Glynne-Jones R, Nilsson P J, Aschele C, Goh V, Peiffert D, Cervantes A, Arnold D
Centre for Cancer Treatment, Mount Vernon Hospital, Northwood, Middlesex, United Kingdom.
Department of Molecular Medicine and Surgery, Karolinska Instituet and Center for Surgical Gastroenterology, Karolinska University Hospital, Stockholm, Sweden.
Eur J Surg Oncol. 2014 Oct;40(10):1165-76. doi: 10.1016/j.ejso.2014.07.030.
Squamous cell carcinoma of the anus (SCCA) is a rare cancer but its incidence is increasing throughout the world, and is particularly high in the human immunodeficiency virus positive (HIV+) population. A multidisciplinary approach is mandatory (involving radiation therapists, medical oncologists, surgeons, radiologists and pathologists). SCCA usually spreads in a loco-regional manner within and outside the anal canal. Lymph node involvement at diagnosis is observed in 30%-40% of cases while systemic spread is uncommon with distant extrapelvic metastases recorded in 5%-8% at onset, and rates of metastatic progression after primary treatment between 10 and 20%. SCCA is strongly associated with human papilloma virus (HPV, types 16-18) infection. The primary aim of treatment is to achieve cure with loco-regional control and preservation of anal function, with the best possible quality of life. Treatment dramatically differs from adenocarcinomas of the lower rectum. Combinations of 5FU-based chemoradiation and other cytotoxic agents (mitomycin C) have been established as the standard of care, leading to complete tumour regression in 80%-90% of patients with locoregional failures in the region of 15%. There is an accepted role for surgical salvage. Assessment and treatment should be carried out in specialised centres treating a high number of patients as early as possible in the clinical diagnosis. To date, the limited evidence from only 6 randomised trials [1,2,3,4,5,6,7], the rarity of the cancer, and the different behaviour/natural history depending on the predominant site of origin, (the anal margin, anal canal or above the dentate line) provide scanty direction for any individual oncologist. Here we aim to provide guidelines which can assist medical, radiation and surgical oncologists in the practical management of this unusual cancer.
肛管鳞状细胞癌(SCCA)是一种罕见的癌症,但其发病率在全球范围内呈上升趋势,在人类免疫缺陷病毒阳性(HIV+)人群中尤其高。多学科方法是必不可少的(涉及放射治疗师、医学肿瘤学家、外科医生、放射科医生和病理学家)。SCCA通常以局部区域方式在肛管内外扩散。诊断时30%-40%的病例有淋巴结受累,而全身扩散不常见,初发时盆腔外远处转移记录为5%-8%,初次治疗后转移进展率在10%至20%之间。SCCA与人类乳头瘤病毒(HPV,16-18型)感染密切相关。治疗的主要目标是实现局部区域控制和肛门功能保留的治愈,同时尽可能提高生活质量。治疗与低位直肠癌有很大不同。基于5-氟尿嘧啶的放化疗与其他细胞毒性药物(丝裂霉素C)联合已被确立为标准治疗方法,可使80%-90%局部区域失败的患者肿瘤完全消退,局部复发率在15%左右。手术挽救有公认的作用。评估和治疗应在临床诊断后尽早在治疗大量患者的专业中心进行。迄今为止,仅6项随机试验[1,2,3,4,5,6,7]的有限证据、该癌症的罕见性以及取决于主要起源部位(肛门边缘、肛管或齿状线以上)的不同行为/自然史,为任何个体肿瘤学家提供的指导很少。在此,我们旨在提供指南,以协助医学、放射和外科肿瘤学家对这种罕见癌症进行实际管理。