头颈部癌中的FGFR3::TACC3融合:对九个病例的研究,突出了表型异质性、与HPV的频繁关联以及形态上独特的亚群,有利于形成一个假定实体。

IF 3.4 3区 医学 Q1 PATHOLOGY
Abbas Agaimy, Cristina R Antonescu, Diana Bell, Gerben E Breimer, Josephine K Dermawan, Lennart A Kester, Jan Laco, Johannes A Rijken, Rumeal D Whaley, Robert Stoehr, Thomas Cramer, Justin A Bishop
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引用次数: 0

摘要

据报道,FGFR3::TACC3融合存在于多种癌症中,包括尿路上皮癌和鳞状细胞癌(SCC)。然而,FGFR3::TACC3阳性头颈部癌的形态学尚未得到很好的研究,目前还不清楚这种融合是一种随机事件,还是可能是一种形态独特的肿瘤类型的特征。我们描述了9例FGFR3::TACC3融合阳性头颈癌,6男3女,年龄在38至89岁之间(中位59岁)。肿瘤起源于鼻窦道(4 例)、腮腺(2 例),口咽、颌下腺和喉部各一例。在最后一次随访(9-21个月;中位数为11个月)时,4名患者出现局部复发和/或远处转移,2名患者在11个月和12个月时因病死亡,1名患者死于其他原因,1名患者带病生存,2名患者无病。六例肿瘤中有三例携带高危致癌人乳头瘤病毒感染(HPV33、HPV18,一例未说明)。组织学上,三个肿瘤呈非角化性过渡细胞样或非描述性形态,伴有可变的混合炎症浸润,让人联想到粘液表皮样癌或 DEK::AFF2 癌(均为 HPV 阴性),三个肿瘤与 HPV 相关(均为鼻窦肿瘤),分别呈多型(1)和非肠腺癌(2)形态。其中一个唾液腺肿瘤显示凝聚力差的大上皮样细胞,背景炎症突出,并表达AR和GATA3,可能是唾液腺导管癌变种。两个肿瘤是传统的 SCC。靶向 RNA 测序发现所有病例均存在框架内 FGFR3::TACC3 融合。该系列病例凸显了携带FGFR3::TACC3融合的头颈部癌的异质性,可分为三类:(1)未分类的HPV阴性类,形态上有别于SCC和其他实体;(2)HPV相关癌的异质性组;以及(3)传统SCC。FGFR3::TACC3融合在第一类(作为潜在的独特实体)中的驱动作用仍有待进一步研究。鉴于现有的表皮生长因子受体靶向疗法,建议对这些肿瘤进行分类并加强识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FGFR3::TACC3 fusions in head and neck carcinomas: a study of nine cases highlighting phenotypic heterogeneity, frequent HPV association, and a morphologically distinct subset in favor of a putative entity.

The FGFR3::TACC3 fusion has been reported in subsets of diverse cancers including urothelial and squamous cell carcinomas (SCC). However, the morphology of FGFR3::TACC3-positive head and neck carcinomas has not been well studied and it is unclear if this fusion represents a random event, or if it might characterize a morphologically distinct tumor type. We describe nine FGFR3::TACC3 fusion-positive head and neck carcinomas affecting six males and three females aged 38 to 89 years (median, 59). The tumors originated in the sinonasal tract (n = 4), parotid gland (n = 2), and one case each in the oropharynx, submandibular gland, and larynx. At last follow-up (9-21 months; median, 11), four patients developed local recurrence and/or distant metastases, two died of disease at 11 and 12 months, one died of other cause, one was alive with disease, and two were disease-free. Three of six tumors harbored high risk oncogenic HPV infection (HPV33, HPV18, one unspecified). Histologically, three tumors revealed non-keratinizing transitional cell-like or non-descript morphology with variable mixed inflammatory infiltrate reminiscent of mucoepidermoid or DEK::AFF2 carcinoma (all were HPV-negative), and three were HPV-associated (all sinonasal) with multiphenotypic (1) and non-intestinal adenocarcinoma (2) pattern, respectively. One salivary gland tumor showed poorly cohesive large epithelioid cells with prominent background inflammation and expressed AR and GATA3, in line with a possible salivary duct carcinoma variant. Two tumors were conventional SCC. Targeted RNA sequencing revealed an in-frame FGFR3::TACC3 fusion in all cases. This series highlights heterogeneity of head and neck carcinomas harboring FGFR3::TACC3 fusions, which segregates into three categories: (1) unclassified HPV-negative category, morphologically distinct from SCC and other entities; (2) heterogeneous group of HPV-associated carcinomas; and (3) conventional SCC. A driver role of the FGFR3::TACC3 fusion in the first category (as a potential distinct entity) remains to be further studied. In the light of available FGFR-targeting therapies, delineation of these tumors and enhanced recognition is recommended.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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