Hooiveld-Noeken J S, Fehrmann R S N, de Vries E G E, Jalving M
Department of Medical Oncology, University Medical Centre Groningen, the Netherlands.
Immunooncol Technol. 2019 Nov 27;4:1-7. doi: 10.1016/j.iotech.2019.11.002. eCollection 2019 Dec.
Metastatic Merkel cell carcinoma (MCC) and cutaneous squamous cell carcinoma (cSCC) are rare and both show impressive responses to immune checkpoint inhibitor treatment. However, at least 40% of patients do not respond to these expensive and potentially toxic drugs. Development of predictive biomarkers of response and rational, effective combination treatment strategies in these rare, often frail patient populations is challenging. This review discusses the pathophysiology and treatment of MCC and cSCC, with a particular focus on potential biomarkers of response to immunotherapy, and discusses how transfer learning using big data collected from patients with common tumours can be used in combination with deep phenotyping of rare tumours to develop predictive biomarkers and elucidate novel treatment targets.
转移性默克尔细胞癌(MCC)和皮肤鳞状细胞癌(cSCC)较为罕见,且二者对免疫检查点抑制剂治疗均显示出显著疗效。然而,至少40%的患者对这些昂贵且具有潜在毒性的药物无反应。在这些罕见且通常身体虚弱的患者群体中,开发反应预测生物标志物以及合理、有效的联合治疗策略具有挑战性。本综述讨论了MCC和cSCC的病理生理学及治疗方法,特别关注免疫治疗反应的潜在生物标志物,并探讨如何将从常见肿瘤患者收集的大数据进行迁移学习,与罕见肿瘤的深度表型分析相结合,以开发预测生物标志物并阐明新的治疗靶点。