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评估2003年至2018年支持新皮肤科药物获批的临床试验中的发表偏倚。

Evaluating publication bias for clinical trials supporting new dermatologic drug approvals from 2003 to 2018.

作者信息

Ravichandran Sairekha, Mulligan Kathleen M, Ezaldein Harib H, Scott Jeffrey F

机构信息

Department of Dermatology, University Hospitals Cleveland Medical Center, Cleveland, OH, USA.

Northeast Ohio Medical University, Rootstown, OH, USA.

出版信息

Arch Dermatol Res. 2023 May;315(4):831-838. doi: 10.1007/s00403-022-02449-6. Epub 2022 Nov 4.

DOI:10.1007/s00403-022-02449-6
PMID:36333459
Abstract

The degree of publication bias and impact of the Food and Drug Administration Amendments Act (FDAAA) of 2007, which aimed to improve clinical trial transparency, has yet to be examined for recent dermatologic drugs. The objective of our study was to estimate the degree of publication bias for clinical trials supporting FDA approval of new dermatologic drugs. This retrospective cohort study examined all phase II and III efficacy trials supporting approval of new dermatologic drugs from 2003 to 2018. FDA drug approval documents were reviewed for supportive clinical trial information, and publications were matched using PubMed and Google Scholar searches. Ratios of relative risks (RRR) comparing positive versus non-positive trials before and after FDAAA enactment served to estimate publication bias. We found that the likelihood of publishing positive versus non-positive drug trials in dermatology was unchanged before and after FDAAA enactment (RRR 0.87, 95% CI 0.37-2.08), as was the likelihood of publishing without misleading interpretation (RRR 1.51, 95% CI 0.22-10.50). There was no measurable publication bias for efficacy trials supporting new drug approvals in dermatology over the past 15 years. Fewer pre-FDAAA trials (n = 21) compared to post-FDAAA trials (n = 106) met inclusion criteria. Though not analyzed in this study, safety and secondary efficacy results are other potential sources for publication bias.

摘要

2007年的《食品药品管理局修订法案》(FDAAA)旨在提高临床试验透明度,其导致的发表偏倚程度及影响,针对近期皮肤科药物尚未进行过研究。我们研究的目的是评估支持美国食品药品监督管理局(FDA)批准新皮肤科药物的临床试验中的发表偏倚程度。这项回顾性队列研究考察了2003年至2018年期间支持新皮肤科药物获批的所有II期和III期疗效试验。查阅FDA药物批准文件以获取支持性临床试验信息,并通过PubMed和谷歌学术搜索来匹配相关出版物。比较FDAAA颁布前后阳性试验与非阳性试验的相对风险比(RRR),用以评估发表偏倚。我们发现,在FDAAA颁布前后,皮肤科药物阳性试验与非阳性试验发表的可能性没有变化(RRR 0.87,95%置信区间0.37-2.08),没有误导性解读而发表的可能性也没有变化(RRR 1.51,95%置信区间0.22-10.50)。在过去15年中,支持皮肤科新药获批的疗效试验没有可测量的发表偏倚。与FDAAA颁布后的试验(n = 106)相比,符合纳入标准的FDAAA颁布前的试验较少(n = 21)。尽管本研究未对此进行分析,但安全性和次要疗效结果是发表偏倚的其他潜在来源。

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