Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, 60 Murray St, Rm L6-201, Toronto, ON, Canada M5T 3L9.
J Natl Cancer Inst. 2010 Oct 6;102(19):1462-7. doi: 10.1093/jnci/djq306. Epub 2010 Aug 12.
Disease biomarkers are used widely in medicine. But very few biomarkers are useful for cancer diagnosis and monitoring. Over the past 15 years, major investments have been made to discover and validate cancer biomarkers. Despite such investments, no new major cancer biomarkers have been approved for clinical use for at least 25 years. In the last decade, many reports have described new cancer biomarkers that promised to revolutionize the diagnosis of cancer and the management of cancer patients. However, many initially promising biomarkers have not been validated for clinical use. In this commentary, a plethora of parameters before sample analysis, during sample analysis, and after sample analysis that can complicate biomarker discovery and validation and lead to "false discovery" are discussed. Several examples of biomarker discoveries that were published in high-profile journals are also presented, as well as why they were not validated and the lessons learned from these false discoveries, so that similar mistakes can be avoided in the future.
疾病生物标志物在医学中被广泛应用。但很少有生物标志物可用于癌症的诊断和监测。在过去的 15 年中,已经投入了大量资金来发现和验证癌症生物标志物。尽管有这样的投资,但至少在过去 25 年中,没有新的主要癌症生物标志物被批准用于临床应用。在过去的十年中,许多报告描述了新的癌症生物标志物,这些标志物有望彻底改变癌症的诊断和癌症患者的管理。然而,许多最初有希望的生物标志物尚未经过临床验证。在这篇评论中,讨论了在样本分析之前、期间和之后可能使生物标志物的发现和验证复杂化并导致“错误发现”的大量参数。还介绍了一些在高影响力期刊上发表的生物标志物发现的例子,以及为什么它们没有得到验证,以及从这些错误发现中吸取的教训,以便在未来避免类似的错误。