Camacho Luis H, Bacik Jennifer, Cheung Alexander, Spriggs David R
Developmental Chemotherapy Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Cancer. 2005 Oct 1;104(7):1497-504. doi: 10.1002/cncr.21337.
Many trials submitted to scientific meetings are not reported in peer-reviewed journals. Results may vary substantially and the lack of final publication constitutes a form of reporting bias. The authors sought to determine the presentation and publication rates of Phase I trials submitted to a major oncology meeting and the factors impeding their subsequent publication.
The authors identified all Phase I studies submitted to the annual meeting of the American Society of Clinical Oncology in 1997, categorizing them as novel (agents not approved by the Food and Drug Administration at the time of submission) or nonnovel (at least one agent approved), and as industry sponsored or not. MEDLINE searches and an E-mailed questionnaire confirmed publication in peer-reviewed literature and the reasons for nonpublication.
Approximately 54% of the 275 Phase I studies were selected for presentation. Abstracts reporting novel agents were more likely selected for presentation than those reporting nonnovel compounds (68% vs. 38%; P < 0.0001). Seventy-two percent of the presented abstracts were subsequently published, compared with 62% of those not presented (P = 0.08). The overall publication rate was 67% at 7.5 years. Presentation status was associated with time to publication (P = 0.01), with abstracts chosen for presentation being published sooner. The median time from presentation to publication was found to be 3.4 years. Lack of time and author relocation were the major obstacles to publication.
The underreporting of final results of Phase I oncology trials remains a serious problem. In the future, investigators must commit to the publication of final results in a timely manner. Journals should provide mechanisms for rapid reporting of Phase I trials.
提交至科学会议的许多试验未在同行评审期刊上发表。结果可能存在很大差异,且缺乏最终发表构成了一种报告偏倚形式。作者试图确定提交至一次主要肿瘤学会议的I期试验的展示率和发表率,以及阻碍其后续发表的因素。
作者识别了1997年提交至美国临床肿瘤学会年会的所有I期研究,将它们分类为新型(提交时未获美国食品药品监督管理局批准的药物)或非新型(至少有一种药物已获批准),以及是否由行业赞助。通过医学主题词数据库检索和电子邮件问卷确认在同行评审文献中的发表情况及未发表的原因。
275项I期研究中约54%被选中进行展示。报告新型药物的摘要比报告非新型化合物的摘要更有可能被选中进行展示(68%对38%;P<0.0001)。展示的摘要中有72%随后发表,未展示的摘要中这一比例为62%(P=0.08)。7.5年时的总体发表率为67%。展示状态与发表时间相关(P=0.01),被选中进行展示的摘要发表得更快。从展示到发表的中位时间为3.4年。时间不足和作者变动是发表的主要障碍。
I期肿瘤学试验最终结果报告不足仍然是一个严重问题。未来,研究者必须致力于及时发表最终结果。期刊应提供快速报告I期试验的机制。