Yamamoto Hirofumi, Tomita Naohiro, Inomata Masafumi, Furuhata Tomohisa, Miyake Yasuhiro, Noura Shingo, Kato Takeshi, Murata Kohei, Hayashi Shigeoki, Igarashi Seiji, Itabashi Michio, Kameoka Shingo, Matsuura Nariaki
Division of Health Sciences, Department of Molecular Pathology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Ann Surg Oncol. 2016 Feb;23(2):391-6. doi: 10.1245/s10434-015-4880-x. Epub 2015 Oct 5.
We previously reported that the one-step nucleic acid amplification (OSNA) assay provided a judgment performance for colorectal cancer equivalent to a 2-mm-interval histopathological examination of lymph nodes (concordance 97.1 %, n = 385 lymph nodes). In this prospective multicenter study, we uncovered an OSNA-assisted pathology to detect lymph node metastasis.
A total of 204 (50 stage I, 74 stage II, and 80 stage III) colorectal cancer patients. All 4324 lymph nodes were examined by the standard histology (one-slice H&E staining) and 1925 lymph nodes (44.5 %) of them were also subject to the OSNA analysis.
The concordance rate between 1 slice hematoxylin/eosin and OSNA assay was 95.7 % (1,842/1925 lymph nodes). The sensitivity and specificity of the OSNA assay were 86.2 % (125/145) and 96.5 % (1717/1780), respectively. Among 124 node-negative patients (pN0), the respective upstaging rates of pStages I, IIA, IIB, and IIC were 2.0 % (1/50), 17.7 % (11/62), 12.5 % (1/8), and 25 % (1/4). OSNA-positive patients had deeper invasion to the colonic wall and severe lymphatic invasion (P = 0.048 and P = 0.004, respectively). The sum of the quantitative results of OSNA and total tumor load increased as the number of metastasized lymph nodes increased: 1550 copies/μL in pN0, 24,050 copies/μL in pN1, and 90,600 copies/μL in pN2.
The present study on colorectal cancer provided fundamental data regarding OSNA-assisted pathology of lymph node metastasis in Japan.
我们之前报道过,一步核酸扩增(OSNA)检测法对结直肠癌的判断性能等同于对淋巴结进行间隔2毫米的组织病理学检查(一致性为97.1%,n = 385个淋巴结)。在这项前瞻性多中心研究中,我们发现了一种OSNA辅助病理学方法来检测淋巴结转移。
共有204例(50例I期、74例II期和80例III期)结直肠癌患者。所有4324个淋巴结均接受标准组织学检查(单切片苏木精/伊红染色),其中1925个淋巴结(44.5%)还进行了OSNA分析。
单切片苏木精/伊红染色与OSNA检测法之间的一致性率为95.7%(1842/1925个淋巴结)。OSNA检测法的敏感性和特异性分别为86.2%(125/145)和96.5%(1717/1780)。在124例淋巴结阴性患者(pN0)中,I期、IIA期、IIB期和IIC期的各自分期上调率分别为2.0%(1/50)、17.7%(11/62)、12.5%(1/8)和25%(1/4)。OSNA阳性患者对结肠壁的浸润更深且有严重的淋巴管浸润(分别为P = 0.048和P = 0.004)。随着转移淋巴结数量的增加,OSNA定量结果与总肿瘤负荷之和也增加:pN0为1550拷贝/微升,pN1为24050拷贝/微升,pN2为90600拷贝/微升。
本项关于结直肠癌的研究提供了日本OSNA辅助淋巴结转移病理学的基础数据。