Agaimy Abbas, Antonescu Cristina R, Bell Diana, Breimer Gerben E, Dermawan Josephine K, Kester Lennart A, Laco Jan, Rijken Johannes A, Whaley Rumeal D, Stoehr Robert, Cramer Thomas, Bishop Justin A
Institute of Pathology, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, Krankenhausstrasse 8-10, 91054, Erlangen, Germany.
Comprehensive Cancer Center, European Metropolitan Area Erlangen-Nuremberg (CCC ER-EMN), Friedrich Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Virchows Arch. 2025 Mar;486(3):499-510. doi: 10.1007/s00428-024-03940-3. Epub 2024 Oct 10.
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.
FGFR3::TACC3融合已在多种癌症的亚组中被报道,包括尿路上皮癌和鳞状细胞癌(SCC)。然而,FGFR3::TACC3阳性的头颈癌的形态学尚未得到充分研究,目前尚不清楚这种融合是随机事件,还是可能代表一种形态学上独特的肿瘤类型。我们描述了9例FGFR3::TACC3融合阳性的头颈癌,患者年龄在38至89岁之间(中位数为59岁),其中男性6例,女性3例。肿瘤起源于鼻窦(n = 4)、腮腺(n = 2),口咽、下颌下腺和喉各1例。在最后一次随访时(9至21个月;中位数为11个月),4例患者出现局部复发和/或远处转移,2例分别在11个月和12个月时死于疾病,1例死于其他原因,1例带瘤生存,2例无疾病生存。6例肿瘤中有3例存在高危致癌性人乳头瘤病毒(HPV)感染(HPV33、HPV18,1例未明确)。组织学上,3例肿瘤表现为非角化的移行细胞样或形态不典型,伴有不同程度的混合性炎症浸润,类似于黏液表皮样癌或DEK::AFF2癌(均为HPV阴性),3例为HPV相关(均为鼻窦),分别具有多表型(1例)和非肠型腺癌(2例)模式。1例涎腺肿瘤表现为细胞黏附性差的大上皮样细胞,背景炎症明显,并表达AR和GATA3,符合涎腺导管癌变异型的可能表现。2例为传统SCC。靶向RNA测序显示所有病例均存在框内FGFR3::TACC3融合。该系列研究突出了携带FGFR3::TACC3融合的头颈癌的异质性,可分为三类:(1)未分类的HPV阴性类型,形态学上与SCC和其他实体不同;(2)HPV相关癌的异质性组;(3)传统SCC。FGFR3::TACC3融合在第一类(作为一种潜在的独特实体)中的驱动作用仍有待进一步研究。鉴于现有的FGFR靶向治疗方法,建议对这些肿瘤进行明确诊断并提高识别率。