Department of Radiotherapy and Oncology, University of Frankfurt, Germany.
Department of Radiotherapy and Oncology, University of Frankfurt, Germany; German Cancer Research Center (DKFZ), Heidelberg, Germany; German Cancer Consortium (DKTK), partner site: Frankfurt a. M., Germany.
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):221-230. doi: 10.1016/j.bbcan.2017.05.001. Epub 2017 May 10.
Anal squamous cell carcinomas (ASCC) are increasing in frequency across the developed world, and 70-90% of all cases originate from infection with human papilloma viruses (HPV). Primary chemoradiotherapy (CRT) is the standard treatment for ASCC, but local and/or distant failure still occurs in up to 30% of patients. HPV-associated ASCC and tumors with a higher density of tumor infiltrating lymphocytes (TIL) carry a better prognosis. Furthermore, HPV can render tumors more immunogenic, whereas it correlates with elevated TIL densities. This comprehensive review highlights the progress made in understanding the immune microenvironment of anal intraepithelial neoplasias and ASCC in the context of HPV. Here, we discuss the immunomodulatory potential of CRT, the prognostic impact of immune checkpoint markers, and the rationale for including immunotherapies to further improve the clinical outcome in patients with ASCC.
分析性鳞状细胞癌(ASCC)在发达国家的发病率正在上升,70-90%的病例源自人乳头瘤病毒(HPV)感染。原发性放化疗(CRT)是 ASCC 的标准治疗方法,但仍有多达 30%的患者发生局部和/或远处失败。HPV 相关的 ASCC 和肿瘤中浸润淋巴细胞(TIL)密度较高的患者预后较好。此外,HPV 可使肿瘤更具免疫原性,而 TIL 密度升高与之相关。这篇综述强调了在 HPV 背景下理解肛门上皮内瘤变和 ASCC 免疫微环境方面所取得的进展。在这里,我们讨论 CRT 的免疫调节潜力、免疫检查点标志物的预后影响,以及将免疫疗法纳入以进一步改善 ASCC 患者临床结果的合理性。