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替代标志物:下一代的经验教训?

Surrogate Markers: Lessons from the Next Gen?

机构信息

Divisions of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington. Departments of Genome Sciences and Medicine, University of Washington, Seattle, Washington.

出版信息

Cancer Prev Res (Phila). 2016 Jul;9(7):512-7. doi: 10.1158/1940-6207.CAPR-16-0059. Epub 2016 May 2.

Abstract

The article by Banerjee and colleagues published in this issue of the journal involving a randomized control prevention trial of ursodeoxycholic acid (UDCA) in Barrett esophagus reported a null outcome despite being well designed and executed. Possible reasons for this null outcome are discussed focusing on use of surrogate endpoints in the trial. The trial is especially topical because it comes at a time when there are calls for a Pre-Cancer Genome Atlas (PCGA) for "understanding the earliest molecular and cellular events associated with cancer initiation…" This commentary discusses current concepts in prevention research including branched evolution that leads to therapeutic resistance. Length bias sampling postulates underdiagnosis is due to rapidly progressing disease that is difficult to detect by screening because it progresses to cancer too rapidly and that overdiagnosis is the result of very slowly or nonprogressing disease that is easy to detect by screening because it persists for a lifetime and the patient dies of unrelated causes. Finally, it also explores study designs, including surrogate endpoints in Barrett esophagus trials, and opportunities and pitfalls for a PCGA in the context of high levels of over and underdiagnosis of Barrett esophagus as well as many other cancers and their precursors. Cancer Prev Res; 9(7); 512-7. ©2016 AACRSee related article by Banerjee, et al., p. 528.

摘要

本期杂志上 Banerjee 及其同事发表的一篇文章涉及熊去氧胆酸(UDCA)在 Barrett 食管中的随机对照预防试验,尽管设计和执行良好,但结果却为阴性。针对这种阴性结果,讨论了可能的原因,重点是试验中使用替代终点。该试验特别具有针对性,因为它恰逢呼吁为“了解与癌症起始相关的最早分子和细胞事件......”制定癌症前基因组图谱(PCGA)之时。本评论讨论了预防研究中的当前概念,包括导致治疗耐药性的分支进化。长度偏倚采样假说认为,诊断不足是由于疾病快速进展导致的,因为疾病进展到癌症太快,难以通过筛查检测到,而过度诊断是由于疾病非常缓慢或非进展导致的,因为疾病容易通过筛查检测到,因为它持续一生,患者死于无关原因。最后,它还探讨了研究设计,包括 Barrett 食管试验中的替代终点,以及在 Barrett 食管以及许多其他癌症及其前体过度和诊断不足程度较高的情况下进行 PCGA 的机会和陷阱。癌症预防研究; 9(7); 512-7. ©2016 AACR 参见 Banerjee 等人在第 528 页的相关文章。

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引用本文的文献

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The Case for a Pre-Cancer Genome Atlas (PCGA).
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Magnitude of Missed Esophageal Adenocarcinoma After Barrett's Esophagus Diagnosis: A Systematic Review and Meta-analysis.
Gastroenterology. 2016 Mar;150(3):599-607.e7; quiz e14-5. doi: 10.1053/j.gastro.2015.11.040. Epub 2015 Nov 24.
3
Genetic Insights in Barrett's Esophagus and Esophageal Adenocarcinoma.
Gastroenterology. 2015 Oct;149(5):1142-1152.e3. doi: 10.1053/j.gastro.2015.07.010. Epub 2015 Jul 21.
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Paired exome analysis of Barrett's esophagus and adenocarcinoma.
Nat Genet. 2015 Sep;47(9):1047-55. doi: 10.1038/ng.3343. Epub 2015 Jul 20.
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Assessment of Esophageal Adenocarcinoma Risk Using Somatic Chromosome Alterations in Longitudinal Samples in Barrett's Esophagus.
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Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis.
Nat Genet. 2014 Aug;46(8):837-843. doi: 10.1038/ng.3013. Epub 2014 Jun 22.
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Addressing overdiagnosis and overtreatment in cancer: a prescription for change.
Lancet Oncol. 2014 May;15(6):e234-42. doi: 10.1016/S1470-2045(13)70598-9.

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