Head and neck squamous cell carcinomas of unknown primary: Can ancillary studies help identify more primary tumor sites?

IF 2.8 4区 医学 Q2 PATHOLOGY
Troy Hutchens , Wade Thorstad , Xiaowei Wang , Yuanxiang Li , Eric J. Duncavage , Lulu Sun , Rebecca D. Chernock
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引用次数: 0

Abstract

A subset of head and neck squamous cell carcinomas present solely as metastatic disease in the neck and are of unknown primary origin (SCCUP). Most primary tumors will ultimately be identified, usually in the oropharynx. In a minority of cases, the primary site remains elusive. Here, we examine the role of ancillary testing, including mutational signature analysis (MSA), to help identify likely primary sites in such cases. Twenty-two cases of SCCUP in the neck, collected over a 10-year period, were classified by morphology and viral status; including human papillomavirus (HPV) testing by p16 immunohistochemistry (IHC) and RT-qPCR, as well as Epstein-Barr virus (EBV) testing by EBER-ISH. CD5 and c-KIT (CD117) IHC was done to evaluate for possible thymic origin in all virus-negative cases. Whole exome sequencing, followed by MSA, was used to identify UV signature mutations indicative of cutaneous origin. HPV was identified in 12 of 22 tumors (54.5%), favoring an oropharyngeal origin, and closely associated with nonkeratinizing tumor morphology (Fisher's exact test; p = 0.0002). One tumor with indeterminant morphology had discordant HPV and p16 status (p16+/HPV-). All tumors were EBV-negative. Diffuse expression of CD5 and c-KIT was identified in 1 of 10 virus-negative SCCUPs (10%), suggesting a possible ectopic thymic origin rather than a metastasis. A UV mutational signature, indicating cutaneous origin, was identified in 1 of 10 (10%) virus-negative SCCUPs. A cutaneous auricular primary emerged 3 months after treatment in this patient. Primary tumors became clinically apparent in 2 others (1 hypopharynx, 1 hypopharynx/larynx). Thus, after follow-up, 6 tumors remained unclassifiable as to the possible site of origin (27%). Most SCCUPs of the neck in our series were HPV-associated and thus likely of oropharyngeal origin. UV signature mutation analysis and additional IHC for CD5 and c-KIT for possible thymic origin may aid in further classifying virus-negative unknown primaries. Close clinical inspection of hypopharyngeal mucosa may also be helpful, as a subset of primary tumors later emerged at this site.

原发部位不明的头颈部鳞状细胞癌:辅助研究能否帮助确定更多的原发肿瘤部位?
有一部分头颈部鳞状细胞癌仅表现为颈部转移性疾病,原发来源不明(SCCUP)。大多数原发肿瘤最终会被确定,通常是在口咽部。在少数病例中,原发部位仍然难以确定。在此,我们研究了突变特征分析(MSA)等辅助检查在帮助确定此类病例可能的原发部位方面所起的作用。我们对 10 年间收集的 22 例颈部 SCCUP 病例进行了形态学和病毒状态分类,包括通过 p16 免疫组化 (IHC) 和 RT-qPCR 进行的人类乳头瘤病毒 (HPV) 检测,以及通过 EBER-ISH 进行的 Epstein-Barr 病毒 (EBV) 检测。对所有病毒阴性病例进行了 CD5 和 c-KIT (CD117) IHC 检测,以评估可能的胸腺来源。通过全外显子组测序和 MSA,确定了表明皮肤来源的紫外线标志性突变。在 22 例肿瘤中的 12 例(54.5%)中发现了 HPV,倾向于口咽起源,并与非角化性肿瘤形态密切相关(费雪精确检验;P = 0.0002)。一个形态不确定的肿瘤具有不一致的 HPV 和 p16 状态(p16+/HPV-)。所有肿瘤均为 EBV 阴性。在 10 例病毒阴性的 SCCUP 中,有 1 例(10%)发现了 CD5 和 c-KIT 的弥漫表达,这表明肿瘤可能来自胸腺异位而非转移。在 10 例病毒阴性的 SCCUP 中,有 1 例(10%)发现了紫外线突变特征,表明其来源于皮肤。该患者在治疗 3 个月后出现了耳廓皮肤原发肿瘤。另外 2 例患者(1 例下咽,1 例下咽/喉)的原发肿瘤在临床上变得明显。因此,在随访后,仍有 6 例肿瘤无法确定可能的起源部位(27%)。在我们的系列研究中,大多数颈部SCCUP都与HPV相关,因此很可能起源于口咽部。紫外线特征突变分析和额外的CD5和c-KIT IHC检查可能有助于进一步对病毒阴性的未知原发病灶进行分类。对下咽粘膜进行仔细的临床检查也会有所帮助,因为一部分原发肿瘤后来出现在这个部位。
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来源期刊
CiteScore
8.90
自引率
0.00%
发文量
78
审稿时长
11.5 weeks
期刊介绍: Under new editorial leadership, Experimental and Molecular Pathology presents original articles on disease processes in relation to structural and biochemical alterations in mammalian tissues and fluids and on the application of newer techniques of molecular biology to problems of pathology in humans and other animals. The journal also publishes selected interpretive synthesis reviews by bench level investigators working at the "cutting edge" of contemporary research in pathology. In addition, special thematic issues present original research reports that unravel some of Nature''s most jealously guarded secrets on the pathologic basis of disease. Research Areas include: Stem cells; Neoangiogenesis; Molecular diagnostics; Polymerase chain reaction; In situ hybridization; DNA sequencing; Cell receptors; Carcinogenesis; Pathobiology of neoplasia; Complex infectious diseases; Transplantation; Cytokines; Flow cytomeric analysis; Inflammation; Cellular injury; Immunology and hypersensitivity; Athersclerosis.
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