Li Xiang, Shi Hui, Zhang Wei, Bai Chong, He Miaoxia, Ta Na, Huang Haidong, Ning Yunye, Fang Chen, Qin Hao, Dong Yuchao
Department of Respiratory and Critical Care Medicine, Changhai Hospital (The First Affiliated Hospital of Naval Medical University), Naval Medical University (Second Military Medical University), Shanghai, China.
Department of Pathology, Changhai Hospital (The First Affiliated Hospital of Naval Medical University), Naval Medical University (Second Military Medical University), Shanghai, China.
Front Oncol. 2021 Sep 30;11:690115. doi: 10.3389/fonc.2021.690115. eCollection 2021.
Primary pulmonary nuclear protein of testis carcinoma is a rare and highly aggressive malignant tumor. It accounts for approximately 0.22% of primary thoracic tumors and is little known, so it is often misdiagnosed as pulmonary squamous cell carcinoma. No effective treatment has been formed yet, and the prognosis is extremely poor. This review aims to summarize the etiology, pathogenesis, diagnosis, treatment, and prognosis of primary pulmonary nuclear protein of testis carcinoma in order to better recognize it and discuss the current and innovative strategies to overcome it. With the increasing importance of cancer immunotherapy and tumor microenvironment, the review also discusses whether immunotherapy and targeting the tumor microenvironment can improve the prognosis of primary pulmonary nuclear protein of testis carcinoma and possible treatment strategies. We reviewed and summarized the clinicopathological features of all patients with primary pulmonary nuclear protein of testis carcinoma who received immunotherapy, including initial misdiagnosis, disease stage, immunohistochemical markers related to tumor neovascularization, and biomarkers related to immunotherapy, such as PD-L1 (programmed death-ligand 1) and TMB (tumor mutational burden). In the meanwhile, we summarized and analyzed the progression-free survival (PFS) and the overall survival (OS) of patients with primary pulmonary nuclear protein of testis carcinoma treated with PD-1 (programmed cell death protein 1)/PD-L1 inhibitors and explored potential population that may benefit from immunotherapy. To the best of our knowledge, this is the first review on the exploration of the tumor microenvironment and immunotherapy effectiveness in primary pulmonary nuclear protein of testis carcinoma.
原发性睾丸癌肺核蛋白癌是一种罕见且侵袭性很强的恶性肿瘤。它约占原发性胸部肿瘤的0.22%,人们对其了解甚少,因此常被误诊为肺鳞状细胞癌。目前尚未形成有效的治疗方法,预后极差。本综述旨在总结原发性睾丸癌肺核蛋白癌的病因、发病机制、诊断、治疗及预后,以便更好地认识该病,并探讨攻克该病的现有及创新策略。随着癌症免疫治疗和肿瘤微环境的重要性日益增加,本综述还讨论了免疫治疗和针对肿瘤微环境是否能改善原发性睾丸癌肺核蛋白癌的预后以及可能的治疗策略。我们回顾并总结了所有接受免疫治疗的原发性睾丸癌肺核蛋白癌患者的临床病理特征,包括初始误诊、疾病分期、与肿瘤新生血管相关的免疫组化标志物以及与免疫治疗相关的生物标志物,如程序性死亡配体1(PD-L1)和肿瘤突变负荷(TMB)。同时,我们总结并分析了接受程序性细胞死亡蛋白1(PD-1)/PD-L1抑制剂治疗的原发性睾丸癌肺核蛋白癌患者的无进展生存期(PFS)和总生存期(OS),并探索了可能从免疫治疗中获益的潜在人群。据我们所知,这是第一篇关于原发性睾丸癌肺核蛋白癌肿瘤微环境及免疫治疗疗效探索的综述。