Pekarek Leonel, Sánchez Cedra Alicia, Jaudenes Yumna Dbouk Y, Ospino Linda Rocío, Iglesias Pedrejón Beatriz, Bernier Loreto, Roberts Cervantes Eduardo David, Sánchez Cendra Cristina, Cassinello Javier, Trasobares Lidia, Quesada-Cortés Alicia, Sáez Miguel A, Álvarez-Mon Melchor, Ortega Miguel A
Department of Medicine and Medical Specialties, Biomedical Network Research Center on Liver and Digestive Diseases, Faculty of Medicine and Health Sciences, University of Alcalá, 28801 Alcalá de Henares, Spain.
Oncology Service, University Hospital of Guadalajara, 19002 Guadalajara, Spain.
Oncol Lett. 2024 Nov 26;29(2):78. doi: 10.3892/ol.2024.14824. eCollection 2025 Feb.
Metastatic melanoma is an aggressive and deadly form of skin cancer, known for its rapid ability to spread to other organs. Melanoma metastasis involves several steps: Local invasion, lymphovascular invasion and proliferation to new sites. This process is facilitated by genetic alterations, interactions with the tumor microenvironment and evasion of the immune system. Despite advances in therapies, the 5-year survival rate remains low at ~22.5%. Notably, current research is focused on identifying patients who may benefit from specific treatments, considering factors such as mutational load and programmed death ligand 1 expression. BRAF inhibitors and immune checkpoint inhibitors have improved survival, although numerous patients do not respond or develop resistance, underscoring the need for novel biomarkers to optimize treatment and monitoring of the disease. In summary, the purpose of the present article is to review the different serological, histological, microRNA and circulating tumor cell biomarkers that have proven useful in the diagnosis, follow-up and prognosis of metastatic melanoma. These biomarkers represent a promising area for research and clinical application, with the aim of offering more precise and personalized treatments.
转移性黑色素瘤是一种侵袭性和致命性的皮肤癌,以其迅速扩散至其他器官的能力而闻名。黑色素瘤转移涉及多个步骤:局部侵袭、淋巴管侵袭以及在新部位的增殖。这一过程由基因改变、与肿瘤微环境的相互作用以及对免疫系统的逃避所促成。尽管治疗取得了进展,但5年生存率仍很低,约为22.5%。值得注意的是,当前的研究集中在识别可能从特定治疗中获益的患者,同时考虑诸如突变负荷和程序性死亡配体1表达等因素。BRAF抑制剂和免疫检查点抑制剂已改善了生存率,尽管许多患者没有反应或产生耐药性,这突出了需要新的生物标志物来优化疾病的治疗和监测。总之,本文的目的是综述已被证明在转移性黑色素瘤的诊断、随访和预后中有用的不同血清学、组织学、微小RNA和循环肿瘤细胞生物标志物。这些生物标志物代表了一个有前景的研究和临床应用领域,旨在提供更精确和个性化的治疗。