2009⁶⁴	68	Esomeprazole 40 mg qd	57.4 ± 12.8	48.5	LA A–D	32.1	NR	NR	65	68
24	Zheng, 2009⁶⁴	69	Lansoprazole 30 mg qd	58.1 ± 13.0	50.7	LA A–D		NR	NR	62	69
24	Zheng, 2009⁶⁴	68	Omeprazole 20 mg qd	57.9 ± 14.1	48.5	LA A–D		NR	NR	60	68
24	Zheng, 2009⁶⁴	69	Pantoprazole 40 mg qd	57.8 ± 13.2	49.3	LA A–D		NR	NR	63	69
25	Ashida et al., 2015³⁰	140	Lansoprazole 30 mg qd	55.8 ± 13.92	70.7	LA A–D	33.6	123	132	126	132
25	Ashida et al., 2015³⁰	154	Vonoprazan 20 mg qd	58.3 ± 13.86	74.7	LA A–D		136	144	139	144
25	Ashida et al., 2015³⁰	146	Vonoprazan 40 mg qd	57.6 ± 12.83	78.1	LA A–D		130	134	130	134
26	Ashida et al., 2016²⁹	202	Lansoprazole 30 mg qd	57.4 ± 13.2	76.2	LA A–D	36.2	184	199	190	199
26	Ashida et al., 2016²⁹	207	Vonoprazan 20 mg qd	58.3 ± 13.8	66.2	LA A–D		198	205	203	205
27	Xue et al., 2016⁶⁵	105	Esomeprazole 40 mg qd	47.8 ± 11.65	68.6	LA A–D	10.8	75	105	89	105
27	Xue et al., 2016⁶⁵	107	Ilaprazole 10 mg qd	48.9 ± 12.63	70.1	LA A–D		87	107	95	107
28	Xue et al., 2018⁶⁶	215	Esomeprazole 40 mg qd	47.5 ± 12.32	70.7	LA A–D	6.1	167	215	178	215
28	Xue et al., 2018⁶⁶	322	Ilaprazole 10 mg qd	48.2 ± 11.96	72.0	LA A–D		245	322	269	322
29	Xiao et al., 2020⁶⁷	237	Lansoprazole 30 mg qd	53.8 ± 12.53	75.5	LA A–D	29.9	192	230	210	230
29	Xiao et al., 2020⁶⁷	244	Vonoprazan 20 mg qd	54.1 ± 13.16	72.1	LA A–D		203	238	220	238
30	Lee et al., 2019³¹	99	Esomeprazole 40 mg qd	50.4 (21.0–75.0)	53.5	LA A–D	4.3	87	99	92	99
30	Lee et al., 2019³¹	102	Tegoprazan 100 mg qd	52.8 (20.0–74.0)	64.7	LA A–D		92	102	97	102
30	Lee et al., 2019³¹	99	Tegoprazan 50 mg qd	52.7 (21.0–74.0)	62.6	LA A–D		87	99	95	99
31	Chen et al., 2022²³	119	Keverprazan 20 mg qd	49.7 ± 12.1	83.2	LA A–D	20.6	98	119	114	119
31	Chen et al., 2022²³	119	Lansoprazole 30 mg qd	48.8 ± 12.3	76.5	LA A–D		97	119	107	119
32	Laine et al., 2023⁶⁸	510	Lansoprazole 30 mg qd	51.7 ± 14.1	45.7	LA A–D	34.3	NR	NR	431	510
32	Laine et al., 2023⁶⁸	514	Vonoprazan 20 mg qd	51.0 ± 13.4	50.2	LA A–D		NR	NR	478	514
33	Lee et al., 2022⁶⁹	115	Esomeprazole 40 mg qd	55.05 ± 12.89	64.3	LA A–D	6.9	92	104	110	111
33	Lee et al., 2022⁶⁹	116	Fexuprazan 40 mg qd	53.70 ± 12.44	67.2	LA A–D		93	103	106	107
34	Lightdale et al., 2006⁶⁰	588	Omeprazole 20 mg qd	45.3 ± 13.0	63.9	LA A–D	26.2	NR	NR	484	588

These articles do not specify the endoscopic grading scale.

HD, Hetzel–Dent; LA, Los Angeles; SM, Savary–Miller; NR, not report.

Data on the healing rate at 8 weeks were reported in 34 studies. Of these, 31 studies were originally conducted for both patients with and without severe EE at baseline but 3 studies included a proportion of severe EE at a baseline of >0–10%, 2 studies only included patients without severe EE at baseline, and 1 study only included patients with severe EE at baseline.

For the subgroup analysis, 11 studies reported a 4-week healing rate for patients without severe EE at baseline, 11 reported a 4-week healing rate for patients with severe EE at baseline, 14 studies reported an 8-week healing rate for patients without severe EE at baseline, and 14 studies reported an 8-week healing rate for patients with severe EE at baseline.

Quality assessment of the included studies

As shown in Supplemental Figure S1, 18 studies had a low risk of bias in random sequence generation; 28 used appropriate allocation concealment; and 32 studies had a low risk of blinding participants, personnel, and outcome assessment. All 34 studies had complete data and none selectively reported the findings, and it was unclear whether other sources of bias existed.

Pooled 4- versus 8-week healing rates

As shown in Supplemental Table S9, the pooled 4-week healing rate was significantly statistically lower than the pooled 8-week healing rate for most drugs, except for Tegoprazan 100 qd (OR: 0.474, 95% CI: 0.156–1.440), Vonoprazan 40 mg qd (OR: 1.000, 95% CI: 0.245–4.084), and Rabeprazole 10 mg bid (OR: 0.562, 95% CI: 0.234–1.349).

4-Week healing rate

The network plot is shown in Figure 2, the area of nodes indicates the number of studies included in the corresponding nodes, and the width of the lines connecting nodes suggests the number of relevant data. No inconsistency was detected in the main, sensitivity, or subgroup analysis (Table 2). The funnel plot is shown in Supplemental Figure S2, indicating that publication bias was acceptable.

Figure 2.

Network plots for 4-week healing rate. (a) Main analysis. (b) Sensitivity analysis. (c) Subgroup analysis on patients without severe baseline grade. (d) Subgroup analysis on patients with severe baseline grade.

Table 2.

Results of inconsistency testing.

Outcomes	Wald χ²	p Value
4-Week healing rate
Main analysis	4.63	0.865
Sensitivity analysis	0.65	0.741
Subgroup analysis
Patients without severe baseline grade	1.03	0.470
Patients with a severe baseline grade	1.07	0.499
8-Week healing rate
Main analysis	0.49	0.893
Sensitivity analysis	0.51	0.886
Subgroup analysis
Patients without severe baseline grade	0.81	0.552
Patients with a severe baseline grade	1.33	0.382

In the main analysis, 25 studies were included with the proportions of severe EE at a baseline of >10%. For all relative treatment pairwise comparisons, all PPIs and P-CABs showed a significantly better 4-week healing rate than the placebo (Supplemental Table S1). Ilaprazole 10 mg qd and Esomeprazole 40 mg qd showed significantly higher rates than Rabeprazole 10 mg bid, Pantoprazole 40 mg qd, Omeprazole 20 mg qd, and Lansoprazole 30 mg qd. Ilaprazole 10 mg qd was also significantly superior to Rabeprazole 20 mg qd on a 4-week healing rate. Vonoprazan 40 mg qd showed significantly higher rates than Rabeprazole 10 mg bid. Ilaprazole 10 mg qd was ranked as the best treatment with a SUCRA value of 89.3, followed by Vonoprazan 40 mg qd with a SUCRA value of 86.7 (Table 3).

Table 3.

The results of SUCRA in the main analysis.

Treatment	4-Week healing rate			8-Week healing rate
Treatment	SUCRA	PrBest	MeanBank	SUCRA	PrBest	MeanBank
Kev20	54.6	2.6	6.5	84.7	41.0	2.8
Ila10	89.3	35.8	2.3	82	28.4	3.2
Vpz20	73.9	4.9	4.1	80.4	7.2	3.3
Eso40	68.6	0.3	4.8	72.5	0.7	4.3
Vpz40	86.7	49.8	2.6	72.7	20.7	4.3
Pan40	45.9	0.0	7.5	56.3	0.1	6.2
Lan30	49.9	0.0	7.0	42	0.0	8.0
Ome40	49.4	1.5	7.1	39.9	0.6	8.2
Lan60	60.0	4.7	5.8	34	0.6	8.9
Ome20	30.9	0.0	7.5	33.3	0.0	9.0
Rab20	25.1	0.3	10.0	26.5	0.1	9.8
Rab10	15.4	0.1	11.2	25.8	0.5	9.9
Placebo	0.3	0.0	13.0	0.0	0.0	13.0

Eso40, Esomeprazole 40 mg qd; Fex40, Fexuprazan 40 mg qd; Ila10, Ilaprazole 10 mg qd; Kev20, Keverprazan 20 mg qd; Lan30, Lansoprazole 30 mg qd; Lan60, Lansoprazole 60 mg qd; Ome 40, Omeprazole 40 mg qd; Ome 20, Omeprazole 20 mg qd; Pan40, Pantoprazole 40 mg qd; Rab10, Rabeprazole 10 mg bid; Rab20, Rabeprazole 20 mg qd; SUCRA, surface under the cumulative ranking curve; Teg100, Tegoprazan 100 mg qd; Teg50, Tegoprazan 50 mg qd; Vpz20, Vonoprazan 20 mg qd; Vpz40, Vonoprazan 40 mg qd.

In the sensitivity analysis, 28 studies were included with the proportions of both severe and non-severe EE at a baseline of >0%. The results showed that all PPIs and P-CABs showed a significantly better 4-week healing rate than the placebo. The superiority was observed in respective groups: Ilaprazole 10 mg qd versus Rabeprazole 10 mg bid and Omeprazole 20 mg qd; Esomeprazole 40 mg qd versus Pantoprazole 40 mg, Omeprazole 20 mg qd and Lansoprazole 30 mg qd; Vonoprazan 40 mg qd versus Rabeprazole 10 mg bid (Supplemental Table S2). Vonoprazan 40 mg qd was ranked as the best treatment with a SUCRA value of 87.3, followed by Ilaprazole 10 mg qd with a SUCRA value of 75.8 (Table 4).

Table 4.

The results of SUCRA in the sensitivity analysis.

Treatment	4-Week healing rate			8-Week healing rate
Treatment	SUCRA	PrBest	MeanBank	SUCRA	PrBest	MeanBank
Teg50	61.4	5.7	6.8	81.3	26.5	3.8
Kev20	47.2	2	8.9	79.3	21.3	4.1
Teg100	75	17.1	4.7	74.9	14.6	4.8
Vpz20	66.9	1.6	6	73.7	2.2	4.9
Ila10	75.8	4.1	4.6	71.7	2.5	5.3
Vpz40	87.3	51.4	2.9	67.4	9.9	5.9
Eso40	68.3	0.1	5.8	64.9	0.1	6.3
Fex40	72.6	15.8	5.1	55.6	22.6	7.7
Pan40	43.1	0	9.5	50.0	0	8.5
Lan30	40.3	0	9.9	37.2	0	10.4
Ome40	50.3	1.5	8.4	36.4	0.1	10.5
Lan60	36.5	0.5	10.5	30.3	0.1	11.5
Ome20	28.3	0	11.8	29.8	0	11.5
Rab20	31.4	0.1	11.3	24.0	0	12.4
Rab10	15.7	0.1	13.6	23.4	0.2	12.5
Placebo	0	0	16	0.2	0	16

In the subgroup analysis on patients without severe EE at baseline, all PPIs and P-CABs showed a significantly better 4-week healing rate than the placebo, and no significant differences were observed between any other two groups (Supplemental Table S3). Vonoprazan 40 mg qd was ranked as the best treatment with a SUCRA value of 90.7, followed by Lansoprazole 30 mg qd with a SUCRA value of 74.2, and Keverprazan 20 mg qd with a SUCRA value of 73.7 (Table 5).

Table 5.

The results of SUCRA in the subgroup analysis on patients without severe baseline grade.

Treatment	4-Week healing rate			8-Week healing rate
Treatment	SUCRA	PrBest	MeanBank	SUCRA	PrBest	MeanBank
Kev20	73.7	20.5	2.8	91.3	70.2	1.7
Vpz40	90.7	73	1.7	76.2	14	2.9
Lan30	74.2	4.5	2.8	66.6	0.7	3.7
Rab20	–	–	–	63.7	14.5	3.9
Vpz20	50	1.1	4.5	57.1	0.6	4.4
Ome20	45.4	0.2	4.8	45.0	0.0	5.4
Eso40	36.5	0.5	5.4	34.4	0.0	6.2
Pan40	29.6	0.3	5.9	15.6	0.0	7.7
Placebo	0.0	0.0	8.0	0.1	0.0	9.0

In the subgroup analysis on patients with severe EE at baseline, all PPIs and P-CABs showed a significantly better 4-week healing rate than the placebo, and Vonoprazan 20 mg qd and Esomeprazole 40 mg qd showed a significantly higher rate than Lansoprazole 30 mg qd and Omeprazole 20 mg qd (Supplemental Table S4). Vonoprazan 20 mg qd was ranked as the best treatment with a SUCRA value of 85.1, followed by Vonoprazan 40 mg qd with a SUCRA value of 84.1 (Table 6).

Table 6.

The results of SUCRA in the subgroup analysis on patients with severe baseline grade.

Treatment	4-Week healing rate			8-Week healing rate
Treatment	SUCRA	PrBest	MeanBank	SUCRA	PrBest	MeanBank
Kev20	57.1	11.9	4.4	89.6	71.0	1.9
Vpz20	85.1	27.2	2.2	75.8	11.0	3.2
Eso40	70.8	2.1	3.3	74.4	3.8	3.3
Vpz40	84.1	55.3	2.3	55.0	8.6	5.0
Pan40	47.9	3.2	5.2	48.8	0.7	5.6
Rab20	–	–	–	44.4	4.1	6.0
Lan30	41.2	0.0	5.7	41.8	0.0	6.2
Ome20	33.8	0.0	6.3	40.1	0.0	6.4
Lan60	30.1	0.3	6.6	30.0	0.7	7.3
Placebo	0.0	0.0	9.0	0.0	0.0	10.0

8-Week healing rate

The network plot is shown in Figure 3. No inconsistency was detected in the main, sensitivity, or subgroup analysis (Table 2). The funnel plot is shown in Supplemental Figure S3, indicating that publication bias was acceptable.

Figure 3.

Network plots for 8-week healing rate. (a) Main analysis. (b) Sensitivity analysis. (c) Subgroup analysis on patients without severe baseline grade. (d) Subgroup analysis on patients with severe baseline grade.

In the main analysis, 28 studies were included with the proportions of severe EE at a baseline of >10%. All PPIs and P-CABs showed a significantly better 8-week healing rate than the placebo; Vonoprazan 20 mg qd (OR: 2.11, 95% CI: 1.16–3.85) and Esomeprazole 40 mg qd (OR: 1.73, 95% CI: 1.27–2.36) showed significantly higher rates than Omeprazole 20 mg qd; Vonoprazan 20 mg qd (OR: 1.88, 95% CI: 1.15–3.07) and Esomeprazole 40 mg qd (OR: 1.54, 95% CI: 1.09–2.18) also showed significantly higher rates than Lansoprazole 30 mg qd (Supplemental Table S5). Vonoprazan 20 mg qd (OR: 2.60, 95% CI: 1.01–6.68) also showed significantly higher rates than Rabeprazole 20 mg qd; Keverprazan 20 mg qd ranked best with a SUCRA value of 84.7, followed by Ilaprazole 10 mg qd with a SUCRA value of 82.0 (Table 3).

In the sensitivity analysis, 31 studies were included with the proportions of both severe and non-severe EE at baseline of >0%. All PPIs and P-CABs showed a significantly better 8-week healing rate than the placebo; Vonoprazan 20 mg qd (OR: 2.12, 95% CI: 1.17–3.82), Ilaprazole 10 mg qd (OR: 2.04, 95% CI: 1.06–3.94), and Esomeprazole 40 mg qd (OR: 1.74, 95% CI: 1.28–2.36) showed significantly higher rates than Omeprazole 20 mg qd; Vonoprazan 20 mg qd (OR: 1.88, 95% CI: 1.16–3.05) and Esomeprazole 40 mg qd (OR: 1.54, 95% CI: 1.10–2.17) also showed significantly higher rates than Lansoprazole 30 mg qd; Vonoprazan 20 mg qd showed a significantly better healing rate than Rabeprazole 20 mg qd (Supplemental Table S6). Tegoprazan 50 mg qd ranked best with a SUCRA value of 81.3, followed by Keverprazan 20 mg qd with a SUCRA value of 79.3 (Table 4).

In the subgroup analysis on patients without severe EE at baseline, all PPIs and P-CABs showed a significantly better 8-week healing rate than the placebo; Keverprazan 20 mg qd (OR: 23.82, 95% CI: 1.11–508.71), Lansoprazole 30 mg qd (OR: 3.18, 95% CI: 1.56–6.47), Omeprazole 20 mg qd (OR: 2.06, 95% CI: 1.19–3.57), and Esomeprazole 40 mg qd (OR: 1.69, 95% CI: 1.14–2.50) showed significantly higher rates than Pantoprazole 40 mg qd; Lansoprazole 30 mg qd (OR: 1.88, 95% CI: 1.02–3.47) also showed significantly higher rates than Esomeprazole 40 mg qd (Supplemental Table S7). Keverprazan 20 mg qd ranked best with a SUCRA value of 91.3, followed by Vonoprazan 40 mg qd with a SUCRA value of 76.2 (Table 5).

In the subgroup analysis on patients with severe EE at baseline, all PPIs and P-CABs showed a significantly better 8-week healing rate than the placebo, and no significant differences were observed between any other two groups (Supplemental Table S8). Keverprazan 20 mg qd ranked best with a SUCRA value of 89.6, followed by Vonoprazan 20 mg qd with a SUCRA value of 75.8 (Table 6).

Discussion

The results of this network meta-analysis demonstrated the efficacy of all kinds of P-CABs and PPIs in treating EE. All P-CABs and PPIs were more effective than placebo. Keverprazan 20 mg qd was found to have the highest healing rate in 8-week treatment, for both severe and non-severe EE patients, and Vonoprazan 40 mg had a relatively higher healing rate in 4-week treatment. To our knowledge, this is the first network meta-analysis including all types and the usual and double dosage of P-CABs and PPIs in treating EE. This analysis may therefore provide evidence for clinicians, enabling them to offer better treatment choices to patients with EE.

This network meta-analysis showed a higher efficacy for most P-CABs than PPIs, particularly in patients with severe EE. This finding may support the hypothesis that patients with severe EE benefit more from P-CABs than those with mild-to-moderate EE.⁷⁰ P-CABs may have an advantage over PPIs because of their special mechanism of action, but the evidence is insufficient. In the current guideline or consensus, PPIs are still recommended as the first-choice treatment; P-CABs or the optimization of PPI therapy are suggested for patients with PPI resistance.^71,72 Further studies were needed, to help inform the appropriate treatment of patients with complaints of differing severity.

In terms of healing rates at 4- and 8-week, the results showed that the pooled 4-week healing rate was significantly statistically lower than the pooled 8-week healing rate for most drugs. Thus, an 8-week treatment may be preferable for treating EE. Under this condition, Keverprazan 20 mg qd is recommended to be the best choice, despite that the sensitivity analysis revealed Keverprazan 20 mg qd was slightly less effective than Tegoprazan 50 mg qd. Only one study included Tegoprazan 50 mg qd, and the proportion of patients with severe EE was much lower (4.3%) than that in the study including Keverprazan 20 mg qd (20.6%). This may be why Tegoprazan 50 mg qd ranked better than Keverprazan 20 mg qd in the 8-week sensitivity analysis. Keverprazan, a new oral P-CAB, was launched in China in February 2023. It was designed based on the structure of Vonoprazan and has a high distribution in the stomach, providing better control of stomach acid.⁷³ A published clinical trial (ChiCTR2100050136) indicated that the percentages of time of intragastric pH greater than 4 [pH >4 holding-time ratio (HTR)] in Placebo, 20 mg Vonoprazan, and 20 mg Keverprazan groups were 5.6 ± 2.4%, 82.2 ± 12.6%, and 85.0 ± 3.0% on day 1, respectively, and the corresponding night-time HTR values were 3.9 ± 4.7%, 87.9 ± 15.7%, and 99.9 ± 0.0%, respectively.⁶⁷ Another phase I study showed that starting 4 h after administration, the pH levels in the 20–60 mg dose groups of Keverprazan were consistently higher than those in the 30 mg Lansoprazole group. Specifically, pH levels were maintained above 6 in the Keverprazan groups after 16 h of administration, which was remarkably higher when compared to Lansoprazole. This head-to-head study therefore demonstrated that the acid suppression effect of Keverprazan at a dose of 20 mg was more potent and stable than 30 mg of Lansoprazole.⁷⁴ Tegoprazan was also a novel P-CAB. The pharmacodynamic data showed that the 50, 100, and 200 mg doses of Tegoprazan demonstrated longer HTRs above pH >4 up to 12 h after evening dosing than the Dexlansoprazole group.⁷⁵ A randomized, open-label, three-period, six-sequence crossover study showed that night-time intragastric pH greater than four HTRs in 50 mg Tegoprazan, 20 mg Vonoprazan, and 40 mg Esomeprazole groups were 66.0 ± 15.7%, 60.5 ± 13.5%, and 36.1 ± 14.7%, respectively.⁷⁶ Further RCT studies, particularly head-to-head studies, are needed to compare Keverprazan and Tegoprazan, to inform the better choice for patients with EE.

In the main analysis, although some drugs, such as Omeprazole showed higher healing rates using double dose compared to standard dose after 4- and 8-week treatment, some drugs such as Vonoprazan and Lansoprazole demonstrated healing rate results unrelated to the dosage after 8-week treatment. Thus, the healing rate of a double dose may not necessarily be higher than that of a standard dose in the initial treatment. In some clinical practice guidelines, a standard dose is often recommended as an initial treatment choice, and a double dose is recommended as a therapeutic strategy for PPI-resistant GERD.^71,72 The EE population included in this network meta-analysis only received initial treatment; therefore, the therapeutic advantage of a double dose might not have been observed. Further research is needed to confirm the optimal dosage at different treatment stages.

This study has several limitations. First, literature-based network meta-analysis included heterogeneity and bias based on each study. We integrated RCTs using variable grading scales to identify the severity for sensitivity and subgroup analyses. Thus, the analyses might be biased by the individual grading criteria adopted in each grading scale. Second, the majority of included studies did not report the outcomes according to severity grading under endoscopy so we could not assess the efficacy of all PPIs and P-CABs with different severity of EE. Finally, as the P-CABs are novel, there are few head-to-head trials comparing their efficacy. For example, only one RCT study assessed the efficacy of Keverprazan, Tegoprazan, and Fexuprazan, respectively, which meant a statistically significant difference in the efficacy of different drugs could not be determined. Therefore, further high-quality RCTs of P-CABs are required to confirm the efficacy in treating EE.

Conclusion

Our network meta-analysis suggests that the healing effect of Keverprazan (20 mg qd) ranked best in 8-week treatment, for both severe and non-severe EE patients. Most P-CABs showed a higher healing rate than PPIs, particularly for patients with severe EE. As current evidence comparing PPIs and P-CABs for EE is insufficient, our results may help inform future directions of treatment for EE patients. Furthermore, high-quality RCTs of P-CABs are required to confirm the healing effect in patients with EE.

Supplemental Material

sj-pdf-1-tag-10.1177_17562848241251567 – Supplemental material for Potassium-competitive acid blockers and proton-pump inhibitors for healing of erosive esophagitis: a systematic review and network meta-analysis

Supplemental material, sj-pdf-1-tag-10.1177_17562848241251567 for Potassium-competitive acid blockers and proton-pump inhibitors for healing of erosive esophagitis: a systematic review and network meta-analysis by Yin Liu, Zhifeng Gao and XiaoHua Hou in Therapeutic Advances in Gastroenterology

Supplemental Material

sj-pdf-2-tag-10.1177_17562848241251567 – Supplemental material for Potassium-competitive acid blockers and proton-pump inhibitors for healing of erosive esophagitis: a systematic review and network meta-analysis

Supplemental material, sj-pdf-2-tag-10.1177_17562848241251567 for Potassium-competitive acid blockers and proton-pump inhibitors for healing of erosive esophagitis: a systematic review and network meta-analysis by Yin Liu, Zhifeng Gao and XiaoHua Hou in Therapeutic Advances in Gastroenterology

Footnotes

Acknowledgements

None.

Declarations

ORCID iD

Yin Liu

Supplemental material

Supplemental material for this article is available online.

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