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转移性葡萄膜黑色素瘤治疗的分子见解与新兴策略

Molecular Insights and Emerging Strategies for Treatment of Metastatic Uveal Melanoma.

作者信息

Mallone Fabiana, Sacchetti Marta, Lambiase Alessandro, Moramarco Antonietta

机构信息

Department of Sense Organs, Sapienza University of Rome, 00161 Rome, Italy.

出版信息

Cancers (Basel). 2020 Sep 25;12(10):2761. doi: 10.3390/cancers12102761.

Abstract

Uveal melanoma (UM) is the most common intraocular cancer. In recent decades, major advances have been achieved in the diagnosis and prognosis of UM allowing for tailored treatments. However, nearly 50% of patients still develop metastatic disease with survival rates of less than 1 year. There is currently no standard of adjuvant and metastatic treatment in UM, and available therapies are ineffective resulting from cutaneous melanoma protocols. Advances and novel treatment options including liver-directed therapies, immunotherapy, and targeted-therapy have been investigated in UM-dedicated clinical trials on single compounds or combinational therapies, with promising results. Therapies aimed at prolonging or targeting metastatic tumor dormancy provided encouraging results in other cancers, and need to be explored in UM. In this review, the latest progress in the diagnosis, prognosis, and treatment of UM in adjuvant and metastatic settings are discussed. In addition, novel insights into tumor genetics, biology and immunology, and the mechanisms underlying metastatic dormancy are discussed. As evident from the numerous studies discussed in this review, the increasing knowledge of this disease and the promising results from testing of novel individualized therapies could offer future perspectives for translating in clinical use.

摘要

葡萄膜黑色素瘤(UM)是最常见的眼内癌。近几十年来,UM的诊断和预后取得了重大进展,从而能够进行个性化治疗。然而,仍有近50%的患者会发生转移性疾病,生存率不到1年。目前UM尚无辅助治疗和转移性治疗的标准,现有的疗法因皮肤黑色素瘤方案而无效。在专门针对UM的关于单一化合物或联合疗法的临床试验中,已经研究了包括肝导向疗法、免疫疗法和靶向疗法在内的进展和新的治疗选择,取得了令人鼓舞的结果。旨在延长或靶向转移性肿瘤休眠的疗法在其他癌症中取得了令人鼓舞的结果,需要在UM中进行探索。在这篇综述中,讨论了UM在辅助和转移情况下诊断、预后和治疗的最新进展。此外,还讨论了对肿瘤遗传学、生物学和免疫学以及转移性休眠潜在机制的新见解。从本综述中讨论的众多研究可以明显看出,对这种疾病的了解不断增加以及新型个体化疗法测试取得的令人鼓舞的结果,可能为转化为临床应用提供未来前景。

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