Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada.
Head of Clinical Biochemistry, Mount Sinai Hospital and University Health Network, 60 Murray St. Box 32, Floor 6, Rm L6-201, Toronto, ON M5T 3L9, Canada.
Clin Chem Lab Med. 2020 Sep 25;58(10):1651-1653. doi: 10.1515/cclm-2020-0083.
The important conclusion that ctDNA is a mediocre proxy for liquid biopsies of tumor tissues for early detection was reached after new data were published recently in Nature Genetics. These data have shown that most mutations found in ctDNA are not related to tumor tissues but rather to the precancerous condition clonal hematopoiesis. Previously, our group has analyzed the sensitivity of the ctDNA test for early detection of cancer and concluded that the achievable sensitivity, especially for small tumors, is not enough to have clinical value. Now, the new data have shown a serious compromise in specificity. We believe that scientists who are interested in early cancer diagnostics should be aware of the limitations of this test, in both sensitivity and specificity. Our work may prompt further work aiming to alleviate these important issues in the cancer diagnostics field.
最近在《自然遗传学》上发表的新数据得出了一个重要结论,即 ctDNA 是肿瘤组织液体活检的一个平庸替代品,用于早期检测。这些数据表明,ctDNA 中发现的大多数突变与肿瘤组织无关,而是与癌前状态克隆性造血有关。此前,我们的研究小组分析了 ctDNA 检测对癌症早期检测的灵敏度,并得出结论,即可实现的灵敏度,特别是对于小肿瘤,不足以具有临床价值。现在,新数据显示特异性存在严重缺陷。我们认为,对早期癌症诊断感兴趣的科学家应该意识到该测试在灵敏度和特异性方面的局限性。我们的工作可能会促使进一步的工作,旨在缓解癌症诊断领域的这些重要问题。