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. 2019 Jun 27;59(2):153–161. doi: 10.2169/internalmedicine.2521-18

Table 1.

Comparative Studies of H. Pylori First-line Eradication Therapy with Vonoprazan and Proton Pump Inhibitors.

References Study design Triple therapy regimen Eradication rate (95% CI) Adverse events (discontinuation)
Vonoprazan PPI Vonoprazan PPI
ITT/FAS PP ITT/FAS PP Vonoprazan PPI
(24) Prospective, non-randomized, open-label, multicenter VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=1,688 RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=76 (RPZ), 71 (EPZ) NA 90.8% NA RPZ 68.4%, EPZ 77.5% NA (0%) NA (0%)
(27) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=111 RPZ 10 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=98 94.6% (88.6-98.0) 95.5% (89.7-98.5) 86.7% (78.4-92.7) 86.7% (78.4-92.7) 2.7% (NA) 3.1% (NA)
(23) Randomized, single-blind, single-center, parallel-group comparison VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=72 RPZ 20 mg or LPZ 30 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=69 95.8% (88.3-99.1) 95.7% (88.0-99.1) 69.6% (57.3-80.1) 71.4% (58.7-82.1) 26.3% (NA) 37.7% (NA)
(28) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=125 LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=295 89.6% (84-95) 89.6% (84-95) 71.9% (67-77) 73.1% (68-78) 11.9% (0%) 10.7% (5 dropouts)
(21) Randomized, double-blind, multicenter, parallel-group comparison VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=329 LPZ 30 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=321 92.6% (89.2-95.2) NA 75.9% (70.9-80.5) NA 34.0% (0.9%) 41.4% (0.6%)
(38) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=308 LPZ 30 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=272 NA 91.0% NA 84.7% NA (2 dropouts) NA (2 dropouts)
(29) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=353 LPZ 30 mg or RPZ 10 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=2,173 62.3% 89.4% 47.1% 66.8% 8.4% (NA) 5.7% (NA)
(30) Prospective and retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 400 mg, twice-daily, 7 days, n=146 LPZ 30 mg, RPZ 10 mg, OPZ 20 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=1,305 NA 89.7% (87.9-91.3) NA 73.9% (66.0-80.8) NA NA
(31) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=546 LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=211 (LPZ), 89 (RPZ), 507 (EPZ) 87.9% (84.9-90.5) NA LPZ 57.3% (50.4-64.1), RPZ 62.9% (52.0-72.9), EPZ 71.6% (67.5-75.5) NA 11.2% (0%) LPZ 5.7%, RPZ 10.1%, EPZ 7.7% (0%)
(32) Retrospective, multicenter VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=422 LPZ 30 mg, RPZ 10 mg, OPZ 20 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=2,293 87.2% NA 72.4% NA 6.2% (NA) 6.2% (NA)
(33) Retrospective, two-institution VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=117 LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=198 (LPZ), 138 (RPZ), 120 (EPZ) 83% (75-89) 85% (77-91) LPZ 66% (59-72), RPZ 67% (58-74), EPZ 83% (75-89) LPZ 69% (62-76), RPZ 70% (61-77), EPZ 87% (79-93) 5% (NA) LPZ 11%, RPZ 6%, EPZ 3% (NA)
(22) Non-randomized, open-label, multicenter, parallel-group comparison VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=623 LPZ 30 mg, RPZ 10 mg, OPZ 20 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=608 84.9% (81.9-87.6) 86.4% (83.5-89.1) 78.8% (75.3-82.0) 79.4% (76.0-82.6) NA NA
(25) Randomized, open-label, multicenter VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=55 [CAM-susceptible H. pylori] LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=42 (LPZ), 4 (RPZ), 5 (EPZ) [CAM-susceptible H. pylori] 87.3% (75.5-94.7) 88.9% (77.4-95.8) 76.5% (62.5-87.2) 86.7% (73.2-94.9) NA (0%) NA (1 dropout)
VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=41 [CAM-resistant H. pylori] 82.9% (67.9-92.8) 82.9% (67.9-92.8)
(34) Retrospective, single-center, propensity score matching analysis VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=181 LPZ 30 mg or RPZ 10 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=480 89.0% (84.4-93.5) [89.1% (84.5-93.8) in propensity score matching] 91.5% (87.3-95.6) [91.2% (87.0-95.5)] 74.2% (70.3-78.1) [70.9% (64.1-77.6)] 77.9% (74.1-81.7) [71.7% (64.9-78.4)] 12.7% (0%) 14.4% (0%)
(37) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=363 LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 or 400 mg, twice-daily, 7 days, n=207 (LPZ), 450 (RPZ), 123 (EPZ) 91.5% (88.6-94.3) 97.4% (95.7-99.1) LPZ 77.3% (71.6-83.0), RPZ 79.8% (76.1-83.5), EPZ 81.3% (74.4-88.2) LPZ 85.6% (80.5-90.6), RPZ 86.1% (82.8-89.4), EPZ 88.5% (82.6-94.4) NA NA
(35) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=443 EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=431 84.6% 86.3% 79.1% 79.9% 0.68% (1 dropout) 1.17% (3 dropouts)
(36) Retrospective, single-center VPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=335 LPZ 30 mg, RPZ 10 mg, or EPZ 20 mg + AMX 750 mg + CAM 200 mg, twice-daily, 7 days, n=1,720 85.7% 90.3% 73.2% 76.4% NA (0%) NA (0.4%)

PPI: proton pump inhibitor, CI: confidence interval, ITT: intention to treat analysis, FAS: full analysis set, PP: per protocol analysis, VPZ: vonoprazan, AMX: amoxicillin, CAM: clarithromycin, LPZ: lansoprazole, RPZ: rabeprazole, OPZ: omeprazole, EPZ: esomeprazole, NA: not available