Pilla Lorenzo, Alberti Andrea, Di Mauro Pierluigi, Gemelli Maria, Cogliati Viola, Cazzaniga Marina Elena, Bidoli Paolo, Maccalli Cristina
Division of Medical Oncology, San Gerardo Hospital, University of Milano-Bicocca School of Medicine, 20900 Monza, Italy.
Medical Oncology Unit, Department of Medical and Surgical Specialties, Radiological Health Science and Public Health, University of Brescia, ASST Ospedali Civili, 25123 Brescia, Italy.
Cancers (Basel). 2020 Nov 20;12(11):3456. doi: 10.3390/cancers12113456.
Advances in the genomic, molecular and immunological make-up of melanoma allowed the development of novel targeted therapy and of immunotherapy, leading to changes in the paradigm of therapeutic interventions and improvement of patients' overall survival. Nevertheless, the mechanisms regulating either the responsiveness or the resistance of melanoma patients to therapies are still mostly unknown. The development of either the combinations or of the sequential treatment of different agents has been investigated but without a strongly molecularly motivated rationale. The need for robust biomarkers to predict patients' responsiveness to defined therapies and for their stratification is still unmet. Progress in immunological assays and genomic techniques as long as improvement in designing and performing studies monitoring the expression of these markers along with the evolution of the disease allowed to identify candidate biomarkers. However, none of them achieved a definitive role in predicting patients' clinical outcomes. Along this line, the cross-talk of melanoma cells with tumor microenvironment plays an important role in the evolution of the disease and needs to be considered in light of the role of predictive biomarkers. The overview of the relationship between the molecular basis of melanoma and targeted therapies is provided in this review, highlighting the benefit for clinical responses and the limitations. Moreover, the role of different candidate biomarkers is described together with the technical approaches for their identification. The provided evidence shows that progress has been achieved in understanding the molecular basis of melanoma and in designing advanced therapeutic strategies. Nevertheless, the molecular determinants of melanoma and their role as biomarkers predicting patients' responsiveness to therapies warrant further investigation with the vision of developing more effective precision medicine.
黑色素瘤在基因组、分子和免疫学构成方面的进展促使了新型靶向治疗和免疫治疗的发展,从而改变了治疗干预的模式并提高了患者的总生存率。然而,调节黑色素瘤患者对治疗的反应性或耐药性的机制仍大多未知。不同药物联合或序贯治疗的研发已得到研究,但缺乏强有力的分子学依据。预测患者对特定治疗的反应性并对其进行分层的可靠生物标志物的需求仍未得到满足。免疫测定和基因组技术的进展以及设计和开展监测这些标志物表达与疾病进展的研究方面的改进,使得能够识别候选生物标志物。然而,它们均未在预测患者临床结局方面发挥决定性作用。在此背景下,黑色素瘤细胞与肿瘤微环境的相互作用在疾病进展中起着重要作用,需要结合预测性生物标志物的作用来加以考虑。本综述提供了黑色素瘤分子基础与靶向治疗之间关系的概述,强调了临床反应的益处和局限性。此外,还描述了不同候选生物标志物的作用及其识别的技术方法。所提供的证据表明,在理解黑色素瘤的分子基础和设计先进治疗策略方面已取得进展。然而,黑色素瘤的分子决定因素及其作为预测患者对治疗反应性的生物标志物的作用仍有待进一步研究,以期开发更有效的精准医学。