National Clinical Research Center for Oral Disease, Shanghai, China.
Department of Oral and Maxillofacial-Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Histol Histopathol. 2021 Aug;36(8):889-898. doi: 10.14670/HH-18-359. Epub 2021 Jul 20.
Undifferentiated pleomorphic sarcoma (UPS) in oral-maxillary area is rarely reported. Herein, we aimed to investigate the clinical characteristics, treatment strategies, prognosis, and molecular features of the oral-maxillary UPS. In total, 10 cases with primary oral-maxillary UPS were included. The rapidly progressive UPS can easily develop to an advanced and life-threatening stage, especially concerning the complex anatomical structures and spaces in the oral-maxillary area. The final diagnosis for UPS greatly depended on histological findings and immunohistochemistry staining after the exclusion of all possible differential diagnoses. Retrospectively, the treatment strategies for the included cases still referred to those of oral squamous cell carcinoma (OSCC). Statistically, the median overall survival (OS) for all the included cases was 7.75 months (range: 5-17 months). Comparatively, 3 cases had improved OS (median survival: 17 months, range: 17-18 months) and experienced PR/SD with neoadjuvant chemotherapy (anlotinib). The molecular features were demonstrated by using whole exonic sequencing for 1 included case. Cancer driver gene detection revealed GBP4 as a candidate driver gene for the primary oral-maxillary UPS. Additionally, a missense mutation in gene PIK3CA (p.E545K) was also identified. Our findings could greatly expand the knowledge about primary oral-maxillary UPS, and provide molecular evidences to improve the therapeutic options for primary oral-maxillary UPS.
口腔颌面部未分化多形性肉瘤(UPS)很少见报道。在此,我们旨在研究口腔颌面部 UPS 的临床特征、治疗策略、预后和分子特征。共纳入 10 例原发性口腔颌面部 UPS 患者。进展迅速的 UPS 很容易发展到晚期和危及生命的阶段,尤其是在口腔颌面部复杂的解剖结构和空间中。UPS 的最终诊断很大程度上取决于组织学发现和免疫组织化学染色,排除所有可能的鉴别诊断后。回顾性分析,纳入病例的治疗策略仍参照口腔鳞状细胞癌(OSCC)。统计学上,所有纳入病例的中位总生存期(OS)为 7.75 个月(范围:5-17 个月)。相比之下,3 例患者经新辅助化疗(安罗替尼)后 OS 得到改善(中位生存时间:17 个月,范围:17-18 个月),并获得 PR/SD。通过对 1 例纳入病例进行全外显子测序来检测分子特征。癌症驱动基因检测显示 GBP4 是原发性口腔颌面部 UPS 的候选驱动基因。此外,还发现了 PIK3CA 基因(p.E545K)的错义突变。我们的研究结果可以大大扩展对原发性口腔颌面部 UPS 的认识,并为原发性口腔颌面部 UPS 的治疗选择提供分子证据。