Queen Alaxendra Hospital, Portsmouth NHS Trust, Portsmouth, UK.
University Hospital Birmingham, NHS Foundation Trust, Birmingham, UK.
Cancer Treat Res. 2023;185:79-89. doi: 10.1007/978-3-031-27156-4_5.
There is no denying that many revolutions took place in the fight against cancer during the last decades. However, cancers have always managed to find new ways to challenge humankinds. Variable genomic epidemiology, socio-economic differences and limitations of widespread screening are the major concerns in cancer diagnosis and early treatment. A multidisciplinary approach is essentially to manage a cancer patient efficiently. Thoracic malignancies including lung cancers and pleural mesothelioma are accountable for little more than 11.6% of the global cancer burden [4]. Mesothelioma is one of the rare cancers, but concern is the incidences are increasing globally. However, the good news is first-line chemotherapy with the combination of immune checkpoints inhibitors (ICIs) in non-small cell lung cancer (NSCLC) and mesothelioma has showed promising respond and improved overall survival (OS) in pivotal clinical trials [10]. ICIs are commonly referred as immunotherapy are antigens on the cancer cells, and inhibitors are the antibodies produce by the T cell defence system. By inhibiting immune checkpoints, the cancer cells become visible to be identified as abnormal cells and attack by the body's defence system [17]. The programmed death receptor-1 (PD-1) and programmed death receptor ligand-1 (PD-L1) inhibitors are commonly used immune checkpoint blockers for anti-cancer treatment. PD-1/PD-L1 are proteins produced by immune cells and mimic by cancer cells that are implicated in inhibiting T cell response to regulate our immune system, which results tumour cells escaping the defence mechanism to achieve immune surveillance. Therefore, inhibiting immune checkpoints as well as monoclonal antibodies can lead to effective apoptosis of tumour cells [17]. Mesothelioma is an industrial disease caused by significant asbestos exposure. It is the cancer of the mesothelial tissue which presents in the lining of the mediastinum of pleura, pericardium and peritoneum, most commonly affected sites are pleura of the lung or chest wall lining [9] as route of asbestos exposure is inhalation. Calretinin is a calcium binding protein, typically over exposed in malignant mesotheliomas and the most useful marker even while initial changes take place [5]. On the other hand, Wilm's tumour 1 (WT-1) gene expression on the tumour cells can be related to prognosis as it can elicit immune response, thereby inhibit cell apoptosis. A systematic review and meta-analysis study conducted by Qi et al. has suggested that expression of WT-1 in a solid tumour is fatal however, it gives the tumour cell a feature of immune sensitivity which then acts positively towards the treatment with immunotherapy. Clinical significance of WT-1 oncogene in treatment is still hugely debatable and needs further attention [21]. Recently, Japan has reinstated Nivolumab in patients with chemo-refractory mesothelioma. According to NCCN guidelines, the salvage therapies include Pembrolizumab in PD-L1 positive patients and Nivolumab alone or with Ipilimumab in cancers irrespective of PD-L1 expression [9]. The checkpoint blockers have taken over the biomarker-based research and demonstrated impressive treatment options in immune sensitive and asbestos-related cancers. It can be expected that in near future the immune checkpoint inhibitors will be considered as approved first-line cancer treatment universally.
不可否认,在过去几十年的癌症抗争中发生了许多革命。然而,癌症总是设法找到新的方法来挑战人类。基因组流行病学的变化、社会经济差异以及广泛筛查的局限性是癌症诊断和早期治疗的主要关注点。多学科方法对于有效地管理癌症患者至关重要。包括肺癌和胸膜间皮瘤在内的胸部恶性肿瘤仅占全球癌症负担的 11.6%以上[4]。间皮瘤是一种罕见的癌症,但令人担忧的是其发病率在全球范围内正在增加。然而,好消息是,在非小细胞肺癌(NSCLC)和间皮瘤的一线化疗中联合使用免疫检查点抑制剂(ICIs),在关键性临床试验中显示出了有希望的反应,并改善了总体生存率(OS)[10]。ICI 通常被称为免疫疗法,是癌细胞上的抗原,而抑制剂是 T 细胞防御系统产生的抗体。通过抑制免疫检查点,癌细胞变得可见,被识别为异常细胞,并被身体的防御系统攻击[17]。程序性死亡受体-1(PD-1)和程序性死亡受体配体-1(PD-L1)抑制剂是常用于癌症治疗的免疫检查点阻断剂。PD-1/PD-L1 是免疫细胞产生的蛋白质,被癌细胞模拟,它们参与抑制 T 细胞反应,以调节我们的免疫系统,从而导致肿瘤细胞逃避防御机制,实现免疫监视。因此,抑制免疫检查点和单克隆抗体可以导致肿瘤细胞的有效凋亡[17]。间皮瘤是一种由大量石棉暴露引起的工业疾病。它是间皮组织的癌症,存在于纵隔、胸膜、心包和腹膜的衬里,最常见的受累部位是肺或胸壁衬里的胸膜[9],因为石棉暴露的途径是吸入。钙结合蛋白 calretinin 在恶性间皮瘤中过度表达,即使在最初发生变化时也是最有用的标志物[5]。另一方面,Wilms 肿瘤 1 (WT-1)基因在肿瘤细胞中的表达与预后有关,因为它可以引发免疫反应,从而抑制细胞凋亡。Qi 等人进行的一项系统评价和荟萃分析表明,实体肿瘤中 WT-1 的表达是致命的,但它使肿瘤细胞具有免疫敏感性的特征,从而对免疫治疗产生积极影响。WT-1 癌基因在治疗中的临床意义仍存在很大争议,需要进一步关注[21]。最近,日本重新批准了纳武单抗用于化疗耐药性间皮瘤患者。根据 NCCN 指南,挽救疗法包括 PD-L1 阳性患者的 Pembrolizumab 以及癌症的 Nivolumab 单独或与 Ipilimumab 联合治疗,无论 PD-L1 表达如何[9]。检查点阻滞剂已经取代了基于生物标志物的研究,并在免疫敏感和石棉相关癌症中展示了令人印象深刻的治疗选择。可以预期,在不久的将来,免疫检查点抑制剂将被普遍视为批准的一线癌症治疗方法。