Mathias-Machado Maria Cecília, Peixoto Renata D'Alpino, Moniz Camila Motta Venchiarutti, Jácome Alexandre A
Department of Gastrointestinal Medical Oncology, Oncoclinicas, São Paulo 04538-132, Brazil.
Department of Oncology, ICESP-Instituto do Cancer do Estado de São Paulo, University of São Paulo, São Paulo 01246-000, Brazil.
Biomedicines. 2022 Aug 20;10(8):2029. doi: 10.3390/biomedicines10082029.
Squamous cell carcinoma of the anal canal (SCCA) is a rare neoplasm, but with rising incidence rates in the past few decades; it is etiologically linked with the human papillomavirus (HPV) infection and is especially prevalent in immunocompromised patients, mainly those infected with HIV. Fluoropyrimidine-based chemoradiotherapy remains the cornerstone of the treatment of non-metastatic disease, but the locally advanced disease still presents high rates of disease recurrence and systemic therapy of SCCA is an unmet clinical need. Despite sharing common molecular aspects with other HPV-related malignancies, such as cervical and head and neck cancers, SCCA presents specific epigenomic, genomic, and transcriptomic abnormalities, which suggest that genome-guided personalized therapies should be specifically designed for this disease. Actionable mutations are rare in SCCA and immune checkpoint inhibition has not yet been proven useful in an unselected population of patients. Therefore, advances in systemic therapy of SCCA will only be possible with the identification of predictive biomarkers and the subsequent development of targeted therapies or immunotherapeutic approaches that consider the unique tumor microenvironment and the intra- and inter-tumoral heterogeneity. In the present review, we address the molecular characterization of SCCA and discuss potential diagnostic, predictive and prognostic biomarkers of this complex and challenging disease.
肛管鳞状细胞癌(SCCA)是一种罕见的肿瘤,但在过去几十年中发病率呈上升趋势;其病因与人类乳头瘤病毒(HPV)感染有关,在免疫功能低下的患者中尤为普遍,主要是感染HIV的患者。基于氟嘧啶的放化疗仍然是非转移性疾病治疗的基石,但局部晚期疾病的疾病复发率仍然很高,SCCA的全身治疗是一项尚未满足的临床需求。尽管SCCA与其他HPV相关恶性肿瘤(如宫颈癌和头颈癌)有共同的分子特征,但SCCA存在特定的表观基因组、基因组和转录组异常,这表明应针对该疾病专门设计基于基因组的个性化疗法。SCCA中可操作的突变很少见,免疫检查点抑制在未经过筛选的患者群体中尚未被证明有效。因此,只有通过识别预测性生物标志物以及随后开发考虑独特肿瘤微环境和肿瘤内及肿瘤间异质性的靶向治疗或免疫治疗方法,SCCA的全身治疗才有可能取得进展。在本综述中,我们阐述了SCCA的分子特征,并讨论了这种复杂且具有挑战性的疾病潜在的诊断、预测和预后生物标志物。