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系统评价:英夫利昔单抗治疗溃疡性结肠炎

Systematic review: Infliximab therapy in ulcerative colitis.

作者信息

Gisbert J P, González-Lama Y, Maté J

机构信息

Gastroenterology Unit, La Princesa University Hospital, Autonomous University, Madrid, Spain.

出版信息

Aliment Pharmacol Ther. 2007 Jan 1;25(1):19-37. doi: 10.1111/j.1365-2036.2006.03131.x.

DOI:10.1111/j.1365-2036.2006.03131.x
PMID:17229218
Abstract

AIM

To perform a systematic review and meta-analysis on the efficacy and tolerance of infliximab in ulcerative colitis.

SELECTION OF STUDIES

evaluating efficacy of infliximab in ulcerative colitis. For the meta-analysis, randomized clinical trials comparing infliximab vs. placebo/steroids.

SEARCH STRATEGY

electronic and manual. Study quality: independently assessed by two reviewers.

DATA SYNTHESIS

meta-analysis combining the odds ratios (OR).

RESULTS

Thirty-four studies (896 patients) evaluated infliximab therapy in UC, with heterogeneous results. Mean short-term (2.3 weeks) response and remission with infliximab was 68% (95% CI 65-71%) and 40% (36-44%). Mean long-term (8.9 months) response and remission was 53% (49-56%) and 39% (35-42%). Five randomized double-blind studies compared infliximab with placebo, the meta-analysis showing an advantage (P < 0.001) of infliximab in all endpoints (short-/long-term response/remission): ORs from 2.7 to 4.6, and number-needed-to-treat (NNT) from 3 to 5. Similar infliximab response was calculated independently of the indication (steroid-refractory/non-steroid-refractory) or the dose (5/10 mg/kg). Adverse effects were reported in 83% and 75% of the infliximab and placebo-treated patients (OR = 1.52; 95% CI 1.03-2.24; number-needed-to-harm (NNH) was 14).

CONCLUSION

Infliximab is more effective than placebo, with an NNT from 3 to 5, for the treatment of moderate-to-severe UC, achieving clinical remission in 40% of the patients at approximately 9 months of follow-up. Further studies are necessary to confirm the long-term efficacy of infliximab in ulcerative colitis.

摘要

目的

对英夫利昔单抗治疗溃疡性结肠炎的疗效和耐受性进行系统评价和荟萃分析。

研究选择

评估英夫利昔单抗治疗溃疡性结肠炎的疗效。对于荟萃分析,纳入比较英夫利昔单抗与安慰剂/类固醇的随机临床试验。

检索策略

电子检索和手工检索。研究质量:由两名评价者独立评估。

数据合成

采用比值比(OR)进行荟萃分析。

结果

34项研究(896例患者)评估了英夫利昔单抗治疗溃疡性结肠炎的疗效,结果存在异质性。英夫利昔单抗治疗的短期(2.3周)平均缓解率和应答率分别为68%(95%CI 65-71%)和40%(36-44%)。长期(8.9个月)平均缓解率和应答率分别为53%(49-56%)和39%(35-42%)。五项随机双盲研究比较了英夫利昔单抗与安慰剂,荟萃分析显示英夫利昔单抗在所有终点(短期/长期缓解/应答)均具有优势(P<0.001):OR为2.7至4.6,需治疗人数(NNT)为3至5。无论适应证(激素难治性/非激素难治性)或剂量(5/10mg/kg)如何,英夫利昔单抗的应答情况相似。英夫利昔单抗治疗组和安慰剂治疗组分别有83%和75%的患者报告了不良反应(OR=1.52;95%CI 1.03-2.24;伤害需治疗人数(NNH)为14)。

结论

英夫利昔单抗治疗中重度溃疡性结肠炎比安慰剂更有效,NNT为3至5,在随访约9个月时40%的患者实现临床缓解。有必要进一步研究以证实英夫利昔单抗治疗溃疡性结肠炎的长期疗效。

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