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克服黑色素瘤免疫疗法的耐药机制

Overcoming Resistance Mechanisms to Melanoma Immunotherapy.

作者信息

Zheng David X, Bozym David J, Tarantino Giuseppe, Sullivan Ryan J, Liu David, Jenkins Russell W

机构信息

Mass General Cancer Center, Krantz Family Center for Cancer Research, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

出版信息

Am J Clin Dermatol. 2025 Jan;26(1):77-96. doi: 10.1007/s40257-024-00907-7. Epub 2024 Dec 5.

DOI:10.1007/s40257-024-00907-7
PMID:39636504
Abstract

The advent of immune checkpoint inhibition has revolutionized treatment of advanced melanoma. While most patients derive survival benefit from established immunotherapies, notably monoclonal antibodies blocking cytotoxic T-lymphocyte antigen 4 and programmed cell death protein 1, a subset does not optimally respond due to the manifestation of innate or acquired resistance to these therapies. Combination regimens have proven efficacious relative to single-agent blockade, but also yield high-grade treatment toxicities that are often dose-limiting for patients. In this review, we discuss the significant strides made in the past half-decade toward expanding the melanoma immunotherapy treatment paradigm. These include newly approved therapies, adoption of neoadjuvant immunotherapy, and studies in the clinical trials pipeline targeting alternative immune checkpoints and key immunoregulatory molecules. We then review how developments in molecular and functional diagnostics have furthered our understanding of the tumor-intrinsic and -extrinsic mechanisms driving immunotherapy resistance, as well as highlight novel biomarkers for predicting treatment response. Throughout, we discuss potential approaches for targeting these resistance mechanisms in rational combination with established immunotherapies to improve outcomes for patients with melanoma.

摘要

免疫检查点抑制的出现彻底改变了晚期黑色素瘤的治疗方式。虽然大多数患者从既定的免疫疗法中获得生存益处,尤其是阻断细胞毒性T淋巴细胞抗原4和程序性细胞死亡蛋白1的单克隆抗体,但由于对这些疗法表现出先天性或获得性耐药,一部分患者并未获得最佳反应。相对于单药阻断,联合方案已被证明有效,但也会产生高级别治疗毒性,这对患者来说往往是剂量限制性的。在本综述中,我们讨论了过去五年在扩大黑色素瘤免疫治疗模式方面取得的重大进展。这些进展包括新批准的疗法、新辅助免疫疗法的采用,以及针对替代免疫检查点和关键免疫调节分子的临床试验研究。然后,我们回顾了分子和功能诊断方面的进展如何进一步加深了我们对驱动免疫治疗耐药的肿瘤内在和外在机制的理解,并强调了预测治疗反应的新型生物标志物。在整个过程中,我们讨论了与既定免疫疗法合理联合靶向这些耐药机制的潜在方法,以改善黑色素瘤患者的治疗结果。

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本文引用的文献

1
Sequencing of Checkpoint or BRAF/MEK Inhibitors on Brain Metastases in Melanoma.黑色素瘤脑转移患者中检查点或 BRAF/MEK 抑制剂的测序。
NEJM Evid. 2024 Oct;3(10):EVIDoa2400087. doi: 10.1056/EVIDoa2400087. Epub 2024 Sep 24.
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Final, 10-Year Outcomes with Nivolumab plus Ipilimumab in Advanced Melanoma.纳武利尤单抗联合伊匹木单抗治疗晚期黑色素瘤的10年最终结果
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Adverse Events in Anti-PD-1-Treated Adjuvant and First-Line Advanced Melanoma Patients.
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Enhancing melanoma therapy with hydrogel microneedles.用水凝胶微针增强黑色素瘤治疗效果。
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Dual role of interferon-gamma in the response of melanoma patients to immunotherapy with immune checkpoint inhibitors.γ干扰素在黑色素瘤患者对免疫检查点抑制剂免疫治疗反应中的双重作用
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Neoadjuvant pembrolizumab, dabrafenib and trametinib in BRAF-mutant resectable melanoma: the randomized phase 2 NeoTrio trial.新辅助帕博利珠单抗、达拉非尼和曲美替尼治疗 BRAF 突变可切除黑色素瘤:随机 2 期 NeoTrio 试验。
Nat Med. 2024 Sep;30(9):2540-2548. doi: 10.1038/s41591-024-03077-5. Epub 2024 Jun 21.
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Advances and prospects of biomarkers for immune checkpoint inhibitors.免疫检查点抑制剂生物标志物的研究进展与展望
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Neoadjuvant Nivolumab and Ipilimumab in Resectable Stage III Melanoma.新辅助纳武利尤单抗和伊匹单抗治疗可切除 III 期黑色素瘤。
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Molecular patterns of resistance to immune checkpoint blockade in melanoma.黑色素瘤免疫检查点阻断治疗耐药的分子模式。
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Adjuvant dendritic cell therapy in stage IIIB/C melanoma: the MIND-DC randomized phase III trial.辅助树突状细胞治疗 IIIB/C 期黑色素瘤:MIND-DC 随机 III 期试验。
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Dendritic cells as orchestrators of anticancer immunity and immunotherapy.树突状细胞作为抗癌免疫和免疫治疗的协调者。
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