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黑色素瘤:分子靶向治疗与免疫检查点抑制的交集。

Melanoma: the intersection of molecular targeted therapy and immune checkpoint inhibition.

机构信息

Department of Cancer Medicine, Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, Victoria 3002, Australia.

Melanoma, Cancer Immunotherapy, and Innovative Therapy Unit, Istituto Nazionale Tumori Fondazione "G. Pascale", Via Mariano Semmola, 80131 Napoli, Italy.

出版信息

Curr Opin Immunol. 2016 Apr;39:30-8. doi: 10.1016/j.coi.2015.12.006. Epub 2016 Jan 5.

DOI:10.1016/j.coi.2015.12.006
PMID:26765776
Abstract

Melanoma is at the forefront of development of systemic therapeutics with both molecular targeted therapies and immune checkpoint inhibitors as cornerstones of treatment. Although responses to molecularly targeted therapy is largely from blockade of oncogenic pathways, evidence is emerging of the immunomodulatory effects from BRAF inhibition. Additionally programmed-death-1 (PD-1) inhibitors have revolutionized the treatment of melanoma and are set to pave future improvements in other solid tumors. Combinations of PD-1 inhibitors with novel immune checkpoints or with molecularly targeted therapies are under investigation and may improve on the considerable progress made.

摘要

黑色素瘤是系统治疗学发展的前沿,分子靶向治疗和免疫检查点抑制剂是治疗的基石。虽然分子靶向治疗的反应主要来自于阻断致癌途径,但 BRAF 抑制的免疫调节作用的证据正在出现。此外,程序性死亡受体-1(PD-1)抑制剂彻底改变了黑色素瘤的治疗方法,并有望为其他实体瘤的未来改善铺平道路。PD-1 抑制剂与新型免疫检查点或与分子靶向治疗的联合应用正在研究中,可能会进一步提高疗效。

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The Role of Treatment Sequencing with Immune-Checkpoint Inhibitors and BRAF/MEK Inhibitors for Response and Survival of Patients with BRAFV600-Mutant Metastatic Melanoma-A Retrospective, Real-World Cohort Study.免疫检查点抑制剂与BRAF/MEK抑制剂序贯治疗对BRAFV600突变转移性黑色素瘤患者反应和生存的作用——一项回顾性真实世界队列研究
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Enhancing Adoptive Cell Transfer with Combination BRAF-MEK and CDK4/6 Inhibitors in Melanoma.
联合BRAF-MEK和CDK4/6抑制剂增强黑色素瘤的过继性细胞转移
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Targeting Replication Stress Using CHK1 Inhibitor Promotes Innate and NKT Cell Immune Responses and Tumour Regression.使用CHK1抑制剂靶向复制应激可促进先天性和NKT细胞免疫反应以及肿瘤消退。
Cancers (Basel). 2021 Jul 25;13(15):3733. doi: 10.3390/cancers13153733.
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Myosin II Reactivation and Cytoskeletal Remodeling as a Hallmark and a Vulnerability in Melanoma Therapy Resistance.肌球蛋白 II 的重新激活和细胞骨架重塑作为黑色素瘤治疗耐药性的标志和弱点。
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