Immunotherapy for locally advanced and metastatic basal cell carcinoma: a narrative review.

IF 1.5 4区 医学 Q4 ONCOLOGY Translational cancer research Pub Date : 2024-11-30 Epub Date: 2024-11-06 DOI:10.21037/tcr-24-742
Xiaoqing Li, Hongru Wang, Qingli Lu
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Abstract

Background and objective: Basal cell carcinoma (BCC) is the most common malignancy of humankind, characterized by its low propensity for metastasis and its high recurrence rate. Surgical intervention is the predominant therapeutic approach. However, for cases of locally advanced BCC (laBCC) and metastatic BCC (mBCC), systematic therapy may be the first option. In recent years, tumor immunotherapy has garnered significant attention within the scientific community. And it has progressively demonstrated its efficacy in the treatment of laBCC and mBCC. This review aims to summarize the characteristics of immune microenvironment, biomarkers, and immunotherapies of BCC, and provide a reference for further research on BCC immunotherapy.

Methods: We searched literature in PubMed database and Web of Science and considered all study types written in English from 2013 to 2024.

Key content and findings: The alteration of the immune microenvironment is a pivotal factor in the progression of BCC. The expression levels of sex determining region Y (SRY)-box 2 (SOX2) and matrix metalloproteinases (MMPs) have emerged as potential prognostic biomarkers for BCC. And they are promising therapeutic targets for laBCC and mBCC. For patients presenting with laBCC or mBCC, a spectrum of immunotherapeutic approaches is being explored, including inhibition of the programmed death receptor 1 (PD-1) and programmed death ligand 1 (PD-L1), blockade of cytotoxic T-lymphocyte antigen 4 (CTLA-4), lymphocyte activation gene 3 (LAG-3) inhibition therapy, the use of chimeric antigen receptor (CAR)-T cells, and vaccination. Cemiplimab is the first immune checkpoint inhibitor (ICI) approved by the Food and Drug Administration for refractory BCC, marking a major breakthrough in BCC immunotherapy.

Conclusions: Immunotherapies have shown efficacy in clinical studies. In the future, more multicenter studies with large samples are needed to further explore the efficacy and safety of immunotherapy for BCC.

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局部晚期和转移性基底细胞癌的免疫治疗:叙述回顾。
背景与目的:基底细胞癌(Basal cell carcinoma, BCC)是人类最常见的恶性肿瘤,具有低转移倾向和高复发率的特点。手术干预是主要的治疗方法。然而,对于局部晚期BCC (laBCC)和转移性BCC (mBCC)病例,系统治疗可能是第一选择。近年来,肿瘤免疫治疗在科学界引起了极大的关注。在laBCC和mBCC的治疗中已逐渐显示出其疗效。本文就BCC的免疫微环境、生物标志物、免疫治疗等方面的特点进行综述,为BCC免疫治疗的进一步研究提供参考。方法:检索2013年至2024年PubMed数据库和Web of Science的文献,考虑所有用英文撰写的研究类型。关键内容和发现:免疫微环境的改变是BCC发展的关键因素。性别决定区Y (SRY)-box 2 (SOX2)和基质金属蛋白酶(MMPs)的表达水平已成为BCC的潜在预后生物标志物。它们是laBCC和mBCC的有希望的治疗靶点。对于出现laBCC或mBCC的患者,正在探索一系列免疫治疗方法,包括抑制程序性死亡受体1 (PD-1)和程序性死亡配体1 (PD-L1),阻断细胞毒性t淋巴细胞抗原4 (CTLA-4),淋巴细胞活化基因3 (LAG-3)抑制治疗,使用嵌合抗原受体(CAR)-T细胞,以及接种疫苗。Cemiplimab是美国食品和药物管理局(fda)批准用于难治性BCC的首个免疫检查点抑制剂(ICI),标志着BCC免疫治疗的重大突破。结论:免疫疗法在临床研究中显示出疗效。未来需要更多的多中心大样本研究来进一步探讨免疫治疗BCC的有效性和安全性。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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