Schwartz H, Krause R, Sahba B, Haber M, Weissfeld A, Rose P, Siepman N, Freston J
Baptist Hospital, Miami, Florida, USA.
Am J Gastroenterol. 1998 Apr;93(4):584-90. doi: 10.1111/j.1572-0241.1998.169_b.x.
The efficacy and safety of dual and triple therapies with a proton pump inhibitor and antibiotic(s) for therapy of Helicobacter pylori-associated duodenal ulcer disease have been compared using results from independent studies using different methods and regimens, making interpretation difficult. In a large, double-blind, multicenter study conducted in the United States, we compared a triple therapy regimen with four dual therapy and one monotherapy regimens in the eradication of H. pylori and the prevention of ulcer recurrence.
Patients with active duodenal ulcer disease or history of duodenal ulcer disease within the past year and H. pylori infection were randomized to receive one of six 14-day treatment regimens: lansoprazole 30 mg, clarithromycin 500 mg, and amoxicillin 1 gm b.i.d.; lansoprazole 30 mg b.id. and either clarithromycin 500 mg b.i.d. or t.i.d.; lansoprazole 30 mg b.i.d. or t.i.d. with amoxicillin 1 gm t.i.d.; or lansoprazole 30 mg t.i.d. alone. No additional acid suppression therapy followed eradication therapy. Primary efficacy endpoints were eradication of H. pylori and ulcer recurrence.
Of 396 patients enrolled in the study, 352 met the entry criteria for duodenal ulcer status and H. pylori positivity. At 4-6 wk after the end of therapy, H. pylori was eradicated from 94% (44 of 47) of patients receiving lansoprazole, clarithromycin, and amoxicillin triple therapy, 77% (39 of 51) of those receiving lansoprazole t.i.d./amoxicillin t.i.d., 75% (36 of 48) of those receiving lansoprazole b.i.d./clarithromycin t.i.d., 57% (28 of 49) of those receiving lansoprazole b.i.d./clarithromycin b.i.d., 53% (26 of 49) of those receiving lansoprazole b.i.d./amoxicillin t.i.d., and 2% (1 of 53) of those receiving lansoprazole monotherapy (p < or = 0.05, triple therapy vs each dual therapy and each dual therapy vs monotherapy). Of those patients who were documented as free of ulcer at 4-6 wk after treatment, ulcers recurred within 6 months in 7% of patients receiving triple therapy, as compared with 13-23% of patients receiving dual therapy, and 69% of patients receiving lansoprazole monotherapy. Patients who were H. pylori negative at 4-6 wk after treatment were less likely to have an ulcer recurrence than were patients who were H. pylori positive (11% [10 of 95] vs 47% [20 of 43], respectively, across treatment groups). For triple therapy and dual therapy, a similar proportion of patients reported a drug-related adverse event (23% vs 17-33%, respectively).
In patients with active or a recent history of duodenal ulcer, a 14-day course of lansoprazole-based triple therapy without additional acid suppression therapy is highly effective in the eradication of H. pylori and in preventing ulcer recurrence. Among the dual therapies, higher eradication rates occurred when lansoprazole (with amoxicillin) or clarithromycin (with lansoprazole) was administered t.i.d. vs b.i.d., but the rates were still significantly lower than with lansoprazole triple therapy with all three drugs administered b.i.d.
使用不同方法和方案的独立研究结果比较了质子泵抑制剂与抗生素的双重和三重疗法治疗幽门螺杆菌相关性十二指肠溃疡疾病的疗效和安全性,这使得解读变得困难。在美国进行的一项大型双盲多中心研究中,我们比较了一种三联疗法方案与四种双重疗法和一种单一疗法方案在根除幽门螺杆菌及预防溃疡复发方面的效果。
患有活动性十二指肠溃疡疾病或在过去一年内有十二指肠溃疡疾病史且感染幽门螺杆菌的患者被随机分配接受六种14天治疗方案中的一种:兰索拉唑30毫克、克拉霉素500毫克和阿莫西林1克,每日两次;兰索拉唑30毫克,每日两次,联合克拉霉素500毫克,每日两次或每日三次;兰索拉唑30毫克,每日两次或每日三次,联合阿莫西林1克,每日三次;或仅兰索拉唑30毫克,每日三次。根除治疗后不进行额外的抑酸治疗。主要疗效终点是幽门螺杆菌的根除和溃疡复发。
在该研究纳入的396例患者中,352例符合十二指肠溃疡状态和幽门螺杆菌阳性的入选标准。在治疗结束后4至6周,接受兰索拉唑、克拉霉素和阿莫西林三联疗法的患者中,94%(47例中的44例)的幽门螺杆菌被根除;接受兰索拉唑每日三次/阿莫西林每日三次的患者中,77%(51例中的39例)的幽门螺杆菌被根除;接受兰索拉唑每日两次/克拉霉素每日三次的患者中,75%(48例中的36例)的幽门螺杆菌被根除;接受兰索拉唑每日两次/克拉霉素每日两次的患者中,57%(49例中的28例)的幽门螺杆菌被根除;接受兰索拉唑每日两次/阿莫西林每日三次的患者中,53%(49例中的26例)的幽门螺杆菌被根除;接受兰索拉唑单一疗法的患者中,2%(53例中的1例)的幽门螺杆菌被根除(p≤0.05,三联疗法与每种双重疗法相比,每种双重疗法与单一疗法相比)。在治疗后4至6周记录为无溃疡的患者中,接受三联疗法的患者在6个月内溃疡复发的比例为7%,而接受双重疗法的患者为13%至23%,接受兰索拉唑单一疗法的患者为69%。治疗后4至6周幽门螺杆菌阴性的患者比幽门螺杆菌阳性的患者溃疡复发的可能性更小(各治疗组分别为11%[95例中的10例]和47%[43例中的20例])。对于三联疗法和双重疗法,报告药物相关不良事件的患者比例相似(分别为23%和17%至33%)。
对于患有活动性十二指肠溃疡或近期有十二指肠溃疡病史的患者,为期14天的基于兰索拉唑的三联疗法且不进行额外的抑酸治疗在根除幽门螺杆菌和预防溃疡复发方面非常有效。在双重疗法中,兰索拉唑(与阿莫西林联合)或克拉霉素(与兰索拉唑联合)每日三次给药时的根除率高于每日两次给药,但仍显著低于三种药物均每日两次给药的兰索拉唑三联疗法。