Tanese Keiji, Nakamura Yoshio, Hirai Ikuko, Funakoshi Takeru
Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Front Med (Lausanne). 2019 Jul 10;6:160. doi: 10.3389/fmed.2019.00160. eCollection 2019.
Non-melanoma skin cancers (NMSCs), which represent a diverse group of cutaneous malignancies, are the most common forms of human neoplasia. The incidence of these diseases is increasing due to a number of factors, including that of increasing human lifespans. The majority of NMSCs are basal cell carcinomas (BCC) and cutaneous squamous cell carcinomas (cSCC), with the remainder being various rare skin cancers, including extramammary Paget's disease (EMPD), Merkel cell carcinoma (MCC), and several skin adnexal carcinomas. Of these, MCC usually shows aggressive behavior with a high mortality rate. On the other hand, BCC, cSCC, EMPD, and skin adnexal tumors usually show an indolent clinical course and metastasize only rarely. Nevertheless, the metastatic forms of these tumors commonly lead to poor patient outcome. A definitive management strategy for the treatment of advanced NMSC has not been established, mainly due to their rarity and lack of reliable information based on well-controlled randomized trials. Chemotherapeutic regimens for treatment of these diseases have been mainly based on the observations of isolated, small case series or clinical trials with a limited numbers of patients. However, accumulating evidence regarding their pathobiological backgrounds as well as recent advances in molecular biotechnology have facilitated the development of novel drugs for treatment of these diseases. Over the past decade, the U.S. Food and Drug Administration has approved several molecular targeting therapies, including Hedgehog inhibitors for BCC, monoclonal antibodies targeting anti-programmed death ligand-1 and anti- programmed cell death 1 (PD-1) for MCC, and anti-PD-1 for cSCC. Here, we review their clinical utility and discuss updated systemic treatment strategies for advanced NMSC.
非黑色素瘤皮肤癌(NMSCs)是一组多样的皮肤恶性肿瘤,是人类肿瘤最常见的形式。由于多种因素,包括人类寿命的延长,这些疾病的发病率正在上升。大多数NMSCs是基底细胞癌(BCC)和皮肤鳞状细胞癌(cSCC),其余为各种罕见的皮肤癌,包括乳腺外佩吉特病(EMPD)、默克尔细胞癌(MCC)和几种皮肤附属器癌。其中,MCC通常表现出侵袭性,死亡率很高。另一方面,BCC、cSCC、EMPD和皮肤附属器肿瘤通常临床病程较为惰性,很少发生转移。然而,这些肿瘤的转移形式通常会导致患者预后不良。由于晚期NMSC的罕见性以及缺乏基于严格对照随机试验的可靠信息,尚未确立明确的治疗策略。治疗这些疾病的化疗方案主要基于孤立的小病例系列观察或患者数量有限的临床试验。然而,关于其病理生物学背景的证据不断积累以及分子生物技术的最新进展促进了治疗这些疾病的新药开发。在过去十年中,美国食品药品监督管理局已批准了几种分子靶向疗法,包括用于BCC的刺猬因子抑制剂、用于MCC的靶向抗程序性死亡配体-1和抗程序性细胞死亡1(PD-1)的单克隆抗体,以及用于cSCC的抗PD-1。在此,我们综述它们的临床应用,并讨论晚期NMSC的最新全身治疗策略。