Goto Taichiro, Hirotsu Yosuke, Oyama Toshio, Amemiya Kenji, Omata Masao
Department of General Thoracic Surgery, Yamanashi Prefectural Central Hospital, Yamanashi, Japan.
Genome Analysis Center, Yamanashi Prefectural Central Hospital, Yamanashi, 400-8506, Japan.
Med Oncol. 2016 Mar;33(3):29. doi: 10.1007/s12032-016-0744-x. Epub 2016 Feb 20.
Liquid biopsies such as circulating tumor DNA in plasma and disseminated tumor cells in the bone marrow are currently available. However, it is unclear which types of samples are appropriate for detecting tumor DNA in these biopsies. Here, we collected primary tumors, pulmonary venous blood, peripheral blood, and rib bone marrow fluid from 10 lung cancer patients. Targeted deep sequencing was performed to identify mutations across 70 specimens. As a result, a total of 43 mutations were identified in the primary tumors. The mutation in the tumors was also identified in circulating tumor DNA in the pulmonary venous and peripheral blood in two patients. These patients showed poor prognosis, as compared to the other patients. However, no mutation was identified in the bone marrow in any of the patients. These results demonstrated that circulating tumor DNA in plasma is more sensitive and clinically useful as a biomarker as compared to DNA in bone marrow fluid.
目前已有液体活检技术,如检测血浆中的循环肿瘤DNA和骨髓中的播散肿瘤细胞。然而,尚不清楚在这些活检中哪些类型的样本适合检测肿瘤DNA。在此,我们收集了10例肺癌患者的原发性肿瘤、肺静脉血、外周血和肋骨骨髓液。进行靶向深度测序以鉴定70个样本中的突变。结果,在原发性肿瘤中总共鉴定出43个突变。在两名患者的肺静脉和外周血的循环肿瘤DNA中也鉴定出肿瘤中的突变。与其他患者相比,这些患者预后较差。然而,在任何患者的骨髓中均未鉴定出突变。这些结果表明,与骨髓液中的DNA相比,血浆中的循环肿瘤DNA作为生物标志物更敏感且在临床上更有用。