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治疗罕见和难治性黑色素瘤亚型的新兴策略。

Emerging strategies to treat rare and intractable subtypes of melanoma.

机构信息

The Wistar Institute, Philadelphia, PA, USA.

出版信息

Pigment Cell Melanoma Res. 2021 Jan;34(1):44-58. doi: 10.1111/pcmr.12880. Epub 2020 Apr 24.

Abstract

Melanoma is the deadliest form of skin cancer, possessing a diverse landscape of subtypes with distinct molecular signatures and levels of aggressiveness. Although immense progress has been achieved therapeutically for patients with the most common forms of this disease, little is known of how to effectively treat patients with rarer subtypes of melanoma. These subtypes include acral lentiginous (the rarest form of cutaneous melanoma; AL), uveal, and mucosal melanomas, which display variations in distribution across (a) the world, (b) patient age-groups, and (c) anatomic sites. Unfortunately, patients with these relatively rare subtypes of melanoma typically respond worse to therapies approved for the more common, non-AL cutaneous melanoma and do not have effective alternatives, and thus consequently have worse overall survival rates. Achieving durable therapeutic responses in these high-risk melanoma subtypes represents one of the greatest challenges of the field. This review aims to collate and highlight effective preclinical and/or clinical strategies against these rare forms of melanoma.

摘要

黑色素瘤是最致命的皮肤癌形式,具有不同的亚型,具有不同的分子特征和侵袭程度。尽管在治疗最常见形式的黑色素瘤患者方面取得了巨大进展,但对于如何有效治疗罕见亚型的黑色素瘤患者却知之甚少。这些亚型包括肢端雀斑样黑色素瘤(最罕见的皮肤黑色素瘤形式;AL)、葡萄膜和黏膜黑色素瘤,它们在(a)世界各地、(b)患者年龄组和(c)解剖部位的分布上存在差异。不幸的是,这些相对罕见的黑色素瘤亚型的患者通常对批准用于更常见的非 AL 皮肤黑色素瘤的治疗方法反应更差,而且没有有效的替代方法,因此总体生存率更差。在这些高危黑色素瘤亚型中实现持久的治疗反应是该领域面临的最大挑战之一。本综述旨在收集和强调针对这些罕见形式黑色素瘤的有效临床前和/或临床策略。

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Real-World Impact of Immune Checkpoint Inhibitors in Metastatic Uveal Melanoma.
Cancers (Basel). 2019 Oct 3;11(10):1489. doi: 10.3390/cancers11101489.
3
Tumour-intrinsic resistance to immune checkpoint blockade.
Nat Rev Immunol. 2020 Jan;20(1):25-39. doi: 10.1038/s41577-019-0218-4. Epub 2019 Sep 30.
4
Clinical and genetic analysis of melanomas arising in acral sites.
Eur J Cancer. 2019 Sep;119:66-76. doi: 10.1016/j.ejca.2019.07.008. Epub 2019 Aug 14.
6
Atypical and Mutations in Mucosal Melanoma.
Cancers (Basel). 2019 Aug 8;11(8):1133. doi: 10.3390/cancers11081133.
7
Immunological Backbone of Uveal Melanoma: Is There a Rationale for Immunotherapy?
Cancers (Basel). 2019 Jul 26;11(8):1055. doi: 10.3390/cancers11081055.
8
Whole-genome landscape of mucosal melanoma reveals diverse drivers and therapeutic targets.
Nat Commun. 2019 Jul 18;10(1):3163. doi: 10.1038/s41467-019-11107-x.
9
Evaluation of the efficacy of immunotherapy for non-resectable mucosal melanoma.
Cancer Immunol Immunother. 2019 Jul;68(7):1171-1178. doi: 10.1007/s00262-019-02351-7. Epub 2019 Jun 7.
10

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