Department of Pathology, Cleveland Clinic, Cleveland, Ohio.
Cancer Cytopathol. 2018 Apr;126(4):243-252. doi: 10.1002/cncy.21972. Epub 2018 Jan 23.
Recent studies suggest that insulinoma-associated protein 1 (INSM1) is a sensitive and specific marker of neuroendocrine neoplasms. The aims of this study were to determine whether INSM1 can be reliably used in cytology (Cellient) cell blocks, to ascertain whether staining correlates with paired surgical pathology specimens, and to compare its sensitivity and specificity with those of synaptophysin (SYN), chromogranin (CHR), and CD56 for neuroendocrine lung tumors.
Seventy-four primary lung neoplasms diagnosed on cytology were stained with INSM1, SYN, CHR, and CD56: 41 small cell lung carcinomas (SCLCs), 1 large cell neuroendocrine carcinoma (LCNEC), 10 carcinoid tumors, 11 adenocarcinomas, 9 squamous cell carcinomas, 1 mesothelioma and 1 poorly differentiated non-small cell lung carcinoma, not otherwise specified. In 20 cases, a paired surgical pathology specimen was also stained with INSM1.
INSM1 was positive in 48 of 52 primary lung neuroendocrine neoplasms (92%), including 38 of 41 SCLCs (93%), the only LCNEC (100%), and 9 of 10 carcinoid tumors (90%), and it was negative in all 22 non-neuroendocrine primary lung tumors. For SCLC, the sensitivity of INSM1 (93%) was lower than the sensitivity of CD56 (100%), equal to the sensitivity of SYN (93%), and higher than the sensitivity of CHR (35%). For carcinoid tumors, the sensitivity of INSM1 (90%) was lower than the sensitivity of all other markers (100% each). The specificity of INSM1 for neuroendocrine neoplasms as a group was 100%. INSM1 staining was concordant with surgical pathology specimens in all 20 paired cases.
INSM1 can be used in cytopathology cell blocks, and it is sensitive and highly specific for neuroendocrine lung tumors. INSM1 staining in cytology cell blocks correlates well with surgical pathology specimens. Cancer Cytopathol 2018;126:243-52. © 2018 American Cancer Society.
最近的研究表明,胰岛素瘤相关蛋白 1(INSM1)是神经内分泌肿瘤的敏感和特异性标志物。本研究的目的是确定 INSM1 是否可以在细胞学(Cellient)细胞块中可靠地使用,确定染色是否与配对的手术病理标本相关,并比较其敏感性和特异性与突触素(SYN)、嗜铬粒蛋白(CHR)和 CD56 用于神经内分泌肺肿瘤。
对 74 例细胞学诊断的原发性肺肿瘤进行 INSM1、SYN、CHR 和 CD56 染色:41 例小细胞肺癌(SCLC)、1 例大细胞神经内分泌癌(LCNEC)、10 例类癌肿瘤、11 例腺癌、9 例鳞状细胞癌、1 例间皮瘤和 1 例低分化非小细胞肺癌,未另作说明。在 20 例病例中,还对配对的手术病理标本进行了 INSM1 染色。
52 例原发性肺神经内分泌肿瘤中有 48 例(92%)INSM1 阳性,包括 41 例 SCLC 中的 38 例(93%)、唯一的 LCNEC(100%)和 10 例类癌中的 9 例(90%),所有 22 例非神经内分泌原发性肺肿瘤均为阴性。对于 SCLC,INSM1(93%)的敏感性低于 CD56(100%)、与 SYN(93%)相同,高于 CHR(35%)。对于类癌,INSM1(90%)的敏感性低于所有其他标志物(均为 100%)。作为一组神经内分泌肿瘤,INSM1 的特异性为 100%。在 20 例配对病例中,INSM1 染色均与手术病理标本一致。
INSM1 可用于细胞学病理细胞块,对神经内分泌肺肿瘤具有敏感性和高度特异性。INSM1 在细胞学细胞块中的染色与手术病理标本相关性良好。癌症细胞病理学 2018;126:243-52. © 2018 美国癌症协会。