Xiao Ningping, Lin Cheng, Yu Tingjie, Bi Feng, Tan Pingping, Tan Jiahui, Zhang Rong, Lou Fan, Xie Xiaoxue, Xu Zi, Yang Jingru, Jin Hekun, Yang Pei, Jin Yi
Department of Radiation Oncology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Hunan Cancer Hospital, Central South University, Changsha, 410013, Hunan, China.
Department of Radiation Oncology, General Hospital of Pingxiang Mining Group Company, Pingxiang, 337000, China.
Discov Oncol. 2025 Jul 26;16(1):1415. doi: 10.1007/s12672-025-03227-2.
Nuclear protein in testis carcinoma (NUTc) is a rare and highly aggressive salivary gland tumor predominantly affecting young patients. It typically involves midline head and neck structures, progresses rapidly, and is associated with a median survival of 6 to 9 months, resulting in an 80% mortality rate within the first year post-diagnosis. In this study, we present a rapidly progressing case of a 28-year-old male diagnosed with NUTc localized to the right nasal cavity (clinical stage cT4bN2M0, IVb). The patient underwent four cycles of cetuximab (anti-EGFR) combined with albumin-bound paclitaxel and cisplatin, achieving transient partial remission before experiencing rapid disease progression. During the observation period, his clinical condition deteriorated precipitously, rendering surgical intervention unfeasible and necessitating a transition to second-line chemotherapy (cisplatin + etoposide, EC regimen). Following one cycle of EC, the patient received symptomatic supportive care; however, during the two-month follow-up, he reported worsening headaches and was subsequently lost to follow-up. This case highlights the critical need for innovative diagnostic and therapeutic approaches, including prompt immunohistochemical staining and molecular testing in symptomatic patients, early tumor burden reduction, and rigorous follow-up protocols to improve survival outcomes.
睾丸癌核蛋白(NUTc)是一种罕见且侵袭性很强的唾液腺肿瘤,主要影响年轻患者。它通常累及头颈部中线结构,进展迅速,中位生存期为6至9个月,确诊后第一年内死亡率达80%。在本研究中,我们报告了一例快速进展的病例,一名28岁男性被诊断为NUTc,肿瘤局限于右侧鼻腔(临床分期cT4bN2M0,IVb期)。该患者接受了四个周期的西妥昔单抗(抗表皮生长因子受体)联合白蛋白结合型紫杉醇和顺铂治疗,在疾病快速进展前实现了短暂的部分缓解。在观察期内,他的临床状况急剧恶化,无法进行手术干预,因此必须转为二线化疗(顺铂+依托泊苷,EC方案)。在接受一个周期的EC方案治疗后,患者接受了对症支持治疗;然而,在两个月的随访期间,他报告头痛加重,随后失访。该病例凸显了创新诊断和治疗方法的迫切需求,包括对有症状患者及时进行免疫组化染色和分子检测、早期减轻肿瘤负荷以及严格的随访方案,以改善生存结局。